材料科学
阴极
杂原子
电化学
水溶液
熔盐
钒
热稳定性
溶解
电池(电)
离子
化学工程
无机化学
兴奋剂
储能
电极
物理化学
化学
冶金
有机化学
热力学
光电子学
戒指(化学)
工程类
物理
功率(物理)
作者
Weiyan Jiang,Huizhong Shi,Miao Shen,Rui Tang,Zhongfeng Tang,Jian‐Qiang Wang
标识
DOI:10.1021/acsami.2c00201
摘要
The lack of suitable cathode materials with a high capacity and good stability is a crucial problem affecting the development of aqueous Zn-ion batteries. Herein, a novel strategy for the modification of V2CTx through molten salt thermal treatment is proposed. In the novel route, S heteroatoms were introduced into V2CTx through a substitution reaction during the dissolution of Li2S in LiCl-KCl molten salts. Then, surface V2O5 was obtained through the in situ electrochemical charging/discharging of the S-doped V2CTx (MS-S-V2CTx) cathode. The assembled Zn/MS-S-V2CTx battery showed a high reversible discharge capacity of 411.3 mAh g-1 at a current density of 0.5 A g-1, an 80% capacitance retention after long cycle stability tests at 10 A g-1 for 3000 cycles, and a high energy density of 375.5 Wh kg-1 in 2M ZnSO4. Density functional theory calculations demonstrate that the improved electrochemical performance of the cathode can be attributed to the introduced S heteroatoms, which considerably reduced the ion diffusion energy barrier for Zn2+ ions and improved the stability of V2O5. This work provides a novel method to produce highly active and stable vanadium-based cathodes for aqueous Zn-ion batteries.
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