Abstract
Two-dimensional (2D) ternary materials recently generated interest in optoelectronics and energy-related applications, alongside their binary counterparts. To date, only a few naturally occurring layered 2D ternary materials have been explored. The plethora of benefits owed to reduced dimensionality prompted exploration of expanding non-layered ternary chalcogenides into the 2D realm. This work presents a templating method that uses 2D transition metal dichalcogenides as initiators to be converted into the corresponding ternary chalcogenide upon addition of copper, via a solution-phase synthesis, conducted in high boiling point solvents. The process starts with preparation of VSe2 nanosheets, which are next converted into Cu3VSe4 sulvanite nanosheets (NSs) which retain the 2D geometry while presenting an X-ray diffraction pattern identical with the one for the bulk Cu3VSe4. Both the scanning electron microscopy and transmission microscopy electron microscopy show the presence of quasi-2D morphology. Recent studies of the sulfur-containing sulvanite Cu3VS4 highlight the presence of an intermediate bandgap, associated with enhanced photovoltaic (PV) performance. The Cu3VSe4 nanosheets reported herein exhibit multiple UV–Vis absorption peaks, related to the intermediate bandgaps similar to Cu3VS4 and Cu3VSe4 nanocrystals. To test the potential of Cu3VSe4 NSs as an absorber for solar photovoltaic devices, Cu3VSe4 NSs thin-films deposited on FTO were subjected to photoelectrochemical testing, showing p-type behavior and stable photocurrents of up to ~ 0.036 mA/cm2. The photocurrent shows a ninefold increase in comparison to reported performance of Cu3VSe4 nanocrystals. This proves that quasi-2D sulvanite nanosheets are amenable to thin-film deposition and could show superior PV performance in comparison to nanocrystal thin-films. The obtained electrical impedance spectroscopy signal of the Cu3VSe4 NSs-FTO based electrochemical cell fits an equivalent circuit with the circuit elements of solution resistance (Rs), charge-transfer resistance (Rct), double-layer capacitance (Cdl), and Warburg impedance (W). The estimated charge transfer resistance value of 300 Ω cm2 obtained from the Nyquist plot provides an insight into the rate of charge transfer on the electrode/electrolyte interface.
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Introduction
A major advantage of the 2D materials, whether intrinsically layered in structure or not, is their amenability to solution processing and deposition on flexible substrates. Ultra-thin films fabricated from 2D materials could survive sustained stress and strain compliance on flexible supports, and thus, could revolutionize diverse applications such as optoelectronics, valleytronics, energy harvesting, conversion and storage, and biomedicine1,2,3.
Among several classes of 2D compounds, transition metal dichalcogenides (TMDCs) gained considerable interest4,5,6 after graphene isolation7 in 2004. While graphene features a zero-band-gap, the plethora of 2D inorganic materials in the TMD family could act as insulators (e.g., hexagonal boron nitride–hBN), semiconductors (e.g., MoS2, WS2, WSe2), or superconductors (e.g., NbSe2, NbS2), on the account of their various crystal structures and polytypism. Structurally, TMDCs with the general formula of MX2, have an individual layer of transition metal atoms (M = Mo, W, Ta, etc.) sandwiched between two chalcogen layers (X = Se, S, Te)8. The plethora of metal–chalcogen combinations and the large number of synthetic methods to fabricate these useful materials make TMDCs a rich platform for further chemical transformations, and we aim to demonstrate synthetic methods to convert them into 2D ternary materials.
Recently, 2D ternary materials raised interest in optoelectronics and energy-related applications, given the degree of freedom added through introduction of the third element9. Four types of 2D ternary metal chalcogenides have been identified and synthesized in the past few years: 2D ternary chalcogenides with well-defined ternary layered crystal structures (e.g., TaNiS5 and Cu2WS4), alloyed TMD nanosheets (e.g., MoS2xSe2(1−x) and MoxW1−xS2, where x = 0.5), heteroatom-doped TMD nanosheets (e.g., Re-, Co-, V-, Cr-, or Pt-doped MoS2), and lateral or vertical metal chalcogenide hetero-nanostructures (e.g., MoS2–MoSe2 and MoS2–WS2)10.
