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Ultrastable atomic copper nanosheets for selective electrochemical reduction of carbon dioxide
Author(s) -
Lei Dai,
Qing Qin,
Pei Wang,
Xiaojing Zhao,
Chengyi Hu,
Pengxin Liu,
Ruixuan Qin,
Mei Chen,
Daohui Ou,
Chaofa Xu,
Shiguang Mo,
Binghui Wu,
Gang Fu,
Peng Zhang,
Nanfeng Zheng
Publication year - 2017
Publication title -
science advances
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 5.928
H-Index - 146
ISSN - 2375-2548
DOI - 10.1126/sciadv.1701069
Subject(s) - copper , carbon dioxide , electrochemistry , electrochemical reduction of carbon dioxide , reduction (mathematics) , materials science , nanotechnology , carbon fibers , environmental chemistry , chemistry , electrode , metallurgy , catalysis , composite material , organic chemistry , carbon monoxide , geometry , mathematics , composite number
The electrochemical conversion of CO2 and H2O into syngas using renewably generated electricity is an attractive approach to simultaneously achieve chemical fixation of CO2 and storage of renewable energy. Developing cost-effective catalysts for selective electroreduction of CO2 into CO is essential to the practical applications of the approach. We report a simple synthetic strategy for the preparation of ultrathin Cu/Ni(OH)2 nanosheets as an excellent cost-effective catalyst for the electrochemical conversion of CO2 and H2O into tunable syngas under low overpotentials. These hybrid nanosheets with Cu(0)-enriched surface behave like noble metal nanocatalysts in both air stability and catalysis. Uniquely, Cu(0) within the nanosheets is stable against air oxidation for months because of the presence of formate on their surface. With the presence of atomically thick ultrastable Cu nanosheets, the hybrid Cu/Ni(OH)2 nanosheets display both excellent activity and selectivity in the electroreduction of CO2 to CO. At a low overpotential of 0.39 V, the nanosheets provide a current density of 4.3 mA/cm2 with a CO faradaic efficiency of 92%. No decay in the current is observed for more than 22 hours. The catalysts developed in this work are promising for building low-cost CO2 electrolyzers to produce CO.

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