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用于高性能柔性锂硫电池的金属有机框架衍生三维分级基体

Metal-Organic-Framework-Derived 3D Hierarchical Matrixes for High-Performance Flexible Li-S Batteries.

作者信息

Jiang Shunqiong, Li Xue Liang, Fang Daliang, Lieu Wei Ying, Chen Chen, Khan M Shahnawaz, Li Dong-Sheng, Tian Bingbing, Shi Yumeng, Yang Hui Ying

机构信息

International Collaborative Laboratory of 2D Materials for Optoelectronics Science and Technology of Ministry of Education, Institute of Microscale Optoelectronics, Shenzhen University, Shenzhen 518060, P. R. China.

Pillar of Engineering Product Development, Singapore University of Technology and Design, 8 Somapah Road, Singapore 487372, Singapore.

出版信息

ACS Appl Mater Interfaces. 2023 Apr 26;15(16):20064-20074. doi: 10.1021/acsami.2c22999. Epub 2023 Apr 12.

Abstract

Lithium-sulfur (Li-S) batteries have shown exceptional theoretical energy densities, making them a promising candidate for next-generation energy storage systems. However, their practical application is limited by several challenging issues, such as uncontrollable Li dendrite growth, sluggish electrochemical kinetics, and the shuttling effect of lithium polysulfides (LiPSs). To overcome these issues, we designed and synthesized hierarchical matrixes on carbon cloth (CC) by using metal-organic frameworks (MOFs). ZnO nanosheet arrays were used as anode hosts (CC-ZnO) to enable stable Li plating and stripping. The symmetric cell with CC-ZnO@Li was demonstrated to have enhanced cycling stability, with a voltage hysteresis of ∼25 mV for over 800 h at 1 mA cm and 1 mAh cm. To address the cathode challenges, we developed a multifunctional CC-NC-Co cathode host with physical confinement, chemical anchoring, and excellent electrocatalysis. The full cells with CC-ZnO@Li anodes and CC-NC-Co@S cathodes exhibited excellent electrochemical performance, with long cycling life (0.02% and 0.03% capacity decay per cycle when cycling 900 times at 0.5 C and 600 times at 1 C, respectively) and outstanding rate performance (793 mAh g at 4 C). Additionally, the pouch cell based on the flexible CC-ZnO@Li anode and CC-NC-Co@S cathode showed good stability in different bending states. Overall, our study presents an effective strategy for preparing flexible Li and S hosts with hierarchical structures derived from MOF, which can pave the way for high-performance Li-S batteries.

摘要

锂硫(Li-S)电池已展现出卓越的理论能量密度,使其成为下一代储能系统的有力候选者。然而,其实际应用受到若干挑战性问题的限制,例如不可控的锂枝晶生长、缓慢的电化学动力学以及多硫化锂(LiPSs)的穿梭效应。为克服这些问题,我们利用金属有机框架(MOF)在碳布(CC)上设计并合成了分级结构的基体。氧化锌纳米片阵列用作阳极主体(CC-ZnO)以实现稳定的锂电镀和脱镀。具有CC-ZnO@Li的对称电池被证明具有增强的循环稳定性,在1 mA cm和1 mAh cm下,超过800小时的电压滞后约为25 mV。为解决阴极挑战,我们开发了一种具有物理限制、化学锚定和优异电催化性能的多功能CC-NC-Co阴极主体。具有CC-ZnO@Li阳极和CC-NC-Co@S阴极的全电池表现出优异的电化学性能,具有长循环寿命(在0.5 C下循环900次和在1 C下循环600次时,每循环的容量衰减分别为0.02%和0.03%)和出色的倍率性能(在4 C下为793 mAh g)。此外,基于柔性CC-ZnO@Li阳极和CC-NC-Co@S阴极的软包电池在不同弯曲状态下显示出良好的稳定性。总体而言,我们的研究提出了一种有效的策略,用于制备具有源自MOF的分级结构的柔性锂和硫主体,这可为高性能锂硫电池铺平道路。

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