Open Access Article
This Open Access Article is licensed under a Creative Commons Attribution-Non Commercial 3.0 Unported Licence

Photocurrent of BiVO4 is limited by surface recombination, not surface catalysis

Carolin Zachäus a, Fatwa F. Abdi*a, Laurence M. Peterb and Roel van de Krol*a
aHelmholtz-Zentrum Berlin für Materialien und Energie GmbH, Institute for Solar Fuels, Hahn-Meitner-Platz 1, 14109 Berlin, Germany. E-mail:;
bDepartment of Chemistry, University of Bath, Bath BA2, 7AY, UK

Received 24th January 2017 , Accepted 9th March 2017

First published on the web 9th March 2017

Bismuth vanadate is one of the most promising photoanode materials for photoelectrochemical water splitting. In order to achieve high photocurrents the surface of BiVO4 always has to be modified with water oxidation catalysts, such as cobalt phosphate (CoPi), FeOOH, or NiFeOx. While this has generally been attributed to the poor intrinsic catalytic activity of BiVO4, detailed insight into the fate of the photogenerated charge carriers at the surface is still lacking. We used intensity modulated photocurrent spectroscopy (IMPS) to investigate the surface carrier dynamics of bare and CoPi-modified spray-deposited BiVO4 films. Using a model developed by Peter et al., it was possible to distinguish the reaction rate constants for surface recombination and charge transfer to the electrolyte. We found that modification with CoPi reduced the surface recombination of BiVO4 with a factor of 10–20, without significantly influencing the charge transfer kinetics. Control experiments with RuOx, one of the best known OER electrocatalysts, did not affect surface recombination and led to an actual decrease of the photocurrent. These results show that the main role of the CoPi is to passivate the surface of BiVO4 and that, contrary to earlier assumptions, the photocurrent of BiVO4 is limited by surface recombination instead of charge transfer. The importance of surface recombination is well recognized for conventional semiconductors in the field of photovoltaics; these findings show that it may also play a crucial role in oxide-based semiconductors for photoelectrochemical energy conversion.


The potential application of metal oxides as semiconductor photoelectrodes for water splitting critically depends on the development of efficient, inexpensive water oxidation catalysts to enhance the surface reaction kinetics. For example, BiVO4—currently the most promising metal oxide photoanode—suffered from having low hole transfer efficiency for a long time,1,2 but this problem has been shown to be easily solved by modifying its surface with CoPi, RhO2, FeOOH, NiFeOx, or MnOx catalysts.2–6 In the past few years, many more studies on modified semiconductor surfaces have been reported. A particularly versatile example is cobalt phosphate (CoPi), a water oxidation catalyst that was initially developed by Nocera and co-workers7 and has been shown to greatly enhance the photocurrents of e.g., Fe2O3,8–11 WO3,12 BiVO4,5,13,14 and TaON.15,16 Despite these successes, the true nature of the enhancement is unclear. In BiVO4 it is usually assumed that the low charge injection efficiency is related to the poor surface catalytic activity of the material, but this is not necessarily true. For example, a high density of surface recombination centers can also lead to a low charge injection efficiency. This raises some intriguing questions: (i) what really limits the charge injection efficiency in BiVO4? (ii) How do the so-called co-catalysts solve the charge injection problem: is it a true catalytic effect or passivation of surface recombination centers? (iii) What is the mechanism behind the improvement in photocurrent?

A few years ago, Gamelin pointed out that there are two conflicting views on the mechanism of photocurrent enhancement in the same CoPi/hematite (α-Fe2O3) photoanode system.8 Barroso et al. reported enhanced charge separation and carrier life time in the semiconductor by introducing CoPi,9 which was attributed to increased band bending. In contrast, Klahr et al. found no indications for a change in band bending, and instead suggested that CoPi rapidly extracts photogenerated holes from hematite, thereby reducing the electron–hole recombination at the surface.17 Boettcher and co-workers made a first general attempt to reconcile these observations by proposing the concept of an ‘adaptive’ junction.18 They showed that redox-active ion-permeable electrocatalysts (e.g., NiOOH and possibly CoPi) yield ‘adaptive’ semiconductor/electrocatalyst junctions where the effective Schottky barrier height changes dynamically with potential as a consequence of changes in the oxidation state of the electrocatalyst. Even before these studies, Zhong and Gamelin already suggested that CoPi reduces the surface recombination of BiVO4.5 However, their experiments could not distinguish whether the increase in photocurrent was indeed due to a decrease in surface recombination, or to enhanced oxygen evolution kinetics.

These considerations illustrate that further studies are needed to understand the role of CoPi—and co-catalysts in general—on a semiconductor photoanode for water oxidation. We consider three different roles for a co-catalyst. First, it can improve the water oxidation kinetics by reducing the activation energy of the rate-determining step of the four electron oxidation process, which results in a faster charge transfer to the electrolyte; this is the ‘classical’ role of an electrocatalyst. The second possible mechanism of a co-catalyst on a photoabsorber is the passivation of surface recombination centers and therefore the inhibition of surface recombination. Finally, as mentioned above, the co-catalyst can influence the band bending of the semiconductor by forming a Schottky-type junction, thereby enhancing the charge separation. As a result, we need a technique that can distinguish these different effects on the semiconductor/electrolyte and semiconductor/co-catalyst/electrolyte interfaces.

