1. Multivalent Cu sites synergistically adjust carbonaceous intermediates adsorption for electrocatalytic ethanol production.
- Author
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Chen, Xiao, Jia, Shuaiqiang, Zhai, Jianxin, Jiao, Jiapeng, Dong, Mengke, Xue, Cheng, Deng, Ting, Cheng, Hailian, Xia, Zhanghui, Chen, Chunjun, Xing, Xueqing, Zeng, Jianrong, Wu, Haihong, He, Mingyuan, and Han, Buxing
- Subjects
COPPER ,FUNCTIONAL groups ,CATALYSTS ,HYDROCARBONS ,ETHYLENE ,ETHANOL - Abstract
Copper (Cu)-based catalysts show promise for electrocatalytic CO
2 reduction (CO2 RR) to multi-carbon alcohols, but thermodynamic constraints lead to competitive hydrocarbon (e.g., ethylene) production. Achieving selective ethanol production with high Faradaic efficiency (FE) and current density is still challenging. Here we show a multivalent Cu-based catalyst, Cu-2,3,7,8-tetraaminophenazine-1,4,6,9-tetraone (Cu-TAPT) with Cu2+ and Cu+ atomic ratio of about 1:2 for CO2 RR. Cu-TAPT exhibits an ethanol FE of 54.3 ± 3% at an industrial-scale current density of 429 mA cm−2 , with the ethanol-to-ethylene ratio reaching 3.14:1. Experimental and theoretical calculations collectively unveil that the catalyst is stable during CO2 RR, resulting from suitable coordination of the Cu2+ and Cu+ with the functional groups in TAPT. Additionally, mechanism studies show that the increased ethanol selectivity originates from synergy of multivalent Cu sites, which can promote asymmetric C–C coupling and adjust the adsorption strength of different carbonaceous intermediates, favoring hydroxy-containing C2 intermediate (*HCCHOH) formation and formation of ethanol. This study proposes a multivalent Cu-based catalyst (Cu-TAPT) for electrocatalytic CO2 RR, which promotes specific intermediate formation by the synergy of Cu2+ and Cu+ sites, thereby achieving a 54.3% Faradaic efficiency of ethanol at 429 mA cm−2 . [ABSTRACT FROM AUTHOR]- Published
- 2024
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