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Electrodeposited Co-Substituted LaFeO3 for Enhancing the Photoelectrochemical Activity of BiVO4
Yangqin Gao1,2,3, Guoqing Yang1,2,3, Yanjie Dai1,2
1State Key Laboratory of Heavy Oil Processing, College of New Energy and Materials, China University of Petroleum Beijing, No. 18 Fuxue Road, Beijing 102249, People's Republic of China.
Abstract:
Co-substituted LaFeO3 was electrodeposited on the surface of BiVO4 as a co-catalyst to enhance the water splitting performance. Compared to bare BiVO4, the BiVO4/Co-LaFeO3 composite photoanode shows a water oxidation photocurrent of 3.4 mA/cm2 at 1.23 V versus reverse hydrogen electrode, accompanied by a notable cathodic shift in the onset potential for 300 mV. Combined optical and electrochemical characterizations show that the solid/electrolyte charge transfer efficiency of BiVO4 are dramatically improved by the incorporation of Co-substituted LaFeO3. From the surface kinetic study of charge carriers by intensity-modulated photocurrent spectroscopy, a suppressed surface recombination rate constant is observed and the enhanced photoelectrochemical water splitting performance observed in the BiVO4/Co-LaFeO3 photoanode is attributed to the surface passivation effect of Co-substituted LaFeO3.
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