In this study, we use intensity modulated photocurrent spectroscopy (IMPS) to investigate the role of CoPi on spray-deposited BiVO4 photoanodes.5,13,14 With IMPS, the charge transfer and the surface recombination at the semiconductor/electrolyte interface can be clearly distinguished. This technique is increasingly utilized in the literature to understand the surface carrier dynamics at the semiconductor/electrolyte interface.19–23 We will show that CoPi, despite being a dark electrocatalyst, does not enhance the charge transfer rate constant on the surface of BiVO4, but instead suppresses surface recombination. Moreover, we find that a conventional electrocatalyst, such as RuOx, does not significantly improve the photoactivity of BiVO4, suggesting that BiVO4 by itself is already thermodynamically active towards water oxidation. This conclusively shows that the photocurrent of BiVO4 is limited by surface recombination, and not by slow oxygen evolution kinetics. The implications of these findings will be discussed.


Preparation of BiVO4 thin film photoanodes

Thin films of BiVO4 were deposited by spray pyrolysis. Bi(NO3)3·5H2O (98%, Alfa Aesar) and VO(AcAc) (99%, Alfa Aesar) were dissolved in acetic acid (98%, Sigma Aldrich) and absolute ethanol (Sigma Aldrich), respectively. The Bi solution was then added to the V solution (Bi[thin space (1/6-em)]:[thin space (1/6-em)]V = 1[thin space (1/6-em)]:[thin space (1/6-em)]1), and the mixture was diluted to 4 mM with excess ethanol. The acetic acid to ethanol volume ratio in the final solution is 1[thin space (1/6-em)]:[thin space (1/6-em)]9. The final solution was then ultrasonicated for 15 minutes. The FTO substrate was heated to 450 °C during deposition. The precursor solution was sprayed in a pulsed deposition mode onto the FTO, with one spray cycle consisting of 5 s spray time followed by 55 s delay time to allow the solvent to evaporate. After deposition, the films were annealed for 2 hours at 450 °C in air. More details can be found in previous reports.24,25

Co-catalyst deposition

The CoPi catalyst was electrodeposited (in the dark) on the surface of BiVO4 in an electrochemical cell using a three-electrode configuration, according to the recipe from Kanan and Nocera.7 The electrolyte is made by dissolving 0.5 mM Co(NO3)2·6H2O (99%, Acros Organics) in a 0.1 M potassium phosphate (KPi) buffer solution (made by dissolving 0.034 M KH2PO4 and 0.066 M K2HPO4 to obtain pH ∼ 7). The potential of the working electrode was controlled by a potentiostat (EG&G PAR 283). A coiled Pt wire and an Ag/AgCl electrode (XR300, saturated KCl/AgCl solution, Radiometer Analytical) were used as the counter and reference electrodes, respectively. The electrodeposition was performed at a constant voltage of 1.1 VNHE (1.5 VRHE) for 30 s. This resulted in a thickness of the Co–Pi layer of ∼1 nm.24

The RuOx catalyst was photoelectrodeposited on the surface of BiVO4 in the same electrochemical cell that was used for the CoPi deposition. Based on the recipes from Gui and Tsuji,26,27 an aqueous solution of 5 mM RuCl3 (Ru content 45–55%, Sigma Aldrich) was used as the deposition bath with a pH ∼ 7. The photo-electrodeposition was performed under AM 1.5 illumination at a constant potential of 0.6 VNHE (1.0 VRHE) for 400 s.

IMPS and photocurrent measurements

IMPS and photocurrent measurements were carried out in an aqueous solution of 0.1 M KPi (buffer, pH ∼ 7). The measurements were performed on bare and CoPi modified BiVO4 films for a bias range of 0.6 to 1.5 VRHE and a frequency range of 0.1 Hz to 10 kHz. The electrochemical cell was the same as that used for the CoPi deposition, and was fitted with a quartz window to allow illumination of the sample surface. IMPS measurements were performed with modulated illumination provided by a light-emitting diode with a wavelength of 455 nm (Thorlabs M455L3) driven by an LED driver (Thorlabs DC2100). Using a beam splitter, the light was split into two beams: one onto the PEC cell, and the other onto a high-speed Si photodiode (Thorlabs PDA10A-EC). The signal output of a frequency response analyzer (FRA, Solartron 1250, Schlumberger) was used to modulate the light intensity sinusoidally, with an rms amplitude of 0.6 mW cm−2 superimposed on a 4 mW cm−2 DC background intensity. An EG&G PAR 283 potentiostat was used to control the potential, and its current monitor output was fed into the channel 1 of the FRA. The voltage signal of the high-speed Si photodiode was fed into the channel 2 of the FRA. The FRA then reported the real and imaginary components of the opto-electrical gain of the sample by dividing the measured photocurrent density (jphoto) through the voltage of the Si photodiode (channel 1/channel 2). This can be converted to the absolute (dimensionless) complex gain of the photoelectrode28 by multiplying with a conversion factor. The conversion factor was determined by measuring the absolute intensity of the light using a calibrated photodiode (PD300UV + Ophir Nova II), and the voltage reading of the high-speed Si photodiode. The conversion factor for our setup was 0.00314 V cm2 mA−1. A schematic diagram of the setup is shown in Fig. 1.
image file: c7sc00363c-f1.tif
Fig. 1 Schematic diagram of the intensity modulated photocurrent spectroscopy (IMPS) setup. Modulated illumination is provided by a light emitting diode (λ = 455 nm), and the modulated photocurrent response of the sample is measured and analyzed.

