Yun Li†
ab,
Jiamin Amanda Ong†
ab and
Pooi See Lee
*ab
aSchool of Materials Science and Engineering, Nanyang Technological University, 50 Nanyang Avenue, 639798, Singapore. E-mail: pslee@ntu.edu.sg
bSingapore-HUJ Alliance for Research and Enterprise, The Smart Grippers for Soft Robotics (SGSR) Programme, Campus for Research Excellence and Technological Enterprise (CREATE), 138602, Singapore
First published on 23rd June 2025
Two-dimensional (2D) materials are critical for applications in tactile perception, health monitoring, virtual reality (VR), augmented reality (AR) and human–machine interfaces. In particular, recent advances in materials science, device fabrication, and machine learning have significantly propelled the applications of 2D materials for multifunctional soft robots owing to their flexible and conformal nature. In this review, we provide an overview of the fundamental mechanisms and recent breakthroughs in 2D materials for soft robotic systems, with a focus on their fabrication techniques, actuation mechanisms, and multiple sensing approaches. Subsequently, we highlight the significance of 2D materials in multimodal devices and feedback loop control for intelligent and smart robotics with self-adaptive manipulation. We then explore innovations such as multimodal sensing, human–robot interaction and artificial intelligence (AI)-promoted fast recognition. Finally, we summarize the future research directions and challenges, such as the reliable preparation roadmap for 2D materials and streamlined configuration to eradicate heavy wiring and enhance the dexterity of soft robots.
Wider impactFlexible, multimodal, adaptive devices are pivotal to the integration of soft robots, offering a revolutionary approach to various bio-mimetic functions. Primary factors limiting the development of soft robotics include material preparation and device integration. The breakthroughs in two-dimensional (2D) materials have introduced new vitality in this field, allowing devices with higher performance without loss in their flexibility and conformability. This review explores the recent advances in 2D material-based actuators and sensors tailored for soft robotics, with a focus on their fabrication strategies, and their integration towards human–mimic motion and perception. Through an in-depth discussion on the advantages and disadvantages of each functional mechanism, a roadmap for further development of 2D material-based device integration is provided. This review not only summarizes the progress in this research field but also enriches the practical guidance for intelligent devices in soft robotics. These insights will help shape the next generation of 2D materials and devices, bridging the gap between materials science and advancing practical soft robots. |
The recent advances in two-dimensional (2D) materials, originating from graphene,6 have accelerated development in various fields owing to their unique physical and mechanical properties, such as high conductivity, large surface area, good flexibility, excellent mechanical strength and tunable electrical structures. Benefiting from these properties, flexible electronic devices, actuators and sensors in particular, have been greatly developed.7–11 With the exploration of material properties and device integration, these devices have offered various potentials to soft robotics. Despite the revolutionary development of 2D materials and their abilities to create an intelligent soft robot system, several critical technological challenges need to be addressed. The technological limitations arise primarily from the mismatch between the mechanical properties of 2D materials and the soft substrates/matrix, as well as the poor compatibility between the preparation process of the 2D materials and the soft substrates/matrices. There are some technological and design breakthroughs that have provided solutions to these problems, such as 2D material–polymer composites,12,13 low-temperature fabrication of 2D materials8,14 and device encapsulation.15–17 Moreover, the recent strides in multimodal device and closed-loop feedback control enable a more complete intelligent soft robot system.18–20
In this review, we focus on the representative works on 2D materials that potentially serve as actuators and sensors in soft robotics. First, we discuss the importance of 2D materials in soft robotics applications, by comparing different fabrication techniques of 2D materials and highlighting the most suitable fabrication techniques for different requirements. At the actuator frontier, an overview of the various actuation mechanisms and motion types based on 2D materials is provided. At the sensor frontier, we categorize the sensors by five representative human–mimic perceptions (sight, taste, smell, sound and tactile), alongside multimodal sensing and the integration attempts towards artificial intelligence (AI) and human–machine interface (HMI). Importantly, we highlight the current limitations of integrating 2D materials into soft robots, and the possible solutions. These challenges include low-temperature integration, device integration (multiple functions in one device instead of device arrays) and adaptive control.
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Fig. 2 Mechanical properties of 2D materials: (a) Young's modulus. (b) Fracture strain limit. Reproduced with permission.21 Copyright 2024, American Chemical Society. |
Therefore, the first advantage of 2D materials in soft robotics is their flexibility, which however poses a challenge to the fabrication process. The thinner and larger the 2D materials, the better their performance. However, a freestanding larger 2D film of centimetre scale is too fragile to work with dynamic robots. Due to their intrinsic mechanical properties and ultrathin nature, the freestanding large 2D films without any substrate support have limited capacity to distribute and absorb mechanical stresses, making them susceptible to deformation and fracture.26 Integrating them onto flexible substrates such as elastomers or hydrogels is a good option. The second demand for this application is conformability and self-adhesion to these soft substrates. Due to the low bending stiffness and high strain limit of 2D materials, this second requirement is met, providing good conformal contact ability. This underlines the near-perfect contact interface between 2D materials and support substrates, such as the 2D electronic tattoos on polyimide (PI)27 or tattoo paper,28 enabling a high signal-to-noise ratio during operation.25 The extremely thin characteristics will not affect the deformation and rebound of the bottom support polymer, and hence, the entire device has good motion deformation ability.
Besides, the large surface-to-volume ratio of 2D materials enables efficient light–matter interactions, allowing higher photocurrent in optoelectronic devices. A single-layer MoS2-based flexible photodetector showed tunable photoresponsivity (by 2–3 orders of magnitude) and response time (as fast as 80 ms). The adjustable performance can be attributed to modified strain in MoS2 films.30 For thermal and photothermal applications, 2D materials have attracted more attention due to their excellent thermal conductivity and significant photothermal effects.31,32 For example, Ti3C2Tx can be integrated into a thermal indicator from 20 to 160 °C due to its high photothermal conversion efficiency.33
Hence, the atomic thickness, outstanding electrical and thermal conductivity as well as the extensive surface-to-volume ratio of 2D materials confer exceptional sensitivity and rapid responsiveness to various stimuli (including strain, molecular interactions, light, and thermal changes), making them highly promising for applications in soft robotics, particularly in sensing components.
Understanding the stability profiles of 2D materials is critical for their successful application in soft robotics. Materials such as h-BN and MoS2 offer promising stability, making them suitable for integration into flexible actuators and sensors. Specifically, the exceptional thermal stability and chemical inertness make h-BN an ideal candidate for insulating layers in flexible electronic components, protecting sensitive elements from thermal and oxidative damage. MoS2 can serve as a suitable material for photodetectors and transistors in soft robotic systems due to its robustness under ambient conditions and relative photostability. In contrast, materials with inherent environmental sensitivities necessitate protective measures to enhance their viability. Ongoing research into stabilization techniques, encapsulation procedures, and a deeper comprehension of degradation mechanisms will further expand the potential of 2D materials in the realm of soft robotics.
Method | Temperature | Advantages | Disadvantages | Application | Ref. |
---|---|---|---|---|---|
Mechanical exfoliation | Room temperature | Simple, high-quality monolayers, minimal defects | Low yield, small flake size, non-scalable | Graphene, TMDs, Xenes | 56 |
Sputtering | <50 °C | Large-area deposition, good uniformity, compatible with industrial processes | High defect density, limited to specific materials | Oxides, nitrides, carbides | 57 |
Thermal evaporation | <100 °C | High-purity films, good thickness control | Poor adhesion, limited to low-melting-point materials | Metals, conductors | 58 |
Composite | <150 °C | Scalable, flexible substrates, low thermal budget, roll-to-roll compatible | Poor flake alignment, agglomeration, low conductivity | Graphene, h-BN, TMDs, MXenes | 44 |
ALD | 50–300 °C | Atomic-level thickness control, excellent conformality, low defect density | Extremely slow, limited material selection | h-BN, TMDs, TMOs | 59 |
Thermal decomposition | 300–400 °C | Low-cost, solution-processable, flexible substrate compatibility | Non-uniform layers, residual impurities, limited crystallinity | Oxides, TMDs | 51 |
Low-thermal-budget CVD | 300–500 °C | BEOL-compatible (<400 °C), direct growth on CMOS/flexible substrates, high uniformity | Requires precursor engineering, reactor design complexity | TMDs | 8 |
MOCVD | 500–800 °C | Precise layer control, doping compatibility, scalable | Expensive precursors, toxic byproducts, complex setup | Graphene, h-BN, TMDs, | 60 |
Conventional CVD | 600–900 °C | High crystallinity, large-area growth, versatile for various 2D materials | High energy cost, substrate limitations, slow cooling required | Graphene, h-BN, TMDs, | 60 |
Devices made by solution-based processing involve the preparation of 2D flake solutions (2D inks), followed by dispensing inks on desired substrates using printing or casting (such as inkjet printing, screen printing, drop-casting, spin coating and spray coating). This strategy is compatible with soft robotics due to their reduced cost and scalability. However, flake or layer aggregation is the primary challenge to limit the development of this method. The concentration and rheological properties of 2D inks must be adjustable for compatibility with different deposition techniques. Otherwise, film defects will significantly decrease the device performance. For example, suitable rheology and concentration of inks are always required to prevent flake aggregation, solvent evaporation, and nozzle clogging.44 To enable their use in soft robotic applications, 2D inks are often mixed with a polymeric network to achieve enhance network cohesion and substrate adhesion. Chemical coupling is often used to compatibilize the functionalized 2D inks with the polymer matrix. Pinilla et al. reviewed the main scientific and technical limitations currently faced by 2D inks and the related printing technologies.45 The optimization of the 2D ink formulation is the key to fabricate devices using solution-based approaches.
