A bifunctional lead–iron oxyfluoride, PbFeO2F, that functions as a visible-light-responsive photoanode and an electrocatalyst for water oxidation

The oxyfluoride PbFeO2F was investigated as a photoanode material and as an electrocatalyst for water oxidation. PbFeO2F powder, which was synthesized by a high-pressure method and had an estimated bandgap of 2.1 eV, was deposited onto a fluorine-doped tin oxide (FTO) substrate. Mott–Schottky plot measurements for the PbFeO2F/FTO electrode showed n-type semiconductivity of PbFeO2F, with a flat-band potential of +0.53 ± 0.05 V vs. reversible hydrogen electrode (RHE). The PbFeO2F/FTO electrode, which was modified with a conductive TiO2 layer and a cobalt phosphate water-oxidation cocatalyst, showed a clear anodic photocurrent in aqueous K3PO4 solution under visible-light irradiation (λ < 600 nm). The PbFeO2F/FTO electrode without any modification functioned as a stable water-oxidation electrocatalyst to form O2 with a faradaic efficiency of close to unity. This study demonstrates that PbFeO2F is a bifunctional material, serving as a water-oxidation photoanode under a wide range of visible-light wavelengths and as an electrocatalyst that operates at a relatively low overpotential for water oxidation.


Introduction
Hydrogen is expected to be used as a renewable energy carrier. Water splitting using semiconductor photoelectrodes or photocatalysts has attracted attention as a method of generating clean hydrogen using solar energy. 1-6 Titanium-based metal oxides (e.g., TiO 2 (ref. 7) and SrTiO 3 (ref. 8)) have been developed as stable photoanode materials for solar water oxidation but are not capable of efficiently utilizing visible light, which represents the majority of solar energy, because of their wide bandgaps (>3 eV). By contrast, visible-light-responsive metal oxides (e.g., a-Fe 2 O 3 (ref. [9][10][11] and BiVO 4 (ref. [12][13][14]) unavoidably require an additional electrochemical (or external) bias for operation because their conduction-band minimum (CBM) is more positive than the H + /H 2 reduction potential [0 V vs. standard hydrogen electrode (SHE) at pH 0].
Compared with the aforementioned oxide materials, mixedanion compounds such as oxynitrides and oxysuldes have relatively small bandgaps and negative CBM potentials, making them good candidate photoanode materials for water oxidation under visible light. 3,[15][16][17] Some of them (e.g., TaON 18,19 ) theoretically enable water splitting to be driven under visible light without requiring an external bias because the CBM and the valence-band maximum (VBM) straddle the water reduction/ oxidation potentials. However, the N 2p orbitals that constitute the VBM of oxynitrides are less stable than the O 2p orbitals, undergoing self-oxidation by holes generated during visible-light irradiation. This self-oxidation occurs with oxy-suldes, in which the VBM is formed by S 3p orbitals. Thus, although the high-energy p-orbitals of anions are essential for providing small bandgaps, they are the main factor preventing more stable water oxidation by mixed-anion compounds.
Recently, the oxyuoride Pb 2 Ti 2 O 5.4 F 1.2 , which is a mixedanion compound, has been reported as a visible-lightabsorbing photocatalyst with a narrow bandgap ($2.4 eV) and n-type semiconductivity. [20][21][22] Pb 2 Ti 2 O 5.4 F 1.2 has a CBM at approximately À1.0 AE 0.1 V vs. SHE, which is sufficiently more negative than the water reduction potential. 21 Thus, this oxy-uoride can drive standalone visible-light water splitting. Moreover, both the F 2p and O 2p orbitals are essentially stable toward self-oxidation by holes generated during visible-light irradiation of the oxyuoride. Indeed, a Pb 2 Ti 2 O 5.4 F 1.2 photoanode with visible-light responsivity and a relatively negative photocurrent onset potential has been reported. 23 However, the literature includes only one example of a visible-lightresponsive oxyuoride photoelectrode (i.e., Pb 2 Ti 2 O 5.4 F 1.2 ) that can utilize a limited portion of visible light at wavelengths as long as 500 nm. Therefore, exploration of a new oxyuoride photoelectrode that can absorb a greater range of visible-light wavelengths is important for enabling the design of visiblelight-responsive photoelectrode materials.
Fe(III)-containing materials are potentially useful as not only semiconductor photoanodes 9,11 but also catalysts for water oxidation. 24 In the present work, the oxyuoride PbFeO 2 F is examined as an electrode material for water splitting with and without irradiation. PbFeO 2 F, which can be synthesized by a high-pressure method, 30 is an anion-disordered cubic perovskite with space group Pm 3m (Fig. 1, drawn by the VESTA program 31 ). PbFeO 2 F has been reported to exhibit antiferromagnetic behavior. 32 It has also been reported to exhibit a yellow colour and is therefore expected to function as a photoelectrode material under visible light. In addition, the fact that PbFeO 2 F contains iron, an element that may provide active sites for water oxidation, suggests another functionality of electrocatalyst. Herein, we report that PbFeO 2 F can indeed function as both a semiconductor photoanode and electrocatalyst for water oxidation.