Introduction of a heteroatom into a ultrathin 2D TMDC nanosheets to construct a 2D ternary metal chalcogenide nanosheet is a compelling way to obtain unprecedented morphologies of compounds known only in bulk10. Ternary 2D nanosheets are of recent interest in important applications, including energy storage (e.g. TiNb2O7—due to its high theoretical specific capacity)11,12; high-performance photodetectors (e.g. CuInSe2), and highly-sensitive/selective fluorescence DNA sensors (e.g. Ta2NiS5)13.
Various synthetic strategies have been explored to produce 2D ternary materials with well-defined ternary 2D crystal structures, comprising top-down exfoliation, bottom-up chemical vapor deposition (CVD), and solution synthesis methods14; often, a combination of two different methods, e.g., chemical vapor transport (CVT) and mechanical exfoliation, is required for preparation of the final product9. Several challenges, including harsh preparation conditions, and subsequently safety of the process, along with reproducibility and preparation time9,10,13,15 are encountered in all of the aforementioned approaches. To advance the field of 2D ternary materials and accommodate an increasing demand for a number of applications, versatile synthetic methods that are robust, simple, safe and time-effective, became a practical necessity. Solution-based methods have several significant advantages over solid-state methods to synthesize nanomaterials including: (1) low reaction temperatures; (2) size-selective growth; and (3) morphological control16.
The class of sulvanites Cu3MX4 (M = V, Nb, Ta; X = S, Se, Te), received recent attention for the outstanding optoelectronic properties and promising thermoelectric properties17,18,19,20, making these compounds attractive for application as solar photovoltaic absorbers, transparent conductors, ion conductors and photocatalysts19,21,22.
The ability to generate such materials in 2D could enable fabrication of ultra-thin-films that would revolutionize a variety of applications. However, typical one-pot solution-based synthesis utilized for synthesizing copper chalcogenides for many of these materials result in nanoparticles23,24.
The sulvanite family is known for decades, but it was only recently explored at the nanoscale. Solution-phase synthesized Cu3VS4 nanocrystals23,25 show an interesting UV–Vis absorption, with three absorption peaks in the visible range, attributed to the presence of the intermediate band gap (IB) in their electronic structure25. We recently showed that Cu3VSe4 nanocrystals, synthesized through a solution process, showcase a similar UV–Vis absorption pattern, suggesting the presence of the IB in the nanoscale vanadium-sulvanites26.
Intermediate band semiconductors recently raised special attention for their potential to exceed the Shockley–Queisser limits in thin-film solar photovoltaics. Semiconductors with an intermediate band can absorb energies below the bandgap energy through two optical transitions from the valence to the intermediate band and from the intermediate to the conduction band, resulting in enhanced conversion efficiency27,28,29. Besides, the three optical transitions caused by the intermediate band can also lower the energy losses relying on thermal relaxation of optically excited carriers30. Theoretical predictions for a solar cell using an intermediate band semiconductor as absorber, could reach an efficiency of 63.1% in a single junction, exceeding the Shockley–Queisser barrier31.
We recently demonstrated that kesterite Cu2ZnSn(S,Se)4 (CZTSSe) could be prepared in a quasi-2D morphology through a cascade reaction starting from a binary chalcogenide SnSe2 with nanosheet morphology. Upon addition of copper and subsequently zinc, quasi-2D CZTSSe with inherited nanosheet morphology formed32. Our recent report on synthesizing Cu3VSe4 cubic nanocrystals using a hot-injection method, paved the road toward obtaining nanoscale Cu3VSe4. The method involves temperatures up to 260 °C, and leads to a high purity material in matter of hours26, in comparison with the six weeks required by the solid state synthesis conducted at 600 °C33.
Our hypothesis was that Cu3VSe4 could be synthesized in nanosheet morphology, and that the approach is amenable to other multinary chalcogenides, including other sulvanites. In this work, we demonstrate a facile synthesis of Cu3VSe4 nanosheets (NSs) using the same template approach that allows a seamless morphing of the nanosheet from the binary compound to the ternary one. The solution-phase process involves synthesis of VSe2 nanosheets followed by insertion of Cu(II) cations in the same reaction vessel, leading to Cu3VSe4 nanosheets.
