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Wang, Xue; Wang, Ziyun; Zhuang, Tao-Tao; Dinh, Cao-Thang; Li, Jun; Nam, Dae-Hyun; Li, Fengwang; Huang, Chun-Wei; Tan, Chih-Shan; Chen, Zitao; Chi, Miaofang; Gabardo, Christine M.; Seifitokaldani, Ali; Todorović, Petar; Proppe, Andrew; Pang, Yuanjie; Kirmani, Ahmad R.; Wang, Yuhang; Ip, Alexander H.; Richter, Lee J.; Scheffel, Benjamin; Xu, Aoni; Lo, Shen-Chuan; Kelley, Shana O.; Sinton, David; Sargent, Edward H.
Nature communications, 11/2019, Letnik: 10, Številka: 1Journal Article
Abstract The electroreduction of C 1 feedgas to high-energy-density fuels provides an attractive avenue to the storage of renewable electricity. Much progress has been made to improve selectivity to C 1 and C 2 products, however, the selectivity to desirable high-energy-density C 3 products remains relatively low. We reason that C 3 electrosynthesis relies on a higher-order reaction pathway that requires the formation of multiple carbon-carbon (C-C) bonds, and thus pursue a strategy explicitly designed to couple C 2 with C 1 intermediates. We develop an approach wherein neighboring copper atoms having distinct electronic structures interact with two adsorbates to catalyze an asymmetric reaction. We achieve a record n -propanol Faradaic efficiency (FE) of (33 ± 1)% with a conversion rate of (4.5 ± 0.1) mA cm −2 , and a record n -propanol cathodic energy conversion efficiency (EE cathodic half-cell ) of 21%. The FE and EE cathodic half-cell represent a 1.3× improvement relative to previously-published CO-to- n -propanol electroreduction reports.
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in: SICRIS
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