Selective CO2 electroreduction to ethanol on encapsulated nickel nanoparticles by N-doped carbon nanotubes

被引:28
作者
Liu, Xing [1 ]
Hou, Yunpeng [2 ]
Yang, Fangqi [1 ]
Liu, Yueyue [1 ]
Yu, Haoming [1 ]
Han, Xinxin [1 ]
Chen, Jingwen [1 ]
Chen, Shixia [1 ]
Zhou, Shaodong [2 ]
Deng, Shuguang [3 ]
Wang, Jun [1 ]
机构
[1] Nanchang Univ, Sch Chem & Chem Engn, Nanchang 330031, Jiangxi, Peoples R China
[2] Zhejiang Univ, Coll Chem & Biol Engn, Hangzhou 310058, Zhejiang, Peoples R China
[3] Arizona State Univ, Sch Engn Matter Transport & Energy, 551 E Tyler Mall, Tempe, AZ 85287 USA
基金
中国国家自然科学基金;
关键词
CO2; electroreduction; Ethanol electrosynthesis; C2+products; In-situ Raman; Confinement effect; ELECTROCHEMICAL REDUCTION; STABLE ELECTROREDUCTION; HIGHLY EFFICIENT; DIOXIDE; FUNDAMENTALS; CONFINEMENT; CONVERSION; CATALYSTS; ELECTRODE; CH4;
D O I
10.1016/j.carbon.2022.09.010
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 electrosynthesis of ethanol by CO2 reduction is mostly achieved on metallic copper electrocatalysts, but confronts low Faradic efficiency (FE) and selectivity. Herein, we report novel electrocatalysts in which Ni nanoparticles are encapsulated in N-rich carbon nanotubes (Ni@NCNT) by chemical vapor deposition method. The optimized Ni@NCNT-700 exhibits a high ethanol FE of 38.5% at-0.5 V and remains over 30% in a wide potential range of-0.5 --1.2V. Notably, ethanol is the only liquid product and the total FE for CO and ethanol keeps above 90% in a potential range of-0.6 --1.2V vs. reversible hydrogen electrode. A high current density of 128 mA cm-2 is obtained in a 1 M KOH electrolyte at-2.0 V in a flow-cell device. Moreover, In-situ Raman and density functional theory calculations demonstrate that the confinement and synergistic effects of Ni NPs and NCNTs sufficiently lower the energy barrier for C-C coupling and suppressed the *CO desorption.
引用
收藏
页码:460 / 466
页数:7
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