VSe2 nanosheets were prepared at 250 ℃ by hot injection synthesis and characterized by X-ray diffraction and transmission electron microscopy (TEM), demonstrating the 2D morphology. Upon introducing Cu cations into VSe2 nanosheets, the quasi-2D Cu3VSe4 formed, exhibiting large surface area (micron size) nanosheets, thus retaining the template morphology. The Cu3VSe4 formation mechanism was investigated by X-ray diffraction, indicating that the insertion and new compound formation happens within minutes. It is remarkable that the Cu3VSe4 nanosheets maintain the crystal structure of bulk sulvanites (cubic), as identified by XRD. The 2D morphology was confirmed by TEM and SEM. Three distinct absorption bands similar to Cu3VS4 NCs were investigated by UV–Vis–NIR measurements. Additionally, the photocurrent generated by a Cu3VSe4 NSs thin film on FTO evidences the potential of Cu3VSe4 NSs in solar photovoltaic applications.
Results and discussion
VSe2 nanosheets characterization
The VSe2 nanosheets, obtained through a modified literature procedure34, show high crystallinity; the X-ray diffraction pattern of the synthesized VSe2 corresponds to the 1 T-VSe2 polytype35 belonging to the P ¯3m1 space group (PDF# 40723) (Fig. 1a). The Raman spectrum of the synthesized VSe2 (Fig. 1b) exhibits two primary peaks (254.3 cm−1 and 282.3 cm−1) where the primary peak (around 251.3 cm−1) corresponds to E2g in-plane vibration mode while the peak at 286 cm−1 is consistent with A1g out-of-plane vibrational mode. The slight redshift (5–10 cm−1) when compared with literature reported data could be attributed to the layered structure34,36. The TEM image in Fig. 1c shows micrometer-size lateral dimension VSe2 NSs. The SEM image of the synthesized VSe2 nanosheets (Fig. 1d), further confirms the nanosheet morphology. The powder subjected to SEM was not subjected to exfoliation and shows an aggregate of VSe2 nanosheets.
Cu3VSe4 nanosheets characterization
The preparation of Cu3VSe4 NSs presented herein demonstrates the ability to maintain the morphology and the large dimension of the template upon copper introduction into VSe2 NSs. By contrast, a similar copper insertion, done at 25 °C, was reported for In2Se3; however, the experiment rendered wrinkled CuInSe2 nanosheets which did not resemble the template. Further, the same reaction conducted at elevated temperatures results in nanodisks37.
The X-ray diffraction pattern in Fig. 2a, agrees with the bulk XRD, showing cubic Cu3VSe4 structure (PDF# 40125, a = b = c = 5.572 Å) in the P ¯43m space group. Raman spectra of as-synthesized Cu3VSe4 in Fig. 2b presents five peaks (134.3 cm−1, 158.3 cm−1, 185.6 cm−1, 219.6 cm−1, and 343.3 cm−1), consistent with the Cu3VSe4 nanocrystals Raman26. The intensity ratio of the peaks of Cu3VSe4 NSs is different from the ones attributed to the nanocrystals could be attributed to the morphology change34,38.
To investigate the thermal stability of the Cu3VSe4 nanosheets, thermogravimetric analysis (TGA) was performed in the temperature interval 25–800 ℃ at a ramping rate of 20 ℃ min−1, under argon atmosphere. Figure 2c displays the TGA curve of the synthesized Cu3VSe4 nanosheets, showing a rapid weight loss that starts at 362 ℃, indicating the decomposition onset. As expected, Cu3VSe4 with nanosheet morphology have much lower thermal stability than Cu3VSe4 nanocrystals. The slight weight loss between 200 and 350 ℃ is characteristic to the decomposition of the organic ligand residues originated from the synthesis.
The morphology of the Cu3VSe4 NSs was evaluated by TEM and SEM. At low magnification, TEM imaging (Fig. 3a) reveal a nanosheet morphology with Cu3VSe4 NSs possessing a large lateral dimension (several hundred nanometers). At higher magnification (Fig. 3b) the images suggest a belt-shape concatenation of small a square-shaped nanocrystal, which self-assemble to render the quasi-2D nanosheets. The d-spacing of ~ 5.32 nm and 3.21 nm, determined by electron diffraction (Fig. 3c,d) correspond to the (100) and (111) facets of cubic Cu3VSe4. The nanosheet morphology is further supported by SEM imaging (Figs. 4a and 5); the nanosheets self-assembly in an arrangement reminiscent of flower petals. The uniform distributions of Cu, V, Se is reflected in the elemental maps collected by SEM–EDS (Fig. 4b–d, respectively). Importantly, the thickness of the nanosheets subjected to AFM is in the vicinity of 10 nm, as illustrated in Figure S1 (“Supporting Information”). As shown in Fig. 5, using VSe2 NSs as template, we obtained Cu3VSe4 NSs, demonstrating the ability of the synthetic method to maintain the morphology and the large dimension of the starting materials. To assess the chemical and electronic structures of the synthesized Cu3VSe4 nanosheets, XPS was performed as shown in Supplementary Figure S2, indicating that the oxidation states of Cu and Se in Cu3VSe4 NSs are + 1 and − 2, respectively, as the same in the Cu3VSe4 nanocrystals, and the vanadium is in presence of V5+ but with a negative shift of 2.5 eV in the binding energy of V5+ (The detailed discussion can be found in “Supporting Information”)26.
