Driving Fast‐Charging for Sodium Ion Batteries in Wide Temperature Range by Metallic 1 <i>T</i> Phase ReSe <sub>2</sub>

ABSTRACT To enable fast sodium ion battery charging in a wide temperature range, the local structures of anode materials must be optimized to reduce the Na + diffusion resistance at the interface and inside the electrode. Guided by theoretical predictions, isotropic ReSe 2 with a 1 T phase crystal structure (1 T ReSe 2 ) is developed herein to exhibit enhanced electrical conductivity for efficient charge transfer compared to the 1 T' ReSe 2 phase. Enabled by its metallic characteristic and longer Re─Se bonds, 1 T ReSe 2 achieves a lower Na + diffusion barrier and lower adsorption energy than 1 T' ReSe 2 , facilitating faster Na + storage reaction kinetics. Operando spectroscopy characterization confirms that the 1 T ReSe 2 electrode can directly produce Na x ReSe 2 without undergoing a significant phase transition. This inhibits volume expansion, leading to improved cycling stability. As a result, 1 T ReSe 2 exhibits good fast‐charging performance in a wide temperature range. A capacity of 197 mAh g −1 @20 A g −1 is maintained after 8000 cycles at room temperature, and a capacity of 136 mAh g −1 @1 A g −1 (corresponding to a capacity retention rate of 60%) is retained after 465 cycles at −40°C.

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Publication Details

Journal
Advanced Functional Materials
Published
2026-01-07
DOI
https://doi.org/10.1002/adfm.202528353
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
0.00

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article

Driving Fast‐Charging for Sodium Ion Batteries in Wide Temperature Range by Metallic 1 T Phase ReSe 2

R. Wang, Tai Yao, XianJie Wang, Jinzhen Huang et al.
Advanced Functional Materials
Advancements in Battery Materials
article

Driving Fast‐Charging for Sodium Ion Batteries in Wide Temperature Range by Metallic 1 T Phase ReSe 2

R. Wang, Tai Yao, XianJie Wang, Jinzhen Huang, Jiecai Han, Xue Li, Bo Song, Qiuxiang Zhang, Sida Jiang
article en

Abstract

ABSTRACT To enable fast sodium ion battery charging in a wide temperature range, the local structures of anode materials must be optimized to reduce the Na + diffusion resistance at the interface and inside the electrode. Guided by theoretical predictions, isotropic ReSe 2 with a 1 T phase crystal structure (1 T ReSe 2 ) is developed herein to exhibit enhanced electrical conductivity for efficient charge transfer compared to the 1 T' ReSe 2 phase. Enabled by its metallic characteristic and longer Re─Se bonds, 1 T ReSe 2 achieves a lower Na + diffusion barrier and lower adsorption energy than 1 T' ReSe 2 , facilitating faster Na + storage reaction kinetics. Operando spectroscopy characterization confirms that the 1 T ReSe 2 electrode can directly produce Na x ReSe 2 without undergoing a significant phase transition. This inhibits volume expansion, leading to improved cycling stability. As a result, 1 T ReSe 2 exhibits good fast‐charging performance in a wide temperature range. A capacity of 197 mAh g −1 @20 A g −1 is maintained after 8000 cycles at room temperature, and a capacity of 136 mAh g −1 @1 A g −1 (corresponding to a capacity retention rate of 60%) is retained after 465 cycles at −40°C.

Advanced Functional Materials
Harbin Institute of Technology (CN), Paul Scherrer Institute (CH)
National Natural Science Foundation of China, China Postdoctoral Science Foundation, Paul Scherrer Institut, Heilongjiang Provincial Postdoctoral Science Foundation, Fundamental Research Funds for the Central Universities, National Science Fund for Distinguished Young Scholars
Affordable and clean energy
Openalex Percentile: Top 95%
Advancements in Battery Materials
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