Cobalt Hexacyanoferrate on BiVO4 Photoanodes for Robust Water Splitting

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 BiVO4 photoactive cores decorated with CoFe Prussian blue-...

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Authors: Hegner, Franziska Simone; Herraiz-Cardona, Isaac; Cardenas-Morcoso, Drialys; López, Núria; Galán-Mascarós, José-Ramón; Gimenez, Sixto
Format: Article
Status:Accepted version
Publication date:2017
Country:España
Institution:Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
Repository:Recercat. Dipósit de la Recerca de Catalunya
OAI Identifier:oai:recercat.cat:2072/359755
Online Access:http://hdl.handle.net/2072/359755
https://doi.org/10.1021/acsami.7b09449
Access Level:Open access
Keyword:54
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author Hegner, Franziska Simone
author2 Herraiz-Cardona, Isaac
Cardenas-Morcoso, Drialys
López, Núria
Galán-Mascarós, José-Ramón
Gimenez, Sixto
author2_role author
author
author
author
author
author_browse Cardenas-Morcoso, Drialys
Galán-Mascarós, José-Ramón
Gimenez, Sixto
Hegner, Franziska Simone
Herraiz-Cardona, Isaac
López, Núria
author_facet Hegner, Franziska Simone
Herraiz-Cardona, Isaac
Cardenas-Morcoso, Drialys
López, Núria
Galán-Mascarós, José-Ramón
Gimenez, Sixto
author_role author
collection Recercat. Dipósit de la Recerca de Catalunya
description 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 BiVO4 photoactive cores decorated with CoFe Prussian blue-type electrocatalysts (CoFe-PB). This combination decreases the onset potential of BiVO4 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 BiVO4. Structural and mechanistic studies indicate that CoFe-PB effectively acts as a true catalyst on BiVO4. 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/BiVO4 junctions and, in addition, leads to noteworthy longterm stability. A bare 10−15% decrease in photocurrent was observed after more than 50 h of operation under light irradiation
eu_rights_str_mv openAccess
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institution Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
instname_str Varias* (Consorci de Biblioteques Universitáries de Catalunya, Centre de Serveis Científics i Acadèmics de Catalunya)
network_acronym_str ES
network_name_str España
oai_identifier_str oai:recercat.cat:2072/359755
publishDate 2017
publishDateSort 2017
reponame_str Recercat. Dipósit de la Recerca de Catalunya
spelling Cobalt Hexacyanoferrate on BiVO4 Photoanodes for Robust Water Splitting Hegner, Franziska Simone Herraiz-Cardona, Isaac Cardenas-Morcoso, Drialys López, Núria Galán-Mascarós, José-Ramón Gimenez, Sixto 54 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 BiVO4 photoactive cores decorated with CoFe Prussian blue-type electrocatalysts (CoFe-PB). This combination decreases the onset potential of BiVO4 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 BiVO4. Structural and mechanistic studies indicate that CoFe-PB effectively acts as a true catalyst on BiVO4. 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/BiVO4 junctions and, in addition, leads to noteworthy longterm stability. A bare 10−15% decrease in photocurrent was observed after more than 50 h of operation under light irradiation http://hdl.handle.net/2072/359755 https://doi.org/10.1021/acsami.7b09449
spellingShingle Cobalt Hexacyanoferrate on BiVO4 Photoanodes for Robust Water Splitting
Hegner, Franziska Simone
54
status_str acceptedVersion
title Cobalt Hexacyanoferrate on BiVO4 Photoanodes for Robust Water Splitting
title_full Cobalt Hexacyanoferrate on BiVO4 Photoanodes for Robust Water Splitting
title_fullStr Cobalt Hexacyanoferrate on BiVO4 Photoanodes for Robust Water Splitting
title_full_unstemmed Cobalt Hexacyanoferrate on BiVO4 Photoanodes for Robust Water Splitting
title_short Cobalt Hexacyanoferrate on BiVO4 Photoanodes for Robust Water Splitting
title_sort Cobalt Hexacyanoferrate on BiVO4 Photoanodes for Robust Water Splitting
topic 54
topic_facet 54
url http://hdl.handle.net/2072/359755
https://doi.org/10.1021/acsami.7b09449