Ni‐Bridged Biphasic Molybdenum Carbide Interfaces: A Synergistic Catalyst for High‐Performance Lithium–Selenium Batteries

J Jiayi Li H Hong Gao (Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry) D Dingyi Zhang L Li Gao S Shijian Wang (Centre for Clean Energy Technology, Faculty of Science) C Congcong Li X Xinyao Yuan (Joint International Laboratory on Environmental and Energy Frontier Materials, School of Environmental and Chemical Engineering Shanghai University Shanghai 200444 China) C Chao Yuan (Department of Preventive Dentistry) X Xinming Nie (School of Physics and Electronic Engineering Jiangsu Normal University Xuzhou Jiangsu 221116 China) J Jinqiang Zhang (Centre for Clean Energy Technology, Faculty of Science) Y Yufei Zhao (State Key Laboratory of Chemical Resource Engineering) G Guoxiu Wang (Center for Clean Energy Technology, School of Mathematical and Physical Sciences, Faculty of Science) H Hao Liu

Abstract

Abstract Transition metal catalysts are key to developing high‐performance lithium‐selenium (Li‐Se) batteries. Herein, we report a rationally designed Ni‐bridged biphasic molybdenum carbide (Mo 2 C) with a multi‐interface structure that exposes abundant active sites and significantly enhances the electrochemically reversibility of Li–Se batteries under high current operation. The synergistic integration of catalytic and conductive functions facilitates the rapid deposition and conversion of Se/Li 2 Se x , effectively preventing electrode passivation caused by inactive accumulation during high‐rate and long‐term cycling. Furthermore, Ni serves dual roles as a structural bridge to link Mo 2 C lattice and an electronic modulator to optimize the d‐orbital configuration of Mo, thereby maximizing the catalytic efficiency of functionalized Mo 2 C. The synergistic effects of adsorption, desorption, and catalysis enable the rationally designed metal carbide/Se electrode to promote not only the rapid conversion of long‐chain Li 2 Se n species but also the solid–solid transformation of Li 2 Se 2 into Li 2 Se. As a result, the electrode achieves full‐process catalytic conversion in Li–Se batteries, delivering excellent cycling stability and high‐rate performance. Even under high Se loading (5.6 mg cm −2 ), the electrode delivers an initial capacity of 400 mAh g −1 at 0.1 C. These results highlight the effectiveness of the synergistic adsorption/desorption/catalysis mechanism in enabling a fast solid–solid conversion pathway for Li–Se batteries.

Article Details

Volume / Issue Vol. 64, Issue 51
Published December 15, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (13)

J

Jiayi Li

H

Hong Gao

Beijing National Laboratory for Molecular Sciences (BNLMS), Institute of Chemistry

D

Dingyi Zhang

L

Li Gao

S

Shijian Wang

Centre for Clean Energy Technology, Faculty of Science

C

Congcong Li

X

Xinyao Yuan

Joint International Laboratory on Environmental and Energy Frontier Materials, School of Environmental and Chemical Engineering Shanghai University Shanghai 200444 China

C

Chao Yuan

Department of Preventive Dentistry

X

Xinming Nie

School of Physics and Electronic Engineering Jiangsu Normal University Xuzhou Jiangsu 221116 China

J

Jinqiang Zhang

Centre for Clean Energy Technology, Faculty of Science

Y

Yufei Zhao

State Key Laboratory of Chemical Resource Engineering

G

Guoxiu Wang

Center for Clean Energy Technology, School of Mathematical and Physical Sciences, Faculty of Science

H

Hao Liu