Experimental
Synthesis of PbFeO 2 F PbFeO 2 F powder was synthesized via solid-state reaction under high pressure using a mixture of PbO (99.9%, Kanto Chemical), PbF 2 (99.999%, Soekawa Chemical) and Fe 2 O 3 (99.99%, Rare Metallic). 32 A stoichiometric mixture of the starting materials was dried under reduced pressure at $573 K overnight. The mixture was sealed in an Au capsule (0.2 mm thick, 3.1 mm inner diameter and 3.2 mm depth), and the loaded capsule was subsequently inserted into a NaCl sleeve. The sleeve and capsule were inserted into a pyrophyllite cube block (one side 13 mm) with a cylindrical graphite heater. The mixture was reacted in a TRY cubic multianvil-type high-pressure apparatus (NAMO 2001) at 6.0 GPa and 1173 K for 30 min and was subsequently quenched to room temperature.

Fabrication of PbFeO 2 F/FTO electrodes
The PbFeO 2 F electrodes were fabricated using an electrophoretic deposition method. 33 Electrophoretic deposition was performed in a 50 mL acetone solution (>99.5%, Kanto Chemical) containing 100 mg of PbFeO 2 F powder and 20 mg of I 2 (>99.8%, FUJI-FILM Wako Pure Chemical). Two parallel uorine-doped tin oxide (FTO) glass substrates were immersed $15 mm apart in the solution, and a potential of 30 V was applied for 30 s using a stabilized DC power supply (PSW 80-13.5, GW Instek). The asfabricated electrodes were then heated at 573 K for 1 h in air in the case of electrodes not subjected to subsequent modications.
Ti(OCH(CH 3 ) 2 ) 4 treatment and Co-Pi electrodeposition for PbFeO 2 F/FTO electrodes According to the previously reported method, 34 Ti(OCH(CH 3 ) 2 ) 4 treatment was carried out by dipping the PbFeO 2 F/FTO electrode in an ethanol solution of 0.1 M Ti(OCH(CH 3 ) 2 ) 4 (>97%, Kanto Chemical), followed by drying on a hotplate at $423 K. The procedure was repeated ve times. Finally, the electrode was heated in air at 573 K for 1 h. Cobalt phosphate (Co-Pi) cocatalyst, known as a water-oxidation promoter, 35 was then electrodeposited onto the TiO 2 /PbFeO 2 F/FTO electrode. 35,36 A threeelectrode cell was used with the TiO 2 /PbFeO 2 F/FTO as the working electrode, a Ag/AgCl electrode as the reference electrode and Pt wire as the counter electrode. An electrochemical bias of +1.0 V vs. Ag/AgCl was applied to the working electrode in 0.1 M potassium phosphate buffered at pH 7 and containing 0.5 mM cobalt nitrate (98%, FUJIFILM Wako Pure Chemical) until the charge passing through the outer circuit reached 100 mC unless otherwise stated. The pH of the phosphate solution was controlled by mixing KH 2 PO 4 (>98.0%, Kanto Chemical), K 2 HPO 4 (>98.0%, Kanto Chemical) and/or K 3 PO 4 ($98%, Sigma-Aldrich), where the concentration was maintained at 0.1 M in total.

