化学
溶剂化
电解质
镁
过电位
化学工程
分离器(采油)
无机化学
氧化物
金属
溶解
锌
溶剂
纤维素
吸附
相间
储能
纳米技术
电池(电)
溶剂化壳
电极
复合数
作者
Shuai Guo,Yi Yang,Siwen Lu,Aobing Du,Longfei Wen,Guochuan Tang,Xiaoniu Guo,Enhui Wang,Jun Luo,Junmin Ge,Gaojie Li,Baihua Qu,Xiaoyuan Zhou,Guanglei Cui,Weihua Chen
摘要
Magnesium metal batteries represent highly promising candidates for sustainable energy storage owing to their extremely high volumetric capacity (3833 mAh cm-3), abundant raw materials, and intrinsic safety. However, their practical viability is severely impeded by uneven Mg deposition, catastrophic interfacial side reactions, and continuous gassing behavior driven by uncontrolled electrolyte decomposition. Herein, we first report an inorganic inter-reinforced organic composite separator, fabricated by pairing cellulose with a zinc oxide (ZnO)-enhanced layer and designed to regulate the electrolyte solvation architecture by effectively anchoring solvent molecules. Spectroscopic and theoretical analyses reveal that the electron-deficient Zn sites on ZnO enhance the solvent-capture ability of the polar hydroxyl groups on cellulose via bidirectional charge transfer. This interaction reconfigures the Mg2+ solvation sheath into a unique single-cluster structure, steering the formation of a dense, ultrathin, inorganic-rich solid electrolyte interphase (SEI) that facilitates rapid Mg2+ desolvation while suppressing parasitic side reactions. Consequently, the as-assembled Mg||Mg symmetric cells deliver an exceptional cycling lifespan exceeding 2000 h with minimal overpotential and exhibit robust compatibility across diverse electrolyte systems. This inorganic inter-reinforced organic strategy for modulating solvation chemistry offers a generalizable avenue toward long-life and high-safety magnesium metal batteries.
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