State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences,

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Electronic Supplementary Material (ESI) for Chemical Science. This journal is The oyal Society of Chemistry 16 Electronic Supplementary Information Insight into the Charge Transfer in Particulate Ta 3 Photoanode with High Photoelectrochemical Performance Zhiliang Wang, ab Yu Qi, ab Chunmei Ding, a Dayong Fan, ab Guiji Liu, ab Yongle Zhao ab and Can Li a* a State Key Laboratory of Catalysis, Dalian Institute of Chemical Physics, Chinese Academy of Sciences, Dalian National Laboratory for Clean Energy, The Collaborative Innovation Center of Chemistry for Energy Materials (ichem), Zhongshan oad 57, Dalian, 1163, China. E-mail: canli@dicp.ac.cn b University of Chinese Academy of Sciences, China. 1

Preparation of different kinds of metal based substrates The Pt and Ta based substrates were prepared by sputtering coating. Generally, metal layer with thickness of 3~5 μm was deposited onto a Ti foil (1 cm cm) with the target (Pt or Ta) on a home-built sputtering coater. Characterization of Photocatalytic water oxidation The powder (13 mg) of necked-ta 3 was peeled off from a large piece of electrode (.7 cm.8 cm). For comparison, similar amount of raw Ta 3 powder (16 mg) was used for the PC reaction. The photocatalytic reactions were carried out in a Pyrex top-irradiation-type reaction vessel connected to a closed gas circulation system. 1 1 ml aqueous solution containing a certain amount of photocatalyst was adopted, and 1 mg AgN 3 (Alfa Aesar, 99.9 %) was used as sacrificial electron acceptor..1 g La 3 (Sinopharm Chemical eagent, 99.95 %) was added to keep the ph value of the reaction solution. Prior to irradiation, the reaction mixture was evacuated to make sure that the air was completely removed. Then a 3 W xenon lamp equipped with an optical filter (Hoya, L-; λ nm) to cut off the ultraviolet light irradiated the system from the top side. A flow of cooling water was used to maintain the system at room temperature. The evolved gases were analyzed by gas chromatography (Agilent; GC-789A, MS-5A column, TCD, Ar carrier). Fabrication of Ta 3 device for TPV test Typically, the Ta 3 device was fabricated by covering the electrode with a piece of FT (Be careful in case of short circuit). During the experiment, it is found the Ti foil is not flat enough, so we used Ti coated glass as substrate. About 1 μm Ti was sputtered onto the glass ( cm 1 cm) in a home-built sputtering coater at the power of 5 W. Then the Ta 3 powder was deposited onto it by EPD. The device was fabricated by clipping a piece of FT (.5 cm.7 cm) on the Ta 3 membrane. And for the device illuminated from frontward and backward direction (Figure S7 a), it is fabricated by depositing raw-ta 3 on FT and further covering another pieces of FT on the electrode. TPV test is conducted with 355 nm pulsed laser (5 ns). The power is 1 mw unless otherwise mentioned. The signals are connected by an oscilloscope (Tektronix TDS 31C). Necking treatment of Ta 3 electrode prepared by oxidation-nitridation Ta 3 electrode was prepared according to the literature. Typically, Ta foil ( cm 1 cm) was oxidized at 58 o C for 7 min to form a layer of tantalum oxide. The raw Ta 3 electrode was prepared by nitriding of the oxidized Ta foil in NH 3 flow (5 sccm) at 95 o C ( o C/min) for 5 h. After that, mm TaCl 5 methanol solution was used for necking treatment with 1 μl per time (five times in total). Then the electrode was heated at 6 o C (5 o C/min) for 1 h in NH 3 flow (1 sccm). Estimation of C bulk and C crystal C bulk here is defined as capacitive charging to the porous Ta 3 matrix. It can be treated as a parallel capacitor, and the capacitance is determined as: C bulk = εε o d (S1) The ε is the permittivity constant of Ta 3, estimated to be 17 ; ε o is the vacuum permittivity constant; d is the distance of two substrates, estimated to be 5 μm from SEM image below. And C bulk is estimated to be 3 1-5 F/cm. C bulk is mainly determined by the intrinsic property of Ta 3 (ε of Ta 3 ). Thus, we assume that the values of C bulk are at the same order of magnitude for raw and necked Ta 3 devices. C crystal can be estimated from the τ 1 (τ=c). Ta 3 has the electric conductivity of 1.3 1 - (Ω cm) -1 3. Thus, the C crystal is estimated to be at the order of 1-8 F/cm.

Figure S1. The SEM image of cross-section of necked-ta 3 electrode. necked-ta 3 TaCl 5 -Ta 3 Intensity (a.u.) heated-ta 3 raw-ta 3 Ti Ta 3 powder 1 3 5 6 (degree) Figure S. XD patterns of as-prepared Ta 3 powder and the fabricated electrodes 3

j (ma/cm ) 6 15 mm TaCl 5-6 o C mm TaCl 5-6 o C 5 mm TaCl 5-6 o C 1 mm TaCl 5-6 o C 5 mm TaCl 5-6 o C mm TaCl 5 raw Ta 3-6 o C raw Ta 3 dark (a) j (ma/cm ) 6 5 o C 55 o C 6 o C 65 o C necked with mm TaCl 5 (b)..6.8 1. 1. 1. 1.6 1.8 E (V vs HE)..6.8 1. 1. 1. 1.6 1.8 E (V vs. HE) Figure S3. The influences of (a) TaCl 5 concentration and (b) necking treatment temperature on the PEC performance of Ta 3 electrodes. 6 Ti j (ma/cm ) Ti Pt Ti Ta..6.8 1. 1. 1. 1.6 E (V vs. HE) Figure S. The influence of substrates on the activity. All the Ta 3 electrodes were necked with mm TaCl 5 and heated at 6 o C in 1 sccm NH 3 flow.

