材料科学
光电流
吸附
热液循环
化学工程
能量转换效率
纳米复合材料
光催化
水热合成
纳米技术
光电子学
催化作用
化学
物理化学
生物化学
工程类
作者
Jianlong Yang,Ning Sun,Ziqing Zhang,Ji Bian,Yang Qu,Zhijun Li,Ming Xie,Weihua Han,Liqiang Jing
标识
DOI:10.1021/acsami.0c06892
摘要
It is a great challenge for achieving efficiently controllable conversion of chlorinated organics through BiVO4-based photoelectrochemical methods by improving the selective adsorption of such organics and charge separation. Herein, we have successfully fabricated SnO2/010 facet-exposed BiVO4 nanocomposites by a series of hydrothermal processes and further used as efficient photoanodes. The resulting photoanode exhibits about 6.3 times higher photoelectrochemical activity than bulk-BiVO4, especially with the efficiently controllable conversion of 2,4-dichlorophenol (2,4-DCP) to the nontoxic valuable intermediates such as catechol and pyrogallol by preferential dechlorination. Based on the 2,4-DCP adsorption curves, in situ diffuse reflectance infrared spectra, transient-state surface photovoltage responses, and photocurrent action spectra, it was clearly confirmed that the exceptional performance could be mainly attributed to the promoted selective adsorption of 2,4-DCP for efficiently modulating holes by the strong coordination interactions between −Cl with lone-pair electrons in 2,4-DCP and Bi– with empty orbits on (010) facet-exposed BiVO4 nanoflakes and to the coupled nano-SnO2 for prolonging the charge lifetime of BiVO4 by acting as the high-energy-level electron-accepting platform. This work provides a feasible strategy to develop excellent BiVO4-based photoelectrochemical methods for efficiently controlling the conversion of chlorinated organics simultaneously with energy production and recovery.
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