期刊
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
卷 42, 期 8, 页码 5496-5504出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.ijhydene.2016.08.168
关键词
Water splitting; Photoanode; Nanorod array; BiVO4
资金
- National Natural Science Foundation of China [51372075, 51472080]
- Research Fund for the Doctoral Program of Higher Education of China (RFDP) [20104208120004]
- Open Research Fund Program of the State Key Laboratory of Low-dimensional Quantum Physics [KF201411]
- Wuhan Youth Chenguang Program of Science and Technology [2013070104010014]
Using TiO2 nanorods as one-dimensional (1D) electron transport tunnel, BiVO4 as light harvester, and Co-Pi (Cobalt-Phosphate) as co-catalyst, TiO2/BiVO4/Co-Pi nanorod arrays were fabricated as efficient photoanode on a FTO substrate for photoelectrochemical (PEC) water splitting cells. It was found that the monoclinic BiVO4 nanoflakes were mainly vertically attached to the side faces of ruffle TiO2 nanorods with an average size of similar to 35 nm and a selective growth direction along < 112 >. By changing the electrodeposited quantity of BiVO4, the effect of the loading density of BiVO4 on the PEC performance was systematically studied, and an optimum photocurrent of similar to 1.86 mA cm(-2) at 1.0 V-RHE with an onset potential as small as 0.3 V-RHE and IPCE of 26% (at 450 nm) was obtained for the TiO2/BiVO4/ Co-Pi anodes. Electrochemical impedance spectroscopy showed that Co-Pi can greatly decrease the charge transfer resistance at the photoanode/electrolyte interface. Along with the band alignment of the 1D nanoarray heterostructure beneficial for the charge separation, a hydrogen production of similar to 7.31 mu mol cm(-2) h(-1) was achieved for the efficient water splitting system. Such a heterostructured 1D nanoarray configuration can be extended to other PEC water splitting systems as well to increase the number of reactive sites and absorption of solar light, and to enhance the OER kinetics. (C) 2016 Hydrogen Energy Publications LLC. Published by Elsevier Ltd. All rights reserved.
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