Livia
Didonè
a,
Yunseok
Shin
b,
Alessandro
Silvestri‡
*c,
Maurizio
Prato
cde,
Sungjin
Park
*b and
Alberto
Bianco
*a
aCNRS, UPR3572, Immunology, Immunopathology and Therapeutic Chemistry, ISIS, University of Strasbourg, 67000 Strasbourg, France. E-mail: a.bianco@ibmc-cnrs.unistra.fr
bDepartment of Chemistry and Chemical Engineering, Inha University, 100 Inha-ro, Nam-gu, Incheon 22212, Korea. E-mail: sungjinpark@inha.ac.kr
cCenter for Cooperative Research in Biomaterials (CIC biomaGUNE), Basque Research and Technology, Alliance (BRTA), Paseo de Miramón 194, 20014 Donostia, San Sebastián, Spain
dIkerbasque, Basque Foundation for Science, 48013 Bilbao, Spain
eDipartimento di Scienze Chimiche e Farmaceutiche, INSTM UdR Trieste, University of Trieste Via Licio Giorgieri 1, 34127 Trieste, Italy
First published on 15th December 2023
Carbon nitride (C3N4) is an innovative material with a high potential in many applications including energy storage, catalysis, composites, and biomedicine. C3N4 appears remarkably interesting not only for its properties but also because its simple preparation routes involve low-cost starting materials and reagents. However, there is still a lack of information on its degradability. For this reason, in this study, we evaluate the environmental persistence of C3N4 and its oxidized form by applying the photo-Fenton reaction. The morphological and structural changes of both materials were monitored by transmission electron microscopy and Raman spectroscopy respectively. In addition, electrochemical impedance spectroscopy has been used as an original technique to validate the degradation process of C3N4.
Graphitic carbon nitrides have drawn a lot of attention due to their features, which can be attributed to their layered structure. Besides the simplicity of its synthesis, this material is characterized by high stability, low toxicity, wide visible light absorption range, and an ideal semiconducting behavior. Different C3N4 are currently applied for photocatalysis and energy storage.3,4 For example, they are used as anodic components in rechargeable lithium-ion batteries.5 Moreover, C3N4 can be used as saturable absorber,6 or in membranes, in solar and fuel cells, and they are effective in removing contaminants from water, air, and soil.7,8 Since C3N4 resulted to be biocompatible, its use in biomedicine, biosensors, for photocatalytic sterilization, photodynamic therapy, and as drug carriers has been exploited.9 Recently, C3N4 was evaluated as an efficient carrier for the anticancer drug cisplatin.10 Nevertheless, it must always be considered that the interaction of nanoparticles with the biological systems or the environment might generate toxic effects due to their small size, large surface area, and high reactivity. Overall, the physicochemical properties of a nanomaterial have a huge influence on its safety. For example, the degree of dispersion of carbon nanomaterials has an impact on their in vitro and in vivo toxicity.11 In order to broaden C3N4 applications in the biomedical and other fields, it is fundamental to examine the degradability profiles of this 2D material. The reported cytotoxicity effects of C3N4 and other carbon-based nanomaterials include reactive oxygen species generation, DNA damage, lysosomal damage, mitochondrial dysfunction, and eventual cell death via necrosis or apoptosis.12,13 Cellular assays on lung epithelial cell lines (e.g., A549) showed that for C3N4 the toxicity resulted to be dose-dependent, and it was generally rated lower than other 2D materials, such as graphene oxide (GO).14
However, no data is available on the (bio)degradability of C3N4. Thus, it is crucial to assess the degradability of this type of carbon-based nanomaterials, to foresee and limit their impact on health and the environment. A substance can undergo a mechanical, chemical, or biological degradation process. Biodegradation aims to bio-transform, recycle, and detoxify the concerned material. For example, in the biomedical field, it is crucial to consider the degradation of a therapeutic nanomaterial, since it should occur at the most proper time and place, namely the targeted pathological site, to allow the pharmacological benefit to take place.15 Through the years, many studies on carbon-based nanomaterial degradation have been reported, but there is a lack of information regarding the degradability of C3N4. Overall, it was demonstrated that carbon-based nanomaterials are sensitive to the treatment with different types of peroxidases, where hydrogen peroxide is involved in the catalytic process. For example, it was shown that the biodegradation of GO by human myeloperoxidase is dispersibility-dependent.16 Moreover, it was proven that the degradation of GO performed by horseradish peroxidase (HRP) is accelerated and more efficient when GO is functionalized with coumarin or catechol, which are specific ligands of HRP.17 In this regard, the concept of degradation-by-design has been proposed, where the chemical functionalization of 2D materials enhances their degradability, and, accordingly, their safety.18 In another study, graphene quantum dots (GQDs) were degraded by myeloperoxidase (MPO) via an oxidative enzymatic process.19
