Affiliation:
1. College of Chemistry, Chemical Engineering and Materials Science Soochow University Suzhou 215006 China
2. Collaborative Innovation Center of Suzhou Nano Science and Technology College of Energy Soochow University Suzhou 215006 China
3. School of Chemistry and Chemical Engineering Nantong University Nantong 226019 China
4. Light Industry Institute of Electrochemical Power Sources Suzhou 215600 China
Abstract
AbstractElectrochemical reduction of CO2 (CO2RR) and nitrogen (NRR) constitute alternatives to fossil fuel‐based technologies for the production of high‐value‐added chemicals. Yet their practical application is still hampered by the low energy and Faradaic efficiencies although numerous efforts have been paid to overcome the fatal shortcomings. To date, most studies have focused on designing and developing advanced electrocatalysts, while the understanding of electrolyte, which would significantly influence the reaction microenvironment, are still not enough to provide insight to construct highly active and selective electrochemical systems. Here, a comprehensive review of the different electrolytes participating in the CO2RR and NRR is provided, including acidic, neutral, alkaline, and water‐in‐salt electrolyte as aqueous electrolytes, as well as organic electrolyte, ionic‐liquids electrolyte, and the mixture of the two as non‐aqueous electrolytes. Through the discussion of the roles of these various electrolytes, it is aimed to grasp their essential function during the electrochemical process and how these functions can be used as design parameters for improving electrocatalytic performance. Finally, priorities for future studies are suggested to support the in‐depth understanding of the electrolyte effects and thus guide efficient selection for next‐generation gas‐involving electrochemical reactions.
Funder
National Natural Science Foundation of China
China Postdoctoral Science Foundation
Subject
Electrochemistry,Condensed Matter Physics,Biomaterials,Electronic, Optical and Magnetic Materials
Cited by
50 articles.
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