Absorption (a.u.) LHE 1.5 1..5. 1..8.6 (a) raw-ta3n5 3 necked-ta3n5 neck-ta 3 5 6 7 8 Wavelength (nm) (c) 3 1 6 8 Wavelength (nm) Absorbed Photon Flux AM 1.5G (W m - nm -1 ) Current Flux (A m - nm -1 ). 1.5 1..5..6.. 6 8 1 1 (d) Wavelength (nm) 5 1.6mA/cm (b) 5 3 1. 3 5 6 7 8 Wavelength (nm) 15 1 5 Photon Flux (1 17 m - s -1 nm -1 ) Integrated Current (ma/cm ) Figure S5. The calculation (blue) of integrated current of Ta 3 electrode. (a) The light absorption spectra of raw-ta 3 (black) and necked-ta 3 (orange) electrode. (b) The spectrum of simulated sunlight (AM 1.5 G). (c) The light harvest efficiency (LHE) and absorbed photons. LHE can be got from the absorption with this expression : LHE (λ)=1-1 -A(λ). (d) The calculated integrated current. All the dates are for raw-ta 3 except that in (a). 5

Figure S6. Current-bias response of the Ta 3 device under dark (red) and illumination (black). The light source used here is simulated AM 1.5G sunlight (1 sun). (a) 8 (b) Photovoltage (mv) frontward illumination backward illumination Photovoltage (mv) 6 1 mw mw 1 3 Time ( s)..5 1. 1.5 Time ( s) Figure S7. (a) The responses of photovoltage upon frontward illumination (black, solid) and backward illumination (black, dashed line). The red dashed line indicates the mv level. (b) The responses of the photovoltage with different laser power: 1 mw (black) and mw (red) 6

Current (ma/cm ) Current (ma/cm ) 6 - - 5-5 -1-15 - -5 (a) on Pt in 1 M NaH+.5 M K 3 Fe(CN) 6 H evolution -...6 1. 1. 1.8 (c) Fe(CN) - 6 /Fe(CN)3-6 Potential (V vs HE) in 1 M NaH+.5 M K 3 Fe(CN) 6 substrate necked Ta 3 -....8 1. Potential (V vs HE) evolution Current (ma/cm ) Current (ma/cm ) - - -6-1. -.5..5 1. 1.5. 1-1 - (b) (d) in 1 M NaH H evolution necked Ta 3 substrate Potential (V vs HE) in 1 M NaH+.5 M K 3 Fe(CN) nd 6 3rd th/5th 1st CoPi/necked-Ta 3 Fe(CN) -/3-6 Co +/3+ -3 -....8 1. 1.6 Potential (V vs HE) Figure S8. (a) The CV on Pt foil in NaH (1 M)+K 3 Fe(CN) 6 (.5 M) aqueous solution to show the redox peaks of ferri/ferrocyanide. (b) and (c) The CV of necked Ta 3 electrode (black) and its substrate (nitridized Ti foil, red) in NaH (1 M) and NaH (1 M)+K 3 Fe(CN) 6 (.5 M) aqueous solution, respectively. (d) The CV of CoPi/necked-Ta 3 electrode in NaH (1 M)+K 3 Fe(CN) 6 (.5 M) aqueous solution. The scan is repeated for 5 circles and the first circles is found to be influenced by the reduction of CoPi. At the last circle of scan, the CV curve is similar to that of necked-ta 3 electrode in the current and potential of the reduction peak. 7

: oxidation state, Fe(CN) 6 3- - : reduction state, Fe(CN) necking 6 e - e - e - e - raw-ta 3 poor contact e - e - e - e - e - necked-ta 3 good contact Figure S9. The schematic illustration of electrochemical reduction of K 3 Fe(CN) 6 on raw-ta 3 and necked-ta 3 electrode. Capacity current ( A/cm ) 15 1 5-5 -1-15 in NaH Scan rate: mv/s 5 3 1 -.1..1. Potential (V vs SCE) Figure S1. The CV of necked-ta 3 electrode in NaH (1 M) at different scan rates (-5 mv/s) in NaH (1 M) aqueous solution. 8

6 necking treatment j (ma/cm ) thermal oxide Ta 3.6.8 1. 1. 1. 1.6 1.8 E (V vs HE) Figure S11. The j-e curves for Ta 3 electrode made from oxidation-nitridation (black) with further necking treatment (red). Electrolyte: 1 M NaH aqueous solution. Illumination: 1 mw/cm, AM 1.5G. 6 necked-ta3n5 injection efficiency (%)8 CoPi/necked-Ta3N5.5.7.9 1.1 1.3 E (V vs HE) Figrue S1. The injection efficiency of necked-ta 3 (black) and CoPi/necked-Ta 3 (red) electrodes. eferences 1. S. Chen, S. Shen, G. Liu, Y. Qi, F. Zhang and C. Li, Angewandte Chemie International Edition, 15, 5, 37-351.. A. Ziani, E. Nurlaela, D. S. Dhawale, D. A. Silva, E. Alarousu,. F. Mohammed and K. Takanabe, Physical Chemistry Chemical Physics, 15, 17, 67-677. 3. J. Swisher and M. ead, Metallurgical Transactions, 197, 3, 93-98.. T. W. Kim and K.-S. Choi, Science, 1, 33, 99-99. 9