Although deposition techniques provide reliable quality and controllable thickness of 2D material films, their high thermal budget and often the need of vacuum is incompatible with the polymeric substrate/matrix that are needed for soft robotics. For example, polydimethylsiloxane (PDMS) and Ecoflex are the widely used elastomers for stretchable devices, while PET and PI are the most popular substrates/matrices for bendable devices with operation temperatures below 300 °C.46–49 Hence, temperature is the primary factor determining the selection of integration techniques for soft robotic applications. With the intensive studies on the fabrication techniques for 2D materials, from mechanical exfoliation to physical vapor deposition (PVD) to chemical vapor deposition (CVD), the methods can be categorized to two types: direct growth and indirect transfer. Fig. 3 illustrates the processing temperatures for different fabrication methods. At the growth frontier, the processing temperature varies from ∼100 °C for PVD (including sputtering and thermal evaporation) to 600–900 °C for CVD.50–52 The PVD process provides high uniformity at a wafer scale with low thermal budget, but introduces high defect density, lowering the device performance. The primary defects are grain boundaries and vacancies, which often need post-treatment to mitigate, thereby enhancing thermal budget (e.g., mitigate oxygen vacancies by annealing in an oxygen atmosphere at high temperatures). The high processing temperature for CVD makes it a non-preferable method to integrate a soft device although it is more reliable to control the thickness and crystallinity on a large scale among other direct growth methods. To use the high-quality deposited 2D films by CVD, an indirect transfer process is widely used.53 For example, CVD-grown TMDs are widely integrated into field-effect transistors by wet-transfer or dry-transfer processes.52 However, devices made with transfer processes tend to suffer from four main challenges: mechanical damage, contamination, scalability and high variability in performance. Cheliotis et al. reviewed the transfer techniques of 2D materials.54 Therefore, devices made by transfer process are compatible with soft robotic applications but achieving near-clean transfer with large area is inevitable.
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Fig. 3 Comparison of different preparation methods for 2D materials with a focus on the processing temperature. |
To overcome the high thermal budget in the CVD process, low thermal budget CVD (low-T CVD) and atomic layer deposition (ALD) are promising in directing 2D material's growth onto polymeric substrates, suppressing the contamination and unwanted defects/damages during the transfer process.8,55 For example, MoS2 can be deposited under 300 °C via low-T CVD and ALD, which is compatible with the back-end-of-line (BEOL) integration and soft robot integration.14 Despite the successful attempts, the increased defect density (mainly grain boundaries) might be detrimental for some applications although the thickness and crystallinity of deposited films are still high. Overall, each fabrication technique has its unique advantages and disadvantages (Table 1), and the best process should be selected based on actual requirements.
Several factors still impede the further deployment of 2D materials in soft robotics. The primary issue is effectively scaling up the fabrication of 2D materials with acceptable defect density. The promising roadmap for fabrication is discussed in the perspective part. The second limitation is the durability of the integrated devices based on 2D materials. Key factors leading to the poor durability of devices primarily include the limited stability of 2D materials in a harsh environment with high temperature and/or high humidity, in which the mismatch of thermal expansion coefficients between 2D materials and the supportive substrates affects the film stability. Encapsulation is a simple but effective method to prevent potential oxidation and unwanted water absorption. Hence, a light-transparent, flexible encapsulation layer with high dielectric coefficient is preferred to endure the responsiveness of 2D materials. Among the encapsulation materials, PDMS, styrene–ethylene–butylene–styrene (SEBS) and parylene are promising for protecting 2D materials.61–63
For the energy transducers in soft robots (mainly actuators), the failure in devices based on 2D materials can be primarily attributed to their structural defects and the interaction with polymer substrates. Their structural defects such as vacancies, dislocations, and grain boundaries act as stress concentrators, in turn, leading to mechanical failures.64 The mismatch in elastic moduli can induce mechanical failures in those applications where 2D materials are integrated with polymer substrates. As the polymer substrate deforms, it can impose strains on the 2D material, leading to crack initiation and propagation.65 Self-healing materials and fatigue-resistant polymer supportive networks are promising to address these challenges.66
Atomically thin 2D flakes with microscale area can be actuated by optical or electrostatic stimuli to move on the horizontal surfaces. Optical actuation refers to a mechanism in soft robotics where light energy (e.g., visible, infrared, or ultraviolet radiation) is converted into mechanical motion or deformation in an actuator. For example, 2D VSe2 and TiSe2 nanoflakes were actuated by femtosecond pulsed laser to achieve movement on sapphire and quartz substrates with large vdW interactions in between (Fig. 4a).68 The actuation is attributed to the surface acoustic effect and thermal stress, which unfortunately has been proved unworkable in other 2D TMD materials. This actuation mechanism with non-touch and non-invasive properties offers potential in drug delivery and biology applications. Ultrathin 2D flakes are used in electrostatic actuators leveraging their exceptional electrical conductivity, enabling micro actuator applications in microelectromechanical systems (MEMS). Electrostatic actuation is a mechanism to attract or repel actuating component by electrostatic forces. For example, a micro-scale graphite flake (15 × 15 μm2) was actuated by an applied DC voltage and the moving direction could be adjusted by changing the form of applied voltage, showing a robust reliability over 10000 reciprocating actuation cycles (Fig. 4b).69
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Fig. 4 Various actuation mechanisms for 2D materials. (a) Optical actuation. Reproduced with permission.68 Copyright 2023, Springer Nature. (b) Electrostatic actuation. Reproduced with permission.69 Copyright 2025, Springer Nature. (c) Photothermal actuation. Reproduced with permission.11 Copyright 2025, Springer Nature. (d) Electrochemical actuation. Reproduced with permission.77 Copyright 2024, John Wiley and Sons. |
Generally, microscale actuators are suited for various applications such as microsurgery,70 imaging, sensing,71 drug delivery72 and lab-on-chip devices.73 Their small size, non-touch actuation, and compliance allow for gentle interaction with fragile biological materials without causing damage. The development of lithographic techniques and novel material platforms enables microrobots, artificial cilia, and cell-scale manipulation.74 Drug delivery is one of the promising applications in this field due to the increasing demand for efficient therapy. Microscale actuators can serve as active platforms to deliver and release drug, thereby significantly accelerating the process in comparison with traditional targeted drug delivery systems, which relies on the fluxes of blood and diffusion. For example, a reduced nanographene oxide (n-rGO)-based electrochemical actuator was reported to achieve ultrafast release of doxorubicin (DOX) at the tumor site within a few seconds.72 In addition, microscale actuators can be used as pumps and valves in microfluidic systems for lab-on-chip (LoC) systems. LoC platforms with small size and reduced costs enable the fast analysis in medical applications.75 Microscale actuators are required to control the flow of various liquids (buffer, drug, etc.) at microscale by performing as microvalves. For example, an actuator based on GO–hydrogel composites was developed to block the channels in LoC systems. Upon optothermal heating with a laser, the actuator reduces its volume to open a flow of solutions at microscale. Moreover, the flow rate can be adjusted between 10 and 20 μL min−1 by adjusting the power supply of the light source.73
Unlike microscale actuators, macroscale actuators provide programmable bending, folding and grasping with substantial deformation and blocking force in soft robots. The high deformation at the macroscale requires the preparation of large-scale 2D materials and their integration into devices. Photothermal actuation and Joule thermal actuation are widely applied to fabricate artificial muscles. Light-responsive graphene and MXenes are used in photothermal actuators due to their broad light absorption spectra.18,76 A single-fibre actuator with graphene fillers was demonstrated as an artificial worm to self-crawl by photothermal actuation (Fig. 4c).11 Moreover, a 1000-strand bundle of fabricated fibres was able to lift a 1kg dumbbell, showing supreme high actuation power. Electrochemical actuation, based on the movement of ions (e.g., Li+, H+, or OH−) into or out of a material, causes volume changes and also offers macroscale actuation with a relatively low voltage applied. Chen et al. developed a large-scale TBA-functionalized MXene-based film with a peak-to-peak strain difference of 0.771% under a voltage of ±1 V, demonstrating a macroscale actuation by lifting objects effectively (Fig. 4d).77
Table 2 summarizes the key parameters of various actuation mechanisms for 2D materials. Each actuation mechanism exhibits unique advantages that can be tailored to specific applications. Optical and electrostatic actuation are ideal for high-speed and precision tasks at microscale, while photothermal and Joule thermal approaches offer balanced performance for flexible electronics and wearable devices at macroscale. Electrochemical actuation, though slower, delivers high deformation, making it highly suitable for artificial muscles.
