木质素
分解
电化学
光电化学
化学
化学工程
材料科学
纳米技术
有机化学
电极
物理化学
工程类
作者
Tengfei Li,Jia Yi Mo,David M. Weekes,Kevan E. Dettelbach,Ryan P. Jansonius,Glenn M. Sammis,Curtis P. Berlinguette
出处
期刊:Chemsuschem
[Wiley]
日期:2020-05-05
卷期号:13 (14): 3622-3626
被引量:31
标识
DOI:10.1002/cssc.202001134
摘要
Abstract The photoelectrochemical decomposition of lignin model compounds at a BiVO 4 photoanode is demonstrated with simulated sunlight and an applied bias of 2.0 V. These prototypical lignin model compounds are photoelectrochemically converted into the corresponding aryl aldehyde and phenol derivatives in a single step with conversion of up to ≈64 % over 20 h. Control experiments suggest that vanadium sites are electrocatalytically active, which precludes the need for a redox mediator in solution. This feature of the system is corroborated by a layer of V 2 O 5 deposited on BiVO 4 serving to boost the conversion by 10 %. Our methodology capitalizes on the reactive power of sunlight to drive reactions that have only been studied previously by electrochemical or catalytic methods. The use of a BiVO 4 photoanode to drive lignin model decomposition therefore provides a new platform to extract valuable aromatic chemical feedstocks using solar energy, electricity and biomass as the only inputs.
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