Solution-phase phosphorus substitution for enhanced oxygen evolution reaction in Cu2WS4.

Transition metal phosphides are among the most promising materials for achieving efficient electrocatalytic performance without the use of rare or expensive noble metals. However, previous research into phosphides for the hydrogen evolution reaction (HER) or oxygen evolution reaction (OER) has focused on high-temperature vapor-phase processes, which are not practical for large-scale applications. Here, we introduce a simple, one-step solution-phase method of phosphide synthesis by modifying Cu2WS4 using triphenylphosphine (TPP), which serves to substitute S with P and transform the normally inactive basal plane of Cu2WS4 into a defect-rich, activated basal plane. The OER activity was significantly enhanced by phosphorus substitution, with the resulting Tafel slope of the sample with ∼8 at% phosphorus reaching 194 mV dec-1, a result close to that of the best OER catalyst (RuO2, 151 mV dec-1). The sample possessed stable OER performance, showing no degradation in current density over ∼24 hours (500 cycles), proving the robust and stable nature of the phosphorus substitution. These results open the possibility for further phosphide catalyst development using this low-cost, solution-phase method. This journal is © The Royal Society of Chemistry.

Introduction

In efforts to develop alternative fuels and expand the feasibility of the “hydrogen economy”, researchers have focused on developing new catalysts to drive water-splitting reactions. Of the two reactions, the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER), the latter is more difficult to achieve due to the higher kinetic barrier.[1] Currently, the best OER catalysts are IrO2 and RuO2,[2] but the high cost of both metals severely limits their commercial viability. For this reason, the development of new catalysts requires an emphasis on low-cost, low-temperature approaches that do not require rare or expensive elements.

Recently, phosphides have jumped to the forefront of HER and OER catalyst research. These include pyrite structures based on Fe, Co, and Ni[3-5] as well as Mo and W based phosphides[6-8] and phosphosulfides.[9,10] In both cases, remarkable improvements in catalytic activity have been achieved by phosphidation, with the enhancement often being attributed to an increase in active sites and improved adsorption. For layered transition metal chalcogenides (TMCs), this strategy could be particularly useful because the basal planes are normally catalytically inactive.[11,12] For this reason, much of the research into TMCs for OER or HER has focused on the formation of defects, edge sites, or localized lattice strain in an effort to increase the active sites.[13-18] In particular, heteroatom doping, such as substituting S with Se, has proven to be an effective strategy to increase the catalytic activity.[19-21]

However, nearly all of current research on these phosphides involves a high-temperature, vapor-phase process, with the most common conditions seeming to be a temperature of over 300 °C with sodium hypophosphite or red phosphorus in a tube furnace.[8,22-26] A notable exception is a solution-phase method reported by McEnaney et al.[27] to produce tungsten phosphide with trioctylphosphine, but the resulting product was entirely amorphous. The need for both high temperatures and an additional synthesis step to create crystalline phosphides significantly undermines the claims of low-cost and scalability in these works, making the development of alternative routes for phosphide synthesis crucial.

In this work, we introduce a novel solution-phase method for P substitution by using triphenylphosphine (TPP) in the Cu2WS4 system. Unlike the aforementioned works, this method achieves stable phosphide synthesis through a one-step, low-temperature, solution-phase process. Through this method, the normally inactive basal plane of Cu2WS4 was transformed into a defect-rich, highly-active structure, resulting in a dramatic improvement in OER properties. The best composition (Cu2WS3.4P0.6) shows a Tafel slope of 194 mV dec−1, close to the value of RuO2 (151 mV dec−1). The result comes from the decreased adsorption energy of –OH on Cu2WS4, which was further analyzed with DFT simulations. These results show the potential of this novel solution-phase phosphorus substitution method for use in OER electrocatalysts.

