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Cobalt Hexacyanoferrate on BiVO4 Photoanodes for Robust Water Splitting
Author(s) -
Franziska Simone Hegner,
Isaac HerrãizCardona,
Drialys Cárdenas-Morcoso,
Núria López,
José Ramón GalánMascarós,
Sixto Giménez
Publication year - 2017
Publication title -
acs applied materials and interfaces
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 2.535
H-Index - 228
eISSN - 1944-8252
pISSN - 1944-8244
DOI - 10.1021/acsami.7b09449
Subject(s) - photocurrent , water splitting , materials science , catalysis , reversible hydrogen electrode , prussian blue , cobalt , photocatalysis , chemical engineering , irradiation , density functional theory , electrode , nanotechnology , optoelectronics , electrochemistry , chemistry , working electrode , computational chemistry , biochemistry , engineering , metallurgy , physics , nuclear physics
The efficient integration of photoactive and catalytic materials is key to promoting photoelectrochemical water splitting as a sustainable energy technology built on solar power. Here, we report highly stable water splitting photoanodes from BiVO 4 photoactive cores decorated with CoFe Prussian blue-type electrocatalysts (CoFe-PB). This combination decreases the onset potential of BiVO 4 by ∼0.8 V (down to 0.3 V vs reversible hydrogen electrode (RHE)) and increases the photovoltage by 0.45 V. The presence of the catalyst also leads to a remarkable 6-fold enhancement of the photocurrent at 1.23 V versus RHE, while keeping the light-harvesting ability of BiVO 4 . Structural and mechanistic studies indicate that CoFe-PB effectively acts as a true catalyst on BiVO 4 . This mechanism, stemming from the adequate alignment of the energy levels, as showed by density functional theory calculations, allows CoFe-PB to outperform all previous catalyst/BiVO 4 junctions and, in addition, leads to noteworthy long-term stability. A bare 10-15% decrease in photocurrent was observed after more than 50 h of operation under light irradiation.

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