Warood Kream
Alaarage
a,
Abbas H.
Abo Nasria
*b,
Tamadhur Alaa
Hussein
b and
Hamid Ibrahim
Abbood
c
aFaculty of Dentistry, University of Kufa, Najaf, Iraq. E-mail: Wuroodk.olaiwi@uokufa.edu.iq
bDepartment of Physics, Faculty of Science, University of Kufa, Najaf, Iraq. E-mail: abbas.abonasiriya@uokufa.edu.iq
cAl-Zahraa University for Women, Iraq. E-mail: hamid.ibrahim@alzahraa.edu.iq
First published on 15th February 2024
We utilised first-principles computations based on density functional theory to investigate the optical and electronic properties of bilayer CdS before and after the adsorption of gas molecules. Initially, we examined four candidate adsorption sites to determine the best site for adsorbing CO, CO2, SO2, H2S, and SO. In order to achieve the optimal adsorption configurations, we analysed the adsorption energy, distance, and total charge. Our findings reveal that the CdS bilayer forms a unique connection between the O and Cd atoms, as well as the S and Cd atoms, which renders it sensitive to SO2, H2S, and SO through chemical adsorption, and CO and CO2 through strong physical adsorption. The adsorption of gas molecules enhances the optical properties of the CdS bilayer. Consequently, the CdS bilayer proves to be a highly efficient gas sensor for SO2, H2S, and SO gases.
Recent research has shown that CdS-based composites, such as CdS-supramolecular organogel hybrid films39 and CdS–SnO2 composites,40 exhibit high sensitivity to volatile organic compounds. Moreover, sensors have been developed based on n-CdS/p-polyaniline thin film heterojunctions41 and leaf-like CdS micro-/nanostructures.42 They have displayed improved performance, such as response, recovery time, stability, and recognition ability towards various analytes. Several methods have been employed to prepare nanocrystalline CdS thin films, including physical and chemical techniques such as sol–gel,43 gas evaporation,44 and electrostatic deposition,45 among others. Researchers have investigated the interaction of oxygen gas with CdS films prepared through spray pyrolysis46 and reported on the resistive type humidity sensing properties of CdS nanoparticles grown through the chemical bath deposition (CBD) method.47 CdS supramolecular organogel hybrid films have been fabricated through the exposure of a supramolecular organogel film containing Cd(Ac)2 to an H2S atmosphere at room temperature,39 and n-CdS/p-polyaniline thin film heterojunction-based liquefied petroleum gas (LPG) sensors have been produced utilising a simple and cost-effective electrodeposition technique.41 CBD is a favoured option among film deposition methods due to its suitability for large-scale fabrication processes, simplicity, cost-effectiveness, and non-polluting properties. CBD produces homogeneous, hard, adhesive, transparent, and stoichiometric nanocrystalline thin films.48 The availability of cost-effective and simple practical methods for synthesising CdS slabs has motivated the industry and research communities' efforts to look on employing CdS for sensing applications.43,48,49
Recently, cadmium sulfide (CdS) has gained recognition as an exceptional material for optoelectronic devices, primarily due to its position as a significant II–VI compound semiconductor with a direct band gap of 2.42 eV.50–56 Multiple methods for synthesizing CdS have been extensively explored, encompassing chemical bath deposition, thermal evaporation, ultrasonic spray pyrolysis, and atomic layer epitaxy.57–59 CdS is commonly recognized for its application as a pigment; however, its utility extends to various other contexts, including piezoelectric transducers, solar cells, photoresistors, photovoltaics, and transistors. The advantageous characteristics of CdS, such as photoconductivity, electroluminescence, and piezoelectricity, enable these applications to operate effectively in high-frequency ranges.60–66 CdS exhibits chemoresistiveity in addition to its more common uses, yet this intriguing quality has received relatively little attention from researchers. The utilization of CdS as a gas sensor has been documented in only a limited number of publications.
Moreover, it has been observed that light at room temperature can activate the chemoresistiveity in CdS. By energizing electrons into the conduction band, electromagnetic irradiation can modify the surface chemistry of the film and enhance its conductivity. This unique property allows CdS gas sensors to operate effectively at room temperature, eliminating the need for external heating.67,68 Consequently, there is a need to explore CdS as a novel material in the gas sensor field. Therefore, 2D CdS bilayers emerge as excellent candidates for highly sensitive gas sensors, given their potential for exceptional gas-sensing capabilities.
