材料科学
过电位
镁
氟化物
法拉第效率
阳极
化学工程
无机化学
阴极
电极
冶金
电化学
化学
工程类
物理化学
作者
NULL AUTHOR_ID,NULL AUTHOR_ID,NULL AUTHOR_ID,NULL AUTHOR_ID,Ming Hu,Chilin Li
标识
DOI:10.1002/aenm.202401507
摘要
Abstract Rechargeable magnesium batteries (RMBs) have the potentials in terms of high energy density, resource abundancy and safety beyond current lithium‐ion batteries. However, the bare Mg metal electrode is prone to be passivated by solvents, suffering from the extremely high overpotential and short life during cycling. Herein, a facile chloride‐free solution pretreatment method for Mg anode is developed to construct the fluoride‐rich artificial interphase. Driven by the strong‐Lewis‐acidity trifluoromethanesulfonate anion, the interphase consisting of magnesiophilic and fluoride‐rich components are constructed by the substitution reaction of Mg metal with antimony trifluoride. The formed porous Sb‐based skeletons can uniform the electric‐field distribution and Mg ions flux at anode side, inducing the self‐adapting dendrite‐free Mg deposition even under large current density. The generated alloyable metal fluoride enables to lower the desolvation energy barrier for Mg ions and sustainedly release metallic antimony to compensate for the potentially invalid magnesiophilic sites during cycling. Therefore the symmetric cells with modified Mg anodes achieve the excellent cycling over 2000 h at 1 mA cm −2 and under a high areal capacity of 5 mAh cm −2 . The full cells with CuS cathodes exhibit a superior high voltage stability (2.6 V vs Mg/Mg 2+ ) and high coulombic efficiency close to 100%.
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