Actuation mechanism | Scale | Deformation (strain) | Blocking force | Speed | Materials | Ref. |
---|---|---|---|---|---|---|
Optical actuation | Micro/nanoscale | Low to moderate | <5 mN | Very fast (<ms) | Graphene, TMDs | 68 |
Electrostatic actuation | Micro/nanoscale | Low | ∼50 nN | Very fast (μs–ms) | Graphene, h-BN, TMDs | 69 |
Photothermal actuation | Micro- to macroscale | Moderate | 4.1 N with 100![]() |
Fast (ms to s) | Graphene, MoS2, WS2, black phosphorus | 11 |
Joule thermal actuation (electrothermal actuation) | Micro/nanoscale | Moderate | 5 mN | Moderate (s) | Graphene, MXenes | 77 and 82 |
Electrochemical actuation | Micro- to macroscale | High | 0.5–10.0 mN | Slow (s to min) | Graphene oxide, MXenes | 77 and 83 |
Pneumatic actuation | Macroscale | High | 1–100 N (depending on the pressure and the contact area) | Moderate (s) | N/A | 84 and 85 |
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Fig. 5 Various functional applications enabled by 2D material-based actuators. (a) Crawling. Reproduced with permission.80 Copyright 2019, AAAS. (b) Jumping. Reproduced with permission.81 Copyright 2022, Elsevier. (c) Swinging. Reproduced with permission.86 Copyright 2019, AAAS. (d) Flying. Reproduced with permission.87 Copyright 2023, Springer Nature. (e) Grasping. Reproduced with permission.88 Copyright 2017, John Wiley and Sons. (f) Multimodal rolling. Reproduced with permission.89 Copyright 2020, Springer Nature. |
Leveraging the outstanding electrochemical and photothermal actuation performance of 2D materials, such as graphene and MXenes, swinging and flying robots are integrated. Umrao et al. reported an ionically cross-linked Ti3C2Tx electrode for artificial muscle with an ultrafast response time within 1 s and decent durability of 97% up to 18000 cycles. Based on the robust performance of the artificial muscle, “dancing” butterflies with moving wings can be fabricated (Fig. 5c).86 Inspired by the vine maple seed, Wang et al. reported a rotary flying photoactuator (actuated under near-NIR light) with a rapid response of around 650 ms and an ultrafast rotation speed of ∼7200 rpm, enabling controlled flight and steering behaviors (Fig. 5d).87 This can be attributed to the synergistic interactions between the photothermal graphene and the hygroscopic agar/silk fibroin components. The key parameters for the flying motion, such as rotation speed, flight height and flight direction, can be controlled by varying the irradiation intensity and position. This flying robot is expected to be deployed in unstructured environments for high-resolution aerial digital imaging.
Soft grippers attract intensive attention due to their light weight, high weight-to-gripper ratio and flexibility, enabling grasping, fragile objects in particular, for intelligent sorting and adaptive gripping. Although most studies focus on pneumatic grippers, the cumbersome pump and complicate gas tubes might not be suitable for a complex environment, especially small space. Therefore, 2D materials show potential in soft grippers due to their non-contact actuation mechanisms, such as photothermal conversion. For example, a WS2-based gripper can lift a steel ball with a weight 500 times heavier than the gripper itself (Fig. 5e).88 This high griping force can be attributed to the effective exfoliation of WS2 in sodium alginate, which, in turn, ensures tunable filler-loading levels in their composites without aggregation.
Unlike the bio-inspired motions, rolling robot, usually in cylindrical geometry, refers to roll autonomously under a stimulus, offering significant potential in conveyors and motors. This motion is driven by an unstable center of gravity under an external stimulus. Fig. 5f shows the rolling robot with a double layer of stacked graphene assembly and polyethylene film. Under lateral IR irradiation, the robot can roll with an increasing rolling speed due to the localized photothermal effect of the propeller. Under vertical IR irradiation, the robot will uncoil instead of roll due to the design of the structure. The rolling robot triggered by non-contact irradiation is expected to work on a wavy sandy ground.89
The fundamental approaches for sensors to mimic the five senses mainly revolve around piezoelectricity, piezoresistivity, capacitivity, triboelectricity, chemosensitivity, ion sensing, photoconductor, phototransistor and photodiode (Fig. 6). In the following section, detailed working principles of each mechanism will be discussed. Additionally, Table 3 lists the overall comparison of each mechanism behind the perception sensors, highlighting the advantages and limitations of each approach.
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Fig. 6 Schematic of the different approaches to mimic human perceptions. Illustrations of human–mimic perceptions were created using BioRender: https://BioRender.com. |
Perception | Approach | Advantages | Limitations |
---|---|---|---|
Vision | Photoconductor | Low power consumption | Possibility of suffering from high dark current when not properly shielded |
Limited response to certain wavelengths | |||
Phototransistor | High gain and sensitivity to light | Requires complex circuit | |
Improved signal-to-noise ratio due to amplified signals | Slow response time | ||
Photodiode | Fast response time | High cost to assemble device | |
High sensitivity to light | Limited dynamic range | ||
Low power consumption | |||
Tactile | Piezoresistive | Easy fabrication | Requires power to operate |
High sensitivity to stress/strain | Signal output affected by external factors such as temperature | ||
Fast response time | Static sensing | ||
Low sensing frequency (0–10 kHz) | |||
Signal drift | |||
Lag effect | |||
Piezoelectric | Self-powered sensor | Can only be used for dynamic sensing | |
High sensitivity to mechanical stress/strain | |||
High sensing frequency (10 Hz to MHz) | |||
High signal to noise ratio | |||
Capacitive | Easy fabrication | Nonlinearity | |
Low power consumption | Susceptible to parasitic effects and electromagnetic interference | ||
Response to both dynamic and static stimuli | Require careful electrode design | ||
Fast response time | Low sensing frequency (0–100 Hz) | ||
Triboelectric | Easy fabrication | Wear and tear of material can reduce performance | |
Self-powered sensor | High output impedance | ||
Wide selection of material | Low sensing frequency (3 Hz–10 kHz) | ||
Fast response time | |||
Sound | Piezoresistive | Easy fabrication | Requires power to operate |
High sensitivity to stress/strain | Signal output affected by external factors such as temperature | ||
Fast response time | Static sensing | ||
Low sensing frequency (0–10 kHz) | Signal drift | ||
Lag effect | |||
Piezoelectric | Self-powered sensor | High noise level | |
High sensitivity to strain | |||
Olfactory | Chemiresistive | High selectivity to target chemical species | Limited device lifespan |
Able to detect low gas concentration | Potential interference from other chemicals | ||
Gustatory | Ion sensing | Detect ions in very low concentration | Drift over time and loss of selectivity |
High selectivity to ionic species |
Piezoelectric sensors work based on the piezoelectric effect, where it converts applied mechanical force into electrical voltage output. Piezoelectric effect was first discovered in 1880 by the Curie brothers in quartz.96 It can exist as either a pressure or strain sensor, depending on the sensing material, as well as the device structure. Hence, piezoelectric sensors are highly responsive to dynamic mechanical changes, making them ideal for applications such as tactile and acoustic sensors.97,98 Furthermore, due to their energy harvesting nature, piezoelectric sensors can exist as self-powered sensors with no power consumption required.
Piezoresistive sensors work based on the principle of converting applied pressure into electrical resistance variation.99 This effect is particularly pronounced in semiconductors such as silicon, where strain alters the mobility of charge carriers, thereby modulating resistivity. Different from piezoelectric sensors, piezoresistive sensors are static sensors. More than often, piezoresistive sensors are found in both tactile and acoustic sensor applications due to their fast response time. The resistance of the sensor can be calculated as follows:
The structures of capacitive sensors are usually composed of top and bottom electrodes sandwiched between a substrate and an insulator. When pressure is applied perpendicularly to the device, it resulted in a deformation of the active area, thus changing the distance between the two electrodes, hence capacitance change. Capacitive sensors have garnered extensive attention for flexible electronics, especially as a tactile sensor, due to their large detection range, high sensitivity, and minimal response to temperature drift. They are also suitable for a wide range of applications since they possess good sensitivity to both static and dynamic pressures, fast response time, and low power consumption. The capacitance of the sensor can be calculated as follows:
Triboelectric sensors have been gaining research interest due to their wide material selection, simple configurations, and high output voltage. First proposed by Fan et al., based on the mechanism of transducing mechanical energy into electrical signals through the coupling of the triboelectric effect, also known as contact electrification, and electrostatic induction.100 Upon applying a mechanical compression, an electric potential difference between the top and bottom electrodes is produced, which results in a charge transfer between the two triboelectric material surfaces. Similarly, triboelectric sensors are mostly presented as tactile sensors due to their high sensitivity and fast response time.101–103 Furthermore, similar to piezoelectric sensors, triboelectric sensors can exist as self-powered sensors.