Characterization
A crystalline phase of the PbFeO 2 F powder was conrmed by Xray diffraction (XRD) measurements with a Malvern Panalytical X'Pert 3 powder diffractometer (monochromated Cu Ka). The light-absorption properties of the PbFeO 2 F powder were characterized via UV-vis diffuse-reectance spectroscopy (DRS) with a JASCO V-565 spectrophotometer. Scanning electron microscopy (SEM) observations combined with energy-dispersive X-ray spectroscopy (EDS) measurements were conducted on a HITA-CHI S4700 equipped with an EDAX Genesis apparatus at the Materials Analysis Division, Open Facility Center, Tokyo Institute of Technology. Inductively coupled plasma optical emission spectrometry (ICP-OES) measurements were conducted with a 5100 VDV apparatus (Agilent Technologies). Measurements for Mott-Schottky plots were carried out using a BAS ALS/ CHI760E electrochemical analyser. Electrochemical impedance spectroscopy measurements were performed using a potentiostat (pocketSTAT, Ivium Technologies). Mott-Schottky plots were recorded at a frequency of 100 Hz with a three-electrodetype system using the PbFeO 2 F/FTO as the working electrode, a Ag/AgCl electrode as the reference electrode (in saturated KCl aqueous solution) and Pt wire as the counter electrode in 0.1 M aqueous potassium phosphate solutions. The solutions were stirred and purged with Ar gas for 30 min before the measurements were conducted.

Photoelectrochemical measurements
The photoelectrochemical measurements were performed with a potentiostat (HSV-110, Hokuto Denko) and an electrochemical cell with a three-electrode conguration using the as-prepared PbFeO 2 F working electrode, an Ag/AgCl reference electrode and a Pt-coil counter electrode. The cell was made of Pyrex glass. An aqueous solution of 0.1 M K 3 PO 4 ($98%, Sigma-Aldrich) was used as the electrolyte, which was stirred and purged with Ar gas for 30 min before the measurements were conducted. It is known that coexistence of phosphate ions in an electrolyte solution has a positive effect on electrochemical water oxidation activity of the Co-Pi catalyst, 35,37 that and basic conditions are generally preferable for water oxidation. The light source was a 300 W Xe lamp (PE300BF, Cermax) tted with an L42, Y48, O54, O58, R62 or R70 cutoff lter (HOYA) to emit visible light of each wavelength range. The irradiation area was 3 cm 2 . The light intensity was approximately 0.31 W cm À2 in the wavelength range 350-700 nm unless otherwise stated. The potentials measured against the Ag/AgCl reference (saturated KCl aqueous solution) were converted to potentials vs. RHE (E RHE ¼ E Ag/AgCl + 0.059 pH + 0.197 at 298 K).
Incident photon to current conversion efficiency (IPCE) was measured in a similar manner using the same 300 W xenon lamp tted with an L38 cutoff lter and a band-pass lter centred at 420 nm (HOYA). The IPCE was calculated by the following equation: where i, l, and 4 is the photocurrent density measured under an irradiation of incident light, the incident light wavelength, and the intensity of incident photon (11 mW cm À2 ), respectively. The irradiation area was 0.28 cm 2 .

Quantifying electrochemical O 2 evolution
To quantify the O 2 evolved during controlled-potential electrolysis, electrochemical measurements were performed in a gastight H-type electrochemical cell with two chambers divided by a peruorinated membrane (Naon 117, Sigma-Aldrich). The PbFeO 2 F/FTO working electrode and an Ag/AgCl reference electrode were separated from a Pt-wire counter electrode in each chamber. The other conditions were identical to those mentioned in the description of the photoelectrochemical measurements. The evolved O 2 was detected using a gas chromatograph (MGC3000A, Incon) equipped with a thermal conductivity detector and an MS-5A column. Ar gas was used as the carrier gas.

