化学
锂(药物)
阴极
顺磁性
限制
卤化物
化学物理
核磁共振波谱
分子动力学
动力学(音乐)
降级(电信)
共振(粒子物理)
同位素标记
锂同位素
工作(物理)
核磁共振
分析化学(期刊)
二维核磁共振波谱
碘化锂
合理设计
核磁共振谱数据库
块(置换群论)
表征(材料科学)
磁场
作者
Houyi Liu,Bao Zhang,Yuhao Duan,Jiuwei Lei,Wen Yin,Wei Xia,Hongzhang Zhang,Kuizhi Chen,Xiaofei Yang,Guangjin Hou,Xianfeng Li
摘要
Abstract The decisive chemistry of iron-based halide cathodes─where lithium resides, how it evolves, and how disorder governs multielectron redox─has remained largely inaccessible, limiting the rational design of catholyte-free composite cathodes in all-solid-state lithium batteries. Here we make the lithium sublattice directly visible in paramagnetic LiFeCl3 using a 6Li solid-state NMR strategy combining high isotopic enrichment, optimized acquisition, and variable-temperature control. This method resolves and quantifies three Li+ environments, revealing that local Li/Fe disorder drives in-place Fe2+ reduction as the root cause of highly reversible intercalation-conversion chemistry. It further uncovers trace irreversible Fe0 species invisible to conventional spectroscopic and imaging techniques. Guided by this hidden degradation signature, optimization of the voltage window enables 85.9% capacity retention after 500 cycles with a 16.3% energy-density penalty, whereas full-depth cycling retains 68.6% after 100 cycles. Our work establishes lithium-resolved NMR as a platform linking disorder, hidden redox, and reversibility in paramagnetic cathodes.
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