Oct 2026· Inorganics· Vol 14, pp. 260· 0 citations· 113 references
Abstract
Catalytic CO2 reduction reaction (CO2RR) offers a promising approach for converting CO2 into value-added chemicals and fuels. However, its practical development remains limited by unfavorable reaction energetics, competition from the hydrogen evolution reaction (HER), and complex product selectivity. Conventional catalyst regulation strategies predominantly rely on static structural design, whereas magnetic regulation introduces an additional degree of freedom through intrinsic spin-state engineering or external magnetic fields. This review systematically summarizes the recent research progress in magnetic regulation of CO2RR with emphasis on the links among spin states, spin-resolved electronic structures, intermediate adsorption, reaction thermodynamics, product selectivity, competing reactions, and charge-carrier dynamics. Importantly, catalytic changes induced by an external magnetic field are not automatically equivalent to spin-mediated effects because magnetohydrodynamic transport, Lorentz-force-driven mass transfer, thermal perturbations, and interfacial transport can also contribute. The review therefore discusses both intrinsic magnetic regulation and field-induced effects while highlighting the evidence required to distinguish spin-associated mechanisms from non-spin contributions, including direct magnetic or spin characterization, spectroscopic evidence, and electrochemical controls that assess transport and thermal effects. Strategies including doping, vacancies, heterojunctions, axial coordination, defect engineering, and applied magnetic fields are summarized, followed by perspectives on physics-informed machine learning, artificial intelligence, and operando sensing for catalyst screening and dynamic regulation.
Catalytic activity, selectivity, and durability arise from coupled electronic, structural, interfacial, transport, and spin-related processes. Conventional catalyst design has relied largely on electronic effects, strain or stress engineering, active-site construction, and local reaction environment control. Although...
Ting-Yu Lu, Yuan Huang, Ang Cao et al.· Accounts of Materials Resear...· 0 citations
Multi-electron-proton coupling reactions are fundamental in renewable energy conversion and environmental cleanup. However, achieving high catalytic efficiency and product selectivity remains a formidable challenge, primarily due to the complex transformations of intermediates, sluggish reaction kinetics, and intense c...
Electrocatalytic carbon dioxide reduction reaction (CO2RR), driven by renewable energy sources, has provided a promising route to convert CO2 into value-added fuels and feedstocks for carbon neutrality. However, its selectivity and conversion efficiency are severely constrained by the chemical inertness of CO2, the com...
You-Zeng Li, Huan Wang, Ke Chen· The Catalyst· 0 citations
Electrochemical carbon dioxide reduction reaction (CO2RR) provides a sustainable pathway to convert the greenhouse gas CO2 into value-added fuels and feedstocks, yet its practical deployment is largely constrained by sluggish reaction kinetics and unsatisfactory product selectivity. As a core component of the electrode...
Li-Ping Chi, Qi Liu, Min-Rui Gao· Chemical Communications· 0 citations
Electrocatalytic nitrate (NO3 -) reduction reaction (eNO3RR) offers a promising route for NO3 - pollution control and nitrogen resource recovery. However, under conventional potentiostatic electrolysis, limited product selectivity and catalyst deactivation still hinder its practical application. Pulsed electrolysis pro...
Hao Liang, Wei Meng, Shu-Han Qin et al.· Advances in Materials· 0 citations
Electrochemical and photochemical carbon dioxide reduction reactions (CO2RR) represent pivotal strategies for converting CO2 into valuable chemicals, yet their multistep pathways and transient intermediates complicate the identification of the rate‐determining step (RDS). Kinetic isotope effects (KIEs) provide bond‐sen...
Xue-Mei Diao, Yi-Yang Li, Xiao-Wei Zhang et al.· Advanced Energy Materials· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.