纳米技术
材料科学
离子键合
结构稳定性
电化学储能
电化学
纳米尺度
钥匙(锁)
计算机科学
工作(物理)
硫化物
储能
硫化铅
离子电导率
理论(学习稳定性)
组态熵
纳米电子学
材料设计
熵(时间箭头)
数码产品
晶体结构
高能
电导率
生化工程
开发(拓扑)
作者
Tong Yuan,Qisheng Zang,Hao Yu,Yu Yang,Fuqin Zhang
出处
期刊:Nano Letters
[American Chemical Society]
日期:2026-08-03
卷期号:26 (31): 10077-10090
标识
DOI:10.1021/acs.nanolett.6c02489
摘要
High-entropy sulfides (HESs) integrate the high ionic conductivity of sulfide materials with the structural tunability of high-entropy design, demonstrating immense potential in advanced energy storage. This review systematically traces the development trajectories of HESs across four key domains: solid-state electrolytes, lithium-sulfur batteries, lithium/sodium-ion batteries, and supercapacitors. By critically examining the evolving "composition-structure-performance" relationships, we highlight breakthroughs in key metrics, including ionic conductivity, cycle life, rate capability, and specific capacitance. Crucially, insights reveal that crystal structure primarily determines the attainable performance window, whereas configurational entropy mainly improves structural stability and transport homogeneity. Therefore, the most effective design strategy avoids simply maximizing entropy. Instead, it combines favorable structural frameworks with moderate high-entropy engineering, often reinforced by nanoscale architectures. Ultimately, this work provides a clear historical framework and forward-looking guidance, emphasizing the need for rigorous validation in practical full cells to verify the intrinsic contributions of high-entropy effects.
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