光电流
分解水
半导体
过渡金属
光电化学
可逆氢电极
光催化
共形映射
材料科学
电解质
光电化学电池
化学
光化学
化学工程
电极
无机化学
光电子学
电化学
催化作用
工作电极
物理化学
生物化学
工程类
作者
Lu Wang,Tao Zhang,Jing Wang,Liejin Guo
出处
期刊:Nano Research
[Springer Science+Business Media]
日期:2020-01-01
卷期号:13 (1): 231-237
被引量:14
标识
DOI:10.1007/s12274-019-2605-3
摘要
Photoelectrochemical (PEC) water splitting using semiconductors offers a promising way to convert renewable solar energy to clean hydrogen fuels. However, due to the sluggish reaction kinetics of water oxidation, significant charge recombination occurred at the photoanode/electrolyte interface and cause decrease of its PEC performance. To reduce the surface recombination, we deposit different transition metal complexes on BiVO4 nanocone arrays by a versatile light driven in-situ two electrode photodeposition approach without applied bias. Conformal cobalt phosphate “Co-Pi”, nickel borate “Ni-Bi” and manganese phosphate “Mn-Pi” complexes were deposited on BiVO4 nanocone arrays to form core-shell structure photoanode, all of which lead to enhanced photoelectrochemical performance. The photocurrent of the Co-Pi/BiVO4 photoanode under front-side illumination for 5 min is increased by 4 folds comparing to that of bare BiVO4 photoanode at 0.6 V vs. RHE, reaching a hole transfer efficiency as high as 94.5% at 1.23 V vs. RHE. The proposed photodeposition strategy is simple and efficient, and can be extended to deposite cocatalyst on other semiconductors with a valence band edge located at a potential more positive than the oxidation potential of transition metal ion in the cocatalyst.
科研通智能强力驱动
Strongly Powered by AbleSci AI