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用于锂离子电池的具有卓越循环诱导容量增强性能的金属有机框架玻璃负极

Metal-Organic Framework Glass Anode with an Exceptional Cycling-Induced Capacity Enhancement for Lithium-Ion Batteries.

作者信息

Gao Chengwei, Jiang Zhenjing, Qi Shibin, Wang Peixing, Jensen Lars Rosgaard, Johansen Morten, Christensen Christian Kolle, Zhang Yanfei, Ravnsbaek Dorthe Bomholdt, Yue Yuanzheng

机构信息

Department of Chemistry and Bioscience, Aalborg University, Aalborg, 9220, Denmark.

Laboratory of Infrared Material and Devices, The Research Institute of Advanced Technologies, Ningbo University, Ningbo, 315211, China.

出版信息

Adv Mater. 2022 Mar;34(10):e2110048. doi: 10.1002/adma.202110048. Epub 2022 Jan 31.

DOI:10.1002/adma.202110048
PMID:34969158
Abstract

Metal-organic frameworks (MOFs) hold great promise as high-energy anode materials for next-generation lithium-ion batteries (LIBs) due to their tunable chemistry, pore structure and abundant reaction sites. However, the pore structure of crystalline MOFs tends to collapse during lithium-ion insertion and extraction, and hence, their electrochemical performances are rather limited. As a critical breakthrough, a MOF glass anode for LIBs has been developed in the present work. In detail, it is fabricated by melt-quenching Cobalt-ZIF-62 (Co(Im) (bIm) ) to glass, and then by combining glass with carbon black and binder. The derived anode exhibits high lithium storage capacity (306 mAh g after 1000 cycles at of 2 A g ), outstanding cycling stability, and superior rate performance compared with the crystalline Cobalt-ZIF-62 and the amorphous one prepared by high-energy ball-milling. Importantly, it is found that the Li-ion storage capacity of the MOF glass anode continuously rises with charge-discharge cycling and even tripled after 1000 cycles. Combined spectroscopic and structural analyses, along with density functional theory calculations, reveal the origin of the cycling-induced enhancement of the performances of the MOF glass anode, that is, the increased distortion and local breakage of the CoN coordination bonds making the Li-ion intercalation sites more accessible.

摘要

金属有机框架材料(MOFs)因其可调节的化学性质、孔隙结构和丰富的反应位点,有望成为下一代锂离子电池(LIBs)的高能量负极材料。然而,晶体MOFs的孔隙结构在锂离子嵌入和脱出过程中容易坍塌,因此其电化学性能相当有限。作为一个关键突破,本文开发了一种用于LIBs的MOF玻璃负极。具体而言,它是通过将钴-沸石咪唑酯骨架结构材料62(Co(Im) (bIm) )熔融淬火制成玻璃,然后将玻璃与炭黑和粘结剂混合而成。与晶体钴-沸石咪唑酯骨架结构材料62以及通过高能球磨制备的非晶态材料相比,所得负极表现出高储锂容量(在2 A g的电流密度下循环1000次后为306 mAh g)、出色的循环稳定性和优异的倍率性能。重要的是,发现MOF玻璃负极的锂离子存储容量随着充放电循环而持续增加,在1000次循环后甚至增加了两倍。结合光谱和结构分析以及密度泛函理论计算,揭示了循环诱导的MOF玻璃负极性能增强的起源,即CoN配位键的畸变增加和局部断裂使锂离子嵌入位点更容易接近。

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