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Electronic Metal‐Support Interactions in Atomically Dispersed Fe(III)‐VO2 Nanoribbons for High‐Performance Lithium–Sulfur Batteries.

Authors :
Pang, Yashuai
Xie, Minsen
Lu, Xinghao
Wan, Zhao
Zhong, Zhuohang
Muhammad, Waqas
Huan, Xiang Long
Niu, Yinghua
Zhang, Zhen
Lv, Weiqiang
Source :
Advanced Functional Materials. 1/9/2024, Vol. 34 Issue 2, p1-9. 9p.
Publication Year :
2024

Abstract

Lithium–sulfur (Li–S) batteries have attracted wide attention as high‐energy‐density energy storage devices, but their practical applications are hindered by the severe shuttle effect and sluggish kinetics of lithium polysulfides (LiPSs). To address these challenges, polar mediators are employed to chemisorb and catalyze LiPSs, but most of them suffer from low electronic conductivity and poor catalytic activity. Here, a novel strategy is reported to enhance both properties by dispersing Fe(III) atoms in VO2 nanoribbons(Fe‐VO2), creating electronic metal‐support interactions (EMSI) that modulate the electronic structure and charge transfer of VO2. Theoretical calculations reveal that EMSI lowers the energy barrier for the decomposition of Li2S from 1.60 to 1.32 eV and increases the electronic conductivity of VO2. Fe doping reduces the Li‐ions diffusion barrier from 1.42 eV in VO2 to 0.99 eV in Fe‐VO2. The Fe‐VO2 catalyst shows strong adsorption and fast converstion of LiPSs, resulting in high energy density and long cycling life of Li‐S batteries. The cathode with Fe‐VO2 maintains a higher capacity retention of 67% after 500 cycles at 1 C, compared with 52.4% and 53.6% for the carbon black based cathode and VO2 based cathode, respectively. This work demonstrates the potential of EMSI for designing efficient catalysts for Li–S batteries and provides new insights into the electronic structure engineering of polar mediators. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1616301X
Volume :
34
Issue :
2
Database :
Academic Search Index
Journal :
Advanced Functional Materials
Publication Type :
Academic Journal
Accession number :
174713235
Full Text :
https://doi.org/10.1002/adfm.202308849