The enhancement of the surface performance for several adsorption systems has previously been confirmed through employing double-layers of the slab.69–71 Here, we have employed a two layers of CdS to replicate the surface behaviour and properties to reproduce the experimental measured structures of the system which would be typical of a semi-infinite CdS slab. The efficacy of replicating a CdS surface behavior and properties using two layers was investigated in the study72 by Qasrawi and Abed. The use of a pre-assembled CdS seed layer prior to CdSe deposition has been reported to improve the performance of quantum dot-sensitized solar cells.73
In this study, we aimed to explore the potential of CdS bilayers as gas sensors for CO, CO2, SO2, H2S, and SO gases. To achieve this, we conducted first-principle calculations using density functional theory (DFT) to analyze the adsorption behavior of these gases on the CdS bilayer. Additionally, we systematically investigated the adsorption of CO, CO2, SO2, H2S, and SO gas molecules on CdS bilayers to facilitate a comprehensive and comparative discussion. Our investigation encompassed the adsorption of gas molecules as well as the electronic and optical properties of the bilayer CdS. Based on our findings, CdS bilayers exhibit promising potential as gas sensors, particularly for H2S and SO. It is crucial to acknowledge that the findings of this research are based on no experimental evidence. Therefore, it is imperative for us to produce strong and conclusive results in order to drive additional experimental investigation in the future.
In line with other studies, the system is composed of a CdS bilayer with a 3 × 3 supercell (36 atoms) and a lattice constant of a = b = 12.619605 and c = 25.067658.87 To evaluate a gas molecule's adsorption system on a CdS bilayer is stable, the adsorption energy defined (Ead) as follows:88
Ead = ECdS + gas − ECdS − Egas, | (1) |
To assess the interaction between gases and the CdS bilayer, we have calculated the interaction energies using the following expression:
Eint = ECdS+gas − [ECdS + Egas] − δBSSE, | (2) |
Fig. 2 illustrates the optimized structures of the supercell of the pristine CdS bilayer from both top and side views, as well as the energy band structure of the bilayer CdS. The top view highlights the resemblance between graphene and the double-layer CdS, both exhibiting hexagonal structures. The Cd–S bond length measures 2.571 Å. To explore the gas adsorption behavior in different orientations (parallel or perpendicular to the bilayer), four adsorption sites, namely T1 (Cd), T2 (S), T3 (center), and T4 (bridge), were utilized on the supercell of the bilayer CdS (as shown in Fig. 2). The initial adsorption distance in various adsorption sites was set at approximately 3 Å. The adsorption energy (Ead) serves as an indicator of bilayer stability, with lower values indicating more stable structures. The most stable energetic sites for CO, CO2, SO2, H2S, and SO on the CdS bilayer are the S, Cd, S, Cd, and S sites, respectively, as presented in Table 1.85 For the CdS bilayer, the spacing between the layers (h = 4.2 Å) is greater than the sum of any two atoms' radii in the bilayer (the atomic radii of Cd and S are rCd = 1.51 Å and rS = 1.02 Å).92 The energy band structure of bilayer CdS is shown in Fig. 2. At the G point, the valence band maximum (VBM) and the conduction band minimum (CBM) are both in bilayer CdS, which has a direct band gap (Eg) of 1.499 eV.
