Efficient solar photoelectrolysis by nanoporous Mo: BiVO4 through controlled electron transport

被引:167
作者
Seabold, Jason A. [1 ]
Zhu, Kai [1 ]
Neale, Nathan R. [1 ]
机构
[1] Natl Renewable Energy Lab, Chem & Mat Sci Ctr, Golden, CO 80401 USA
关键词
PHOTOELECTROCHEMICAL WATER OXIDATION; OXYGEN EVOLUTION; VISIBLE-LIGHT; HYDROGEN; CATALYST; RECOMBINATION; PHOTOANODES; COBALT; ELECTROCATALYSTS; SILICON;
D O I
10.1039/c3cp54356k
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
A detailed understanding of doping level, electron diffusion length and coefficient, as well as light capture and charge separation efficiencies in nanoporous Mo-doped BiVO4 (Mo: BiVO4) photoanodes is obtained using photoelectrochemical techniques. Efficient water oxidation is achieved by doping with 1.8% Mo, resulting in a several-fold enhancement in photooxidation rate versus non-doped BiVO4. Two techniques are used to study the effect of Mo doping on the electron transport: (1) an analysis of the front/ back illumination ratio of incident photon-to-current efficiency and (2) intensity modulated photocurrent spectroscopy. These techniques show that Mo doping improves the diffusion coefficient four-fold and increases the diffusion length to ca. 300 nm (from 10 nm for the non-doped material), which is also the empirically-determined optimal Mo: BiVO4 film thickness for photoelectrolysis. These films are found to have a 90% charge separation efficiency and an 80% absorbed photon-to-current efficiency, excellent values for metal oxide photoabsorbers. Among the many oxygen evolution catalysts studied, surface modification with iron oxyhydroxide (FeOOH), a simple earth abundant catalyst, dramatically enhances the water oxidation performance of Mo: BiVO4 to an integrated IPCE of 2.41 mA cm(-2) and a photocurrent density of 2.77 mA cm(-2) in neutral phosphate at 1.23 V vs. RHE.
引用
收藏
页码:1121 / 1131
页数:11
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