Photoelectrochemical oxidation of organic substrates in organic media

被引:128
|
作者
Li, Tengfei [1 ]
Kasahara, Takahito [1 ]
He, Jingfu [1 ]
Dettelbach, Kevan E. [1 ]
Sammis, Glenn M. [1 ]
Berlinguette, Curtis P. [1 ,2 ,3 ,4 ]
机构
[1] Univ British Columbia, Dept Chem, 2036 Main Mall, Vancouver, BC V6T 1Z1, Canada
[2] Univ British Columbia, Dept Chem & Biol Engn, 2036 Main Mall, Vancouver, BC V6T 1Z1, Canada
[3] Univ British Columbia, Stewart Blusson Quantum Matter Inst, 2036 Main Mall, Vancouver, BC V6T 1Z1, Canada
[4] Univ British Columbia, Dept Chem Biol Engn, 2036 Main Mall, Vancouver, BC V6T 1Z1, Canada
来源
NATURE COMMUNICATIONS | 2017年 / 8卷
基金
加拿大自然科学与工程研究理事会; 加拿大创新基金会;
关键词
BIVO4; PHOTOANODES; HYDROGEN-PRODUCTION; CATALYSTS;
D O I
10.1038/s41467-017-00420-y
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
There is a global effort to convert sunlight into fuels by photoelectrochemically splitting water to form hydrogen fuels, but the dioxygen byproduct bears little economic value. This raises the important question of whether higher value commodities can be produced instead of dioxygen. We report here photoelectrochemistry at a BiVO4 photoanode involving the oxidation of substrates in organic media. The use of MeCN instead of water enables a broader set of chemical transformations to be performed (e.g., alcohol oxidation and C-H activation/oxidation), while suppressing photocorrosion of BiVO4 that otherwise occurs readily in water, and sunlight reduces the electrical energy required to drive organic transformations by 60%. These collective results demonstrate the utility of using photoelectrochemical cells to mediate organic transformations that otherwise require expensive and toxic reagents or catalysts.
引用
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页数:5
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