Adsorption systems | Site | E ad (eV) | d (Å) | r (Å) | Q (|e|) | Style |
---|---|---|---|---|---|---|
CO/CdS-bilayer | Cd | −0.40 | 3.07 | 2.28 (C–Cd) | 0.01 | Donor |
S | −0.48 | 2.85 | 2.28 (C–Cd) | 0.02 | Donor | |
Bridge | −0.42 | 3.21 | 2.28 (C–Cd) | 0.01 | Donor | |
Center | −0.42 | 3.22 | 2.28 (C–Cd) | 0.02 | Donor | |
CO2/CdS-bilayer | Cd | −0.44 | 3.04 | 2.24 (O–Cd) | −0.02 | Acceptor |
S | −0.38 | 3.06 | 2.24 (O–Cd) | −0.01 | Acceptor | |
Bridge | −0.39 | 3.12 | 2.24 (O–Cd) | −0.01 | Acceptor | |
Center | −0.42 | 3.35 | 2.24 (O–Cd) | −0.02 | Acceptor | |
SO2/CdS-bilayer | Cd | −1.59 | 3.24 | 2.24 (O–Cd) | −0.03 | Acceptor |
S | −1.75 | 2.46 | 2.24 (O–Cd) | −0.11 | Acceptor | |
Bridge | −1.37 | 3.02 | 2.24 (O–Cd) | −0.07 | Acceptor | |
Center | −1.15 | 3.19 | 2.24 (O–Cd) | −0.05 | Acceptor | |
H2S/CdS-bilayer | Cd | −1.69 | 2.77 | 2.53 (S–Cd) | −0.16 | Acceptor |
S | −1.37 | 2.83 | 2.53 (S–Cd) | 0.12 | Donor | |
Bridge | −1.02 | 3.21 | 2.53 (S–Cd) | 0.11 | Donor | |
Center | −1.12 | 3.29 | 2.53 (S–Cd) | 0.10 | Donor | |
SO/CdS-bilayer | Cd | −1.32 | 2.30 | 2.04 (S–S) | −0.17 | Acceptor |
S | −1.92 | 2.77 | 2.53 (S–Cd) | −0.21 | Acceptor | |
Bridge | −1.39 | 2.52 | 2.53 (S–Cd) | −0.15 | Acceptor | |
Center | −1.58 | 2.58 | 2.53 (S–Cd) | −0.16 | Acceptor |
Adsorption systems | E int (eV) | d (Å) | r (Å) | Q (|e|) | Style | τ (s) |
---|---|---|---|---|---|---|
CO/CdS | −0.48 | 3.27 | 2.28 (C–Cd) | 0.02 | Donor | 1.15 × 10−4 |
CO2/CdS | −0.44 | 3.06 | 2.24 (O–Cd) | −0.02 | Acceptor | 0.24 × 10−4 |
SO2/CdS | −1.75 | 2.46 | 2.24 (O–Cd) | −0.11 | Acceptor | 2.44 × 1017 |
H2S/CdS | −1.69 | 2.77 | 2.53 (S–Cd) | −0.16 | Acceptor | 2.40 × 1016 |
SO/CdS | −1.92 | 2.77 | 2.53 (S–Cd) | −0.21 | Acceptor | 1.75 × 1020 |
![]() | ||
Fig. 3 Adsorption systems for gas molecules absorbed on bilayer CdS: optimal adsorption configurations (CO, CO2, SO2, H2S, SO). |
E ad of SO2, H2S, and SO adsorbed on the CdS bilayer were (−1.75, −1.69, and −1.92) eV, respectively, and the Q values are (−0.11, −0.16 and −0.21) |e|, respectively. These values indicate charge transfer from CdS bilayer to SO2, H2S, and SO. Their interactions are stronger compared with CO and CO2 on the CdS bilayer. In addition, the sum of the covalent radii of the O and Cd atoms (rO–Cd = 2.24 Å) and the S and Cd atoms (rS–Cd = 2.53 Å) remains smaller than their distance (d = 2.46 Å and d = 2.77 Å). Bonding standards are near the theoretical interatomic covalent radius (±0.3 Å); therefore, chemical bonds can occur in these systems.96 Additionally, after these adsorptions, a significant structural deformation was seen on the CdS bilayer, further proving the strong chemical adsorption between these gas and CdS. The results indicate that the CdS bilayer has excellent application potential as SO2, H2S, and SO sensors with clear sensing responses.97,98 As shown in Fig. 3, the adsorption of these gases on CdS has induced significant changes in atomic positions. The adsorption of CO or SO2 gases on CdS has resulted in considerable structural deformations due to the interaction between the gases and Cd surface atoms. The SO molecule has bound to CdS by interacting with the surface S atom, leading to a vertical displacement of atoms and causing a restructuring of the monolayer. Similarly, H2S has interacted with the surface S atom, and its binding has led to the formation of S–S–H bonds, resulting in alterations in the surface chemistry and atomic arrangement. On the other hand, the CO2 molecule has interacted with the surface S atom, leading to the formation of new bonds and surface reconstruction. These deviations significantly affect the electronic structure, surface chemistry, and sensitivity of CdS, enabling it to detect and discriminate between different gases. Through the study of structural and optical changes induced by gas adsorption, it is possible to design and optimize CdS-based sensors for improved gas sensing performance.
A better understanding of the adsorption behaviours of molecules on the bilayer necessitated a further investigation into the band structures of molecules adsorbed on the CdS bilayer; these results are shown in Fig. 4. The Fermi level is represented by the black dashed line (Ef). After CO, CO2, SO2, and H2S adsorption, the band gap of CdS increased to 2.078, 1.847, 1.712, and 1.890 eV, respectively, while the value of the VBM and CBM remained unaltered at G point. Finally, the adsorption of SO molecules lowered the original band gap (0.95 eV), showing that these adsorptions affect the electronic properties of the CdS bilayer.
