分离器(采油)
细菌纤维素
锂(药物)
阳极
纤维素
电解质
化学工程
过电位
多硫化物
化学
阴极
材料科学
无机化学
电化学
有机化学
电极
热力学
物理
工程类
内分泌学
物理化学
医学
作者
Zhihang Fang,Long Tu,Zhijia Zhang,Jiankun Wei,Yinyu Xiang,Wei Guo,Junsheng Li
标识
DOI:10.1016/j.apsusc.2022.153683
摘要
Owing to the ultrahigh theoretical energy density and low-cost, lithium-sulfur (Li-S) batteries hold broad prospects as one of the promising substitutes for commercial lithium-ion batteries. The polysulfides shuttling originated from sulfur cathode and the lithium dendrite growth from lithium anode are the main challenges that hinder the commercial survival of Li-S batteries. Herein, thermal stable bacterial cellulose (BC) separator is successfully fixed with polyethyleneimine (PEI) by a scalable chemical grafting. The hydroxyl groups and amino groups in PEI grafted BC ([email protected]) separator can participate in the formation of Li2O and Li3N, respectively, contributing to robust solid electrolyte interface with high ionic conductivity. Therefore, the lithium deposition is well regulated, resulting in a spherical and dendrite-free Li deposit pattern. The Li/Li symmetrical cell assembled with [email protected] separator exhibits excellent cyclic stability, which can continuously plate/stripe for more than 820 h with an overpotential of ∼ 40 mV at 2 mA cm−2. Meanwhile, the polar amino group can restrain the polysulfides migration via chemosorption. As a consequence of these merits, ultrahigh initial capacity (1402 mAh g−1 at 0.1C) and excellent rate performance (440.5 mAh g−1 at 2C) for Li-S full cell are achieved, presenting new insights into the fabrication of multifunctional separators for Li-S batteries.
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