Study of the Cu3VSe4 formation mechanism
To get insight into the conversion mechanism of VSe2 NSs to Cu3VSe4 NSs, we conducted a time study, involving a series of syntheses with all parameters kept constant, excepting the reaction times. The corresponding XRD patterns of the products are showed in Fig. 6. The study indicated that the primary crystalline phase in all products is cubic Cu3VSe4 with representative 2θ peaks of 15.9°, 27.7°, and 46.03°. Interestingly, Cu3VSe4 NSs forms within 1 min after the Cu2+ injection. A minor amount of Cu2Se and trace amounts of VSe2 were present in the products for the reactions conducted for 1 min, 5 min, and 15 min. When the reaction time exceeded an hour, VSe2 templating material and Cu2Se impurities are no longer present and the sole product was Cu3VSe4 NSs. Likewise, when extending the reaction time to two hours, the product shows the same Cu3VSe4 phase with a slightly higher crystallinity. It is important to note that no decomposition occurs.
We posit that the 2D layering nature of the VSe2 template provides a short diffusion distance for the injected Cu2+ which, along with the large reaction surface area, enables a short reaction time. Provided that the reaction is conducted in a cascade, involving VSe2 formation and further addition of Cu(II), unreacted Se from VSe2 formation could react with Cu(II) resulting in Cu2Se impurities. It is conceivable that as the reaction proceeds, the formed Cu2Se and unreacted VSe2 NSs form Cu3VSe4. In all reactions, the formed Cu3VSe4 maintains the 2D morphology.
Optical properties of Cu3VSe4 NSs
To assess absorption characteristics of Cu3VSe4 nanosheets, UV–Vis–NIR spectra of the synthesized Cu3VSe4 NSs were measured (Fig. 7a; all measurements used Cu3VSe4 NSs ethanol dispersions). All spectra show three absorption peaks located at around 382 nm, 552 nm, and 664 nm. The three peaks are a signature of the nanoscale sulvanites studied to date (Cu3VSe4 and Cu3VSe4 NCs) and it could be inferred from all published work on several ternary chalcogenides that the Cu3VSe4 with the nanosheet morphology present an intermediate bandgap. Similar to reported assignments for Cu3VS4 and Cu3VSe4 NCs, and other ternary chalcogenides26,27,39 the three absorption peaks could be ascribed to the following bandgaps: VB-CB (3.24 eV), VB-IB I (2.24 eV), and VB-IB II (1.86 eV), respectively, when converting wavelength in photon energy.
Photoluminescence (PL) measurements were conducted to determine the bandgap of the nanosheets for comparison with the reported theoretical bandgap. Figure 7b shows the photoluminescence (PL) spectrum of as-synthesized Cu3VSe4 NSs, with a significant emission peak at 690 nm when using 460 nm as the excitation wavelength. Interestingly, the variation of the excitation wavelength from 430 to 520 nm at 10 nm intervals leads to PL emission peak steadily redshift from 650 nm (1.9 eV) to 780 nm (1.59 eV) (Supporting Information Figure S7). The excitation-dependent emission feature could be associated with the thickness distribution of Cu3VSe4 NSs and the effect of different surface functionalization on the NSs40,41,42,43. However, the emission peak at 690 nm has the highest intensity, suggesting that for most of the Cu3VSe4 NSs product, 460 nm is the optimal excitation wavelength, corresponding to a band gap of 1.80 eV.
To interrogate the effect of surface functionalization on the PL spectra of Cu3VSe4 NSs by conducting PL measurements on the Cu3VSe4 NSs that were subjected to ligand exchange. Although the same distribution of emission wavelengths remained, the main peak remained at 690 nm for the 460 nm excitation wavelength (Supporting Information Figure S3). The impact of thickness dependence of PL emission was documented for other materials, including layered 2D MoS2 44 and WS2 45. The FTIR spectra in Figure S4 (“Supporting Information”) demonstrated the complete removal of the organic ligands after the ligand exchange.