Results and discussion

Fig. 1a illustrates the crystal structure of Cu2WS4 and Cu2WS4 with P substitution. Cu2WS4 reference samples were synthesized through a previously reported method.[28,29] Phosphorus substitution was achieved by adding TPP to the mixture in amounts corresponding to 0.1, 0.15, and 0.20 molar ratios relative to the other precursors, which were designated as Cu2WS3.6P0.4, Cu2WS3.4P0.6, Cu2WS3.2P0.8, respectively. The XRD results in Fig. 1b show evidence of successful defect formation through P substitution. The major peaks correspond to Cu2WS4 (JCPDS 81-1159), but at higher concentrations the P substitution appears to add higher lattice strains, as evidenced by the inset showing the significant full-width half max (FWHM) increase. Similar XRD trends have been shown to indicate lattice strain[16] and/or defect formation[30] in previous reports of TMC catalysts. We note that no additional peaks were observed after P-doping, indicating that P substitutes into the Cu2WS4 lattice or forms defect sites rather than forming secondary crystalline phases.

Fig. 1

Illustration of phosphorus substitution and basal plane activation using TPP (a). (b) XRD showing increased lattice strain and decreased crystallinity with increasing phosphorus substitution. (c) XPS showing a shift of the W 4f peaks and increase of P 2p peaks. (d) Raman spectra with vibrational modes labeled.

XPS analysis (Fig. 1c) confirms the presence of phosphorus, reaching a maximum of ∼11 at% in the Cu2WS3.2P0.8 sample. A significant shift of the W 4f peaks is also observed, an expected result due to the electronegativity difference between S and P. Interestingly, the Cu peaks are not shifted, while the S peaks experience a much smaller and less progressive shift, as seen in Fig. S1.† Raman spectroscopy (Fig. 1d) also confirms the changes in the chemical state after P substitution. The standard A1, B2, and E modes are present in all samples, which are characteristic of Cu2WS4, but the intensity decreases with increasing P concentration. Meanwhile, α and β modes appear in samples with P substitution, and increase in prominence with increasing P concentration. The A1, B2, and E modes are characteristic of S vibrations in TMCs[31,32] and often broaden and decrease in intensity with increasing defect formation.[30,33] Therefore, this is strong evidence for both P substitution in the lattice as well as increased defects in P-substituted sample.

The effect of P substitution was also seen in the morphology of the samples. The SEM images indicate only minor changes in the particle shape and size. The pristine sample (Fig. 2a, inset) appears monodisperse and with a small (<50 nm diameter) size, while P-substituted samples appear to have slightly larger average particle sizes, and the Cu2WS3.2P0.8 develops a broader size distribution. However, the changes in crystallinity, as observed by HRTEM, are much more pronounced. Both the pristine Cu2WS4 and the Cu2WS3.6P0.4 samples appear fully crystalline, with no significant defects or amorphous regions. The Cu2WS3.4P0.6 in Fig. 2c sample appears to be slightly less crystalline, as indicated by the FFT pattern and false-color TEM image, where crystalline regions are colored light blue and amorphous regions are colored light pink. The Cu2WS3.2P0.8 sample (Fig. 2d) appears even less crystalline, with large amorphous regions observed and only very faint points appearing in the FFT pattern. The full set of SEM and TEM images are presented in Fig. S2.† A uniform distribution of P was also confirmed by Energy Dispersive X-ray Spectroscopy (EDS), as shown in Fig. S3.† Overall, these data agree well with the previously discussed Raman and XRD data, with both indicating that significant lattice strain and defect formation takes place after P substitution.

Fig. 2

False-color TEM images showing decreased crystallinity with increasing P-substitution (left). SEM images (scale bar = 500 nm) and FFT patterns (right) also show the changes in sample crystallinity and morphology.

The oxygen evolution reaction (OER) performances of as-synthesized pristine and P-substituted Cu2WS4 electrocatalysts were measured by dropping the catalyst slurry onto a rotating disk electrode (RDE) with a mass loading of 0.1 mg cm−2 in the O2-saturated 0.1 M KOH at the rotation of 1600 rpm. As seen in the linear sweep voltammetry (LSV) curves in Fig. 3a, the catalytic activity of the samples significantly improves after P substitution. The pristine Cu2WS4 sample is almost completely inactive for OER, which is typical for TMCs with no basal plane modification or edge structuring.[29,34-37] After P substitution, the material is transformed into a highly active catalyst, with the Cu2WS3.4P0.6 sample showing the best performance (onset potential 1.59 V vs. RHE at 10 mA cm−2). Furthermore, to investigate the OER kinetics of the as-synthesized samples, Tafel plots (Fig. 3b) are fitted according to the polarization curves. As seen in the comparison of Tafel slopes, the value for Cu2WS3.4P0.6 (194 mV dec−1) is close to that of the benchmark RuO2 catalyst (151 mV dec−1) tested under the same conditions. Although the phosphorus content is relatively low compared to the other constituent elements (∼8 at% P for Cu2WS3.4P0.6), we note that many other studies have confirmed that light doping (<10 at%) can produce dramatic improvements in electrocatalytic activity.[35,38,39]

