Document Type
Article
Abstract
Molecular catalysts serve as ideal platforms for studying electrocatalytic reaction mechanisms. While current research mainly focuses on modulating central metals or surrounding ligands, the influence of molecular spatial configuration remains largely unexplored. Herein, we synthesized two cobalt complexes with similar ligand environments but distinct spatial geometries, a planar cobalt hexaazamacrocylic complex (CoHAM) and a non-planar acyclic Co(phen)2Cl2, and evaluated their performance in CO2 reduction reaction (CO2RR). The planar CoHAM exhibited dramatically superior CO2RR performance compared to the non-planar Co(phen)2Cl2. Through a combined analyses using in-situ UV-vis spectroscopy, high-resolution mass spectrometry (HRMS), and Raman spectroscopy, we elucidated the origins of this performance gap by identifying key intermediates and reaction pathways. These findings underscore the critical role of the spatial configuration of molecular catalysts in governing electrocatalytic performance and provide a strategic direction for the rational design of efficient CO2RR catalysts.
Graphical Abstract
Keywords
Molecular catalysts, Spatial configuration, Cobalt hexaazamacrocylic complex, CO2 reduction, Catalytic mechanism
DOI
10.61558/2993-074X.3610
Online Date
4-9-2026
Recommended Citation
Ru Jia, Cheng-Biao Zhu, Zi-Mo Zhang, Tuo Wang, Kai-Cong Yang, Guang-Zhe Wang, Yang Hu, Ting-Ting Zhang, Zhen-Wei Wei, Li Xiao, Gong-Wei Wang, Lin Zhuang. Distinct CO2 Electroreduction Behaviors over Planar and Non-Planar Cobalt Molecular Catalysts[J]. Journal of Electrochemistry, doi: 10.61558/2993-074X.3610.