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使用CoP包覆的N掺杂介孔碳增强多硫化物的吸附和反应动力学用于高能量密度锂硫电池

Enhancing Adsorption and Reaction Kinetics of Polysulfides Using CoP-Coated N-Doped Mesoporous Carbon for High-Energy-Density Lithium-Sulfur Batteries.

作者信息

Cheng Qi, Yin Zhouhong, Pan Siyi, Zhang Guizhi, Pan Zhenxiao, Yu Xiaoyuan, Fang Yueping, Rao Huashang, Zhong Xinhua

机构信息

Key Laboratory for Biobased Materials and Energy of Ministry of Education, College of Materials and Energy, South China Agricultural University, Guangzhou 510642, China.

Guangdong Laboratory for Lingnan Modern Agriculture, Guangzhou 510642, China.

出版信息

ACS Appl Mater Interfaces. 2020 Sep 30;12(39):43844-43853. doi: 10.1021/acsami.0c13601. Epub 2020 Sep 18.

Abstract

Lithium-sulfur (Li-S) batteries have shown great potential in the next-generation energy storage devices due to high theoretical energy density and low cost. To obtain high-performance Li-S batteries, it is important to inhibit the polysulfide shuttle effect and improve the reaction kinetics of polysulfides. Herein, CoP nanoparticles coated by metal-organic framework-derived N-doped mesoporous carbon (CoP@N-C) composites are synthesized and applied in both a cathode for a sulfur host and a modified layer on a separator for high-energy-density Li-S batteries since the CoP component has strong chemical anchoring capability toward soluble polysulfides and high electrochemical activity toward polysulfides transformation. Meanwhile, the porous structure of conductive N-doped mesoporous carbon can not only buffer the volume variation of sulfur during the charge/discharge process but also enhance the charge transport rate in the cathode. The constructed batteries have demonstrated a high specific capacity of 1222 mAh g (8.6 mAh cm) with a high sulfur areal loading of ∼7.0 mg cm on cathodes, and a mass loading of 0.35 mg cm for modified layer on separators. Its average capacity decay is only 0.076% per cycle after 100 cycles. This work presents the highly competitive performance of Li-S batteries on the areal capacity and capacity decay.

摘要

锂硫(Li-S)电池由于具有高理论能量密度和低成本,在下一代储能设备中显示出巨大潜力。为了获得高性能的Li-S电池,抑制多硫化物穿梭效应并改善多硫化物的反应动力学至关重要。在此,合成了由金属有机框架衍生的N掺杂介孔碳包覆的CoP纳米颗粒(CoP@N-C)复合材料,并将其应用于高能量密度Li-S电池的硫宿主阴极和隔膜改性层,因为CoP组分对可溶性多硫化物具有很强的化学锚定能力,对多硫化物转化具有高电化学活性。同时,导电N掺杂介孔碳的多孔结构不仅可以缓冲充放电过程中硫的体积变化,还可以提高阴极中的电荷传输速率。所构建的电池在阴极上具有约7.0 mg cm²的高硫面负载和隔膜改性层0.35 mg cm²的质量负载下,展现出1222 mAh g⁻¹(8.6 mAh cm⁻²)的高比容量。在100次循环后,其平均容量衰减仅为每循环0.076%。这项工作展示了Li-S电池在面积容量和容量衰减方面极具竞争力的性能。

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