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通过协同限制实现自支撑且灵活的硫阴极用于高能量密度锂硫电池

Self-Supported and Flexible Sulfur Cathode Enabled via Synergistic Confinement for High-Energy-Density Lithium-Sulfur Batteries.

作者信息

Wang Zhuosen, Shen Jiadong, Liu Jun, Xu Xijun, Liu Zhengbo, Hu Renzong, Yang Lichun, Feng Yuezhan, Liu Jun, Shi Zhicong, Ouyang Liuzhang, Yu Yan, Zhu Min

机构信息

Guangdong Provincial Key Laboratory of Advanced Energy Storage Materials, School of Materials Science and Engineering, South China University of Technology, Guangzhou, 510641, P. R. China.

Guangdong Provincial Key Laboratory of Functional Soft Condensed Matter, Smart Energy Research Centre, School of Materials and Energy, Guangdong University of Technology, Guangzhou, 510000, P. R. China.

出版信息

Adv Mater. 2019 Aug;31(33):e1902228. doi: 10.1002/adma.201902228. Epub 2019 Jun 20.

Abstract

Lithium-sulfur (Li-S) batteries have attracted much attention in the field of electrochemical energy storage due to their high energy density and low cost. However, the "shuttle effect" of the sulfur cathode, resulting in poor cyclic performance, is a big barrier for the development of Li-S batteries. Herein, a novel sulfur cathode integrating sulfur, flexible carbon cloth, and metal-organic framework (MOF)-derived N-doped carbon nanoarrays with embedded CoP (CC@CoP/C) is designed. These unique flexible nanoarrays with embedded polar CoP nanoparticles not only offer enough voids for volume expansion to maintain the structural stability during the electrochemical process, but also promote the physical encapsulation and chemical entrapment of all sulfur species. Such designed CC@CoP/C cathodes with synergistic confinement (physical adsorption and chemical interactions) for soluble intermediate lithium polysulfides possess high sulfur loadings (as high as 4.17 mg cm ) and exhibit large specific capacities at different C-rates. Specially, an outstanding long-term cycling performance can be reached. For example, an ultralow decay of 0.016% per cycle during the whole 600 cycles at a high current density of 2C is displayed. The current work provides a promising design strategy for high-energy-density Li-S batteries.

摘要

锂硫(Li-S)电池因其高能量密度和低成本而在电化学储能领域备受关注。然而,硫正极的“穿梭效应”导致循环性能较差,这是Li-S电池发展的一大障碍。在此,设计了一种新型硫正极,它将硫、柔性碳布和具有嵌入CoP的金属有机框架(MOF)衍生的N掺杂碳纳米阵列整合在一起(CC@CoP/C)。这些独特的带有嵌入极性CoP纳米颗粒的柔性纳米阵列不仅为体积膨胀提供了足够的空隙,以在电化学过程中保持结构稳定性,还促进了所有硫物种的物理封装和化学捕获。这种设计的CC@CoP/C正极对可溶性中间多硫化锂具有协同限制作用(物理吸附和化学相互作用),具有高硫负载量(高达4.17 mg cm),并在不同C倍率下表现出高比容量。特别地,可以实现出色的长期循环性能。例如,在2C的高电流密度下进行的整个600次循环中,每次循环的衰减率超低,仅为0.016%。当前的工作为高能量密度Li-S电池提供了一种有前景的设计策略。

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