TY - GEN
T1 - Spray-deposited Co-Pi catalyzed BiVO 4
T2 - 2012 MRS Spring Meeting
AU - Abdi, Fatwa F.
AU - Firet, Nienke
AU - Dabirian, Ali
AU - Van De Krol, Roel
N1 - Publication details (e.g. title, author(s), publication statuses and dates) are captured on an “AS IS” and “AS AVAILABLE” basis at the time of record harvesting from the data source. Suggestions for further amendments or supplementary information can be sent to [email protected].
PY - 2012
Y1 - 2012
N2 - Bismuth vanadate (BiVO 4) thin films are deposited by a low-cost and scalable spray pyrolysis method. Its performance under AM1.5 illumination is mainly limited by slow water oxidation kinetics. We confirm that cobalt phosphate (Co-Pi) is an efficient water oxidation catalyst for BiVO 4. The optimum thickness of BiVO 4 is 300 nm, resulting in an AM1.5 photocurrent of 1.9 mA/cm 2 at 1.23 V vs. RHE when catalyzed with Co-Pi. Once the water oxidation limitation is removed, the performance is limited by low charge separation efficiency. This causes more than 60% of the electron-hole pairs to recombine before reaching the respective interfaces. The slow electron transport is shown to be the main cause of this low efficiency, and future efforts should therefore be focused on addressing this key limitation. © 2012 Materials Research Society.
AB - Bismuth vanadate (BiVO 4) thin films are deposited by a low-cost and scalable spray pyrolysis method. Its performance under AM1.5 illumination is mainly limited by slow water oxidation kinetics. We confirm that cobalt phosphate (Co-Pi) is an efficient water oxidation catalyst for BiVO 4. The optimum thickness of BiVO 4 is 300 nm, resulting in an AM1.5 photocurrent of 1.9 mA/cm 2 at 1.23 V vs. RHE when catalyzed with Co-Pi. Once the water oxidation limitation is removed, the performance is limited by low charge separation efficiency. This causes more than 60% of the electron-hole pairs to recombine before reaching the respective interfaces. The slow electron transport is shown to be the main cause of this low efficiency, and future efforts should therefore be focused on addressing this key limitation. © 2012 Materials Research Society.
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U2 - 10.1557/opl.2012.811
DO - 10.1557/opl.2012.811
M3 - RGC 32 - Refereed conference paper (with host publication)
SN - 9781605114231
VL - 1446
T3 - Materials Research Society Symposium Proceedings
SP - 7
EP - 12
BT - Materials for Catalysis in Energy
Y2 - 9 April 2012 through 13 April 2012
ER -