Many of the studies focused on the biodegradation of carbon-based nanomaterials are based on the simulation of oxidative conditions, in order to evaluate the behavior of a particular material when it comes in contact with the environment or a living organism. According to the literature, oxidative enzymes such as HRP and MPO are efficient agents for the biodegradation of carbon-based nanomaterials.20 In addition to enzyme-catalyzed biodegradation, in an environmental context, the photo-Fenton reaction showed also significant results21 and has been widely used to decompose aromatic organic pollutants in water.22
Since there is no sufficient knowledge regarding the degradation of graphitic carbon nitrides, we relied on our previous study conducted on the biodegradation of hexagonal boron nitride (hBN), since this material is known for its chemical inertness and high oxidation resistance.23 The photo-Fenton reaction was applied as a first approach to study C3N4 degradation in environmental conditions. This model reaction was chosen to develop effective tools to monitor the C3N4 degradation process, that in future works will be applied to the enzymatic degradation. The photo-Fenton reaction is a UV-assisted version of the Fenton reaction, where the UV light enhances the degradation rate, by accelerating the production of chemically reactive hydroxyl radicals.
The effects of this reaction were monitored by transmission electron microscopy (TEM) imaging and by electrical impedance spectroscopy (EIS). EIS is a novel technique in the study of 2D material degradation, based on the perturbation of an electrochemical system in the equilibrium state, through the application of an oscillating voltage over a wide range of frequencies. The sinusoidal current response is monitored and the resistance of the material is recorded as a function of the perturbation frequency (impedance). EIS is a powerful technique able to discriminate, in the frequency domain, the electrochemical events occurring contemporarily at the interface between the material and the electrolyte. Therefore, EIS is a unique tool to investigate the changes in the material properties in relation to the surface structure and chemical composition. Based on these principles, EIS is largely used in the study of metal corrosion. Although 2D material degradation is conceptually a similar event, EIS has never been applied in this field.
The second sample (oxCNMel) was synthesized by a two-step process starting from melamine. Heat treatment of melamine generated carbon nitride materials, followed by a chemical modification using H2SO4 and KMnO4 as strong oxidizing reagents, afforded oxCNMel (Scheme 2). The purpose was to obtain a material that would be easier to degrade, owing to the presence of the oxygenated functions. We point out that it was not possible to obtain this oxidized form of carbon nitride from CNUrea because this latter is too sensitive to strong acidic conditions, which lead to complete degradation during the oxidation process. This can be considered a novel route to produce small sheets of water-dispersible and atomically thin oxidized carbon nitride-based materials.25
Both CNUrea and oxCNMel were characterized using complementary spectroscopic and microscopic techniques (see data and discussion in ESI, Fig. S1–S7†). The characterization revealed that CNUrea contains tri-s-triazine-based crystalline C3N4 structures, while oxCNMel contains heavily oxidized C3N4-based structures with significantly damaged sp2 networks.
For the degradability studies, stock water dispersions (0.78 mg mL−1) were prepared using a cup-horn sonicator, operating for 60 min. The photo-Fenton reaction was then applied by incubating the dispersions of the two materials in an acidic aqueous solution, where FeCl3 and H2O2 were regularly added as catalysts. In acidic conditions, Fe3+ mainly exists as Fe(OH)2+, and effectively absorbs UV light. In this way, a disproportionation occurs being Fe(OH)2+ transformed into Fe2+ and hydroxyl radicals, that generate the oxidation conditions of the materials (Fig. S8†). The process is accelerated by UV irradiation at a wavelength of 365 nm. The reaction to degrade both carbon nitride materials was carried out for 100 h at room temperature, by renewing FeCl3 every 35 h and H2O2 every 10 h. TEM is commonly employed to follow the progress of the nanomaterial degradation,20 even though this technique provides qualitative rather than quantitative results. Before starting the degradation process, CNUrea appears round shaped and organized as layered structures. Despite the long sonication process, the particles are not homogeneously distributed on the grid, but they are present as aggregates (Fig. 1).
