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Chemical Immobilization and Conversion of Active Polysulfides Directly by Copper Current Collector: A New Approach to Enabling Stable Room‐Temperature Li‐S and Na‐S Batteries
Author(s) -
Li Peirong,
Ma Lu,
Wu Tianpin,
Ye Hualin,
Zhou Junhua,
Zhao Feipeng,
Han Na,
Wang Yeyun,
Wu Yunling,
Li Yanguang,
Lu Jun
Publication year - 2018
Publication title -
advanced energy materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 10.08
H-Index - 220
eISSN - 1614-6840
pISSN - 1614-6832
DOI - 10.1002/aenm.201800624
Subject(s) - polysulfide , sulfur , cathode , copper , aqueous solution , chemistry , chemical engineering , current collector , electrochemistry , metal , energy storage , materials science , nanotechnology , inorganic chemistry , electrode , electrolyte , organic chemistry , quantum mechanics , engineering , power (physics) , physics
Room‐temperature Li/Na‐S batteries are promising energy storage solutions, but unfortunately suffer from serious cycling problems rooted in their polysulfide intermediates. The conventional strategy to tackle this issue is to design host materials for trapping polysulfides via weak physical confinement and interfacial chemical interactions. Even though beneficial, their capability for the polysulfide immobilization is still limited. Herein, the unique sulfiphilic nature of metallic Cu is revisited. Upon the exposure to polysulfide in aqueous or aprotic solution, the surface sulfidization rapidly takes place, resulting in the formation of Cu 2 S nanoflake arrays with tunable texture. When the sulfidized Cu current collector is directly used as the sulfur‐equivalent cathode, it enables high‐performance Li/Na‐S batteries at room temperature with reasonable high sulfur loading. Specific capacities up to ≈1200 mAh g −1 for Li‐S and ≈400 mAh g −1 for Na‐S are measured when normalized to the amount of equivalent sulfur, and can be readily sustained for >1000 cycles.