Boosting photoelectrochemical water oxidation of hematite in acidic electrolytes by surface state modification

State-of-the-art water-oxidation catalysts (WOCs) in acidic electrolytes usually contain expensive noble metals such as ruthenium and iridium. However, they too expensive to be implemented broadly in semiconductor photoanodes for photoelectrochemical (PEC) water splitting devices. Here, an Earth-abu...

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Detalles Bibliográficos
Autores: Tang, Peng-Yi, Han, Li-Juan, Simone Hegner, Franziska, Paciok, Paul, Biset-Peiró, Martí, Du, Hong-Chu, Wei, Xian-Kui, Jin, Lei, Xie, Haibing, Shi, Qin, Andreu, Teresa, Lira-Cantú, Mónica, Heggen, Marc, Dunin-Borkowski, Rafal E., López, Núria, Galán-Mascarós, José Ramón, Morante, Joan Ramón, Arbiol, Jordi
Tipo de recurso: artículo
Estado:Versión enviada para evaluación y publicación
Fecha de publicación:2019
País:España
Institución:Consejo Superior de Investigaciones Científicas (CSIC)
Repositorio:DIGITAL.CSIC. Repositorio Institucional del CSIC
OAI Identifier:oai:digital.csic.es:10261/200169
Acceso en línea:http://hdl.handle.net/10261/200169
Access Level:acceso abierto
Palabra clave:Acidic electrolyte
Hematite
Photoelectrochemical water splitting
Surface states
Descripción
Sumario:State-of-the-art water-oxidation catalysts (WOCs) in acidic electrolytes usually contain expensive noble metals such as ruthenium and iridium. However, they too expensive to be implemented broadly in semiconductor photoanodes for photoelectrochemical (PEC) water splitting devices. Here, an Earth-abundant CoFe Prussian blue analogue (CoFe-PBA) is incorporated with core–shell Fe2O3/Fe2TiO5 type II heterojunction nanowires as composite photoanodes for PEC water splitting. Those deliver a high photocurrent of 1.25 mA cm−2 at 1.23 V versus reversible reference electrode in acidic electrolytes (pH = 1). The enhancement arises from the synergic behavior between the successive decoration of the hematite surface with nanolayers of Fe2TiO5 and then, CoFe-PBA. The underlying physical mechanism of performance enhancement through formation of the Fe2O3/Fe2TiO5/ CoFe-PBA heterostructure reveals that the surface states’ electronic levels of hematite are modified such that an interfacial charge transfer becomes kinetically favorable. These findings open new pathways for the future design of cheap and efficient hematite-based photoanodes in acidic electrolytes.