The photocurrent–voltage measurements were performed using the same setup. The sample area is 0.283 cm2. The 455 nm LED light source (4 mW cm−2) was chopped by applying a square wave with a frequency of 0.1 Hz. The number of absorbed photons in BiVO4 at this wavelength and intensity is a factor of ∼4 lower compared to full AM1.5 illumination, but this is still within the range of conditions encountered in practice when considering the effects of e.g. clouds.

The open circuit potential measurements as a function of light intensity were carried out using a combination of a 457 nm CW argon ion laser (Coherent Innova 90C Series) and multiple neutral density filters (metal film, OD 0.1–3, Melles Griot). The illumination intensities were measured with a calibrated photodiode (Ophir PD300-UV). Hydrogen peroxide (H2O2, 0.5 M) was added to the phosphate buffer to better define the redox potential of the electrolyte.

In situ UV-Vis measurements

The setup for the in situ UV-Vis measurements consists of a deuterium–halogen lamp (Mikropack DH-2000-BAL), which was used as the light source, an electrochemical cell with the sample under investigation (e.g., BiVO4, CoPi) as the working electrode, and a high sensitivity spectrometer (Ocean Optics Maya 2000 PRO) to measure the light transmitted through the sample. Optical fibers (Ocean Optics QP200-2-SR/BX) were used to guide the light from the deuterium–halogen lamp through the quartz window of the electrochemical cell and onto the spectrometer. The measured transmission spectra (integrated for 1 second) were divided by the reference spectrum (measured in the same cell prior to starting the experiment) to obtain the relative changes in the optical absorption (ΔA) as a function of applied potential and the wavelength of the light. The spectra were recorded while slowly scanning the potential, using a scan rate of 2 mV s−1.


The water oxidation photocurrent in semiconductor photoelectrodes is a product of the illumination intensity, φ, the light harvesting efficiency, ηLH, the bulk charge separation efficiency, ηCS, and the charge-transfer efficiency from the semiconductor to the electrolyte, ηCT (sometimes called the injection efficiency).
Jph = φηLHηCSηCT (1)

The ηLH is determined by the band gap and the absorption coefficient of the material. The ηCS, which is sometimes also called the hole collection efficiency, is defined as the fraction of the photogenerated holes that reaches the surface. Normally this is determined by the width of the space charge layer (SCL) and the minority carrier diffusion length, if we assume that no recombination occurs in the SCL. The ηCT in an n-type material is defined as the fraction of holes that transfers from the semiconductor into the electrolyte, and its value reflects the kinetic competition between charge transfer and surface recombination processes.

As mentioned earlier, the deposition of co-catalysts on the photoanode surface has been shown to either significantly improve the transfer efficiency (catalysis), to suppress the surface recombination, or to modify the band bending, all of which affects ηCT and/or ηCS. In order to determine which surface processes are affected, a measurement technique capable of de-convoluting the charge transfer processes is needed. When studying metal/electrolyte interfaces, methods based on potential variation, such as electrochemical impedance spectroscopy (EIS), are generally used to periodically modulate the reaction rates via the applied potential and in this way study the kinetics of charge transfer processes. However, these methods are not directly applicable for the semiconductor/electrolyte interface, since the potential variations appear mainly across the space charge region of the semiconductor rather than across the Helmholtz layer. Therefore, in IMPS, a modulation of the light intensity is used to modulate the surface concentration of the photo-generated carriers. We thus modulate the concentration of one of the reactants instead of the reaction rate constant itself. A simplified model, illustrated in literature by Peter et al., is then used to analyze the competition between hole transfer (i.e., hole injection into the electrolyte) and surface recombination at the semiconductor/electrolyte interface. From this analysis, one can extract the values of the reaction rate constants for charge transfer, ktr, and surface recombination, krec.29 In the case of simple one-electron charge transfer reactions, these rate constants are true rate constants (s−1). The situation is somewhat more complicated for the case of multi-step charge transfer reactions. One can still use the same expressions to analyze the IMPS response and distinguish the hole injection and surface recombination processes, but ktr and krec are now to be interpreted as phenomenological rate parameters that are functions of the rate constants of the elementary steps.30,31 One can, in principle, derive these expressions if the reaction mechanism is known,31 but so far this has not been attempted for the photo-oxidation of water by holes. We will therefore proceed with the understanding that ktr and krec are to be interpreted as pseudo first-order rate constants.