To further understand how the adsorption of gas molecules changes the bilayer CdS's electronic properties, we analysed its total and partial densities of states. Fig. 5–9 illustrate the density of states (DOS) and projected density of states (PDOS) for the CdS bilayer adsorption systems. These figures reveal that in the CO/CO2/SO2/H2S–CdS adsorption systems, the DOS undergoes a rightward shift at certain locations. However, in the SO–CdS adsorption system, the DOS exhibits a leftward shift. In the case of theSO adsorption system, the conduction band's bottom shifts to the left, making it easier for the charge to be excited from the valence band to the conduction band.
In the case of PDOS, the influence of adsorbed gases on the electronic states near the Fermi energy (Ef) is crucial. The adsorption of CO and CO2 introduces active electronic states in close proximity to Ef. Specifically, in the CO adsorption system, there is an overlap between the s and p orbitals of the Cd atom and the p orbital of the C atom within the energy ranges of 2 to 5 eV and −2 to −5 eV, respectively. Likewise, in the CO2 adsorption system, there is an overlap between the p orbital of the O atom and the s and p orbitals of the Cd atom within the energy ranges of 4 to 6 eV, the s orbital from −2 to −4 eV, and the d orbital from −6 to −9 eV. These overlapping orbitals indicate strong orbital hybridizations, implying the presence of chemical bonding. The electronic densities of SO2, H2S, and SO are all significantly active near Ef, further supporting the existence of chemical bonds with the CdS system. Considering the SO2 adsorption system, the p orbit of the O atom overlaps with the s, p, and d orbits of the Cd atom in the energy range of −2 to −4 eV.
In addition, for the H2S adsorption system, the p orbit of the S atom overlaps with the s and p orbits of the Cd atom in the range of 2 to 12 eV and with the s, p, and d orbits in the range of 0 to −5 eV. Moreover, the s and p orbits of the S atom overlap with the d orbit of Cd in the range of −6 to −8 eV, while the s, p, and d orbits of Cd overlap with the s orbit of the S atom in the range of −10 to −12 eV. For the SO adsorption system, the s and p orbits of the Cd atom overlap with the p orbit of the S atom in the range of 1 to 10 eV and with the s orbit in the range of −9 to −13 eV. Additionally, the s and p orbits of the S atom overlap with the s, p, and d orbits of the Cd atom in the range of 1 to −6 eV, along with the d orbit in the range of −7 to −9 eV. These findings highlight the flexibility and adaptability of CdS to interact with various gas molecules, making it a promising material for potential applications in electronic devices and gas sensing technologies.
By analysing the charge density difference (CDD), the redistribution of charges (ρ) between gas molecules and CdS bilayer has been studied, which is defined as:
ρ = ρCdS+gas − ρCdS − ρgas, | (3) |
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Fig. 10 Electron density difference for bilayer CdS after gas molecules absorption (CO, CO2, SO2, H2S, SO). |
The electron localisation function (ELF) was utilised to support the bond in some adsorption models of high adsorption energy and short adsorption distance.99 ELF was found to be a useful tool for thoroughly comprehending the properties of chemical bonds and pairings of non-bond electrons (lone electrons pairs) by defining the amount of electron localisation qualitatively (Fig. 11).89 The ELF value provides an excellent representation of the localisation or delocalisation of electrons between gas molecules and the CdS bilayer.85 As shown in Fig. 6, the ELF of CO and CO2 on the CdS bilayer displays delocalised electrons in the interlayer region. CO and CO2 interact strongly with CdS bilayer. The atoms have still not bonded, though.100
![]() | ||
Fig. 11 Slices of electron localisation function for bilayer CdS after gas molecules absorption (CO, CO2, SO2, H2S, SO). |
Additionally, this result demonstrates that the gas molecules of CO and CO2 are bound to the CdS bilayer by vdW interactions rather than a chemical bond. When SO2, H2S, and SO are adsorbed on a CdS bilayer, the ELF value in the interlayer areas indicates the establishment of chemical bonds. Considering the substantial ELF plot, quantity of charge transfer, and high adsorption energy, it is shown that ionic bonds, rather than covalent bands, are produced during the adsorption of SO2, H2S, and SO.95 This proves a chemisorption property of the SO2/H2S/SO– CdS system.
