胶体
钾
离子
熵(时间箭头)
金属
无机化学
过渡金属
纳米技术
化学工程
原子单位
化学
二硫键
材料科学
化学物理
热力学
催化作用
物理
物理化学
有机化学
工程类
生物化学
量子力学
作者
Yan-Jie Liao,Wei‐Wen Shen,Che‐Bin Chang,Hsing‐Yu Tuan
标识
DOI:10.1016/j.cej.2023.143942
摘要
High-entropy metal disulfide (HES2) colloid clusters were synthesized through a two-step templated solvothermal method for used as anode materials for potassium-ion storage devices. HES2’s large configuration entropy stabilizes its crystal structure and promotes chemical diversity by introducing multiple cations, thus reducing the impact of the shuttle effect, retaining active materials and extending cycling life up to 1800 cycles. During cycling, crystalline-amorphous grain boundaries formed in situ enhance electrochemical reaction activities and ensure the exposure of active sites. Elements with lower electronegativity allow S to bring more negative charges, improving the electrostatic force between S and K+ and enabling better anchoring of potassium polysulfide. Meanwhile, the retained close-packed cluster structure of HES2 provides a large contact area to accelerate the reduction reaction of the electrolyte in the sphere during the repeating K+ insertion/extraction. We further demonstrate the excellent performance of HES2 anodes on practical potassium-ion full battery and hybrid capacitor applications. The pioneering concept in atomic compositional engineering and structural design of transition metal sulfide electrodes presented in this work marks a significant step forward in the development of chalcogenide electrode systems for energy storage devices.
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