The small amplitude modulation of the light intensity results in a modulation of the photocurrent with the same frequency, but generally different magnitude and phase. The modulated photocurrent response consists of the sum of the hole current (minority carriers) and the electron current (majority carriers) that precedes the hole current. These in-phase and out-of-phase components result in a real and imaginary part of the photocurrent which can be plotted in a Nyquist plot. At low frequencies, this gives a semicircle that is located in the upper quadrant of the complex plane, see ESI Fig. S1. This part is called the “recombination semicircle” because the shape of the semicircle is largely dominated by surface recombination. The imaginary photocurrent reaches a maximum when the frequency matches the characteristic relaxation constant of the system:

ωmax = ktr + krec (2)

As outlined above, ktr and krec are the pseudo-first order charge transfer and recombination rate constants (s−1), respectively. The high and low frequency intercepts of the x-axis (imaginary current = 0) are analogous to the initial maximum (spike) and the steady state photocurrents in a photocurrent transient plot, respectively.

At the high frequency intercept, the recombination is “frozen” due to fast modulation. Detailed analysis shows that the value at this intercept represents the product of the hole current, jh, and the capacitance factor, CH/(CSC + CH).29 CSC is the space charge capacitance, which can be estimated from the lower quadrant semicircle (ESI Fig. S1) that represents the attenuation by the total series resistance of the cell and the combined space charge and Helmholtz capacitances of the sample, and is usually referred to as the RC time constant of the cell.29 The frequency at the minimum of the semicircle, ωmin, corresponds to the product of the series resistance of the cell Rcell and CSC (ωmin = (RcellCSC)−1). The Helmholtz capacitance CH is assumed to be 20 μF cm−2, but can usually even be neglected for standard materials with moderate charge carrier density.32 This means that normalizing the photocurrent at this high frequency intercept against the hole current (jphoto/jh) gives a value of CH/(CSC + CH) ≈ 1, when CSCCH.

The low frequency intercept represents the fraction of the holes that arrive at the surface that is injected into the electrolyte. This is none other than the charge transfer efficiency,

image file: c7sc00363c-t1.tif(3)

It is important to note that the model is based on three main assumptions. First, bulk processes (e.g., band-to-band recombination, trapping) are assumed to be invisible. This is true if bulk recombination occurs before significant charge separation can take place, as the latter will lead to displacement currents. Since bulk recombination processes are much faster (typically <100 ns) than surface processes (typically 100 μs to 1 s), this assumption is likely to hold. Secondly, the relevant processes should occur on the same time scale as the IMPS measurements, which is indeed the case for most surface recombination processes.1,4,33,34 Finally, the band bending is assumed to remain constant during the modulated illumination. This is true if the space charge capacitance and the density of majority carriers do not change significantly during the modulation of the light intensity. For the modest modulation depth used in this study (15%), this assumption is also reasonable. Further details on the theory of IMPS can be found in the literature.28,29,35,36

Results and discussion

Fig. 2 shows the complex IMPS plot for bare BiVO4 at different applied bias potentials. Each spectrum is normalized to ensure that the high frequency intercept with the real axis corresponds to CH/(CSC + CH). As the applied bias is increased, the low frequency intercept also increases. Since the low frequency intercept represents the charge transfer efficiency (ktr/(ktr + krec)), and recombination is expected to decrease at more positive potentials, this is as expected. The decrease in recombination at more positive potentials is also consistent with the overall increase of the photocurrent and the decrease of the transients in the chopped current–voltage curve shown in Fig. 3 (black curve).
image file: c7sc00363c-f2.tif
Fig. 2 IMPS spectra of BiVO4 photoanode under different applied potentials. The increase of low-frequency intercepts with increasing potential, indicate an improvement of the charge transfer efficiency.

image file: c7sc00363c-f3.tif
Fig. 3 Photocurrent–voltage (jV) curve of bare BiVO4 (black) and CoPi modified BiVO4 (red) taken under chopped illumination with a 455 nm LED (Φ = 4 mW cm−2).

Fig. 2 reveals that the high frequency semicircle of the photo response in the lower quadrant (the RC attenuation semicircle) is somewhat flattened. The same observation on hematite has been attributed to the frequency-dependence of the dielectric constant and/or surface inhomogeneities.20 A similar explanation may hold here, as our spray-deposited films show some roughness with typical feature sizes of ∼100 nm.37

Using eqn (2) and (3), the charge transfer rate constant, ktr, and the surface recombination rate constant, krec, are calculated from the IMPS spectra of un-modified and CoPi-modified BiVO4. Fig. 4 shows the results as a function of applied potential. We first analyze the bare BiVO4 and observe two potential ranges with different behaviors. At potentials below 1 VRHE, krec is constant whereas ktr increases with increasing potential. The constant krec suggests that the band bending does not change in this potential regime. Any change in the applied bias thus has to fall across the Helmholtz layer. This is indeed consistent with the observed increase in ktr with potential. Although this resembles metallic behavior (ESI Fig. S2a), it is highly unlikely that these (undoped) BiVO4 films are truly metallic in nature. Instead, we attribute the behavior of krec and ktr to Fermi level pinning at the BiVO4 surface (ESI Fig. S2b).

image file: c7sc00363c-f4.tif
Fig. 4 Charge transfer rate constant (red) and recombination rate constant (black) for the unmodified (open symbols) and the CoPi modified BiVO4 (closed symbols). The error bars represent the spread in the results obtained for different samples at selected potentials; in total, three bare BiVO4 electrodes and two BiVO4/CoPi electrodes were measured.

