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Optimizing Heat-Treated Al-BDC@TiO2 to Improve the Electrochemical Properties of Lithium-Sulfur Batteries.

Authors :
Xue, Kaiyu
Chen, Liping
Wu, Dingding
Bai, Yang
Wang, Juan
Source :
Journal of Electronic Materials; Mar2024, Vol. 53 Issue 3, p1133-1141, 9p
Publication Year :
2024

Abstract

Lithium-sulfur batteries (Li-S) are highly promising due to their high energy density and specific capacity; however, the poor conductivity of the active material leads to slow reaction kinetics, and the shuttle effect of the intermediate product lithium polysulfides leads to rapid capacity decay. Here, the effective encapsulation of Al-BDC by TiO<subscript>2</subscript> particles is achieved by encapsulating an aluminum-based metal organic framework (Al-BDC) with terephthalic acid as the organic ligand and heat-treating at different temperatures. This method shows that the TiO<subscript>2</subscript> particles can effectively encapsulate Al-BDC while maintaining the structural stability of Al-BDC after heat treatment at 400°C. The TiO<subscript>2</subscript> crystallization is disordered after heat treatment at 300°C, and the TiO<subscript>2</subscript> is exfoliated and the Al-BDC is collapsed after heat treatment at 500°C. In addition, TiO<subscript>2</subscript> particles can be partially filled into the pores of Al-BDC. Therefore, Al-BDC@TiO<subscript>2</subscript>-400 can effectively inhibit the shuttle of polysulfides, and the corresponding Li-S batteries can achieve relatively high discharge specific capacity, rate performance and cycling stability. In particular, the Al-BDC@TiO<subscript>2</subscript>-400@S can achieve an initial discharge specific capacity of 907.6 mAh g<superscript>−1</superscript> at 0.1C, and 686.5 mAh g<superscript>−1</superscript> at 2C with remained capacity of 379.8 mAh g<superscript>−1</superscript> after 400 cycles. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
03615235
Volume :
53
Issue :
3
Database :
Complementary Index
Journal :
Journal of Electronic Materials
Publication Type :
Academic Journal
Accession number :
175199765
Full Text :
https://doi.org/10.1007/s11664-023-10888-8