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 SO 4 2- 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 Zn 2+ solvation and protonated water clusters (H 3 O + ). Molecular dynamics simulations and in situ Raman spectroscopy reveal that the hydrated SO 4 2- –H 2 O complexes promote Zn 2+ nucleation and deposition on the (002) plane, with preferential oxygen adsorption inhibiting two-dimensional Zn 2+ diffusion. Moreover, magnetizing the electrolyte disrupts the Grotthuss proton-transfer pathway, suppressing H 2 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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