For potentials more positive than 1 VRHE, the photoanode is behaving more like a ‘normal’ semiconductor (ESI Fig. S2c). Most of the change in the applied bias falls across the space charge region, which affects the concentration of conduction band electrons and, therefore, krec. In this regime, ktr does not depend on the applied potential, which is indeed expected for a semiconductor/liquid junction. To further support these observations, the (external) quantum efficiency (EQE) is plotted as −ln(1 − EQE) as a function of the square root of the applied potential with respect to the flatband potential (ESI Fig. S3). At potentials > 1 VRHE, −ln(1 − EQE) is found to be proportional to the square root of the potential difference. This is in good agreement with the Gärtner equation,38 which expresses the photocurrent for an ideal planar Schottky-type junction:

image file: c7sc00363c-t2.tif(4)
−ln(1 − EQE) = αW + ln(1 + αLp) (5)
image file: c7sc00363c-t3.tif(6)
here, jh is the hole current that arrives at the surface, I0 is the incident photon flux, α is the absorption coefficient of the film, W is the width of the space charge region, and Lp is the hole diffusion length. ε0 and εr are the vacuum permittivity and dielectric constant, respectively, q is the elementary charge, ND is the donor density, φsc is the potential drop across the space charge layer (φsc = VappliedVFB), k is the Boltzmann constant, and T is the temperature. This ideal behavior implies that the Fermi level is no longer pinned at potentials positive of 1 VRHE.

After modification with CoPi, krec and ktr show very different behavior (Fig. 4, closed symbols). Most notably, the surface recombination rate constant is suppressed by a factor of 10–20 over the entire potential range. One possible explanation would be a change in band bending due to the formation of a Schottky-like contact between BiVO4 and CoPi. This in turn would affect the concentration of electrons at the surface (ns), and thus also the surface recombination rate constant. If this were the case, one would expect to observe a higher value of the high frequency photocurrent intercept with the real axis of the IMPS spectra, which corresponds to the flux of holes arriving at the surface before they have a chance to recombine (at these frequencies, recombination is ‘frozen’). A change in band bending would affect the width of the depletion region (where charge separation occurs), and thus the amount of photo-generated holes that reach the surface. As shown in Fig. S4, no significant difference in the high-frequency photocurrent intercept with the real axis is observed for bare and CoPi modified BiVO4. To further study the possibility of a change in band bending upon adding CoPi in more detail, we measured the change of the open circuit potential upon illumination (ΔOCP) using a high intensity cw Ar ion laser source (ESI Fig. S5). The ΔOCP is found to increase by only a small amount (∼24 mV) after adding the CoPi, independent of the light intensity. A 24 mV change in the surface band bending corresponds to a ∼2.5-fold decrease of surface majority carrier concentration, which is much lower than the observed ∼15-fold decrease of the surface recombination rate constant. Thus, while a small change in band bending is indeed observed, we conclude that it plays only a very minor (if any) role in suppressing the recombination in CoPi modified BiVO4.

An alternative explanation for the decrease in krec is that CoPi passivates the surface defects at which recombination occurs. Although the chemical nature of these surface defects and the mechanism by which passivation of such states by CoPi would occur is not clear at this stage, our observations are consistent with such a passivation mechanism.

For a more detailed analysis of the influence of CoPi, we first look at the behavior of CoPi-modified BiVO4 at modest applied potentials (<1 VRHE). The overall trends in Fig. 4 are the same as for bare BiVO4, i.e., ktr increases with potential and krec remains constant. This suggests that Fermi level pinning still occurs at the BiVO4/CoPi surface and that the surface states that are responsible for the Fermi level pinning are not passivated by the CoPi. Within this potential range, krec is reduced by the introduction of CoPi; this is attributed to surface passivation, as discussed above. However, the presence of CoPi does not affect the value of ktr. This is not what one would intuitively expect, since CoPi is expected to act as an electrocatalyst and should thus enhance the charge transfer rate. Instead, the negligible change in ktr suggests that the charge transfer still occurs via the BiVO4 surface. This is consistent with the recent findings of Ma et al.; based on their transient photocurrent/absorption studies, these authors also suggest that charge transfer still predominantly occurs via the BiVO4 in a CoPi-catalyzed BiVO4 film.39 This is actually not so surprising since the oxidation power (i.e., thermodynamic driving force) of holes in the valence band of BiVO4 is higher than that of holes in CoPi. Specifically, the overpotential of CoPi is reported to be ∼0.3–0.4 V, whereas the valence band of BiVO4 is located more than 1 V positive of the water oxidation potential.7,40–42

At potentials >1.0 VRHE, the recombination rate constant of the CoPi-modified BiVO4 is again greatly reduced. However, the charge transfer rate constant, ktr, decreases with increasing potential. We tentatively attribute this counter-intuitive observation to a gradual shift of direct water oxidation at the BiVO4 surface (high driving force) to oxidation via CoPi at more positive potentials. The reason for this shift is that the exposed BiVO4 surface, which is not very catalytically active, can no longer keep up with the increasing flux of photogenerated holes. As a result, an increasing fraction of these holes will now oxidize the CoPi. Although the latter has been reported to have a much higher intrinsic catalytic activity7,43 than the BiVO4 surface, the thermodynamic overpotential available for water oxidation for holes in CoPi is much lower than it is for holes in the BiVO4 valence band. This would explain the decrease in ktr with increasing potential.