Results and discussion
Light absorption behaviour and at-band potential of PbFeO 2 F The single-phase production of the as-synthesized PbFeO 2 F was conrmed by XRD measurement (Fig. S1 †). SEM observations show that the synthesized PbFeO 2 F consisted of 0.1-10 mm particles (Fig. S2 †). The UV-vis DRS spectra of the PbFeO 2 F (Fig. 2) indicate that the material has an absorption edge at $600 nm and substantial absorption in the longer-wavelength region, which might be attributable to anionic defects. As reported for a-Fe 2 O 3 , the longer-wavelength absorption band is assigned to oxygen vacancies. 38,39 The bandgap of the PbFeO 2 F was estimated to be 2.1 eV on the basis of the onset wavelength in the UV-visible DRS spectra. The previously reported PbFeO 2 F exhibited a yellow colour, 30 whereas the as-prepared PbFeO 2 F in the present work was yellow-brown. This difference in colour originates from different concentrations of anionic defects (i.e., different concentrations of reduced metal ions), which commonly affect the appearance of powders. 40 The as-synthesized PbFeO 2 F was deposited onto a FTO substrate via electrophoretic deposition. As shown in Fig. 3, the thickness of the deposited PbFeO 2 F particles was 1-2 mm. In the electrophoresis method, colloidal particles suspended in liquid migrate in an electric eld between two electrodes, undergoing deposition onto one side of the two electrodes. 33 Therefore, light-weight, smaller particles are preferentially deposited onto the electrode. Therefore, it is considered that the size of the deposited PbFeO 2 F particles (0.1-2 mm) were smaller than the as-synthesized PbFeO 2 F ones (0.1-10 mm).
To determine the at-band potential (E FB ) of PbFeO 2 F, Mott-Schottky plots of the PbFeO 2 F/FTO electrode were recorded in aqueous phosphate solutions with different pH values under dark conditions. As shown in Fig. 4A, the Mott-Schottky plots show positive slopes irrespective of pH, which indicates n-type semiconducting behaviour of the PbFeO 2 F. The E FB values, which were obtained by extrapolation of the linear portion to the x-axis intercept, were negatively shied with increasing electrolyte pH. The negative E FB shi corresponds to approximately À0.0591 V per pH, indicating Nernstian behaviour (Fig. 4B). Thus, the E FB of PbFeO 2 F was determined to be +0.53 AE 0.05 V vs. RHE. The CBM of an n-type semiconductor depends  on its conductivity and lies at 0.1-0.3 V negative relative to the E FB . 41 Assuming that the difference between the CBM and the E FB of PbFeO 2 F was 0.2 V because of the unclaried conductivity of PbFeO 2 F, the CBM is estimated to be +0.33 AE 0.05 V vs. RHE. This potential is more positive than the H + /H 2 reduction potential (0 V vs. RHE), as displayed in Fig. 4C. On the basis of the bandgap of PbFeO 2 F (2.1 eV), the VBM of PbFeO 2 F was determined to be +2.43 AE 0.05 V, which is more positive than the water oxidation potential (+1.23 V vs. RHE).

