Electrolyte‐Regulated Conversion of Small Resource Molecules
Electrocatalysis powered by renewable electricity is a promising strategy for clean energy transformation and achieving carbon neutrality goals. In resource molecules conversion (e.g., CO<sub>2</sub> and NO<sub>3</sub> <sup>-</sup>), electrolytes serve multiple roles as reaction media, proton donors, and mass-transport carriers, with their composition and physicochemical properties exerting a significant influence on reaction pathways, intermediate stability, and product selectivity. Most research endeavors have predominantly concentrated on catalyst design, often oversimplifying electrolytes as inert backgrounds. This minireview proposes a classification framework for electrolyte effects into short-, medium-, and long-range interactions, highlighting their active regulatory roles at electrified interfaces. A comprehensive overview is provided of recent advancements in methodologies for investigating solvent effects, accompanied by an in-depth analysis of representative electrocatalytic systems. This analysis elucidates how the composition of electrolytes influences molecular-level elementary reaction steps, the dynamic reorganization and equilibrium of the interfacial microenvironment, as well as macroscopic catalytic performance, through a variety of distinct mechanisms. Finally, the key challenges and opportunities are also discussed, emphasizing electrolyte engineering as a strategic tool to reshape reaction environments and accelerate the practical deployment of electrocatalytic technologies.
Authors
- Ruhan Wang (ORCID: https://orcid.org/0000-0001-5874-4350)
- Lei He (ORCID: https://orcid.org/0000-0003-3485-3995)
- Xiaofu Sun
- Limin Wu
- Buxing Han
Institutions
- Beijing National Laboratory for Molecular Sciences (CN)
- University of Chinese Academy of Sciences (CN)
- Beijing University of Chemical Technology (CN)
Publication Details
- Journal
- Angewandte Chemie International Edition
- Published
- 2026-02-06
- DOI
- https://doi.org/10.1002/anie.202519095
- Primary Topic
- Ammonia Synthesis and Nitrogen Reduction
- Type
- article
- Field-Weighted Citation Impact
- 0.00
Funders
- National Natural Science Foundation of China
- Chinese Academy of Sciences
- National Key Research and Development Program of China