To support this tentative model, we monitored the oxidation of CoPi as a function of the applied potential by in situ UV-Vis absorption measurements. The oxidation of CoPi leads to an absorption around 350 nm (Fig. S6a), while control experiments confirm that no optical changes occur for bare FTO (Fig. S6c) or for FTO/BiVO4 (Fig. S6d). The absorption data for FTO/BiVO4/CoPi, shown in Fig. S6b, reveal that CoPi starts to oxidize at potentials above ∼0.8 VRHE. This is close to the potential at which ktr for CoPi-modified BiVO4 starts to decrease (Fig. 4), and is consistent with our hypothesis (and the recent work of Ma et al.39) that water oxidation indeed shifts gradually from the BiVO4 surface to the CoPi.

The IMPS data clearly indicate that surface recombination limits the photocurrent of bare BiVO4, and that a CoPi layer enhances the photocurrent by passivating surface recombination centers. Although CoPi is well-known to be an efficient (dark) electrocatalyst, this does not seem to be its main function in the BiVO4/CoPi system. To further support the assertion that the photocurrent of BiVO4 is limited by surface recombination, we modified BiVO4 photoelectrodes with RuOx particles. RuOx is known to be an excellent water oxidation catalyst. If BiVO4 is not limited by hole transfer properties, modifying the surface with RuOx should not increase the charge transfer rate constant, ktr. In fact, ktr is expected to decrease due to the lower oxidation power of holes in RuOx compared to holes in the valence band of BiVO4. To test this prediction, we deposited RuOx onto BiVO4 photoanodes. We used a photo-assisted anodic process to ensure that the RuOx is deposited on the surface facets where the photo-generated holes arrive and do their electrochemical work. We also deposited RuOx on FTO to verify its high catalytic activity, see ESI Fig. S7. Fig. 5a shows that the photocurrent of BiVO4 does indeed not improve with the introduction of RuOx; it actually decreases. Moreover, Fig. 5b shows that the charge transfer rate constant is actually smaller than that of the bare BiVO4. The surface recombination is not affected, which shows that RuOx does not passivate the BiVO4 surface. These observations are fully consistent with our model and confirm our hypothesis that the photocurrent of BiVO4 is limited by surface recombination, not water oxidation kinetics.

image file: c7sc00363c-f5.tif
Fig. 5 (a) Photocurrent–voltage (jV) curve of bare BiVO4 (black) and RuOx modified BiVO4 (red) taken under illumination with a 455 nm LED (φ = 4 mW cm−2). (b) Charge transfer rate (red) and recombination rate constant (black) for the unmodified (open symbols) and the RuOx modified BiVO4 (closed symbols).

It should be pointed out that BiVO4 samples prepared by different methods may be limited by other factors. For example, undoped BiVO4 samples made by RF magnetron sputtering consistently show lower onset potentials and higher injection efficiencies than sprayed samples.44 Efforts to improve these sputtered samples by CoPi or RuOx deposition have been unsuccessful (unpublished results), most likely because their performance is limited by bulk recombination at sputter-induced defects.44 For the spray-deposited samples studied here, however, surface recombination is clearly the main performance-limiting factor.

Our understanding of the processes taking place at the bare and co-catalyst modified BiVO4 is summarized in Fig. 6. For the bare BiVO4 shown in Fig. 6a, the valence band holes can either directly oxidize water (1), or move to the surface states and recombine with conduction band electrons (2). The latter means that they do not participate in water oxidation. By functionalizing the BiVO4 with a surface passivating “co-catalyst”, such as CoPi, the surface state is passivated (Fig. 6b). This effectively blocks the surface recombination pathway for the valence band holes, which will instead be injected into the electrolyte to directly oxidize water. We note that the CoPi layer is porous, so part of the BiVO4 is still in direct contact with water. With increasing potentials, however, the surface of BiVO4 can no longer keep up with the photogenerated hole flux, due to its low intrinsic catalytic activity (slow kinetics). This limits the direct injection of holes into the electrolyte (1), and favors the competing pathway of hole transfer to the CoPi (3). Here, the intrinsic (catalytic) activity for water oxidation is higher, but the thermodynamic driving force is much smaller, which leads to an overall decrease in ktr with applied potential, as described above in detail. Finally, a non-passivating co-catalyst, such as RuOx, on BiVO4 (Fig. 6c) does not affect the recombination rate constant. The RuOx does, however, decrease the ktr compared to BiVO4 due to the lower oxidation power of the holes in RuOx.

image file: c7sc00363c-f6.tif
Fig. 6 Simplified model of the elementary processes in a BiVO4 photoanode (a) without a co-catalyst (b) with a surface passivating co-catalyst (e.g. CoPi) and (c) with a non-passivating co-catalyst (e.g. RuOx). Upon illumination, photo-excited carriers move towards the semiconductor–electrolyte interface, where direct water oxidation by valence band holes (1), surface state-mediated recombination (2), and charge transfer via co-catalyst (3) can take place.