Photoelectrochemical response
The as-deposited PbFeO 2 F/FTO electrode was subjected to a post-necking treatment with an ethanol solution of titanium(IV) isopropoxide [Ti(OCH(CH 3 ) 2 ) 4 ], followed by heating at 573 K for 1 h in air. This treatment resulted in the deposition of a TiO 2 layer onto the PbFeO 2 F/FTO electrode (Fig. 5), which is expected to contribute to an enhanced photocurrent because of the reduced resistance of the electrode, as demonstrated in previous works. 34,42 A Co-Pi cocatalyst, known to function as a water-oxidation promoter, 35 was then electrodeposited onto the as-prepared TiO 2 /PbFeO 2 F/FTO electrode. 36 The deposited Co-Pi was observed as islands on the TiO 2 /PbFeO 2 F/FTO electrode surface (Fig. 6A). EDS spectra also show the presence of P and Co species on the electrode surface (Fig. 6B). Peaks of P at 2.0 keV and Co at 6.9 keV were observed, the latter of which was overlapped with an Fe peak at 7.1 keV. In addition, EDS spot analysis demonstrated that the islands contain more P and Co species than the region surrounding the islands (Fig. S3 †). Cyclic voltammetry (CV) of the modied electrodes was conducted in 0.1 M K 3 PO 4 solution under dark conditions (Fig. 7). A TiO 2 /FTO electrode, which was prepared by Ti(OCH(CH 3 ) 2 ) 4 treatment of an FTO substrate, showed little dark current in the examined potential range. By contrast, the PbFeO 2 F/FTO and Co-Pi/TiO 2 /PbFeO 2 F/FTO electrodes exhibited dark current with a redox peak in the range from 0 to +0.6 V vs. RHE. This dark current might be attributable to a redox reaction involving Fe cations in PbFeO 2 F because the dark current was observed when PbFeO 2 F was present. A similar CV prole has been reported for an a-Fe 2 O 3 photoanode in the same potential range investigated in the present study. 43 For the PbFeO 2 F/FTO electrode, a dark current with an irreversible wave in the range from +1.4 V vs. RHE was observed, attributable to the oxygen evolution reaction and/or the oxidation of Fe 3+ to Fe 4+ . 43 The oxidation of Pb 2+ to Pb 4+ can contribute to the dark current as well. 44 The Co-Pi/TiO 2 /PbFeO 2 F/FTO electrode also gave a dark current with a redox peak in the range from +0.9 to +1.8 V. The dark current originated from Co species on the Co-Pi electrodeposited electrode. 35,45,46 This interpretation is supported by an increase in the dark current for electrodes that contained more Co-Pi cocatalyst (Fig. S4 †). Given these results,   photoelectrochemical measurements were conducted in the potential range from +0.5 to +1.3 V to avoid the dark current during the positive sweep scan. The feasibility of using PbFeO 2 F as a water-oxidation electrocatalyst will be discussed in a later section.
Linear-sweep voltammetry of the modied electrodes in 0.1 M K 3 PO 4 solution was conducted under intermittent visiblelight irradiation (Fig. 7). The PbFeO 2 F/FTO electrode exhibited no photocurrent response. By contrast, a slight photocurrent response was observed with the TiO 2 /PbFeO 2 F/FTO electrode, primarily because of reduced interparticle resistance in the electrode. 34,47 As displayed in Fig. S5, † electrochemical impedance spectroscopy conrmed that the charge-transfer resistance of the TiO 2 -deposited electrode was smaller than that of the electrode without TiO 2 , as indicated by the smaller arc of the semicircle in the Nyquist plots. The reduction of the chargetransfer resistance originates from improved conductivity of the electrode, which was achieved as a result of the TiO 2 treatment.
As previously mentioned, the CBM of PbFeO 2 F was located at +0.33 AE 0.05 V vs. RHE (Fig. 4), which is more positive than the reported CBM of TiO 2 (À0.04 V vs. RHE). 48 Therefore, charge transfer from the CBM of PbFeO 2 F to that of TiO 2 is apparently not efficient. However, TiO 2 has midgap states that originate from defective sites ($0.4 V below the CBM). 49 In the shallow defect states, the trapped electrons can be thermally detrapped and exhibit high mobility. 50 This effect is inferred to have improved interparticle conductivity, which is known to function as an electron trapping-detrapping effect in TiO 2 -based dyesensitized solar cells. 51 A clear anodic photocurrent was observed for the Co-Pi/ TiO 2 /PbFeO 2 F/FTO electrode (Fig. 7). Loading the Co-Pi cocatalyst resulted in improved rate of charge transfer at the electrode interface for water oxidation and in charge separation from the surface to the bulk. 35,52 This effect was conrmed by electrochemical impedance spectroscopy measurements (Fig. S5 †). In addition, the anodic photoresponse again showed n-type semiconducting character of PbFeO 2 F, with a photocurrent onset potential of +0.7 V vs. RHE, although an accurate determination was difficult because of an overlap of dark current. The photocurrent onset potential of the Co-Pi/TiO 2 / PbFeO 2 F/FTO electrode, which can be regarded as the at-band potential of PbFeO 2 F, was slightly more positive than that determined from the corresponding Mott-Schottky plot (+0.53 AE 0.05 V, Fig. 4). This result implies that charge recombination in the illuminated PbFeO 2 F surface was substantial and concealed the real at-band potential, similar to the case of a-Fe 2 O 3 photoanodes. 9,53 Photoelectrochemical activity under a wide range of visible light Fig. 8 demonstrates anodic photocurrent densities of the Co-Pi/ TiO 2 /PbFeO 2 F/FTO electrode at +1.0 V vs. RHE in aqueous 0.1 M K 3 PO 4 solution (pH 13.4) under irradiation with light of different wavelengths, which was controlled using different cutoff lters. The UV-vis DRS spectrum of the PbFeO 2 F powder is also shown in Fig. 8. The photocurrent densities decreased with increasing cutoff wavelength and became almost zero under >600 nm irradiation. This change in the anodic photocurrent corresponded to the light-absorption properties of PbFeO 2 F, indicating that the PbFeO 2 F photoanode operated under visible-light irradiation with wavelengths as long as $600 nm and that the anodic photoresponse occurred by light absorption of PbFeO 2 F itself. It was also conrmed that no photocurrent was generated from Co-Pi/TiO 2 /FTO electrode (Fig. S6 †).
The results also indicate that an absorption band of longer wavelengths than 600 nm does not contribute to the generation of anodic photocurrent. As previously mentioned, the absorption band at longer wavelengths originates from anionic defects in PbFeO 2 F, as reported in a-Fe 2 O 3 . 38,39 Lifetimes of charge carriers generated at defect states in a semiconductor are generally short, 54,55 which could be the reason for the negligible photoresponse of PbFeO 2 F under >600 nm irradiation.
The stability of the anodic photocurrent was examined via controlled-potential photoelectrolysis at +1.0 V vs. RHE (Fig. S7A †). This measurement shows that the anodic  photocurrent gradually decayed with increasing reaction time. The O 2 evolution could not be quantied because of the small current that owed during the photoelectrolysis. Nevertheless, the fact that Co-Pi (a well-known water oxidation promoter) improved the anodic photocurrent density of the PbFeO 2 F electrode (Fig. 7) strongly suggests the oxidation of water to O 2 . As previously mentioned, the oxidation of metal cations in the PbFeO 2 F/FTO electrode was suggested; 43,44 however, the concentration of metal cations found in the electrolyte solution by ICP-OES was negligible (below ppm level).
It has been reported that stability of a photoanode for water oxidation is inuenced by various factors (e.g., cocatalyst, electrolyte pH, operating potential and so on). 18,47 It is therefore expected that optimizing these factors will improve photoelectrochemical stability of PbFeO 2 F and also photocurrent density, although it is beyond the scope of this work, which aimed at developing a new electrode material based on oxy-uorides. Nevertheless, more stable, larger photocurrent from the TiO 2 /PbFeO 2 F/FTO electrode was observed in the presence of I À as a reversible electron donor upon visible light than in aqueous solution without I À (Fig. S7B †). This indicates that PbFeO 2 F is essentially stable toward the photooxidation reaction.

