电解质
锂(药物)
储能
合理设计
设计要素和原则
电化学
纳米技术
电压
电化学储能
材料科学
离子键合
离子电导率
金属锂
钥匙(锁)
能量密度
离子
能量(信号处理)
电池(电)
高能
工程物理
电导率
导电体
高压
计算机科学
数码产品
化学
能量转换
电化学能量转换
作者
Yanchen Piao,Yusheng Ye,Youqi Zhang,Feng Wu,Jingmei Lyu,Renjie Chen
出处
期刊:ACS energy letters
[American Chemical Society]
日期:2026-02-23
卷期号:11 (3): 2636-2646
被引量:2
标识
DOI:10.1021/acsenergylett.5c04182
摘要
Enhancing charging rates is pivotal for electrified technologies, motivating the development of “charge-and-go” energy storage systems. High-voltage batteries are particularly attractive as the energy output scales with both voltage and capacity. However, fast-charging at high voltages is fundamentally constrained by sluggish Li + transport and interfacial degradation. Rational electrolyte design is therfore a critical strategy to overcome these limitations. In this Review, we examine the key mechanistic origins of these limitations and summarize electrolyte-driven solutions for high-voltage, fast-charging lithium batteries. We summarize recent advances across five strategies, including fluorinated electrolytes, superconcentrated and localized high-concentration electrolytes, competitive and cooperative coordination, electron-donor molecular design, and asymmetric molecular architectures. We further elucidate the correlation between operating voltage and ionic conductivity in emerging high-voltage fast-charging electrolytes and highlight cathode–electrolyte redox dynamics and structure–property relationships. These insights establish design principles to guide next-generation lithium batteries and broaden the landscape of electrochemical energy storage systems.
科研通智能强力驱动
Strongly Powered by AbleSci AI