| Literature DB >> 30972870 |
Kun Ni1, Xiangyang Wang1, Zhuchen Tao1, Jing Yang2, Na Shu1, Jianglin Ye1, Fei Pan1, Jian Xie1, Ziqi Tan1, Xuemei Sun1, Jie Liu1, Zhikai Qi1, Yanxia Chen2, Xiaojun Wu1, Yanwu Zhu1.
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.Entities:
Keywords: density functional theory; graphene; in operando; lithium-ion storage
Year: 2019 PMID: 30972870 DOI: 10.1002/adma.201808091
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849