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原子分辨率研究锂离子电池金属氧化物电极中的可逆转换反应。

Atomic resolution study of reversible conversion reaction in metal oxide electrodes for lithium-ion battery.

机构信息

Department of Materials Science and Engineering, NUANCE Center, Northwestern University , Evanston, Illinois 60208, United States.

出版信息

ACS Nano. 2014 Nov 25;8(11):11560-6. doi: 10.1021/nn504806h. Epub 2014 Oct 28.

Abstract

Electrode materials based on conversion reactions with lithium ions have shown much higher energy density than those based on intercalation reactions. Here, nanocubes of a typical metal oxide (Co3O4) were grown on few-layer graphene, and their electrochemical lithiation and delithiation were investigated at atomic resolution by in situ transmission electron microscopy to reveal the mechanism of the reversible conversion reaction. During lithiation, a lithium-inserted Co3O4 phase and a phase consisting of nanosized Co-Li-O clusters are identified as the intermediate products prior to the subsequent formation of Li2O crystals. In delithiation, the reduced metal nanoparticles form a network and breakdown into even smaller clusters that act as catalysts to prompt reduction of Li2O, and CoO nanoparticles are identified as the product of the deconversion reaction. Such direct real-space, real-time atomic-scale observations shed light on the phenomena and mechanisms in reaction-based electrochemical energy conversion and provide impetus for further development in electrochemical charge storage devices.

摘要

基于锂离子嵌入反应的电极材料的能量密度比基于转换反应的电极材料高得多。在这里,在几层石墨烯上生长出典型金属氧化物(Co3O4)的纳米立方体,并通过原位透射电子显微镜以原子分辨率研究其电化学嵌锂和脱锂过程,以揭示可逆转换反应的机理。在嵌锂过程中,鉴定出了一个锂离子嵌入的 Co3O4 相和一个由纳米级 Co-Li-O 团簇组成的相,它们是随后形成 Li2O 晶体的中间产物。在脱锂过程中,还原后的金属纳米颗粒形成一个网络并崩解成更小的团簇,作为促使 Li2O 还原的催化剂,而 CoO 纳米颗粒被鉴定为逆转换反应的产物。这种直接的、实时的原子尺度的观察揭示了基于反应的电化学能量转换中的现象和机制,并为电化学电荷存储器件的进一步发展提供了动力。

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