Colloidal zinc oxide-copper(I) oxide nanocatalysts for selective aqueous photocatalytic carbon dioxide conversion into methane

被引:120
|
作者
Bae, Kyung-Lyul [1 ,2 ]
Kim, Jinmo [1 ,2 ]
Lim, Chan Kyu [1 ,2 ]
Nam, Ki Min [3 ]
Song, Hyunjoon [1 ,2 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Chem, Daejeon 34141, South Korea
[2] Inst for Basic Sci Korea, Ctr Nanomat & Chem React, Daejeon 34141, South Korea
[3] Mokpo Natl Univ, Dept Chem, Jeonnam 58554, South Korea
来源
NATURE COMMUNICATIONS | 2017年 / 8卷
基金
新加坡国家研究基金会;
关键词
FIELD-EMISSION; CO2; PHOTOREDUCTION; TIO2; ADSORPTION; REDUCTION; SURFACE; ENERGY; NANOSTRUCTURES; NANOPARTICLES;
D O I
10.1038/s41467-017-01165-4
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
Developing catalytic systems with high efficiency and selectivity is a fundamental issue for photochemical carbon dioxide conversion. In particular, rigorous control of the structure and morphology of photocatalysts is decisive for catalytic performance. Here, we report the synthesis of zinc oxide-copper(I) oxide hybrid nanoparticles as colloidal forms bearing copper (I) oxide nanocubes bound to zinc oxide spherical cores. The zinc oxide-copper(I) oxide nanoparticles behave as photocatalysts for the direct conversion of carbon dioxide to methane in an aqueous medium, under ambient pressure and temperature. The catalysts produce methane with an activity of 1080 mu mol g(cat)(-1) h(-1), a quantum yield of 1.5% and a selectivity for methane of >99%. The catalytic ability of the zinc oxide-copper(I) oxide hybrid catalyst is attributed to excellent band alignment of the zinc-oxide and copper(I) oxide domains, few surface defects which reduce defect-induced charge recombination and enhance electron transfer to the reagents, and a high-surface area colloidal morphology.
引用
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页数:8
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