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Enhanced Polysulfide Conversion with Highly Conductive and Electrocatalytic Iodine‐Doped Bismuth Selenide Nanosheets in Lithium–Sulfur Batteries.

Authors :
Li, Mengyao
Yang, Dawei
Biendicho, Jordi Jacas
Han, Xu
Zhang, Chaoqi
Liu, Kun
Diao, Jiefeng
Li, Junshan
Wang, Jing
Heggen, Marc
Dunin‐Borkowski, Rafal E.
Wang, Jiaao
Henkelman, Graeme
Morante, Joan Ramon
Arbiol, Jordi
Chou, Shu‐Lei
Cabot, Andreu
Source :
Advanced Functional Materials; 6/24/2022, Vol. 32 Issue 26, p1-12, 12p
Publication Year :
2022

Abstract

The shuttling behavior and sluggish conversion kinetics of intermediate lithium polysulfides (LiPS) represent the main obstacles to the practical application of lithium–sulfur batteries (LSBs). Herein, an innovative sulfur host is proposed, based on an iodine‐doped bismuth selenide (I‐Bi2Se3), able to solve these limitations by immobilizing the LiPS and catalytically activating the redox conversion at the cathode. The synthesis of I‐Bi2Se3 nanosheets is detailed here and their morphology, crystal structure, and composition are thoroughly. Density‐functional theory and experimental tools are used to demonstrate that I‐Bi2Se3 nanosheets are characterized by a proper composition and micro‐ and nano‐structure to facilitate Li+ diffusion and fast electron transportation, and to provide numerous surface sites with strong LiPS adsorbability and extraordinary catalytic activity. Overall, I‐Bi2Se3/S electrodes exhibit outstanding initial capacities up to 1500 mAh g−1 at 0.1 C and cycling stability over 1000 cycles, with an average capacity decay rate of only 0.012% per cycle at 1 C. Besides, at a sulfur loading of 5.2 mg cm−2, a high areal capacity of 5.70 mAh cm−2 at 0.1 C is obtained with an electrolyte/sulfur ratio of 12 µL mg−1. This work demonstrated that doping is an effective way to optimize the metal selenide catalysts in LSBs. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
1616301X
Volume :
32
Issue :
26
Database :
Complementary Index
Journal :
Advanced Functional Materials
Publication Type :
Academic Journal
Accession number :
157642545
Full Text :
https://doi.org/10.1002/adfm.202200529