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Two-dimensional molecular brush-functionalized porous bilayer composite separators toward ultrastable high-current density lithium metal anodes

机译:面向超稳定高电流密度锂金属阳极的二维分子刷功能化多孔双层复合隔板

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摘要

Lithium metal batteries have been considerably limited by the problems of uncontrolled dendritic lithium formation and the highly reactive nature of lithium with electrolytes. Herein, we have developed functional porous bilayer composite separators by simply blade-coating polyacrylamide-grafted graphene oxide molecular brushes onto commercial polypropylene separators. Our functional porous bilayer composite separators integrate the lithiophilic feature of hairy polyacrylamide chains and fast electrolyte diffusion pathways with the excellent mechanical strength of graphene oxide nanosheets and thus enable molecular-level homogeneous and fast lithium ionic flux on the surfaces of electrodes. As a result, dendrite-free uniform lithium deposition with a high Coulombic efficiency (98%) and ultralong-term reversible lithium plating/stripping (over 2600 h) at a high current density (2 mA cm−2) are achieved for lithium metal anodes. Remarkably, lithium metal anodes with an unprecedented stability of more than 1900 h cycling at an ultrahigh current density of 20 mA cm−2 are demonstrated.
机译:锂金属电池受到不受控制的树枝状锂形成以及锂与电解质的高反应性的问题的限制。本文中,我们已经通过简单地将聚丙烯酰胺接枝的氧化石墨烯分子刷刮涂到商用聚丙烯隔膜上来开发了功能性多孔双层复合隔膜。我们的功能性多孔双层复合隔板将毛状聚丙烯酰胺链的亲硫特性和快速的电解质扩散路径与氧化石墨烯纳米片的出色机械强度相结合,从而在电极表面上实现了分子级均匀且快速的锂离子通量。结果,在高电流密度(2 mA cm −2 )可实现锂金属阳极。值得注意的是,锂金属阳极在20 mA cm -2 的超高电流密度下具有超过1900 h循环的空前稳定性。

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