化学
阳极
法拉第效率
太阳能燃料
氢
制氢
催化作用
阴极
能量转换效率
生物量(生态学)
化学工程
电解水
无机化学
析氧
分解水
电化学
电解质
有机化学
电极
电解
光催化
材料科学
工程类
地质学
物理化学
海洋学
光电子学
作者
Hyun Gil,Kyoung‐Shin Choi
出处
期刊:Nature Chemistry
[Springer Nature]
日期:2015-03-09
卷期号:7 (4): 328-333
被引量:593
摘要
In a typical hydrogen-producing photoelectrochemical cell (PEC), water reduction at the cathode (producing hydrogen) is accompanied by water oxidation at the anode (producing oxygen). This anode reaction is, however, not kinetically favourable. Here we investigate the possibility of utilizing solar energy for biomass conversion by performing the oxidation of 5-hydroxymethylfurfural (HMF) into 2,5-furandicarboxylic acid (FDCA) at the anode of a PEC. HMF is a key intermediate in biomass conversion, and FDCA is an important monomer for the production of numerous polymers. Using 2,2,6,6-tetramethylpiperidine-1-oxyl as a mediator, we obtained a near-quantitative yield and 100% Faradaic efficiency at ambient conditions without the use of precious-metal catalysts. This reaction is also thermodynamically and kinetically more favourable than water oxidation. Our results suggest that solar-driven biomass conversion can be a viable anode reaction that has the potential to increase both the efficiency and the utility of PECs constructed for solar-fuel production.
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