跳到主要导航 跳到搜索 跳到主要内容

Stabilization of Cu+ sites by amorphous Al2O3 to enhance electrochemical CO2 reduction to C2+ products

  • Hailian Cheng
  • , Shuaiqiang Jia*
  • , Jiapeng Jiao
  • , Xiao Chen
  • , Ting Deng
  • , Cheng Xue
  • , Mengke Dong
  • , Jianrong Zeng
  • , Chunjun Chen
  • , Haihong Wu*
  • , Mingyuan He
  • , Buxing Han*
  • *此作品的通讯作者

科研成果: 期刊稿件文章同行评审

摘要

Catalytic conversion of CO2 to produce fuels and chemicals is of great importance, and the electrocatalytic CO2 reduction reaction (eCO2RR) is considered one of the most attractive pathways. Multi-carbon (C2+) products are more desirable in many cases. To date, Cu-based catalysts, especially Cu+ sites, have been found to be the most efficient for the production of C2+ products. However, the retention of Cu+ sites at high cathodic potentials in the eCO2RR remains a great challenge. In this study, we designed and synthesized CuAl-oxide-derived (CuxAly-OD, x and y are the mass percentages of Cu and Al) catalysts for the eCO2RR to C2+ products. During the eCO2RR process, the predominant Cu species changed to Cu+, and the resulting electrocatalyst showed a high faradaic efficiency (FE) of 81.6% for C2+ products in alkaline aqueous solutions. Experimental studies showed that the presence of a stable amorphous Al2O3 phase stabilized the Cu+ sites by oxidation state control, leading to high selectivity and activity for the production of C2+ products. This work provides a strategy for improving the stability of Cu+ in the catalyst to enhance the performance of the eCO2RR.

源语言英语
页(从-至)2599-2604
页数6
期刊Green Chemistry
26
5
DOI
出版状态已出版 - 15 1月 2024

指纹

探究 'Stabilization of Cu+ sites by amorphous Al2O3 to enhance electrochemical CO2 reduction to C2+ products' 的科研主题。它们共同构成独一无二的指纹。

引用此