Versatile, transferrable 3-dimensionally nanofabricated Au catalysts with high-index crystal planes for highly efficient and robust electrochemical CO2 reduction

被引:29
作者
Cho, Minhyung [1 ]
Kim, Jong Min [1 ]
Kim, Beomil [1 ]
Yim, Soonmin [1 ]
Kim, Ye Ji [1 ]
Jung, Yeon Sik [1 ]
Oh, Jihun [1 ,2 ,3 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Mat Sci & Engn, Daejeon 34141, South Korea
[2] Korea Adv Inst Sci & Technol, Grad Sch Energy Environm Water & Sustainabil EEWS, Daejeon 34141, South Korea
[3] Korea Adv Inst Sci & Technol, KAIST Inst NanoCentury, Daejeon 34141, South Korea
基金
新加坡国家研究基金会;
关键词
CARBON-DIOXIDE; METAL-ELECTRODES; ELECTROREDUCTION; SELECTIVITY; CONVERSION; PLATINUM; INSIGHTS;
D O I
10.1039/c8ta12242c
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Considerable interest has been shown in the electrochemical CO2 reduction reaction (CO2RR) for transforming CO2 into other value-added carbonaceous products such as CO. In this work, we prepared multi-stacked Au (MS-Au) nanowire arrays with tailored active reaction sites and controlled 3-dimensional structures by oblique angle deposition and a sequential solvent-assisted nanotransfer printing (S-nTP) method for highly selective and efficient electrochemical CO2RR. Our MS-Au nanowires exhibit high CO2RR activity in a wide range of overpotentials due to the electrochemically active high index grain faces and high grain boundary density and by controlling local reaction environments. With our 10 layers of MS-Au nanowires, we achieve similar to 13 times higher CO2RR geometric current density (j(CO)) at low overpotential (-0.39 V) compared to the pristine Au thin-film electrode. Finally, the S-nTP method allows versatile transferability of MS-Au nanowires onto a gas diffusion electrode in a flow reactor to maximize CO evolution with an exceptional mass activity of similar to 172.66 A g(-1) at an overpotential of only 80 mV.
引用
收藏
页码:6045 / 6052
页数:8
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