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过渡金属配位化合物用于可逆锂存储的容量和倍率性能洞察。

Insights into the Capacity and Rate Performance of Transition-Metal Coordination Compounds for Reversible Lithium Storage.

作者信息

Du Jia, Ren Jie, Shu Miao, Xu Xiufang, Niu Zhiqiang, Shi Wei, Si Rui, Cheng Peng

机构信息

Key Laboratory of Advanced Energy Materials Chemistry (MOE), Renewable Energy Conversion and Storage Center, College of Chemistry, Nankai University, Tianjin, 300071, China.

Shanghai Synchrotron Radiation Facility, Shanghai Institute of Applied Physics, Chinese Academy of Sciences, Shanghai, 201204, China.

出版信息

Angew Chem Int Ed Engl. 2021 Feb 19;60(8):4142-4149. doi: 10.1002/anie.202013912. Epub 2020 Dec 22.

Abstract

Coordination compounds are well-known compounds that are being used as new materials for lithium storage because of their unique advantages, that is, designable structures, abundant active sites, and facile as well as mild synthetic routes. However, the electrode stability, low rate performance, and cycle life of coordination compounds are currently the main issues preventing their application as electrode materials, and the lithium-storage mechanism in coordination networks is not well understood. Herein, isostructural one-dimensional coordination compounds were synthesized to study their lithium-storage performance. Co-HIPA and Ni-HIPA showed superior electrolyte stability than other M-HIPAs, and Co-HIPA displayed a superior reversible capacity and cycle stability, excellent rate performance, and clear voltage platform. DFT calculations and kinetic analysis revealed the influence of the metal center with different electronic structures on the lithium-storage mechanism.

摘要

配位化合物是众所周知的化合物,由于其独特的优势,即可设计的结构、丰富的活性位点以及简便温和的合成路线,正被用作锂存储的新材料。然而,配位化合物的电极稳定性、低倍率性能和循环寿命目前是阻碍其作为电极材料应用的主要问题,并且配位网络中的锂存储机制尚未得到很好的理解。在此,合成了同构的一维配位化合物以研究其锂存储性能。Co-HIPA和Ni-HIPA比其他M-HIPA表现出更好的电解质稳定性,并且Co-HIPA展现出优异的可逆容量和循环稳定性、出色的倍率性能以及清晰的电压平台。密度泛函理论计算和动力学分析揭示了具有不同电子结构的金属中心对锂存储机制的影响。

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