High-spin state electron configuration in Mn-doped Ni3Se4 for efficient methanol oxidation
Year: 2025
Type: article
Abstract: This work demonstrates that Mn doping in Ni 3 Se 4 modulates spin state and electronic structure, significantly enhancing methanol oxidation to formic acid with excellent catalytic efficiency at a high current density. The methanol oxidation reaction (MOR) to formic acid offers a promising alternative to the anodic oxygen evolution reaction (OER) in water electrolysis. However, the development of efficient and cost-effective catalysts remains a primary challenge. In this study, an enhancement in catalytic MOR performance is achieved through the incorporation of Mn atoms with unsaturated t 2 g orbitals into Ni 3 Se 4 . Comprehensive experimental analyses and theoretical calculations reveal that substituting Ni with Mn induces strong electron-withdrawing effects, effectively modulating the local coordination environment of the metal centers. The presence of Mn also elongates Ni–Se(O) bonds, which reduces e g orbital occupancy and modifies the spin state of the material. Electrochemical measurements demonstrate that electrodes based on this optimized material exhibit a high spin state and deliver excellent catalytic activity, achieving a MOR current density up to ∼190 mA cm −2 at 1.6 V. This performance enhancement is attributed to the favorable electronic configuration and reduced reaction energy barriers associated with the high-spin state.
Source: Journal of Energy Chemistry
Authors: Yong Zhang, Yi Ma, Jing Yu, Canhuang Li, Jordi Arbiol, Xiaoxi Wang, Ning Jian, Huan Ge, Luming Li, Andreu Cabot, Junshan Li
Language: English
Field: Energy
Domain: Physical Sciences
Open Access status: hybrid
Estimated APC paid: $3,750
Funders: Fundación Carmen y Severo Ochoa, European Commission, Generalitat de Catalunya, China Postdoctoral Science Foundation, Natural Science Foundation of Sichuan Province, Sichuan Province Science and Technology Support Program, European Regional Development Fund, Agencia Estatal de Investigación
OpenAlex ID: W7082002824