Chemiresistive sensors are based on the change in electrical resistivity caused by the adsorption of molecules on the surface of the sensing layer or metal electrodes.104 These interactions, influenced by material type, properties of gas, temperature, pressure, and humidity, alter the electron density in the semiconductor. When a metal electrode contacts the semiconductor, their Fermi levels align, creating a Schottky barrier if their work functions differ. For n-type semiconductors, electron-donating gases such as NH3 increase the electron density, thus reducing the resistance, whereas electron-withdrawing gases such as NO2 decrease the electron density, thereby increasing the resistance. Conversely, p-type semiconductors exhibit the opposite behaviour. The Schottky barrier's height and depletion layer thickness depend on the work function difference and doping effects. Adsorbed gases also modify the semiconductor's Fermi level, shifting it toward the conduction or the valence band, thereby altering the built-in potential and resistance at the electrode-semiconductor junction. Generally, n-doping by reducing gases decreases the resistance in n-type materials but increases it in p-type materials, while p-doping by oxidizing gases has the reverse effect. This mechanism enables the detection of specific gases based on resistance changes. For example, the p–n heterojunction, via the incorporation of n-type 2D SnO2 sheet and p-type black phosphorus, introduced oxygen vacancies, thereby amplifying the carrier concentration after the adsorption of H2S. The BP–SnO2 sensor exhibited a larger sensitivity than that of a pure SnO2 sensor (1.3/ppm vs. 0.342/ppm), alongside faster response/recovery speeds.105 Similarly, an rGO–MoS2 composite formed a p–p heterojunction. The synergistic effect of MoS2 and rGO significantly enhances the selectivity toward NH3 compared to other gases by promoting the charge transfer and surface interaction.106
Ion sensing is a type of chemical sensor, which detects small organic or inorganic molecules or ions in the aqueous phase. The main mechanism is driven by the protonation and deprotonation of the functional group that is present on the surface of the 2D materials. It has a similar working mechanism as chemiresistive; however, instead of change in resistance, it is usually reflected by change in current or voltage output. For example, an MXene-based electronic tongue can detect the sourness by generating varying current signals when it is subjected to pH variation. The good performance of this MXene sensor is attributed to the abundant functional groups, mainly –OH, –F, and –O, on MXene surface, allowing effective ion sensing.107 In addition to mimic gustatory and olfactory perceptions, this technique is applied to detect minute concentrations of chemicals in food. Glyphosate, a widely used herbicide, can be selectively detected by a CeO2–graphene oxide chemical sensor with a detection limit of 30 nmol L−1.108
Photoconductor is a device for which electrical conductivity increases upon exposure to light. It operates on the photoconductive effect, where absorbed photons generate electron–hole pairs, resulting in an increase in the number of charge carriers. This device has a lateral structure, which consists of an active layer and two electrodes, and is commonly used in optoelectronic devices, which can also be observed in several 2D material-based photodetectors such as 2D perovskites, TMDs, and graphene.109–111 For example, the hybrid MoS2–graphene photoconductor shows a ultrafast response of ∼17ns and a high responsivity of ∼3
×
104
A W−1 at 635 nm illumination with 16.8 nW power across the broad spectral range. The excellent performance can be attributed to the addition of an MoS2 layer with the abilities of tunnelling, as well as passivating surface states.111 This improvement makes it promising for optoelectronic applications in soft robotics.
Phototransistor is a light-sensitive transistor that amplifies photogenerated current. It can be considered as an extension from photoconductor, whereby it combines the photoconductive effect with the gain mechanism of a transistor. With a similar working principle as the photoconductor, phototransistor can provide photogenerated carriers when exposed to light and form photocurrent via the conductive channel of the active layer, such as MoS2 and 2D perovskites, driven by the source-drain voltage.112,113 Akhil et al. reported a monolayer MoS2 phototransistor array with a responsivity of ∼3.6 × 107 A W−1 and a high dynamic range of ∼80 dB. Interestingly, the MoS2 phototransistor exhibited programmable phototransistor in each pixel, offering a substantial reduction in footprint and energy consumption. This reduction is attributed to the atomic thickness and multifunction nature of MoS2.112 Additionally, due to the gate voltage, the active layer can generate more photogenerated carriers, allowing the electrical signal to be further amplified. Therefore, upon comparison with photoconductors, phototransistors with a gate voltage display a higher external quantum efficiency and an on/off ratio. At the same time, the phototransistors have a slower response speed. For example, the response speed for graphene-based phototransistors was ∼400 ns, whereas its photoconductor counterpart ranged from 10 ns to 3 μs.111,114,115
Lastly, photodiode is a semiconductor device that converts light into an electrical current through the photovoltaic effect. Photodiodes typically exist as vertical devices, which are made up of functional layers sandwiched between the top and bottom electrodes. The photodiode uses the photovoltaic effect of semiconductors that usually work under a reverse bias voltage that promotes the electron–hole pairs to separate, therefore achieving a higher on/off ratio and a faster response speed. Despite the lower external quantum efficiency and responsivity as compared to phototransistors and photoconductors, photodiodes usually exhibit a large linear dynamic range and high detectivity due to the low dark current. Some 2D materials are commonly used as photodiodes including TMDs, black phosphorus (BP) and 2D perovskites.116–120 Photodiodes can be self-powered due to their vertical structure, which reduces the carrier transport distance, thus facilitating a faster response speed and a lower working voltage.
By leveraging the extraordinary properties of 2D materials, researchers are paving the way for a new generation of soft robots that can perceive the world with human–mimic perceptions. Table 4 summarizes the 2D materials used for each perception sensor, at the same time highlighting the challenges they faced, respectively. These advancements not only enhance the functionality of soft robotic systems, allowing them to sense their surroundings with remarkable sensitivity.
Perception | Materials | Challenges |
---|---|---|
Vision | Graphene | Stability under different wavelengths |
TMDs | Long-term performance degradation | |
2D perovskites | ||
Black phosphorus | ||
Tactile | Graphene | Long-term stability |
TMDs | Sensor linearity output | |
MXenes | ||
Black phosphorous | ||
2D perovskites | ||
Sound | Graphene | Limited detection frequency range |
TMDs | ||
MXenes | ||
2D perovskites | ||
Olfactory | Graphene | Selectivity of the gas ions/molecules |
TMD | Detection of unwanted gas ions with similar functional group | |
MXenes | ||
2D MOFs | ||
Gustatory | Graphene | Sensitivity of the ions |
TMDs | Long-term performance degradation of the sensor | |
MXenes | ||
2D MOFs |
Among the five perceptions, vision and tactile are most attractive for soft robots to depict their working environment in real time by capturing and monitoring signals continuously. Further, robots can react and respond to any changes in environments by actuating the motion components, such as circumvent obstacles and grasping objects, if a closed-loop system is equipped. Sensitivity, detection limit and wavelength/frequency range of vision and tactile sensors are primary parameters determining the use case in a soft robot. For example, tactile sensors with a low detection limit are required for monitoring minute strain/deformation (e.g., slippage detection), while tactile sensors with high sensitivity are suitable for circumstances with indistinguishable stimuli (material/texture recognition).
Unlike vision and tactile sensors, which are often needed in soft robots, the other three perceptions are only deployed in certain situations (e.g., gather information about sounds and molecules). Although the mechanisms for tactile and sound perceptions are almost same, the performance stability varies. The primary difficulty lies on sound perception is the signal-to-noise ratio due to the non-contact sensing, which is susceptible to external noise. However, noise is commonly derived from soft robots (e.g., pump and motor) and their working environments. The capability to differentiate signal with a wide detection frequency range is indispensable to solve this issue. Similarly, supreme selectivity of molecules is important for olfactory and gustatory sensing in soft robots.