TEM images of the samples were captured at different time points. To monitor the process of degradation on the material, and to obtain significant information about the morphological changes, the samples were observed first after 50 h (Fig. 2). At this time point, some pores inside the structure started forming, but it is after 100 h that the edges appear jagged and the number of holes in the material becomes more significant (Fig. 3).
We already proved that the treatment of hBN for 100 h in the conditions of the photo-Fenton reaction resulted in the successful degradation of the material, since its 2D layered structure was completely lost at the end of the process. During this experiment with C3N4, we expected to achieve a similar result in the same time frame. However, even if the TEM images allow us to state that the oxidation process has modified the material, the degradation was not completed.
The TEM analysis of oxCNMel before degradation, evidenced a less homogeneous material, with many irregular layers surrounding one another (Fig. 4).
To evaluate the degradation of oxCNMel, the samples were observed again after 50 and 100 h of reaction. In the middle of the process, no significant changes were visible (Fig. 5, left). However, at the end of the photo-Fenton reaction, the morphology of the material showed evident modifications (Fig. 5, right). In facts, there are holes inside the structure, and the edges appear fragmented.
Overall, for both materials, the results of the TEM analysis show an incomplete degradation of the starting material by the end of the experiments. This suggests that the degradation took place, but only partially. Moreover, inspired by the study of hBN degradation,23 Raman spectroscopy was considered as an additional characterization technique to follow the degradation process. This kind of spectroscopy is known to be remarkable not only for being nondestructive, fast and high-resolution, but also for its ability to provide a comprehensive overview of the structural electronic information of a material.26 Carbon-based nanomaterials present diagnostic bands in the Raman spectrum that correspond directly to a specific vibrational frequency of a molecular bond. During the degradation process, it is likely to observe the decrease in intensity of these distinguishing peaks. For example, a complete disappearance of the band was seen at the end of the photo-Fenton degradation of hBN.23 In the case of C3N4 both in powder and on the residue obtained depositing and drying the solution on a silica wafer, CNUrea and oxCNMel revealed a very strong autofluorescence, which hampered the observation and evolution of their characterizing peaks during the photo-Fenton process (Fig. S9†).
Although TEM allowed to see the onset of the biodegradation process of these two types of carbon nitrides, the need to broaden the understanding of this phenomenon was relevant. To this aim, EIS proved to be effective. EIS is an electrochemical technique used to study the phenomena happening at the interface of an electrode and a solution of electrolyte. When an electrode is immersed in an electrolyte and polarized, a series of phenomena take place at the liquid–solid interface. Some of the main phenomena involved include the formation of an electrical double layer at the interface, charge transfer through the materials, and the diffusion of chemical species from the bulk of the electrolyte to the surface.27 Although all these phenomena take place at the same time, EIS can resolve them by applying an oscillating potential to the electrode and measuring the impedance in function of the frequency. The contribution of each of these processes depends on the chemical composition of the material at the interface and on its morphology.28 The photo-Fenton reaction is expected to degrade C3N4 modifying its morphology, oxidation degree and introducing defects in the crystalline structure affecting the behavior of the material at the interface with an electrolyte solution. To confirm our hypothesis and prove that EIS can be used to study the degradation of 2D materials, we drop-cast aliquots of the two types of C3N4 on top of a glassy carbon electrode (GCE), sampled at time 0 and 100 h of the photo-Fenton reaction. Potassium ferricyanide (K3[Fe(CN)6]) was used as an electrochemical mediator to investigate the phenomena happening at the interface with the material. E1/2 of K3[Fe(CN)6] (0.21 V) was selected as operational potential, as at this potential the mediator generates a faradaic current, which is exploited to study the properties of the material. Small perturbations of 10 mV were applied with a range of frequencies between 100 kHz and 10 mHz. In Fig. 6A and C it is possible to see the Bode plots for CNUrea and oxCNMel, representing the impedance of the material in function of applied frequency. At high frequencies (up to 1 kHz) the value of impedance is constant and does correspond to the uncompensated resistance of the electrochemical system. In the middle region, we can see an increase in the impedance due to the charge transfer process across the material. Finally, the rapid increase in the impedance at low frequencies can be attributed to the formation of a depletion layer, due to the consumption of the mediator close to the electrode surface. When this happens, the value of impedance is governed by the diffusion rate of the electrochemical mediator from the bulk of the solution to the surface of the electrode.28
