Efficient Polysulfide Trapping and Conversion on N‐Doped CoTe2 via Enhanced Dual‐Anchoring Effect
Source abstract
Abstract
Abstract Polysulfide shuttling and sluggish sulfur redox kinetics hinder the cyclability and rate capability of lithium–sulfur (Li–S) batteries. The intrinsic redox kinetics of sulfur cathodes strongly depends on the interaction between catalysts and sulfur species. Herein, N‐doped CoTe2 is proposed as an effective dual‐anchoring electrocatalyst, which can simultaneously bind Li and S atoms in lithium polysulfides via ionic Te–Li/N–Li bonding and coordinate covalent Co–S bonding. The incorporated N not only serves as enhanced lithiophilic site, but also an agent to improve the sulfiphilicity of the Co site as revealed by a series of experimental and computational results. Benefiting from these superiorities, the use of N‐doped CoTe2 as a catalytic interlayer enables efficient operation of Li–S batteries in terms of impressive rate capability of 758 mAh g−1 at 4 C and very low capacity decay of 0.021% per cycle over 1000 cycles. The material and strategy demonstrated in this work may open the door toward developing more advanced Li–S electrocatalysts.
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Research context
OpenAlex topics: Advanced Battery Materials and Technologies · Advancements in Battery Materials · Advanced battery technologies research
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Chemistry and Chemical Engineering Harbin Institute of Technology Harbin 150001 China
Academy of Fundamental and Interdisciplinary Sciences Harbin Institute of Technology Harbin 150001 China
State Key Laboratory of Urban Water Resource and Environment Harbin Institute of Technology Harbin 150001 China
Funding
National Natural Science Foundation of China
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