Materials | Response time | Photoresponsivity | Stability | Ref. |
---|---|---|---|---|
Commercial sensor | 0.0125–33 μs | 0.006–0.72 A W−1 | — | https://www.hamamatsu.com/ |
2D perovskite | 5–50 s | — | — | 140 |
2D perovskite | — | 104 A W−1, visible light | — | 141 |
200 A W−1, NIR | ||||
2D perovskite/graphene | 0.08 s | 730 A W−1 | 74 days | 142 |
h-BN encapsulated graphite/WSe2 | — | Up to 2.2 × 106 A W−1 | — | 143 |
Ta2PdS6/MoS2 | 470 ms | 590.36 A W−1, 633 nm | — | 144 |
MoS2 | — | ∼3.6 × 107 A W−1 | — | 112 |
MoS2/graphene | 2.7–6.1 s | 23.95 A W−1, 532 nm, strained condition | 10 days | 145 |
MoS2/black phosphorus | 4.8 μs | Up to 110.68 A W−1 | — | 146 |
MoS2 | 0.044–0.119 s | Up to 119.16 A W−1 | — | 147 |
MXene | — | 0.07 A W−1 | — | 148 |
PbS QD/MXene | 30 ms | 1000 mA W−1 | Bending: 500 cycles | 149 |
Quasi-2D perovskite-MXene | — | ∼151 A W−1 | >50 cycles | 150 |
Black phosphorus | — | — | Bending: 100 cycles | 151 |
Black phosphorus/graphene/InSe | 24.6 ms | Up to 3.02 × 104 A W−1 | — | 152 |
Two-dimensional materials such as graphene, MXenes, TMDs, and 2D perovskites are widely used as optoelectronic materials owing to their semiconductor properties.121–124 Currently, there are a wide variety of 2D-based photodetectors fabricated with a detection range from ultraviolet to the near-infrared reported.125–128 Graphene is the first and highly researched 2D material that exhibited extremely high carrier mobility, high electrical conductivity, wide absorption from ultraviolet to terahertz, and a bandwidth of 40 GHz.129–131 For example, Xu et al. reported a graphene derivative, GO-based for flexible artificial system with 81% accuracy in image recognition via the photoconductive effect.132 Liang et al. also reported that the use of graphene helped to reduce the relaxation time as the conductivity of the artificial vision system increased.133 This reduction of relaxation time is significant as it allows the artificial synapses to achieve short-term plasticity.
The zero bandgap and ultrahigh carrier mobilities at low temperatures of graphene enable its detection from the visible to terahertz range. However, single-layer “zero bandgap” graphene exhibits large dark current and poor absorption of light, thus limiting its practical applications. This results in a shift of research interest towards other 2D materials such as TMDs of decent mobility and strong light coupling from vis to mid-IR.122
As an emerging group of 2D materials, 2D perovskites possess excellent optoelectronic properties, which are especially observed in the field of photovoltaics.134 Two-dimensional perovskites exhibit low defect density, high carrier mobility, strong light absorption, and ease of fabrication, making them promising candidates for flexible and highly performing photodetectors.127,135–137 Wang et al. reported on the use of quasi-2D halide perovskite photodetectors for optical imaging.138 Its performance was comparable to its 3D derivative, MAPbI3 photodiode. Furthermore, the performance of the photodetector was stable even after 100 days of storage under ambient conditions, in the presence of both air and humidity, which was something 3D perovskites cannot achieve thus far. Generally, large organic cation spacers are added to separate octahedral layers to form 2D perovskites.139 The improved stability in air and humidity is attributed to the hydrophobic groups of aromatic or alkyl amines in large organic cation spacers such as butylammonium. This shows the potential of 2D perovskites in optical sensing applications. Wang et al. also demonstrated artificial retina using 2D perovskites for facial recognition purposes with high accuracy (Fig. 7a).140
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Fig. 7 2D materials for vision perception. (a) Artificial retina based on 2D perovskites with high recognition accuracy. Reproduced with permission.140 Copyright 2024, John Wiley and Sons. (b) Representative illustration of the h-BN/WSe2 synaptic device. Reproduced with permission.153 Copyright 2018, Springer Nature. |
To enhance the performances of the optoelectronic devices, heterostructures of the 2D materials are fabricated to tune the material's property. Seo et al. reported an optic-neural synaptic device based on h-BN and WSe2 heterostructures developed by integrating synaptic and optical-sensing functions in a single device (Fig. 7b).153 Polat et al. also reported a flexible graphene-based photodetector as a wearable fitness monitor and a UV sensor, where PbS quantum dots were applied as sensitizers to improve the UV-IR responses.154 Zhang et al. demonstrated the growth of heterostructures perovskite/graphene, which achieved a high responsivity of ∼107 A W−1. With the exceptional high-responsivity photodetector, it can be incorporated into flexible substrates as image sensors.155
However, the key issue with optical sensors is the time-lag response. This time-lag response occurs due to the limited response speed of light absorption and emission in certain 2D materials such as MoS2 or 2D perovskites, which exhibit a lower carrier mobility than that of the other semiconductors. The lower carrier mobility can be attributed to enhanced quantum confinement and reduced dielectric screening, which lead to stronger Coulomb interactions and the formation of tightly bound excitons.156–158 In 2D materials such as MoS2, the energy level separation increases with the reduction in thickness due to quantum confinement, where the motion of charge carriers is restricted in one or more dimensions, leading to discrete energy levels. This results in inefficient phonon emission by hot carriers, thus causing a phonon bottleneck effect. The carriers can relax via emitting optical phonons only with the energy or sum of them equal to that of the energy gap, leading to slower carrier recombination.159,160 For MoS2, it possesses low carrier mobility (1 cm2 V−1 s−1) and indirect bandgap for multilayers, while the carrier mobility can increase to 122.6 cm2 V−1 s−1 for single crystal monolayers after optimizing the preparation recipe.52 Despite the significant improvement, its carrier mobility is still lower than that of traditional semiconductors such as silicon (1350 cm2 V−1 s−1).161,162 Similarly, 2D perovskites exhibit a similar trend. Upon the addition of large organic cations butylammonium and phenethylammonium, there is a mismatch in dielectric constant between the bulky organic cations (ε = ∼4) and the inorganic octahedral layers (ε = ∼7.3), resulting in the formation of quantum wells.163 Furthermore, the large organic cations hinder the carrier mobility between the octahedral layers due to their insulating nature.164,165 Milot et al. reported a reduction in carrier mobility upon the addition of phenethylammonium cations (PEA+) to MAPbI3, where the carrier mobilities for MAPbI3 and (PEA)2PbI4 were 25 cm2 V−1 s−1 and 1 cm2 V−1 s−1, respectively.166 This low carrier mobility hinders the sensor to rapidly detect changes in light intensity, particularly in high-speed or dynamic environments.
Materials | Response time | Detection range | Sensitivity | Stability | Ref. |
---|---|---|---|---|---|
Commercial sensor | <5 ms | 0–5 MPa | — | >1 million times | https://Flexniss.com |
Commercial sensor | <5 μs | 4.4 N | — | >3 million times | https://tekscan.com |
111 N | |||||
445 N | |||||
PDMS/MXene | — | 10–80 Pa | 0.18 V Pa−1 | — | 173 |
80–800 Pa | 0.06 V Pa−1 | ||||
MXene | 70 ms | Up to 117.5 kPa | 3.94 kPa−1 | >7500 cycles | 174 |
MXene nanocomposite | 160 ms | Up to 500 kPa | Gauge factor (0–60% compression): 0.4 | >6700 s | 175 |
Gauge factor (60–80% compression): 2.61 | |||||
Gauge factor (80–90% compression): 1.04 | |||||
MXene/MOFs | 15 ms | 0.0035–100 kPa | 110 kPa−1 | 13![]() |
176 |
MXene/MoS2 | 385 ms | 1.477–3.185 kPa | 14.7 kPa−1 | ∼2500 cycles | 177 |
2D perovskite | — | 1–5 N | — | 4000 cycles | 178 |
MoS2/PDMS | 30–50 ms | <1 kPa | 150.27 kPa−1 | 10![]() |
179 |
1–23 kPa | 1036.04 kPa−1 | ||||
MoS2–rGO based | — | 0.5–5 N | 7.5 V Pa−1 | 100 cycles | 180 |
MnOx/MoS2 | <2 ms | 0–45 kPa | 6601 kPa−1 | 10![]() |
181 |
45–150 kPa | 58![]() |
||||
150–1000 kPa | 22![]() |
||||
h-BN | 15 ms | 0.05–450 kPa | 261.4 kPa−1 | >5000 cycles | 182 |
Borophene | 90 ms | 0–1.2 kPa | 2.16 kPa−1 | >1000 cycles | 183 |
1.2–25 kPa | 0.13 kPa−1 | ||||
25–120 kPa | 0.07 kPa−1 | ||||
Black phosphorus | 200 ms | <1 kPa | 0.06 kPa−1 | 2800 cycles | 184 |
2–40 kPa | 0.02 kPa−1 | ||||
40–100 kPa | |||||
Laser-induced graphene | 12 ms | 0–7 kPa | 52![]() |
10![]() |
185 |
65 Pa–1000 kPa | |||||
Vertical graphene | — | 0–21.5 N | 0.1–1.1 N | >25![]() |
186 |
Graphene | 9 ms | 0.2 Pa–425 kPa | 2297.47 kPa−1 | >10![]() |
187 |
There is a wide material selection to assemble a piezoresistive device, with semiconductors exhibiting higher piezoresistive effects, thus making the 2D material a potential candidate for piezoresistive sensing applications.167 Among the 2D materials, graphene is an ideal material for piezoresistive sensors due to its high conductivity, superior flexibility, large surface area, and robust mechanical strength.168 Niu et al. reported the use of graphene as a flexible piezoresistive tactile sensor for both pressure and strain detection.169 Similarly, Luo et al. demonstrated a 3D hollow structured graphene-based strain sensor with a good sensitivity of 15.9 kPa−1 and a faster response time.170 Other 2D materials used as piezoresistive sensors include TMDs, where Ji et al. demonstrated MoS2-based piezoresistive sensors.171 Tannarana et al. also reported the assembly of a highly stable and high responsivity-functionalized SnSe2 as a piezoresistive sensor (Fig. 8a).172
