磁流体驱动
阴极
材料科学
多硫化物
可控性
锂(药物)
密度泛函理论
储能
磁场
工作(物理)
纳米技术
离子
阳极
硼化物
多物理
磁流体力学
联轴节(管道)
沉积(地质)
领域(数学)
磁芯
电子
化学物理
工程物理
吸附
感应耦合
多收费
凝聚态物理
铁磁性
电流密度
作者
Bin Wang,Beining Guo,Muhammad Mamoor,Yueyue Kong,Linlin Wang,Fengbo Wang,Zhongxin Jing,Guangmeng Qu,Xiyu He,Ling‐Yi Kong,Pengtu Zhang,Liqiang Xu
标识
DOI:10.1002/anie.202519187
摘要
Lithium-sulfur batteries, despite their high specific capacity, high theoretical energy density, environmental benignity, and low cost-related unique advantages, face critical challenges including polysulfide shuttling, sluggish redox kinetics, and uncontrolled lithium dendrite growth. Here, we propose a magnetic field cooperative regulation strategy that concurrently optimizes both sulfur cathode and lithium via spin engineering and magnetohydrodynamic (MHD) effects. Bilayer-hollow FeNi boride bipyramids (FeNi─B) with nanoreactor architectures were designed, in which an external magnetic field triggers 3d-orbital electron spin rearrangement. Simultaneously, the uniform distribution of ions and dendrite-free deposition were achieved by driving lithium-ion spiral convection through MHD effects. It is worth noting that the optimized cells exhibit exceptional cycling stability under extreme conditions (-40°C). Density functional theory and multiphysics simulations jointly reveal two mechanisms: Spin-polarization-enhanced adsorption energy for sulfur species and lithium protection via Lorentz-force-mediated ion transport. This work establishes a novel paradigm for designing magnetic field-responsive electrocatalysts and manipulating spin-orbit coupling, offering broad implications for multiphysical-field strategies in next-generation batteries.
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