非阻塞I/O
甲烷
法拉第效率
煅烧
催化作用
化学工程
可逆氢电极
无机化学
原材料
碳氢化合物
材料科学
乙醇
产量(工程)
化学
电极
电化学
有机化学
冶金
物理化学
工作电极
工程类
作者
Yuxin Song,Yue Zhao,Guizhen Nan,Wei Chen,Zhikai Guo,Shenggang Li,Zhiyong Tang,Wei Wei,Yuhan Sun
标识
DOI:10.1016/j.apcatb.2020.118888
摘要
Electrocatalytic conversion of methane (CH4) to valuable chemicals under mild conditions is an attractive approach that combines the direct utilization of natural gas as a hydrocarbon feedstock and the chemical storage of renewable electricity. However, it remains a great challenge due to the intrinsic chemical inertness of CH4. Here we report that a NiO/Ni interface constructed by calcination can act as the active site for the electrooxidation of CH4 to alcohols especially ethanol. With the optimized NiO/Ni interface catalyst, an 89 % Faradaic efficiency (FE) for ethanol production with a yield of 25 μmol∙gNiO−1∙h−1 at 1.40 V versus reversible hydrogen electrode (RHE) was achieved. Experiments and density functional theory (DFT) calculations demonstrated that the NiO/Ni interface enables efficient CH activation and CC coupling, leading to the highly selective formation of ethanol from CH4 electrooxidation.
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