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Fig. 8 2D materials for tactile perception. (a) Piezoresistive sensor based on 2D SnSe2 with different pressures. Reproduced with permission.172 Copyright 2023, Elsevier. (b) Image and working mechanism of the laser-induced graphene-based triboelectric tactile sensor, along with its sensing performance at different pressures. Reproduced with permission.191 Copyright 2023, Elsevier. (c) Schematic of the h-BN-based capacitive tactile sensor, along with its device performance. Reproduced with permission.182 Copyright 2023, Springer Nature. |
Piezoelectric materials are required to have a non-centrosymmetric crystal structure. Among the 2D materials, TMDs are known to exhibit large in-plane piezoelectricity.188,189 Kim et al. reported a flexible single-crystal monolayer MoS2 flexible strain sensor with an in-plane piezoelectric coefficient as high as 3.78 pm V−1.190 However, graphene and h-BN possess a centrosymmetric crystal structure. To further attain piezoelectric performance, surface engineering of these materials is required. For example, in the case of the graphene-based sensor, Chen et al. reported the use of heterostructures on the graphene-based sensor.192 This heterostructure led to the surface modification of graphene, resulting in the breaking of the centrosymmetric crystal structure, thus successfully bringing the response time of the piezoelectric sensor to as low as 5 ms. Similarly, Tan et al. demonstrated a large piezoelectric effect in MXene-based sensors by oxygen-functionalized MXenes.193 Two-dimensional perovskites have been reported to be promising piezoelectric materials. Upon the addition of the large organic cation spacers, it breaks the centrosymmetric structure of the perovskite, which favors piezoelectricity. Furthermore, in quasi-2D perovskites, there is an enhancement in piezoelectricity as compared to its 3D counterpart due to the presence of defects.194 Ji et al. demonstrated the use of 2D halide perovskite, (CHA)2PbBr4, as a piezoelectric sensor with good voltage output linearity (∼2.5 V N−1, estimated from data) at a low applied pressure (1–5 N with an active area of 1 cm by 1 cm).178
However, for triboelectric sensors, materials with high electronegativity and electrical conductivity are suitable, as the large potential differences and high currents result in better signal outputs. Furthermore, the surface roughness of the material also plays a critical role, since friction between the material surfaces causes electron transfer. Therefore, Zhang et al. assembled an MXene-based triboelectric tactile sensor with leather to increase the surface roughness.195 Ghosh et al. also reported a stretchable MXene-based triboelectric nanogenerator.196 Guo et al. even demonstrated a laser-induced graphene-based triboelectric tactile sensor array, that can achieve pattern recognition and tactile imaging with high device performance stability (Fig. 8b).191 Other 2D materials reported in triboelectric devices are 2D conductive MOFs, as reported by Wu et al.197 With high electrical conductivity, 2D Cu-MOFs exhibited potential candidates in triboelectric sensors.
Lastly, the material selection to assemble a capacitive sensing device is high electrical conductivity to increase the dielectric constant of the sensing material. Zhang et al. reported MXene-based tactile sensors with high permittivity and low dielectric loss.198 Mukherjee et al. also reported the use of printed flexible graphene as a cognitive gripper integrated onto a soft gripper, which facilitated slippage-free and damage-resistant gripping without interference from users.199
The introduction of 2D materials as fillers into a polymer is a common technique to improve the tactile sensor performance. Umapathi et al. demonstrated the use of an h-BN composite film as a pressure sensor, which can effectively detect handwritings.200 The addition of h-BN into PDMS enhanced the output voltage to ∼198.6 V and a maximum peak power density of 7.86 W m−2. Yang et al. also introduced h-BN into an ionic ink, which enhanced the conductivity of the composite film, thus increasing the performance of the capacitive sensor (Fig. 8c).182 Similarly, Rana et al. reported the enhancement of triboelectric sensor performance upon the addition of zirconium-MOFs and hybridized MXenes.201 Kundu et al. also reported the addition of 2D TMOs into PVDF to enhance the piezoelectric properties of the sensor, thus enabling better identification of the shape and size of the object placed onto it.202
However, 2D material-based tactile sensors are also facing the issue of time-lag response. This issue surfaced due to the inherent mechanical properties of the materials and the signal processing mechanisms involved. For example, when 2D materials such as graphene or MoS2 are subjected to compression or stretching deformation, there might be a delay in the real-time transfer of stress or strain information to the sensor's electrical output. Such phenomenon is mainly observed in a composite film, where 2D materials act as fillers. Nuthalapati et al. assembled a piezoresistive pressure sensor by embedding rGO in PDMS, where a delay in recovery time (58 ms) was observed.203 The delay in recovery time was due to the viscoelastic property of the polymeric matrix.204 Such observation is not unique to piezoresistive sensors, and other tactile sensors such as capacitive sensors also face the similar issue. A lag time (a response time of ∼45 ms versus a recovery time of ∼83 ms) has been observed due to the reconstruction of the percolation network in the polymer matrix after release of applied pressure or strain.205,206
The amount of applied pressure plays another key factor in influencing the response speed. In a high-pressure regime, larger deformation is generated, thus requiring a longer time to response and recover from original configuration, resulting in time-lag in tactile responses. For example, the response and recovery times under a pressure of 3 Pa were 37 ms and 14 ms for an rGO-based piezoresistive tactile sensor. However, the response and recovery times increased to 305 ms and 165 ms, respectively, when the applied pressure increased to 2634 Pa.207
Materials | Response time | Detection range | Sensitivity | Stability | Ref. |
---|---|---|---|---|---|
Commercial sensor | — | 50 Hz–20 kHz | 52 dB | — | https://ca.robotshop.com/ |
MXene/MoS2 | ∼4 ms | 40–3000 Hz | 25.8 mV dB−1 | — | 217 |
MXene/bacterial cellulose | 90 ms | 0–0.82 kPa | 51.14 kPa−1 | 5000 cycles | 218 |
0.82–10.92 kPa | 2.62 kPa−1 | ||||
rGO/PDMS | 107 μs | 20–20![]() |
8699 | >10![]() |
46 |
Graphene-based | 0.126 s | — | Gauge factor (tension): 73 | 1000 cycles | 219 |
Gauge factor (compression): 43 | |||||
2D MOF | 5 ms | 20–330 Hz | 0.95 V Pa−1 | — | 220 |
Gou et al. reported a piezoresistive MXene-based artificial eardrum that can detect human voice with high sensitivity and speech recognition accuracy.208 In recent years, perovskites have been attracting attention for being promising piezoelectric materials due to their high stability in air and moisture. Furthermore, the reduction of dimensionality of perovskite has also improved the piezoelectric property of the perovskite.209 Guo et al. demonstrated the 2D halide perovskite as an acoustic sensor, detecting ultrasound with excellent transmission efficiency as high as 12% (Fig. 9a).210
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Fig. 9 2D materials for sound perception. (a) Ultrasound detection via a 2D perovskite-based acoustic sensor. Reproduced with permission.210 Copyright 2023, American Chemical Society. (b) Voice recognition using a piezoelectric acoustic sensor, coupled with machine learning. Reproduced with permission.216 Copyright 2022, American Chemical Society. |
Besides, traditional artificial throat sensors are usually made of graphene-based materials such as laser-induced graphene.211,212 However, graphene-based artificial throat shows limited biocompatibility, sensitivity, accuracy and conductivity.213,214 Therefore, other 2D materials are studied to solve these issues. Jin et al. reported a MXene-based piezoresistive artificial throat with a speech recognition accuracy as high as ∼89%.215 Chen et al. demonstrated MoS2-based piezoelectric artificial throat (Fig. 9b), with a speech recognition accuracy of ∼97%.216
However, the key issue faced by 2D material-based acoustic sensors is achieving the necessary sensitivity across a broad range of frequencies, especially low-frequency sounds, which are critical for applications such as speech recognition or environmental monitoring. Additionally, 2D material-based acoustic sensors face time-lag response due to the slow mechanical and electrical coupling between the sensor material and the acoustic waves. The inherent mass and stiffness of 2D materials such as graphene and TMDs can limit the speed at which the sensor responds to sound vibrations, particularly in low-frequency ranges. Moreover, signal processing delays can occur when extracting acoustic information from the sensor's analogue signals.
