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Engineering stable electrode-separator interfaces with ultrathin conductive polymer layer for high-energy-density Li-S batteries

材料科学 阳极 电解质 多硫化物 化学工程 阴极 分离器(采油) 电极 聚吡咯 聚合物 过电位 复合材料 储能 聚合 电化学 化学 物理化学 量子力学 功率(物理) 工程类 物理 热力学
作者
Yuanjian Li,Wenyu Wang,Xiaoxiao Liu,Eryang Mao,Mintao Wang,Guocheng Li,Lin Fu,Zhen Li,Alex Yong Sheng Eng,Zhi Wei Seh,Yongming Sun
出处
期刊:Energy Storage Materials [Elsevier]
卷期号:23: 261-268 被引量:163
标识
DOI:10.1016/j.ensm.2019.05.005
摘要

Lithium-sulfur (Li-S) battery has been regarded as a promising energy-storage system due to its high theoretical specific capacity of 1675 mAh g−1 and low cost of raw materials. However, several challenges remain to make Li-S batteries viable, including the shuttling of soluble lithium polysulfide intermediates and pulverization of Li metal anode. Engineering stable electrode-separator interfaces without causing large mass/volume increase of inactive materials and electrolyte uptake is an effective approach to improve the cycling stability of Li-S batteries while maintaining high available energy density. Herein, we report the engineering of a stable electrode-separator interface with an ultrathin conductive polymer nanolayer on the pore walls of both surfaces of the separator via a simple and scalable approach using in-situ vapor-phase polymerization of polypyrrole (PPy) on commercial Celgard separator with only a small increase in overall mass and volume. The inherent hydrophilicity of PPy enables the separator to have enhanced electrolyte uptake, which facilitates homogenous Li+ flux and thus uniform plating and stripping of metallic lithium at the anode side during the charge/discharge processes. Meanwhile, the chemical immobilization effect of PPy suppresses the migration of the soluble polysulfides and improves the stability of the sulfur cathode. We showed that a Li||Li symmetrical cell with the PPy modified separator gave a low and stable overpotential of less than 30 mV for over 250 h' stripping and plating test at 1 mA cm−2 with a fixed areal capacity of 3 mAh cm−2, which was significantly better than that using a regular Celgard separator. Using the PPy modified separator, Li-S cell with sulfur/carbon black composite cathode and lithium anode delivered stable cycling for 250 cycles at 0.5 C with a low capacity decay rate of 0.083% per cycle. Even for a Li-S cell with a high-areal-capacity sulfur cathode (4.8 mAh cm−2), good cycling stability was achieved. It gave a reversible areal capacity of 3.6 mAh cm−2 after 150 charge/discharge cycles at 0.2 C with 75.6% capacity retention. Besides, the as-achieved separator showed better thermal stability than the bare counterpart. This work offers an alternative approach for achieving a practical Li-S battery toward high energy density and long cycle life through simple and scalable separator-electrode interface engineering without significant increase in volume and mass.
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