Fig. 3

Electrochemical properties of Cu2WS4 and P-substituted samples: LSV (a) and Tafel slopes (b) show a comparison of the P-substituted samples vs. the reference as well as vs. RuO2. ECSA (c) and impendence spectroscopy (d) indicate decreased charge transfer resistance and increased active sites with P-substitution. The stability test (e) as well as the comparison of LSV curves before and after the test (f) show the robust nature of the sample.

However, the catalytic activity decreases with further P substitution, with the Cu2WS3.2P0.8 sample showing an onset potential of 1.67 V vs. RHE at 10 mA cm−2 with a Tafel slope of 341 mV dec−1. Although a certain degree of defect formation is beneficial for catalytic activity, excessive defects can hinder performance by reducing electrical conductivity.[40,41] Because Cu2WS3.2P0.8 was shown to have many amorphous regions and a heavily strained lattice in the previously discussed XRD and TEM data, we suspect that the electrical conductivity is negatively impacted as a result. However, the catalytic activity of Cu2WS3.6P0.4 (onset potential 1.70 V vs. RHE at 10 mA cm−2 with Tafel slope 272 mV dec−1) sample reveals that ∼6 at% P is not enough to utilize the basal planes of Cu2WS4 for OER activity.

To further analyze the results, the double-layer capacitances (Cdl) are derived from the cyclic voltammetry to evaluate the electrochemical surface area (ECSA) of as-synthesized samples and is shown in Fig. 3c. Here, the Cu2WS3.4P0.6 appears to have superior properties, with the highest Cdl (3.1 mF cm−2) confirming the increased number of active sites after P-substitution. Impedance spectroscopy was also performed to gain insights into the charge transfer resistance of the samples, as seen in Fig. 3d. All samples show a characteristic semicircular shape, and smallest area (lowest resistance 175 Ω) is seen in the Cu2WS3.4P0.6 sample.

Often, non-oxide OER compounds have poor stability in alkaline solutions.[42] Here, we investigated stability of the best performing sample, Cu2WS3.4P0.6, over a period of ∼24 hours. The sample showed a slight increase in current density in the initial stages of the test, followed by stabilization and no significant decay over the remainder of the measured time. As seen in the comparison of LSV curves in Fig. 3f, the catalytic activity is fully maintained after the stability test. XPS was also performed confirm that the phosphorus content remained after the stability test, as see in Fig. S5.† These data indicate that this method of P-substitution is stable and robust in the alkaline environment.

This improved performance after P-substitution can be attributed to increased active sites induced from defect and strain formation in the lattice. Previous research into TMCs for OER has shown that this disruption of the crystal structure can improve catalytic activity by reducing OH− adsorption energy.[14,34] To support our experimental findings, density functional theory (DFT) calculations were employed to calculate the adsorption energy required for OH− on pristine Cu2WS4 and P-substituted Cu2WS4. To determine the adsorption energy of the adsorbent (OH−) on pristine Cu2WS4, and P-substituted Cu2WS4 (Cu2WS3P and Cu2WS2P2), first geometry optimizations were carried out for single molecule of Cu2WS4, Cu2WS3P, and Cu2WS2P2 using the B3PW91 functional (shown in Fig. 4). Using long-range correlated (LC) van der Waals functional ωB97XD, the calculated adsorption energy is −6.75 eV, −6.51 eV, −7.66 eV for Cu2WS4, Cu2WS3P, and Cu2WS2P2, respectively. Since the adsorption process of OH− on pristine Cu2WS4, and P-substituted molecules is physisorption caused by intermolecular van der Waals forces, it is expected the values calculated by functional ωB97XD is in nice agreement.

