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通过ZIF-67的热解和硫化原位形成Co S /N-C空心纳米球用于高性能锂离子电池

In Situ Formation of Co S /N-C Hollow Nanospheres by Pyrolysis and Sulfurization of ZIF-67 for High-Performance Lithium-Ion Batteries.

作者信息

Zeng Peiyuan, Li Jianwen, Ye Ming, Zhuo Kaifeng, Fang Zhen

机构信息

Key Laboratory of Functional Molecular Solids, Ministry of Education, Center for Nano Science and Technology, College of Chemistry and Materials Science, Anhui Normal University, Wuhu, East Beijing Road 1#, 241000, P.R. China.

出版信息

Chemistry. 2017 Jul 18;23(40):9517-9524. doi: 10.1002/chem.201700881. Epub 2017 May 22.

DOI:10.1002/chem.201700881
PMID:28370522
Abstract

Co S is considered a promising candidate as the anode material in lithium-ion batteries (LIBs) because of its remarkable electrical conductivity, high theoretical capacity, and low cost. However, the practical application of Co S is greatly restricted because of its poor cycling stability and rate performance, which result mainly from the large volume expansion and dissolution of the polysulfide intermediates during the charge/discharge process. In this report, Co S embedded in N-rich carbon hollow spheres are successfully designed and synthesized through an in situ pyrolysis and sulfurization process, employing the well-known ZIF-67 as the precursor and ethanethiol as the sulfur source. Co S nanoparticles embedded in the N-rich hollow carbon shell exhibit excellent lithium storage properties at a high charge/discharge rate. A discharge capacity of 784 mAh g is obtained upon battery testing at a current density of 1 C (544 mA g ). Even upon cycling at a current density of 4 C, the as-prepared Co S /N-C can still deliver a discharge capacity of 518 mAh g . The excellent battery performance can be attributed to the hollow structure as well as the N-rich carbon encapsulation. Moreover, this metal-organic framework sulfurization route also shows good generality for the synthesis of other metal sulfide-carbon composites such as ZnS/N-C and Cu S/C.

摘要

由于具有出色的导电性、高理论容量和低成本,CoS被认为是锂离子电池(LIBs)阳极材料的一个有前景的候选者。然而,CoS的实际应用受到极大限制,因为其循环稳定性和倍率性能较差,这主要是由于在充/放电过程中多硫化物中间体的大量体积膨胀和溶解所致。在本报告中,通过原位热解和硫化过程,成功设计并合成了嵌入富氮碳空心球中的CoS,采用著名的ZIF-67作为前驱体,乙硫醇作为硫源。嵌入富氮空心碳壳中的CoS纳米颗粒在高充/放电速率下表现出优异的锂存储性能。在1C(544 mA g)的电流密度下进行电池测试时,获得了784 mAh g的放电容量。即使在4C的电流密度下循环,所制备的CoS/N-C仍能提供518 mAh g的放电容量。优异的电池性能可归因于空心结构以及富氮碳封装。此外,这种金属有机框架硫化路线对于合成其他金属硫化物-碳复合材料(如ZnS/N-C和CuS/C)也显示出良好的通用性。

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