The curves of absorption coefficient (α) of the CdS bilayer before and after adsorption are shown in Fig. 12(a). The pristine bilayer absorption peak is 91682.55 cm−1 at 7.57345 eV. However, the high absorption occurs between 3 and 22 eV, while the edge absorption starts at 0.01 eV (far-IR region) in the pristine CdS bilayer. The absorption coefficients fall within the range of 24
070.17 cm−1 to 12
684.06 cm−1. Thus, the pristine CdS bilayer can absorb light from the IR to the UV regions, and it can be used in a various applications. It is common knowledge that adsorption causes changes to a material's optical properties. Consequently, it is important to further distinguish the unsatisfactory situation of the adsorption of gas molecules by looking into the considerable alteration of optical properties following the adsorption mechanism.
Moreover, SO/CdS has the highest absorption peak (95523.86 cm−1 at 7.70525 eV), followed by CO (93
221.69 cm−1 at 7.60208 eV), H2S (92
399.88 cm−1 at 8.19712 eV), SO2 (89
072.10 cm−1 at 7.75403 eV) and CO2 (84
655.70 cm−1 at 8.19044 eV). Notably, the gas molecules adsorbed on the CdS bilayer cause the UV absorption peak to rise compared to the peak of the pristine bilayer. As shown from the above result, the molecules adsorbed on the CdS bilayer are useful in UV-sensitive optoelectronic and photoelectric devices. Fig. 12(b) shows the refractive index curves for pristine CdS bilayer and adsorption gas. For pristine CdS, the maximum refraction index value is 1.9286 at 1.38763 eV. Following gas adsorption, the refractive index decreases as photon energy increases, settling at a roughly constant value of 0.96 at around 30 eV. The maximum refractive index is for H2S (1.87142), followed by CO2/CdS (1.83241), and then CO (1.81326), SO (1.81236), and SO2 (1.80687), respectively. By summing the real and imaginary components, we will get the dielectric function, which appears like the below:101,102
ε(ω) = ε1(ω) + iε2(ω) | (4) |
![]() | (5) |
![]() | (6) |
Moreover, multiple peaks are observed in the adsorption systems with gas molecules (Fig. 12(c)). These dielectric function curves vary, but at an energy of 29 eV, they approach and remain fixed. When compared to the pristine bilayer's peak, the imaginary dielectric function exhibits the same behaviour as its real component equivalent, with the number of peaks increasing and the maximum peak value decreasing. The H2S molecule possessed the highest peak of the imaginary dielectric function, which equals 3.35205 at 3.10738 eV.
The real and imaginary conductivity curves of the pristine CdS bilayer and the adsorption gas are shown in Fig. 12(e) and (f). The maximum real conductivity of the pristine CdS bilayer is 1.56319 at an energy of 5.76363 eV, which lies in the UV region. Conductivity gradually decreases after the gas molecules adsorption on CdS bilayer.
Where (1.55137) is the highest value for the conductivity of the gas SO, followed by CO (1.52149), H2S (1.46892), CO2 (1.42478), and SO2 (1.40284), respectively. For the imaginary conductivity of the pristine CdS bilayer, The maximum peak is 0.77882 at an energy of 8.14071 eV, and it lower once gas molecules are adsorbed on it.
The loss function curves for a pristine CdS bilayer and adsorption gas as a function of photon energy are shown in Fig. 12(g). The curve of the pristine CdS bilayer exhibits a noticeable peak with a value of 1.11924 at an energy of 8.762 eV, which is in the UV region. Compared to the pristine bilayer's peak, all molecules adsorbed on the CdS bilayer exhibit higher peaks.
The curves of CdS bilayer reflectivity before and after adsorption is shown in Fig. 12(h). Two lower peaks for the pristine CdS bilayer were found at 5.95271 eV (0.13493) and 3.62965 eV (0.12175). In addition, the higher peak lies at 7.73553 eV (0.13518) in the UV region. As gas molecules are absorbed, the maximum reflection peak values rise. The UV region is still displaying large peaks at this time.
![]() | (7) |
In addition, Q of the CO and CO2 adsorption systems are (0.02 and −0.02) |e|, respectively; this indicates that charges are transferred from the CdS bilayer to the CO2, whereas for CO, which is the opposite. However, the covalent radii of the C and Cd atoms (rC–Cd = 2.28 Å) and the O and Cd atoms (rO–Cd = 2.24 Å) are both smaller than the calculated adsorption distance,81 confirming the existence of a weak van der Waals force between the CdS bilayer and the gas molecules.95
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