电解质
离子
枝晶(数学)
材料科学
调制(音乐)
化学物理
化学
电极
物理
物理化学
几何学
声学
数学
有机化学
作者
Xiayan Yao,Zhi Wang,Jianwei Guo,Guoyu Qian,Hongchen Wang,Xuzhong Gong,Dong Wang
标识
DOI:10.1038/s41467-025-61310-2
摘要
Tuning anionic solvation structures and dynamic processes at solid-liquid interfaces is critical yet challenging for stabilizing Zn metal negative electrodes in Zn-ion batteries, particularly due to the issue of dendrite formation and hydrogen evolution reaction. Here, we show that highly hydrated SO42- can be effectively modulated under a strong magnetic field via the Paschen-Back effect on O-H vibrations, which reorients individual water molecules to manipulate Zn2+ solvation and protonated water clusters (H3O+). Molecular dynamics simulations and in situ Raman spectroscopy reveal that the hydrated SO42--H2O complexes promote Zn2+ nucleation and deposition on the (002) plane, with preferential oxygen adsorption inhibiting two-dimensional Zn2+ diffusion. Moreover, magnetizing the electrolyte disrupts the Grotthuss proton-transfer pathway, suppressing H2 evolution and further reducing dendrite formation. By employing inexpensive permanent magnets without external power, this magnetization strategy offers a practical, energy-efficient route to enhance both the stability and performance of zinc-based rechargeable batteries.
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