Theoretical predictions place sulvanites, including Cu3VSe4, in the optically active materials category, holding promise in applications including photodetectors and photovoltaics19,21. A photocurrent evaluation was carried out using Cu3VSe4 thin films obtained by depositing nanosheet dispersions (inks) on conductive, fluorine-doped tin oxide (FTO) substrates, in a photoelectrochemical setting. The fabricated Cu3VSe4 NSs-FTO thin film shows a homogeneous distribution of the nanosheets on the substrate and a uniform thickness of about 604 nm (Supplementary Figure S5). The Cu3VSe4 NSs thin films were further used to investigate the photoresponse of Cu3VSe4 NSs.
Electrolyte pH affects the photoelectrochemical behavior of the semiconductor, impacting the rate of photo-reduction/photo-oxidation as well as the rate of electron–hole recombination in the system46,47. The current density–voltage (J–V) curves of Cu3VSe4 NSs were therefore explored, using a 0.6 M KCl aqueous solution with varying pH as electrolyte (Fig. 8a). The Cu3VSe4 NSs-FTO thin film exhibits a cathodic photocurrent response with highest photocurrent obtained in the electrolyte with pH 4, indicating that Cu3VSe4 is a p-type semiconductor. The cathodic photocurrent generation could be attributed to the H+ reduction26; Cu3VSe4 NSs illumination drives generation of electron/hole pairs, with the photogenerated electrons reaching the electrode/electrolyte interface reducing H+ to H2 32. The effect of pH can be understood in terms of surface reaction on the Cu3VSe4 NSs-FTO thin film. At low pH, namely using acid KCl aqueous solution as the electrolyte, the proposed H+ reduction reaction at cathode (Cu3VSe4 NSs-FTO thin film) is \(2{H}^{+}+2{e}^{-}\to {H}_{2}\), which consumes hydrogen ions; whereas, at high pH (pH = 10), the reaction at cathode consumes water rather than H+, being \({2H}_{2}O+2{e}^{-}\to {H}_{2}+{2OH}^{-}\) 48,49. The consumption of water takes place via an extra water dissociation \({H}_{2}O\leftrightarrow {H}^{+}+{OH}^{-}\), thus, the process of photocatalytic reduction is naturally slowed at higher pHs50, in turn, the larger amount of H+ present at acid pH facilitates the H2 production. Besides, at pH of 4, the surface of Cu3VSe4 NSs-FTO thin film is positively charged by adsorbing H+, facilitating the reduction reaction, whereas, at higher pH (pH of 7 and 10) the electrode/electrolyte interface is neutral or negatively charged, which eliminates the electrostatic interaction, or even creates a strong electrostatic repulsion towards Cl− that results in a lower hole capture rate and in a low production of hydrogen51. The changing trend of photocurrent response is consistent with their photocatalytic H2 evolution. Therefore, the increase of photocurrent response at pH of 4 can be attributed to the larger capture of holes which reduces charge recombination, as well as the large amount of H+ which facilitating the H+ reduction reaction at the cathode/electrolyte interface. A chronoamperometry experiment using the same photoelectrochemical cell setup and the KCl aqueous solution with pH 4 as electrolyte was carried out at − 425 mV through several 10 s light on–off cycles (inset, Fig. 8b); a stable photocurrent of ~ 0.036 mA cm−2 was observed. According to literature, the bare FTO substrate sometimes presents photocurrent response during the electrochemical measurements52,53,54. A control experiment was performed with bare FTO as working electrode and the chronoamperometry experiment being conducted under the same condition with the measurement of Cu3VSe4 NSs-FTO thin film. The photocurrent response of bare FTO substrate is shown in Supplementary Fig S6 (red line), where no significant photocurrent is observed under the same conditions, suggesting that the photocurrent response of Cu3VSe4 NSs-FTO thin film is substantially resulted from the Cu3VSe4 NSs thin film. To investigate the stability of the photocurrent response of Cu3VSe4 NSs, a chronoamperometry measurement was conducted on the Cu3VSe4 NSs-FTO thin film which was kept in air for 6 months after the photoelectrochemical measurement. As shown in Figure S6 (“Supporting Information”) blue line, the Cu3VSe4 NSs-FTO thin film could still display active photoelectrochemical behaviour after 6 months. Furthermore, Cu3VSe4 NSs showed good stability in the electrochemical measurements, as the XRD pattern and TEM (Supporting Information Figure S7) of Cu3VSe4 NSs after the photoelectrochemical test indicate that the Cu3VSe4 preserved the nanosheet morphology and cubic crystals.
