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在单层石墨烯上进行锂离子存储的原位探测

In Operando Probing of Lithium-Ion Storage on Single-Layer Graphene.

作者信息

Ni Kun, Wang Xiangyang, Tao Zhuchen, Yang Jing, Shu Na, Ye Jianglin, Pan Fei, Xie Jian, Tan Ziqi, Sun Xuemei, Liu Jie, Qi Zhikai, Chen Yanxia, Wu Xiaojun, Zhu Yanwu

机构信息

Hefei National Research Center for Physical Sciences at the Microscale, CAS Key Laboratory of Materials for Energy Conversion, Department of Materials Science and Engineering, i-ChEM (Collaborative Innovation Center of Chemistry for Energy Materials), University of Science and Technology of China, 96 Jin Zhai Rd., Hefei, Anhui, 230026, P. R. China.

Hefei National Laboratory for Physical Sciences at Microscale, Department of Chemical Physics, University of Science and Technology of China, 96 Jin Zhai Rd., Hefei, Anhui, 230026, P. R. China.

出版信息

Adv Mater. 2019 Jun;31(23):e1808091. doi: 10.1002/adma.201808091. Epub 2019 Apr 11.

Abstract

Despite high-surface area carbons, e.g., graphene-based materials, being investigated as anodes for lithium (Li)-ion batteries, the fundamental mechanism of Li-ion storage on such carbons is insufficiently understood. In this work, the evolution of the electrode/electrolyte interface is probed on a single-layer graphene (SLG) film by performing Raman spectroscopy and Fourier transform infrared spectroscopy when the SLG film is electrochemically cycled as the anode in a half cell. The utilization of SLG eliminates the inevitable intercalation of Li ions in graphite or few-layer graphene, which may have complicated the discussion in previous work. Combining the in situ studies with ex situ observations and ab initio simulations, the formation of solid electrolyte interphase and the structural evolution of SLG are discussed when the SLG is biased in an electrolyte. This study provides new insights into the understanding of Li-ion storage on SLG and suggests how high-surface-area carbons could play proper roles in anodes for Li-ion batteries.

摘要

尽管高比表面积碳材料,如基于石墨烯的材料,正在被研究用作锂离子电池的负极,但人们对锂离子在这类碳材料上存储的基本机制仍了解不足。在这项工作中,当单层石墨烯(SLG)薄膜在半电池中作为负极进行电化学循环时,通过拉曼光谱和傅里叶变换红外光谱对电极/电解质界面的演变进行了探测。SLG的使用消除了锂离子在石墨或少层石墨烯中不可避免的嵌入,而这可能使先前工作中的讨论变得复杂。将原位研究与非原位观察及从头算模拟相结合,讨论了SLG在电解质中施加偏压时固体电解质界面的形成以及SLG的结构演变。这项研究为理解锂离子在SLG上的存储提供了新的见解,并提出了高比表面积碳材料如何在锂离子电池负极中发挥适当作用。

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