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The Role of TiO2 Doping on RuO2-Coated Electrodes for the Water Oxidation Reaction

Authors :
Näslund, Lars-Åke
Sánchez-Sánchez, Carlos M.
Ingason, Arni Sigurdur
Bäckström, Joakim
Herrero, Enrique
Rosén, Johanna
Holmin, Susanne
Näslund, Lars-Åke
Sánchez-Sánchez, Carlos M.
Ingason, Arni Sigurdur
Bäckström, Joakim
Herrero, Enrique
Rosén, Johanna
Holmin, Susanne
Publication Year :
2013

Abstract

Electrochemical water splitting into H-2 and O-2 presents a significant and challenging energy loss due to the high overpotential required at the anode. Today, in industrially relevant applications, dimensionally stable anodes (DSA) based on the electrocatalytic active RuO2 are conventionally utilized. To enhance the resistance against corrosion, incorporation of TiO2 in the RuO2-coated electrodes is widely employed. In the present work we have used scanning electrochemical microscopy (SECM) to demonstrate that TiO2-doped RuO2-coated electrodes, in addition to being more durable, also show an electrocatalytic activity that is, on average, 13% higher as compared to the pure RuO2-coated electrodes. We also demonstrate that cracks in the pure RuO2 coating are the most active zones, probably because Ti from the Ti support has diffused into the first applied layer of the RuO2 coating. To reveal the nature of this enhanced activity for water oxidation displayed on TiO2-doped RuO2 electrodes, we have employed X-ray photoelectron spectroscopy (XPS) for material characterization. The results show that the electrocatalytic activity enhancement displayed on the mixed (Ru1-x:Ti-x)O-2 coating is promoted through a charge transfer from the RuO2 to the TiO2, which provides new and more reactive sites designated as activated RuO2 delta+.<br />Funding Agencies|European Commission FP7 Initial Training Network "ELCAT"|214936-2|Ministry of Education, Culture, Sports, Science and Technology|2007A20052008A1671/BL-47XU

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1234186934
Document Type :
Electronic Resource
Full Text :
https://doi.org/10.1021.jp308941g