Materials | Response time | Detection range | Stability | Sensing environment | Selectivity | Ref. |
---|---|---|---|---|---|---|
Commercial sensor | — | 1–50 ppm | High | — | Volatile organic compound (VOC) | https://www.winsen-sensor.com/ |
rGO-based | 50 s | 0.25% change in resistance per 1 ppm (1–10 ppm) | — | — | NH3 | 244 |
SnO2/rGO | — | — | H2S: >90 days | — | H2S, NO2, H2 | 245 |
NO2, H2: >15 days | ||||||
Graphene-based | ∼14 s | 0.0579 ppm−1 (5–100 ppm); | <1 year | H2, air, H2O | H2 | 246 |
0.0253 ppm−1 (100–200 ppm) | ||||||
WS2–CuO–C | 37.2 s | — | 25 days | 100.1 °C, 500 ppb | H2S | 247 |
MoS2 | 90–280 s | NH3: 0.084–0.043 ppm−1 | 24 weeks | — | NH3, H2S | 248 |
H2S: 0.079–0.065 ppm−1 | ||||||
MoS2-based | 43 s | Non-linear, 5–80 ppm | >5 weeks | 80 ppm H2 and NH3 | CO | 249 |
20 ppm NO2 | ||||||
150 °C–300 °C | ||||||
WSe2/MWCNT | 32 s | 10–105 ppb | >45 days | — | VOC | 250 |
Black phosphorus | 22 s | Down to 100 ppb | >30 days | Air, NH3 | NH3 | 251 |
Black phosphorus–SnO2 | 39.8 s | 1–9 ppm | 20 days | 5 ppm CO2, SO2, NH3, CO, C3H6O | H2S | 105 |
MXene-based | 112 s | 4–100 ppm | >3 weeks | Air and 100 ppm SO2 | CO, SO2, NH3 | 252 |
MXene/NiO | 279 s | 1–100 ppm | 56 days | — | HCHO | 253 |
MOF@MXene | 55 s | 50–400 ppb | 20 days | H2S, NO2, SO2, CO, NH3, CH4O, C2H6O, C3H6O | H2S | 254 |
MXene/WSe2 | 9.7 s | 1–40 ppm | >1 month, 40 ppm | — | VOC | 255 |
2D MOF | 1.69 min | 1–100 ppm | 10 days | NO2, air | NO2 | 256 |
2D MOF | 57.3 min | 50 ppb–5 ppm | — | C7H8, CO, CO2, dimethyl sulfide, H2S | H2S | 236 |
2D MOF | ∼11 s | 0.1–100 ppm | 60 days | H2S, NO2, MeOH, SO2, CO2, CH4, NH3, CO | NO2 | 257 |
3.5 ppb (limit of detection) |
Graphene-based electronic nose has been demonstrated by Kwon et al., with ultrasensitive and improved selectivity to detect NO2 by the introduction of n-dopants to graphene.225 Naganaboina et al. reported graphene–CeO2-based gas sensors for CO detection with a greater selectivity and better repeatability.226 The performance of the sensor improved due to the presence of oxygen vacancies and the heterojunction between CeO2 and graphene. Similarly, Tung et al. improved the selectivity of the graphene-based sensor using a graphene/MOF heterostructure (Fig. 10a) to detect volatile organic compounds.227
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Fig. 10 2D materials for olfactory and gustatory perception. (a) Illustration of a gas sensor along with its performance to detect volatile organic compounds. Reproduced with permission.227 Copyright 2020, Elsevier. (b) Relationship between the bending angle and the ability to detect NO2 in a flexible gas sensor based on MXene/MOF. Reproduced with permission.232 Copyright 2024, American Chemical Society. (c) Artificial tongue based on a graphene sensor to mimic human taste. Reproduced with permission.259 Copyright 2023, Springer Nature. |
Besides, there has been an increase in interest in other 2D materials such as MXenes and TMDs due to graphene-based gas sensors’ limitations such as low selectivity, long-term drift and long recovery time.228,229 Zhao et al. reported a MXene-cationic polyacrylamide nanocomposite for flexible NH3 gas sensing.230 In order to improve the sensitivity of the gas sensor, Lee et al. developed MXene/graphene hybrid fibers for NH3 sensing.231 The three order higher sensitivity for these hybrid fibers were mainly attributed to the high surface-to-volume ratio. Similarly, Liu et al. reported a flexible and stretchable hybrid MXene/MOF aerogel gas sensor (Fig. 10b) to detect NO2.232 TMDs such as MoS2 are also candidates for gas sensing. For example, functionalized MoS2 gas sensor was demonstrated for NH3 sensing.233 With Au decorated on MoS2, S vacancies were introduced, allowing higher carrier density in MoS2, thereby enhancing the ability to detect NH3.
Besides, 2D MOFs are a group of emerging materials that have gained attention for chemiresistive sensor applications.234,235 The π-conjugated ligands in 2D MOFs allow effective charge delocalization. These ligands are linked to metal nodes via π–d hybridization, forming extended conjugation throughout the frameworks. In 2D MOFs, their porous framework structure favors the interactions between gas and materials, thus making them a highly attractive material for chemiresistive gas sensor applications. In fact, Jeon et al. reported a 2D MOF-based H2S gas sensor with an improved detection limit, where the gas sensor can detect H2S gas concentration as low as 1 ppm.236
Despite attracting attention due to their high sensitivity, the main issue faced by the above-mentioned 2D material-based gas sensors is their poor selectivity due to the limited variety in the adsorption sites, leading to unfavorable to selective response to gases such as H2 and H2S gas.228 Moreover, when exposed to practical applications with a complex gaseous mixture, the 2D material-based gas sensors, such as graphene-based and MXenes-based gas sensors, often exhibit cross-sensitivity, responding to multiple gases. The poor selectivity often leads to false alarms and overlapping signals of gases with similar structures or functional groups. Furthermore, 2D materials such as graphene oxide exhibit a time-lag response primarily due to the slow adsorption and desorption processes of gas molecules on the material's surface, which can be detrimental to timely feedback. The electrical properties of the sensor gradually change as the gas molecules interact with the 2D material. Thus, the sensor performance degrades overtime, making their durability worse.
To address the issue of poor selectivity in gas sensors, one of the promising approaches is the functionalization of 2D materials, where noble metals such as gold, ruthenium, palladium and platinum are widely used to decorate 2D materials.228 For example, Kim et al. demonstrated the tunability of the selectivity of the noble metal-decorated WS2-based gas sensor, where Pt/Pd bimetallic nanoparticle-decorated Ru-implanted WS2 exhibited better selectivity than pristine WS2 and Ru-implanted WS2.237 Additionally, Quan et al. reported a fully flexible gold-decorated MXene-based gas sensor with improved selectivity (4.8% for 1 ppm) towards NO2, which is about 3.2 and 76.0 times as high as that of the Au interdigital electrode integrated with the Ti3C2Tx/WS2 sensor (4.8%) and the MXene electrode integrated with the Ti3C2Tx sensor (0.2%), respectively.238 The improvement in selectivity is due to the catalytic effect of the noble metals, promoting reactions with the targeted gas molecules, resulting in the electron transfer between gas molecules and sensing layers.239 To overcome the issue on cross-sensitivity, assembling sensor arrays with multiple sensing units are used to detect different targeted gases. Yuan et al. demonstrated high selectivity for multiple-gas detection by assembling multiple gas sensing units, where each unit was decorated with specific noble metals (Ru and Ag) or silicon oxide SiOx to enhance selectivity for targeted gases (NH3, H2S and H2O, respectively).240 However, the enhancement in the selectivity of gas sensor based on 2D materials is highly dependent on optimal conditions, such as the type, implantation dose, and quantity of decorated noble metals.
Besides the functionalization of 2D materials and sensor arrays, van der Waals heterostructures can tune the selectivity of gas sensors by controlling the stacking of 2D materials.241,242 Such phenomenon was observed in 2D MOF-based gas sensors, where Yao et al. reported the use of MOF-on-MOF to modify the selectivity of the gas sensor.243 Due to the presence of an electrically non-conductive MOF layer (Cu-TCPP), which acted as the sieving layer, on the electrically conductive MOF layer (Cu-HHTP), the selectivity of the MOF-based gas sensor was tuned from NH3 to benzene. The change in selectivity was a result of the strong interaction between NH3 and the sieve layer (Cu-TCPP), thus refraining NH3 gas molecules to reach the sensing layer (Cu-HHTP).
Materials | Response time | Detection range | Stability | Selectivity | Ref. |
---|---|---|---|---|---|
Commercial sensor | — | — | — | Sourness, sweetness, bitterness, astringency, umami, saltiness | https://www.insentjp.com/ |
MXene-based | 14–22 s | — | <7 days | pH | 107 |
AuNPs@ZIF-8/Ti3C2 MXene | 20 min | 10−11–10−13 M | <7 days | Umami | 263 |
Laser-induced graphene | — | 1–1000 ppm | — | Sourness, sweetness, bitterness, umami, saltiness | 264 |
Graphene-based | — | — | — | Sourness, sweetness, bitterness, umami, saltiness | 259 |
MoS2-based | — | 10–300 μM | — | Tyramine | 265 |
Black phosphorus | — | pH 1.0–8.0 | 6 days | pH | 266 |
Among the 2D materials, graphene and its derivations stand out from other 2D materials as a palate sensor due to its simple, miniaturized, low cost and high performance.222,258 Ghosh et al. reported a graphene-based electronic tongue (Fig. 10c) that can detect taste perception like sweetness and bitterness.259 Yu et al. also reported a high-sensitivity rGO-based e-tongue that can detect and distinguish multi-flavors.260
However, due to the low selectivity of graphenes, there is an increasing interest towards other 2D materials. Zhi et al. reported a MXene-based electronic tongue with good pH-sensitivity, enabling taste perception such as sourness.261 The scope of detection in an electronic tongue is not limited to taste perception, but extended to detect specific foods or drugs. Veeralingam et al. demonstrated a MoS2-based electronic tongue that detects drugs in human saliva.262
Gustatory sensors remain highly unexplored due to challenges in capturing and simulating these signals and the limited pioneering research on integration to soft robots. The main issue arises from the low selectivity of these 2D material-based electronics. Hence, such sensors cannot achieve simultaneous detection and differentiation of signals in complex environments. Besides, gustatory sensors suffer from time-lag response, which is caused by the slow interaction between the target chemical molecules and the 2D material surface, as well as the delay in the subsequent electrical signal change. In the case when the sensors need to detect low concentrations of gases or chemicals, which requires a longer exposure time to accumulate sufficient molecular interactions for a detectable response.