Electrochemical water oxidation by PbFeO 2 F in the dark
The ability of PbFeO 2 F to function as an electrocatalyst for water oxidation was investigated by controlled-potential electrolysis using the as-prepared PbFeO 2 F/FTO electrode at +1.7 V vs. RHE under dark conditions (Fig. 9). Although the onset potential of water oxidation current by the PbFeO 2 F/FTO electrode was more negative than +1.7 V (see Fig. 7), we conducted the electrolysis experiment at +1.7 V in order to obtain more O 2 gas for reliable quantication. GC analysis of the evolved O 2 gas shows that the PbFeO 2 F functions as an electrocatalyst to stably produce O 2 . The amount of O 2 evolved at the initial stage of the electrolysis was slightly smaller than one-fourth the amount of electrons that owed to the outer circuit. This result is attributed primarily to a time lag of gas diffusion from the solution to the gas chromatograph. In fact, the total O 2 evolved reached the value expected on the basis of the reaction stoichiometry, giving a high faradaic efficiency of 97%. This result indicates that water oxidation was the major path at the PbFeO 2 F/FTO electrode. Under the same condition, an a-Fe 2 O 3 /FTO electrode, prepared in a similar manner, did not produce appreciable current, indicative of its large overpotential for water oxidation.

Conclusions
PbFeO 2 F synthesized by a high-pressure method had grain sizes ranging from 0.1 to 10 mm and an estimated bandgap of 2.1 eV. The Mott-Schottky plot measurements showed n-type semiconductivity of PbFeO 2 F with a at-band potential of +0.53 AE 0.05 V vs. RHE. The PbFeO 2 F electrode modied with a conductive TiO 2 layer and a Co-Pi water-oxidation cocatalyst exhibited a clear anodic photocurrent in aqueous K 3 PO 4 solution under visible-light irradiation (l < 600 nm).
At present, the performance of the PbFeO 2 F photoanode is not satisfactory; IPCE at 420 nm was 0.14% at +1.0 V vs. RHE. Nevertheless, it is expected that photoelectrochemical performance of PbFeO 2 F will be improved by further development in materials synthesis and post modication technologies for PbFeO 2 F, as we can learn from the history of the a-Fe 2 O 3 photoanode. [9][10][11] Meanwhile, a PbFeO 2 F/FTO electrode without the modications exhibited anodic current and O 2 evolution in aqueous K 3 PO 4 solution at +1.7 V vs. RHE, where water oxidation did not proceed for an a-Fe 2 O 3 electrode. The present study reveals that PbFeO 2 F becomes a bifunctional material-that is, a photoanode material that can function under a wide range of visiblelight wavelengths and as an electrocatalyst at a relatively low overpotential for water oxidation.

Conflicts of interest
There are no conicts to declare.