Your browser doesn't support javascript.
loading
Constructing Ionic Interfaces for Stable Electrochemical CO2 Reduction.
Liu, Yong; Song, Yun; Huang, Libei; Su, Jianjun; Li, Geng; Zhang, Qiang; Xin, Yinger; Cao, Xiaohu; Guo, Weihua; Dou, Yubing; He, Mingming; Feng, Tanglue; Jin, Zhong; Ye, Ruquan.
Afiliación
  • Liu Y; Department of Chemistry, State Key Laboratory of Marine Pollution, City University of Hong Kong, Hong Kong 999077, P. R. China.
  • Song Y; Department of Chemistry, State Key Laboratory of Marine Pollution, City University of Hong Kong, Hong Kong 999077, P. R. China.
  • Huang L; Division of Science, Engineering and Health Study, School of Professional Education and Executive Development, The Hong Kong Polytechnic University (PolyU SPEED), Hong Kong 999077, P. R. China.
  • Su J; Department of Chemistry, State Key Laboratory of Marine Pollution, City University of Hong Kong, Hong Kong 999077, P. R. China.
  • Li G; Department of Chemistry, State Key Laboratory of Marine Pollution, City University of Hong Kong, Hong Kong 999077, P. R. China.
  • Zhang Q; Department of Chemistry, State Key Laboratory of Marine Pollution, City University of Hong Kong, Hong Kong 999077, P. R. China.
  • Xin Y; Department of Chemistry, State Key Laboratory of Marine Pollution, City University of Hong Kong, Hong Kong 999077, P. R. China.
  • Cao X; Department of Chemistry, State Key Laboratory of Marine Pollution, City University of Hong Kong, Hong Kong 999077, P. R. China.
  • Guo W; Department of Chemistry, State Key Laboratory of Marine Pollution, City University of Hong Kong, Hong Kong 999077, P. R. China.
  • Dou Y; Department of Chemistry, State Key Laboratory of Marine Pollution, City University of Hong Kong, Hong Kong 999077, P. R. China.
  • He M; Department of Chemistry, State Key Laboratory of Marine Pollution, City University of Hong Kong, Hong Kong 999077, P. R. China.
  • Feng T; Department of Chemistry, State Key Laboratory of Marine Pollution, City University of Hong Kong, Hong Kong 999077, P. R. China.
  • Jin Z; State Key Laboratory of Coordination Chemistry, MOE Key Laboratory of Mesoscopic Chemistry, MOE Key Laboratory of High Performance Polymer Materials and Technology, Jiangsu Key Laboratory of Advanced Organic Materials, Tianchang New Materials and Energy Technology Research Center, School of Chemistr
  • Ye R; Department of Chemistry, State Key Laboratory of Marine Pollution, City University of Hong Kong, Hong Kong 999077, P. R. China.
ACS Nano ; 18(22): 14020-14028, 2024 Jun 04.
Article en En | MEDLINE | ID: mdl-38764286
ABSTRACT
The electrochemical CO2 reduction reaction (CO2RR) has emerged as a promising approach for sustainable carbon cycling and valuable chemical production. Various methods and strategies have been explored to boost CO2RR performance. One of the most promising strategies includes the construction of stable ionic interfaces on metallic or molecular catalysts using organic or inorganic cations, which has demonstrated a significant improvement in catalytic performance. The stable ionic interface is instrumental in adjusting adsorption behavior, influencing reactive intermediates, facilitating mass transportation, and suppressing the hydrogen evolution reaction, particularly under acidic conditions. In this Perspective, we provide an overview of the recent advancements in building ionic interfaces in the electrocatalytic process and discuss the application of this strategy to improve the CO2RR performance of metallic and molecular catalysts. We aim to convey the future trends and opportunities in creating ionic interfaces to further enhance carbon utilization efficiency and the productivity of CO2RR products. The emphasis of this Perspective lies in the pivotal role of ionic interfaces in catalysis, providing a valuable reference for future research in this critical field.
Palabras clave

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: ACS Nano / ACS nano Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Idioma: En Revista: ACS Nano / ACS nano Año: 2024 Tipo del documento: Article