Paschen-Back effect modulation of SO<sub>4</sub><sup>2-</sup> hydration in magnetized electrolyte toward dendrite-free Zn-ion batteries.
basic_science · Level V
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- Record sourced from PubMed, PMID 40595737.
- Also identified by DOI 10.1038/s41467-025-61310-2 and PMC identifier 12217354.
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Abstract
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<sub>4</sub><sup>2-</sup> 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<sup>2+</sup> solvation and protonated water clusters (H<sub>3</sub>O<sup>+</sup>). Molecular dynamics simulations and in situ Raman spectroscopy reveal that the hydrated SO<sub>4</sub><sup>2-</sup>-H<sub>2</sub>O complexes promote Zn<sup>2+</sup> nucleation and deposition on the (002) plane, with preferential oxygen adsorption inhibiting two-dimensional Zn<sup>2+</sup> diffusion. Moreover, magnetizing the electrolyte disrupts the Grotthuss proton-transfer pathway, suppressing H<sub>2</sub> 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.