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Co/CoS 2 Heterojunction Embedded in N, S-Doped Hollow Nanocage for Enhanced Polysulfides Conversion in High-Performance Lithium-Sulfur Batteries
Modulating the electronic configuration of the substrate to achieve the optimal chemisorption toward polysulfides (LiPSs) for boosting polysulfide conversion is a promising way to the efficient Li-S batteries but filled with challenges. Herein, a Co/CoS heterostructure is elaborately built to tuning...
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Published in: | Small (Weinheim an der Bergstrasse, Germany) Germany), 2024-01, Vol.20 (3), p.e2303192 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Modulating the electronic configuration of the substrate to achieve the optimal chemisorption toward polysulfides (LiPSs) for boosting polysulfide conversion is a promising way to the efficient Li-S batteries but filled with challenges. Herein, a Co/CoS
heterostructure is elaborately built to tuning d-orbital electronic structure of CoS
for a high-performance electrocatalyst. Theoretical simulations first evidence that Co metal as the electron donator can form a built-in electric field with CoS
and downshift the d-band center, leading to the well-optimized adsorption strength for lithium polysulfides on CoS
, thus contributing a favorable way for expediting the redox reaction kinetics of LiPSs. As verification of prediction, a Co/CoS
heterostructure implanted in porous hollow N, S co-doped carbon nanocage (Co/CoS
@NSC) is designed to realize the electronic configuration regulation and promote the electrochemical performance. Consequently, the batteries assembled with Co/CoS
@NSC cathode display an outstanding specific capacity and an admirable cycling property as well as a salient property of 8.25 mAh cm
under 8.18 mg cm
. The DFT calculation also reveals the synergistic effect of N, S co-doping for enhancing polysulfide adsorption as well as the detriment of excessive sulfur doping. |
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ISSN: | 1613-6810 1613-6829 |
DOI: | 10.1002/smll.202303192 |