Electrochemical Dehydrogenation of Ethane to Ethylene in a Solid Oxide Electrolyzer

被引:81
作者
Zhang, Xirui [1 ]
Ye, Lingting [1 ]
Li, Hao [1 ]
Chen, Fanglin [2 ]
Xie, Kui [1 ]
机构
[1] Chinese Acad Sci, Fujian Inst Res Struct Matter, Key Lab Design & Assembly Funct Nanostruct, Fuzhou 350002, Fujian, Peoples R China
[2] Univ South Carolina, Dept Mech Engn, Columbia, SC 29208 USA
来源
ACS CATALYSIS | 2020年 / 10卷 / 05期
基金
美国国家科学基金会;
关键词
solid oxide electrolyzers; electrochemical dehydrogenation; metal-oxide interface; ethane; ethylene; METALS; PERFORMANCE;
D O I
10.1021/acscatal.9b05409
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
The conversion of ethane, a main component of natural gas, to ethylene feed stock has attracted widespread attention since the worldwide shale gas revolution. Thermal catalysis of ethane to ethylene, mainly oxidative dehydrogenation, faces the fundamental challenge of low conversion, low selectivity, and catalyst coking. This work demonstrates an efficient conversion of ethane to ethylene in a nonoxidative dehydrogenation process in a proton-conducting solid oxide electrolyzer at ambient pressure and 700 degrees C. We show the highest ethane conversion of 75.2% and similar to 100% ethylene selectivity even only at 0.8 V in this electrochemical catalysis process. The electrochemical pumping of protons at anode with active exsolved metal-oxide interfaces enhances anode activity, while the metal-oxide interface interactions further engineer the ethane conversion in the electrochemical dehydrogenation process. We exsolve metal-oxide interface architecture at nanoscale on the electrode scaffold to improve coking resistance and catalyst stability. We further present the reduction of carbon dioxide to carbon monoxide in the cathode combined with ethane conversion in the anode, and we show the higher performance of ethane conversion in the anode with syngas production in the cathode. The electrochemical dehydrogenation process would provide an alternative method for the petrochemical production and a thermochemical practice in a clean energy mode.
引用
收藏
页码:3505 / 3513
页数:17
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