A comparative test was conducted using a thin film fabricated with Cu3VSe4 nanocrystals (NCs) on FTO as the photoelectrode (Supporting Information Figure S6). The observed photocurrent generated by Cu3VSe4 NSs-FTO thin film is around nine fold higher than the photocurrent produced by the reported Cu3VSe4 NCs-FTO thin film26. The photocurrent enhancement in Cu3VSe4 NSs could be ascribed to the higher surface area provided by the 2D geometry of the nanosheets.
The electrochemical cell fabricated with the Cu3VSe4 NSs-FTO thin film was further subjected to an Electrochemical Impedance Spectroscopy (EIS) measurement to study the interfacial charge transfer characteristics at the semiconductor/electrolyte interface. Figure 9 shows the Nyquist plot obtained at the open-circuit potential of 0.215 V vs Ag/AgCl in the frequency range of 1 Hz to 100 KHz. An electrical equivalent circuit, as shown in the inset in Fig. 9, was designed to rationalize the charge-transfer and transport phenomena in the electrochemical cell, where Rs, Rct, Cdl, and W represents solution resistance, charge-transfer resistance, double-layer capacitance, and Warburg impedance, respectively. The first small semicircle at high frequency region is related to the solution resistance Rs, whereas the large semicircle at low frequency region could be assigned to the charge-transfer resistance Rct and the double-layer capacitance Cdl at the electrode/electrolyte interface55,56. Generally, the diameter of semicircle extrapolated in the Nyquist plot represents resistance R, in turn, reflects the reaction rate57,58. Herein, the charge transfer resistance (RCT) of Cu3VSe4 NSs-FTO thin film in 0.6 M KCl aqueous electrolyte was found to be 300 Ω cm2 from the second semicircle of the Nyquist plot. The linear part located at low frequency could be ascribed to the Warburg impedance W that corresponds to the diffusion processes.
Conclusion
Quasi-2D Cu3VSe4 nanosheets with cubic crystal structure have been prepared through a templating method using binary VSe2 NSs as a solid-state precursor in a solution-phase approach, which enabled the preservation of the 2D morphology. Microscopy analyses (TEM, SEM, and AFM) highlighted the large lateral size and thin thickness of the synthesized Cu3VSe4 nanosheets. Three strong absorption bands at 382 nm, 552 nm, and 664 nm were observed for Cu3VSe4 nanosheets, indicating the presence of an intermediate bandgap. The emission peak redshift in the PL spectra, from 650 to 780 nm, when varying the excitation wavelength from 430 to 520 nm, is attributed to the size/thickness distribution and has been observed in other layered materials, including 2D MoS2 44 and WSe2 45. The mechanism study suggested that the formation of Cu3VSe4 nanosheets involves primarily the Cu3VSe4 nanosheets formation as a result of reaction of Cu(II) cations with VSe2 NSs. At the same time, unreacted Se present in the reaction reacts with Cu cations to form a minor Cu2Se is consumed during the reaction by reacting with VSe2 NSs and leads to Cu3VSe4 nanosheets.
To evaluate the conduction type of Cu3VSe4 NS, thin films were made by depositing the nanosheets (after ligand exchange) on FTO substrates. The fabricated Cu3VSe4 NSs thin film exhibited a p-type semiconductor behavior. A photocurrent of ~ 0.036 mA cm−2 was measured in an electrochemical setting, in a KCl aqueous solution at pH 4.0. The electrical impedance spectroscopy was measured assuming that the Cu3VSe4 NSs-FTO based electrochemical cell fits an equivalent circuit with the circuit elements of solution resistance (Rs), charge-transfer resistance (Rct), double-layer capacitance (Cdl), and Warburg impedance (W). The estimated charge transfer resistance value of 300 Ω cm2 obtained from the Nyquist plot provides an insight into the rate of charge transfer at the electrode/electrolyte interface.