Using IMPS, we have shown that modification of the surface of sprayed BiVO4 photoanodes with CoPi reduces surface recombination with a factor of 10–20. The charge transfer rate constant is much less affected, which is surprising in view of the fact that CoPi is a well-known electrocatalyst. The resulting increase in the overall charge transfer efficiency is consistent with the observed increase in photocurrent. Moreover, surface modification with RuOx, one of the best known OER catalysts, does not lead to an increase in the photocurrent. These results provide compelling evidence that the main role of CoPi on BiVO4 is not to enhance the water oxidation kinetics, but to suppress surface recombination. We emphasize that this conclusion is not absolute and recognize that there may be conditions under which CoPi indeed functions as an OER catalyst (as we suggested during the discussion of Fig. 6b).

Our conclusion also implies that the photocurrent of BiVO4 is not limited by surface reaction kinetics, but by surface recombination. Similar conclusions have recently been drawn for CoPi-catalyzed hematite electrodes8 which, perhaps in hindsight, is not so surprising when one considers the strong oxidizing power of the valence band holes in most wide-bandgap metal oxide semiconductors. The importance of surface recombination is very well recognized and established in the field of photovoltaics, but much less so in photoelectrochemistry and photocatalysis. At the moment it is unclear whether surface recombination is particular to BiVO4 (and perhaps certain types of α-Fe2O3), or if it is a more generally occuring limitation in oxide semiconductors. The same is true for the passivating behavior of CoPi; this “catalyst” may also be able to passivate other photoanode materials, and it is likely that there are also other materials that are able to passivate BiVO4 and Fe2O3. Further development of efficient photoelectrochemical solar fuel generators clearly requires a better understanding of semiconductor/catalyst systems and the processes that occur at these interfaces.


The authors thank the Helmholtz-NREL Solar Energy Initiative and the PECDEMO project (funded by the European Fuel Cell and Hydrogen Joint Undertaking (FCH-JU) under Grant Agreement 621252) for financial support of this work.

