4.6 Article

Low-overpotential selective reduction of CO2 to ethanol on electrodeposited CuxAuy nanowire arrays

期刊

JOURNAL OF ENERGY CHEMISTRY
卷 37, 期 -, 页码 176-182

出版社

ELSEVIER
DOI: 10.1016/j.jechem.2019.03.030

关键词

CO2 reduction; Electrocatalysis; Nanowire array; Selectivity; Cu-based catalyst

资金

  1. Natural Science Foundation of Hunan Province [2018JJ2485]
  2. Hunan Provincial Science and Technology Plan Project [2018RS3008, 2017TP1001]
  3. National Natural Science Foundation of China [21872174]
  4. Innovation-Driven Project of Central South University [2016CXS031, 2017CX003]

向作者/读者索取更多资源

Direct electrochemical reduction of CO2 to multicarbon products is highly desirable, yet challenging. Here, we present a potentiostatic pulse-electrodeposition of high-aspect-ratio CuxAuy nanowire arrays (NWAs) as high-performance electrocatalysts for the CO2 reduction reaction (CO2 RR). The surface electronic structure related to the Cu:Au ratio in the CuxAuy NWAs could be facilely modulated by controlling the electrodeposition potential and the as-fabricated CuxAuy NWAs could be directly used as the catalytic electrode for the CO2RR. The morphology of the high-aspect-ratio nanowire array significantly lowers the onset potential of the alcohol formation due to the diffusion-induced enhancement of the local pH and CO concentration near the nanowire surface. Besides, the properly adjusted surface electronic structure of the CuxAuy NWA enables the adsorption of CO and facilitates the subsequent CO reduction to ethanol via the C-C coupling pathway. Owing to the synergistic effect of morphology and electronic structure, the optimized CuxAuy NWA selectively reduces CO2 to ethanol at low potentials of -0.5--0.7 V vs. RHE with a highest Faradaic efficiency of 48%. This work demonstrates the feasibility to optimize the activity and selectivity of the Cu-based electrocatalysts toward multicarbon alcohols for the CO2RR via simultaneous adjustment of the electronic structure and morphology of the catalysts. (C) 2019 Science Press and Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. and Science Press. All rights reserved.

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