Efficient electrically powered CO2-to-ethanol via suppression of deoxygenation

Xue Wang, Ziyun Wang, F. Pelayo García de Arquer, Cao Thang Dinh, Adnan Ozden, Yuguang C. Li, Dae Hyun Nam, Jun Li, Yi Sheng Liu, Joshua Wicks, Zitao Chen, Miaofang Chi, Bin Chen, Ying Wang, Jason Tam, Jane Y. Howe, Andrew Proppe, Petar Todorović, Fengwang Li, Tao Tao ZhuangChristine M. Gabardo, Ahmad R. Kirmani, Christopher McCallum, Sung Fu Hung, Yanwei Lum, Mingchuan Luo, Yimeng Min, Aoni Xu, Colin P. O’Brien, Bello Stephen, Bin Sun, Alexander H. Ip, Lee J. Richter, Shana O. Kelley, David Sinton, Edward H. Sargent*


研究成果: Article同行評審

284 引文 斯高帕斯(Scopus)


The carbon dioxide electroreduction reaction (CO2RR) provides ways to produce ethanol but its Faradaic efficiency could be further improved, especially in CO2RR studies reported at a total current density exceeding 10 mA cm−2. Here we report a class of catalysts that achieve an ethanol Faradaic efficiency of (52 ± 1)% and an ethanol cathodic energy efficiency of 31%. We exploit the fact that suppression of the deoxygenation of the intermediate HOCCH* to ethylene promotes ethanol production, and hence that confinement using capping layers having strong electron-donating ability on active catalysts promotes C–C coupling and increases the reaction energy of HOCCH* deoxygenation. Thus, we have developed an electrocatalyst with confined reaction volume by coating Cu catalysts with nitrogen-doped carbon. Spectroscopy suggests that the strong electron-donating ability and confinement of the nitrogen-doped carbon layers leads to the observed pronounced selectivity towards ethanol.

頁(從 - 到)478-486
期刊Nature Energy
出版狀態Published - 1 6月 2020


深入研究「Efficient electrically powered CO2-to-ethanol via suppression of deoxygenation」主題。共同形成了獨特的指紋。