Practical applications for 2D material-based soft robots are already beginning to emerge. In healthcare, soft robots equipped with flexible sensors can be used in minimally invasive surgeries, where precise manipulation and feedback are critical. These robots can mimic the dexterity and sensitivity of human hands, which can be used for smart collision-aware surgical robots.267
Deng et al. demonstrated a tactile sensor which can achieve multimodal sensing function in a single device using polyimide–MXene/SrTiO3 hybrid aerogel (Fig. 11a),271 where MXene played an important role in achieving the pressure sensing function through the piezoresistive effect. Meanwhile, the heterostructure of MXene/SrTiO3 assisted in detecting thermoelectric and infrared radiation responses. Therefore, this device with heterostructures achieved not only the perception of tactile, but also the ability to sense temperature and differentiate shapes. Similarly, Saeidi-Javash demonstrated the potential of multimodal sensors using MXene/graphene for temperature and strain sensing.272 With these promising results, the integration of such 2D material-based multimodal sensor onto a soft gripper opens up more opportunities to applications such as rescue missions, collaborative robots, fruit sorting, and intelligent prosthetics. Zhang et al. integrated a graphene-based tactile sensor on a soft gripper to classify the size and ripeness of kiwifruit.273 With the graphene-based multimodal sensor, the soft gripper can perform nondestructive evaluation with a grading speed of ∼2.5 s per fruit with a high sensitivity of 23.65 kPa−1, promoting a higher efficiency for fruits in cold chain logistics. This fast response and high sensitivity were attributed to the excellent electrical conductivity of graphene, which enables detectable change in resistivity even with small pressure or strain applied.274
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Fig. 11 Advanced applications of 2D materials in soft robotics. (a) Illustration of the stimuli of a MXene-based multimodal sensor that can simultaneously detect shape and temperature. Reproduced with permission.271 Copyright 2024, Cell Press. (b) Illustration of artificial synapses to mimic the human visual system. Reproduced with permission.140 Copyright 2024, John Wiley and Sons. (c) Demonstration of the potential application of the human–machine interface using a pressure sensor. Reproduced with permission.183 Copyright 2022, Elsevier. |
Despite the above-mentioned successful attempts to multimodal sensing, some challenges still obstruct their deployment in soft robots. The primary issue is the degree of cross-coupling for each sensor unit from different stimuli. For electrical type sensors, electric signals (current, voltage, capacitance, and resistance) are analysed to determine the stimuli. Separate signals responding to different stimuli are ideal to achieve this multimodal sensing. For example, the change in resistance (piezoresistive) and open-circuit voltage (thermoelectric) from MXenes represents the signals triggered by external forces and temperature, respectively, in a low cross-coupling manner.271 In addition, such concern can be mitigated by proper encapsulation and device design of sensor, improving the accuracy.275 A pressure and temperature all-resistive dual-mode sensor based on MXenes without crosstalk in multiple states was reported, which was achieved by simple PDMS encapsulation. A temperature-independent pressure sensor is developed by constructing a more conductive silver film on the PDMS contacted with the MXene film to form a two-phase contact mechanism with different conductivities. Furthermore, a pressure-independent temperature sensor is proposed by designing PDMS with a hollow structure around the MXene film.276 Alternatively, machine learning is promising for the recognition of complex signals after effective training,277 which can be a potential solution to this issue. Therefore, the integration of different active 2D materials and suitable device designs is promising to address the challenge from multimodal sensors.
With the increasing demand for AI, memristive artificial synapses based on 2D materials have attracted intensive attention due to their unique characteristics.299–301 Memristive artificial synapses required low power switching capability, excellent electrical and physical tuning properties and hetero-integration compatibility. Of these, 2D materials such as graphene, TMDs, and h-BN have exhibited to be emerging materials for low-power and high-performance memristive artificial synapses.302–305 While two-terminal memristors exhibit basic synaptic function, three-terminal memristors are able to perform more complexed tasks. The degree of complication of the sensing required directly determines the type of memristors used. Some of the synaptic functions these artificial synapses possess include short-term plasticity, long-term plasticity, short-term depression, long-term depression, spike term-dependent plasticity, and paired pulse facilitation. Some of these artificial synapses were demonstrated by Wang et al., where they integrated the visual sensor with artificial synapses so as to mimic the whole human visual system (Fig. 11b).140
Some of the more common examples to demonstrate the application of HRI are pressure sensors. Hou et al. assembled a borophene pressure sensor with a sensitivity ranging between 0.07 kPa−1 and 2.16 kPa−1, a detection limit of 10 Pa, and a fast response time of 90 ms.183 The demonstration of the pressure sensor towards the application of HRI (Fig. 11c) has also been shown by connecting the pressure to a robotic arm so as to control it. Mukherjee et al. demonstrated a cognitive robotic gripper that can perform cognitive decision-making tasks with a graphene-based multi-array sensor,199 graphene acts the capacitive pressure sensor with a response time of 0.3 s, which provides real-time feedback on the slippage detection thus preventing over-exertion of pressure on the targeted object.
Collaborative robot (cobot) with graphene-based electronic skin has been prototyped, demonstrating the possibility of integrating a 2D material-based tactile sensor with a robotic control system,307 where graphene is the active material of the piezoresistive pressure sensor. However, the reaction time of the soft robot is about 0.2 s due to the measurement and computational delay. One practical application of such sensor in cobot is to avoid its collision with human and its surroundings, which can promote a safer co-workspace between human and soft robots, while boosting the production process. Similarly, Klimaszewski et al. demonstrated an identical function through the integration of a capacitive graphene tactile sensor onto a soft robot.308 The reaction time of the soft robot was ∼2500 ms, which might be slow for collision prevention. Despite the prolonged reaction time resulting from the filtering of undesired environmental noise, the detection quality improved, enabling the sensor to estimate and brake at a proximity distance of approximately 20 mm or less. The primary challenge is to reduce the reaction time while maintaining the precise and robust proximity distance estimation. Integrating a multimodal sensor into the cobot could address this issue by ensuring that the cobot does not rely solely on a single stimulus during the decision-making process.
In practical applications, one of the more investigated applications is in the healthcare industry such as rehabilitation and prosthetic limb feedback and/or control. William et al. reported the use of graphene-based composites for prosthetic upper limb feedback, whereby the prosthetic limb was able to detect pressure, temperature and movement with an accuracy of ∼95% due to excellent stability of the graphene-based piezoresistive sensor.309 Rehabilitation hand for patient suffering from stroke has also been demonstrated by Zhang et al., where an rGO-based piezoresistive pressure sensor was integrated onto a prosthetic hand,310 with a high operation range (2–1200 kPa) and a high sensitivity (6.03 kPa−1). This prosthetic hand with an embedded tactile sensor can help to monitor the compression strength and duration during rehabilitation to prevent muscle atrophy and even promote recovery. Other than 2D material-based tactile sensors, optical sensors are also integrated to retinal prosthesis for rehabilitation. Choi et al. has demonstrated the feasibility of using MoS2–graphene as an implantation optoelectronic device that can be used as a retinal prosthesis.311 The MoS2–graphene photodetector is able to detect the visible light, without capturing IR noises due to the wide bandgap of MoS2, making it promising in soft implantable optoelectronic devices.
Given the multiple steps for the conventional technical route (CVD-transfer-encapsulation), low temperature deposition and composite fabrication are expected to be the alternative solutions. With a thermal process under moderate temperatures (compatible with polymers), transition interfaces between 2D films/flakes and polymeric substrates/matrix are expected to stabilize the structure, enabling higher durability and stability. It should be noted that these two technical routes can be practical only when the defect density of 2D materials is down to an acceptable level.
To solve these challenges, the development of 2D materials including material fabrication, device integration, and system establishment are indispensable. This requires multi-disciplinary development and progress. A breakthrough at any step along the technological route can approach commercial robotic applications.
Footnote |
† These authors contributed equally to this work. |
This journal is © The Royal Society of Chemistry 2025 |