The cascade synthesis method reported herein for the Cu3VSe4 ternary chalcogenides could be expanded to other significant chalcogenides that could benefit from 2D morphology. The lightweight nanostructures could be useful in a plethora of optoelectronic devices that support contemporary applications, including wearable electronics, biosensors and the Internet-of-Things (IoT).
Methods
Materials
All chemicals used in the experiment were used as received, without further purification. Vanadium (IV) oxide acetylacetonate (VO(acac)2, ≥ 98%) was ordered from Merck KGaA. Selenium powder (Se, 99.99%), oleylamine (OLA, 70%), 1-dodecanethiol (1-DDT, ≥ 98%), Copper(II) chloride dihydrate (CuCl2·2H2O, 99.999%), and formamide were bought from Sigma-Aldrich. Sodium sulfide (Na2S, anhydrous) was purchased from Alfa Aesar. ACS grade chloroform (CHCl3, ≥ 99.8%), toluene (C7H8, ≥ 99.5%), and methanol (CH3OH, 99.8%) were bought from Fisher Scientific. Ethanol (C2H5OH, 100%) was ordered from Decon laboratories. FTO Soda Lime glass substrates were purchased from MSE Supplies.
Preparation of VSe2 nanosheets (NSs)
In the preparation of VSe2 NSs synthesis, Vanadium (IV) oxide acetylacetonate was used as the source of V4+ cations, whereas elemental Se served as the source of Se2− anions. Vanadium (IV) oxide acetylacetonate (133 mg, 0.5 mmol) and 15 mL OLA were loaded in a 100 mL two-neck round bottom flask. The mixture was degassed for 30 min at 120 ℃ and flushed with argon. Meanwhile, Se powder (1 mmol, 78.96 mg) was mixed with 1 mL of 1-DDT and 3 mL of OLA in a 25 mL two-neck round bottom glass flask. The Se solution was stirred under vacuum at room temperature for 30 min and then purged with argon. Next, the temperature of vanadium precursor was raised to 140 ℃, followed by the swift injection of the Se solution. The reaction was further heated to 250 ℃ and maintained at this temperature for two hours to form the VSe2 nanosheets. Upon cooling, a mixture of OLA (9 mL) and I-DDT (1 mL) was added to remove the Se residues and the precipitated VSe2 nanosheets were collected by centrifugation. The nanosheets were subsequently washed twice with the same CHCl3 and C2H5OH mixture (V:V, 1:3). The final precipitates were collected and dried overnight in a vacuum oven.
Preparation of Cu3VSe4 nanosheets
In a typical synthesis, the formed VSe2 OLA prepared as described above were not removed from suspension, and upon reaching two hours reaction time at 250 ℃ under argon atmosphere and a Cu (II) solution was rapidly injected. The Cu (II) solution was made by dissolving CuCl2·2H2O (136.4 mg, 0.8 mmol) in 5 mL of OLA. The reaction was kept at 250 ℃ for one hour. Afterward, the heating source was removed, and the reaction allowed to cool down to room temperature. Upon cooling, a mixture of CHCl3 and C2H5OH (V:V, 1:3) was added and the precipitated Cu3VSe4 nanosheets were collected by centrifugation. The product was further purified by washing twice with a mixture of CHCl3 and C2H5OH (V:V, 1:3). The precipitate was dried overnight in a vacuum oven.
Mechanism study
To study the mechanism of Cu3VSe4 formation starting from the VSe2 nanosheets, the experiment described above was conducted with different reaction times from the point of addition of Cu(II) solution. The series included experiments with all parameters held the same and reaction times of 1minute, 5 min, 15 min, 30 min, 1 h, and 2 h.
Ligand exchange with S2−
A ligand exchange process was conducted to replace the OLA coordinated to Cu3VSe4 nanosheet surface with S2−. In a typical experiment, Cu3VSe4 nanosheets were suspended in chloroform (8 mg mL−1) and 10 mL of the suspension was transferred to a 50 mL tube containing 10 mL of Na2S solution in formamide (0.2 M). Next, the mixture was vigorously shaken for 1 min and further allowed to rest until ligand exchange completion, when Cu3VSe4 NSs were fully transferred from the chloroform phase (lower) to the formamide phase (upper). Afterward, the clear chloroform phase was removed, and 5 mL distilled water and 20 mL of ethanol was added to the aqueous phase to precipitate the Cu3VSe4 NSs. The precipitate was purified by washing twice with a mixture of ethanol and distilled water (V:V, 4:1) followed by washing with a mixture of toluene and ethanol (V:V, 1:3). The resulting product was collected and dried in a vacuum oven overnight.
