电解质
电池(电)
锂(药物)
材料科学
储能
离子液体
能量(信号处理)
能量密度
离子键合
电流(流体)
聚合物电解质
纳米技术
计算机科学
离子
静电学
计算模拟
锂离子电池
化学物理
想象
计算模型
密度泛函理论
原子间势
工作(物理)
工作温度
作者
Gunwook Nam,Junyoung Choi,K. I. Jang,Yousung Jung
摘要
Abstract Lithium‐ion batteries have dominated the energy storage landscape for decades, driven by their high energy density and operating voltage. However, increasing demands for wide operating temperature ranges and fast charging push current technologies to their limits, requiring next‐generation lithium batteries with superior safety and extended cycle life. In this context, the rational design of electrolytes remains a major challenge, as intricate bulk and interfacial mechanisms govern system viability. Specifically, solid‐state electrolytes struggle with low ionic conductivity, while liquid electrolytes are limited by complex chemical interactions. Machine learning interatomic potentials (MLIPs) address these issues by combining first‐principles accuracy with computational efficiency. These models allow us to simulate atomistic interactions and interfacial reactions that were previously impractical. We summarize recent advances in the application of MLIPs, focusing on bulk and interfacial phenomena in solid‐state and liquid electrolytes.
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