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Boosting Zn 2+ and NH 4 + Storage in Aqueous Media via In‐Situ Electrochemical Induced VS 2 /VO x Heterostructures
Author(s) -
Yu Dongxu,
Wei Zhixuan,
Zhang Xinyuan,
Zeng Yi,
Wang Chunzhong,
Chen Gang,
Shen Ze Xiang,
Du Fei
Publication year - 2021
Publication title -
advanced functional materials
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 6.069
H-Index - 322
eISSN - 1616-3028
pISSN - 1616-301X
DOI - 10.1002/adfm.202008743
Subject(s) - materials science , vanadium , aqueous solution , electrochemistry , cathode , sulfide , transition metal , electrolyte , chemical stability , intercalation (chemistry) , heterojunction , chemical engineering , nanotechnology , inorganic chemistry , electrode , optoelectronics , metallurgy , chemistry , catalysis , biochemistry , engineering
Aqueous‐ion batteries have received much attention owing to the merits of high safety, low cost, and environmental friendliness. Among potential cathode candidates, transition metal sulfides drew little attention since they suffer from low capacity, low working potential, and fast capacity fading. Here, advantage is taken of the chemical instability of VS 2 in aqueous electrolyte to in situ fabricate a heterostructural VS 2 /VO x material. Benefiting from the internal electric field at heterointerfaces, high conductivity of vanadium sulfide and high chemical stability of vanadium oxides, heterostructural VS 2 /VO x delivers an enhanced working potential by 0.25 V, superior rate capability with specific capacity of 156 mA h g −1 at 10 A g −1 , and long‐term stability over 3000 cycles as Zn 2+ storage electrode. In addition, heterostructural VS 2 /VO x is employed as the cathode for aqueous NH 4 + ion storage with high reversible capacity over 150 mA h g −1 and long lifespan over 1000 cycles, surpassing the state‐of‐the‐art materials. VS 2 /VO x is proved to demonstrate a (de)intercalation process for Zn 2+ storage, while a conversion reaction accompanied by insertion is responsible for nonmetal NH 4 + . The strong insight obtained in this study sheds light on a new methodology of exploring the potential of transition metal sulfides‐based cathode materials for aqueous ion batteries.