In case of both CNUrea and oxCNMel, higher values of impedance were recorded for the samples which underwent the photo-Fenton reaction. However, for oxCNMel the difference is less pronounced, as the starting material was already oxidized and presented a higher impedance compared to CNUrea. The Nyquist plots (Fig. 6B and D) represent the imaginary (Z′′) part of the impedance plotted as a function of the real one (Z′). These graphs give a good visual interpretation of the phenomena taking place at the interface of the electrode. The semicircle at the beginning of the curve confirms the presence of a charge transfer process. The larger is the diameter of the semicircle, the higher is the resistance of the material at the electron transfer. The tail of the curve with a slope of 45° is representative of the diffusion processes taking place from the bulk of the solution to the interface. From the Nyquist plot, it is possible to extrapolate quantitative data, by fitting it with an equivalent circuit. The circuit chosen in this work is represented in Fig. 6E and is composed of a parallel resistance and a constant phase element (CPE) in series with a Warburg (W) element. RS represents the uncompensated resistance. RCT represents the resistance to electron transfer imposed by C3N4. CPE is an imperfect capacitor and represents the formation of a double layer of charges at the interface with the electrolyte. Finally, W is a mathematical equation representing the diffusive process. The most significant value that can be obtained from the fitting is the RCT. For CNUrea, RCT increases drastically after the photo-Fenton process from 1.38 kΩ to 3.06 kΩ indicating that the reaction induces the formation of defects and oxidized sites in the carbon nitride structure, and therefore can partially degrade it. Due to the Hummers oxidative process, the charge transfer resistance of the oxCNMel is instead high already before the photo-Fenton reaction (3.1 kΩ). Control reactions without Fe, H2O2, or UV light treatment were performed. In the three cases no variation of the resistance was detected, confirming that in the absence of one of the three factors the degradation does not take place (Fig. S10†). The evolution in time of the C3N4 degradation process was investigated by taking aliquots from the reaction mixture at the time points 20 h and 50 h (Fig. S11†). Due to the reduced volume of the aliquots, less material was available to perform these time-resolved measurements. Consequently, we drop cast 10 μl of 0.1 mg ml−1 C3N4 solution on the GCE. The lower amount of C3N4 deposited resulted in higher charge transfer resistance values. Nevertheless, the trend seen in Fig. 6 is confirmed: the resistance to the charge transfer of both CNUrea and oxCNMel increases with time, corroborating that this effect is correlated with progressive material degradation. Furthermore, these data confirm that the changes in RCT for oxCNMel are less prominent, since the oxidized material presents higher charge resistance values before the photo-Fenton reaction.
In summary, the results of TEM and EIS evidenced a partial degradation of the two carbon nitrides during the course of the photo-Fenton reaction. While the onset of CNUrea biodegradation was clearly demonstrated, the morphological changes in oxCNMel were more difficult to assess. This is likely because the initial oxidation of this material already disrupted its graphitic structure, resulting in a difficult distinction of the contribution of the Hummers reaction from the oxidative degradation operated by the photo-Fenton reaction. In conclusion, the synergy between the two spectroscopic and microscopic methods used in this study contributed to a better understanding the degradation process of graphitic carbon nitrides and could be applied to other 2D materials.
Footnotes |
† Electronic supplementary information (ESI) available. See DOI: https://doi.org/10.1039/d3nr04502a |
‡ Current address: Department of Molecular Sciences and Nanosystems, Ca’ Foscari University of Venice, 30170, Venice, Italy. E-mail: alessandro.silvestri@unive.it |
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