Notes and references

  1. Y. Ma, S. R. Pendlebury, A. Reynal, F. Le Formal and J. R. Durrant, Chem. Sci., 2014, 5, 2964 RSC.
  2. Y. Park, K. J. McDonald and K.-S. Choi, Chem. Soc. Rev., 2013, 42, 2321–2337 RSC.
  3. T. W. Kim and K.-S. Choi, Science, 2014, 343, 990–994 CrossRef CAS PubMed.
  4. Y. Ma, F. Le Formal, A. Kafizas, S. R. Pendlebury and J. R. Durrant, J. Mater. Chem. A, 2015, 3, 20649–20657 CAS.
  5. D. K. Zhong, S. Choi and D. R. Gamelin, J. Am. Chem. Soc., 2011, 133, 18370–18377 CrossRef CAS PubMed.
  6. L. Trotochaud, S. L. Young, J. K. Ranney and S. W. Boettcher, J. Am. Chem. Soc., 2014, 136, 6744–6753 CrossRef CAS PubMed.
  7. M. W. Kanan and D. G. Nocera, Science, 2008, 321, 1072–1075 CrossRef CAS PubMed.
  8. D. R. Gamelin, Nat. Chem., 2012, 4, 965–967 CrossRef CAS PubMed.
  9. M. Barroso, C. A. Mesa, S. R. Pendlebury, A. J. Cowan, T. Hisatomi, K. Sivula, M. Grätzel, D. R. Klug and J. R. Durrant, Proc. Natl. Acad. Sci. U. S. A., 2012, 109, 15640–15645 CrossRef CAS PubMed.
  10. Y.-R. Hong, Z. Liu, S. F. B. S. A. Al-Bukhari, C. J. J. Lee, D. L. Yung, D. Chi and T. S. A. Hor, Chem. Commun., 2011, 47, 10653 RSC.
  11. C. Y. Cummings, F. Marken, L. M. Peter, A. A. Tahir and K. G. U. Wijayantha, Chem. Commun., 2012, 48, 2027 RSC.
  12. J. A. Seabold and K. S. Choi, Chem. Mater., 2011, 23, 1105–1112 CrossRef CAS.
  13. F. F. Abdi, L. Han, A. H. M. Smets, M. Zeman, B. Dam and R. van de Krol, Nat. Commun., 2013, 4, 1–7 Search PubMed.
  14. H. Ye, H. S. Park and A. J. Bard, J. Phys. Chem. C, 2011, 115, 12464–12470 CAS.
  15. M. Higashi, K. Domen and R. Abe, J. Am. Chem. Soc., 2012, 134, 6968–6971 CrossRef CAS PubMed.
  16. Y. Liu, Y. Zhou, G. Chen, T. Guo, L. Wang, X. Huang and W. Zeng, Mater. Lett., 2015, 148, 155–158 CrossRef CAS.
  17. B. Klahr, S. Gimenez, F. Fabregat-Santiago, J. Bisquert and T. W. Hamann, Energy Environ. Sci., 2012, 5, 7626 CAS.
  18. F. Lin and S. W. Boettcher, Nat. Mater., 2014, 13, 81–86 CrossRef CAS PubMed.
  19. H. K. Dunn, J. M. Feckl, A. Müller, D. Fattakhova-Rohlfing, S. G. Morehead, J. Roos, L. M. Peter, C. Scheu and T. Bein, Phys. Chem. Chem. Phys., 2014, 16, 24610–24620 RSC.
  20. L. M. Peter, K. G. U. Wijayantha and A. A. Tahir, Faraday Discuss., 2012, 155, 309–322 RSC.
  21. W. Li, D. He, S. W. Sheehan, Y. He, J. E. Thorne, X. Yao, G. W. Brudvig and D. Wang, Energy Environ. Sci., 2016, 9, 1794–1802 CAS.
  22. J. E. Thorne, J.-W. Jang, E. Y. Liu and D. Wang, Chem. Sci., 2016, 7, 3347–3354 RSC.
  23. G. Liu, S. Ye, P. Yan, F. Xiong, P. Fu, Z. Wang, Z. Chen, J. Shi and C. Li, Energy Environ. Sci., 2016, 9, 1327–1334 CAS.
  24. F. F. Abdi and R. van de Krol, J. Phys. Chem. C, 2012, 116, 9398–9404 CAS.
  25. F. F. Abdi, N. Firet, A. Dabirian and R. van de Krol, MRS Proc., 2012, 1446 DOI:10.1557/opl.2012.811.
  26. Z. Gui, E. Gillette, J. Duay, J. Hu, N. Kim and S. B. Lee, Phys. Chem. Chem. Phys., 2015, 17, 15173–15180 RSC.
  27. E. Tsuji, A. Imanishi, K. I. Fukui and Y. Nakato, Electrochim. Acta, 2011, 56, 2009–2016 CrossRef CAS.
  28. L. Peter and L. Peter, Chem. Rev., 1990, 90, 753–769 CrossRef CAS.
  29. E. A. Ponomarev and L. M. Peter, J. Electroanal. Chem., 1995, 396, 219–226 CrossRef.
  30. D. J. Fermín, E. A. Ponomarev and L. M. Peter, J. Electroanal. Chem., 1999, 473, 192–203 CrossRef.
  31. L. M. Peter, E. A. Ponomarev and D. J. Fermin, J. Electroanal. Chem., 1997, 427, 79–96 CrossRef CAS.
  32. R. van de Krol and M. Grätzel, Photoelectrochemical Hydrogen Production, Springer-Verlag, 2012 Search PubMed.
  33. F. Le Formal, K. Sivula and M. Grätzel, J. Phys. Chem. C, 2012, 116, 26707–26720 CAS.
  34. S. R. Pendlebury, A. J. Cowan, M. Barroso, K. Sivula, J. Ye, M. Grätzel, D. R. Klug, J. Tang and J. R. Durrant, Energy Environ. Sci., 2012, 5, 6304–6312 CAS.
  35. J. Li and L. M. Peter, J. Electroanal. Chem., 1985, 193, 27–47 CrossRef CAS.
  36. R. Peat and L. M. Peter, J. Electroanal. Chem., 1987, 228, 351–364 CrossRef CAS.
  37. F. F. Abdi, N. Firet and R. van de Krol, ChemCatChem, 2013, 5, 490–496 CrossRef CAS.
  38. W. W. Gärtner, Phys. Rev., 1959, 116, 3 CrossRef.
  39. Y. Ma, A. Kafizas, S. R. Pendlebury, F. Le Formal and J. R. Durrant, Adv. Funct. Mater., 2016, 26, 4951–4960 CrossRef CAS.
  40. K. Ding, B. Chen, Y. Li, Y. Zhang and Z. Chen, J. Mater. Chem. A, 2014, 2, 8294 CAS.
  41. S. Kohtani, K. Yoshida, T. Maekawa, A. Iwase, A. Kudo, H. Miyabe and R. Nakagaki, Phys. Chem. Chem. Phys., 2008, 10, 2986 RSC.
  42. R. Saito, Y. Miseki and K. Sayama, Chem. Commun., 2012, 48, 3833 RSC.
  43. C. C. L. McCrory, S. Jung, J. C. Peters and T. F. Jaramillo, J. Am. Chem. Soc., 2013, 135, 16977–16987 CrossRef CAS PubMed.
  44. H. Gong, N. Freudenberg, M. Nie, R. van de Krol and K. Ellmer, AIP Adv., 2016, 6, 45108 CrossRef.


Electronic supplementary information (ESI) available: IMPS spectra, band diagrams, electrochemical and photoelectrochemical measurements, and absorption spectra Fig. S1–S7. See DOI: 10.1039/c7sc00363c
Equal contribution.

This journal is © The Royal Society of Chemistry 2017