Coupling Se-Vacancy-Rich FeSe<sub>2</sub>/Bi<sub>2</sub>Se<sub>3</sub> Heterojunction and Microhydration-Guided Water-in-Oil Electrolyte for Ultrahigh-Performance Hybrid-Ion Batteries.
basic_science · Level V
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- Record sourced from PubMed, PMID 41773491.
- Also identified by DOI 10.1021/acs.nanolett.5c05603.
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Abstract
Magnesium/sodium hybrid-ion batteries (MNHBs), combining dendrite-free, high-capacity Mg anodes with fast Na<sup>+</sup> cathode kinetics, are appealing for post-lithium-ion storage. However, adoption is limited by sluggish Mg<sup>2+</sup> diffusion and a lack of ideal electrolytes. Here we present a synergistically engineered MNHB coupling a Se-vacancy-rich FeSe<sub>2</sub>/Bi<sub>2</sub>Se<sub>3</sub> heterojunction cathode with an optimized trace water-in-oil electrolyte. The vacancy-tailored heterointerface accelerates Mg<sup>2+</sup>/Na<sup>+</sup> migration, preserving structural integrity, supported by first-principles calculations. Molecular dynamics reveal that controlled microhydration strengthens [Mg(H<sub>2</sub>O)<sub><i>n</i></sub>]<sup>2+</sup> coordination, weakens Mg<sup>2+</sup>-Na<sup>+</sup> pairing, and increases the diffusivity. Electrochemical measurements reveal a high capacity 487 mAh g<sup>-1</sup>, excellent rate capability, a high Coulombic efficiency of >99.7% after 1000 cycles at 1.0 A g<sup>-1</sup>, and ultralong cycling stability ≥ 3500 cycles at 1.5 A g<sup>-1</sup>. <i>In-situ</i>/<i>ex-situ</i> characterizations reveal low polarization, fast diffusion, and reversible phase transitions. These findings establish a clear mechanistic understanding and a broadly applicable strategy to overcome kinetic and interfacial limitations in secondary batteries.