Fig. 4

Illustration of the layered samples (top) with the representative molecules used for DFT calculations and adsorbed –OH shown below.

These DFT data agree well with the experimental results regarding OER activity. Because the –OH adsorption is lowered for the representative Cu2WS3P molecule, it is further evidence of the beneficial effects of P-substitution. However, the increased adsorption energy for the Cu2WS2P2 molecule could indicate an additional reason why the heavily P-substituted sample (Cu2WS3.4P0.6) showed decreased catalytic activity compared to Cu2WS3.2P0.8. It is possible that while light P-substitution decreases adsorption energy, adjacent are closely spaced P atoms interact to produce the opposite effect.

Conclusions

In summary, we have developed a low-temperature, solution-phase method to successfully substitute S with P in Cu2WS4. In contrast to the standard high-temperature, vapor-phase methods, this technique allows for the production of phosphides in a simple, one-step process. It was shown that P substitution creates a highly defective, active basal plane in the samples, which is beneficial for catalytic properties. As a result, the P-substituted samples showed significantly improved OER performance, a result which was attributed to the increased number of active sites and decreased charge transfer resistance compared to the reference sample. These results are of interest for further development of low-cost phosphides for electrochemical catalysts.

Experimental procedures

Pristine Cu2WS4 was synthesized using a solvothermal method.[28,29] In a typical reaction, 1.56 mmol of [Cu(MeCN)]BF4 is added to 20 ml acetonitrile and 0.78 mmol of (NH4)WS4 is added to 20 ml dimethylformamide (DMF). The solutions were then mixed together in an N2 atmosphere and refluxed at 160 °C for 12 hours. The product was then collected using vacuum filtration over a PVDF membrane, rinsed with ethanol and deionized (DI) water, and dried in air at 65 °C overnight. For P substitution, triphenylphosphine (TPP) was added to the mixture prior to refluxing in molar ratios of 0.10, 0.15, and 0.20.

X-ray diffraction (XRD) patterns were obtained using Cu Kα1 radiation (Rigaku, D/MAX-2500) with a scan rate of 2° min−1. Chemical analysis was performed using X-ray photoelectron spectroscopy (Thermo VG Scientific, K-alpha) and Raman spectroscopy using a 532 nm laser source (Bruker, Senterra). Scanning electron microscopy (SEM) images were obtained using a Hitachi SU5000, and high-resolution transmission electron microscopy (HRTEM) was performed by drying the solutions over a carbon grid and imaging using an FEI Titan cubed G2.

Electrodes were fabricated by first sonicating 30 mg of the active material with 8 ml of DI water, 2 ml ethanol, and 100 μl Nafion® 117 solution (5%) for 1 h. Then, 1 μl of the prepared homogenous suspension was drop-cast onto a rotating glassy carbon electrode disc (d = 3 mm). The samples were then dried at 60 °C overnight before use. Electrochemical analyses were performed using a VersaSTAT 3 electrochemical workstation with rotating disc electrode system (AMETEK, 616B). A three electrode system was used, where the working electrode is the active material/glassy carbon disc, the reference electrode is Ag/AgCl in 3 M KCl, and the counter electrode is a Pt mesh in 0.1 M KOH (pH = 11). All of the potentials were calibrated to a RHE, ERHE = EAg/AgCl + 0.196 + 0.0591pH V.

The Gaussian 09 and GaussView 5.0 package was used for density functional theory (DFT) based calculation. To determine the adsorption energy of the adsorbent (OH−) on pristine Cu2WS4, and P-doped Cu2WS4 (Cu2WS3P, Cu2WS2P2, and Cu2WS1P3), first geometry optimizations were carried out for single molecule of Cu2WS4, Cu2WS3P, and Cu2WS2P2, using the B3PW91 functional. The 6-311G(d,p) basis set was used for S, P, O, H atoms and LANL2DZ basis set was used for metals Cu, W. After geometry optimization, the adsorption energy was calculated using functionals B3PW91 and ωB97XD with counterpoise corrections to correct for basis set superposition error (BSSE). The functionals B3PW91 and ωB97XD are local density functional and long-range correlated (LC) van der Waals functionals, respectively.

Conflicts of interest

There are no conflicts to declare.