Cu3VSe4 inks and thin film fabrication
The Cu3VSe4 NSs inks were prepared via dispersing 10 mg of ligand exchanged-Cu3VSe4 NSs into 1 mL of ethanol and ultrasonicating the dispersion for 10 min with a probe sonicator. The substrate used for ink deposition, 1″ × 1″ FTO-coated glass, were freshly cleaned using an ultrasonic bath using, in sequence: distilled water, methanol, and acetone, for 10 min each.
All Cu3VSe4 thin films used in this work were fabricated by bar-coating in ambient conditions. An amount of 20 μL of Cu3VSe4 ink was dispensed and coated on the FTO-coated glass. The film was dried for 1 min in air at 100 ℃, using a hot plate. The coating and drying process was repeated twice to complete the glass/FTO/Cu3VSe4 thin film.
Photoelectrochemical measurements
To evaluate the photoelectrochemical performance, a three-electrode photoelectrochemical cell has been set up, consisting of an Ag/AgCl reference electrode, a platinum counter electrode, and the Cu3VSe4 NSs-FTO thin film as the photoelectrode. An aqueous solution of KCl (0.6 M) was used as the electrolyte. The pH of the KCl electrolyte was adjusted to either 4 or 10 using HCl or 2 M NaOH aqueous solution, respectively. The current density–voltage (J–V) dependence was investigated in the − 0.5 to 0 V range, with a cycle of 10-s light-off and 10-s light-on. The sweep rate was 2 mV s−1 and the LED light power was 2000 lumens. The photocurrent of the Cu3VSe4 NSs-FTO thin film using the same 10 s light-on/10 s light-off cycle recorded with a Pine Research Potentiostat.
Characterization
The crystal structure and purity of prepared VSe2 and Cu3VSe4 nanosheets were determined by X-ray powder diffraction (XRD) using a Siemens Diffractometer D5000 (Cu Kα radiation, λ = 1.5405 Å). To confirm product purity by Raman spectroscopy, Raman spectra were obtained with a Renishaw Raman microscope equipped with a 633 nm laser. The morphology and size of the synthesized VSe2 and Cu3VSe4 were determined by transmission electron microscopy (TEM) imaging, using a Philips CM200, and scanning electron microscopy (SEM) imaging, with a JEOL 6330F. Elemental distribution of the Cu3VSe4 nanosheets was determined with the energy dispersive spectroscopy (EDS) feature of the JEOL 6330F SEM. The oxidation states of the Cu, V, and Se elements of the synthesized Cu3VSe4 nanosheets were confirmed via X-ray photoelectron spectroscopy (XPS) in a VG Escalab 220i-XL equipped with an Al Kα source. Photoluminescence (PL) measurements of Cu3VSe4 nanosheets were carried out with a Perkin Elmer LS-55 Luminescence Spectrometer. The absorption spectrum of Cu3VSe4 nanosheets was collected using an Agilent Cary 5000 UV–Vis–NIR spectrophotometer. The thermal stability of the Cu3VSe4 nanosheets was determined by thermogravimetric analysis (TGA) using a TA Instrument SDT-Q600 Simultaneous TGA/DSC. The WaveNow Potentiostat (PINE research) was used to determine the photoelectrochemical behavior of the Cu3VSe4 NSs-FTO thin film.
Data availability
All data generated or analyzed during this study are included in this article (and its “Supporting Information” file).
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Acknowledgements
This work was funded in part by NASA under Award # 80NSSC19M0201, and by NSF Award #1924412. The authors extend special thanks to Prof. Zhiqun Lin at Georgia Institute of Technology for access to photoluminescence measurements in his laboratory.
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M.L., C.-Y. L. and D.R.R. conceived the study. M.L. performed the synthesis and characterization, except for the PL and impedance measurement conducted by M.Z.; M.L. and D.R.R. wrote the manuscript, and C.-Y.L. and D.R.R. reviewed the manuscript for final submission.
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Liu, M., Lai, CY., Zhang, M. et al. Cascade synthesis and optoelectronic applications of intermediate bandgap Cu3VSe4 nanosheets. Sci Rep 10, 21679 (2020). https://doi.org/10.1038/s41598-020-78649-9
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DOI: https://doi.org/10.1038/s41598-020-78649-9
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