离子液体
石墨烯
电解质
超级电容器
电化学
酰亚胺
无机化学
傅里叶变换红外光谱
四氟硼酸盐
化学
磺酰
电极
材料科学
化学工程
有机化学
纳米技术
物理化学
烷基
工程类
催化作用
作者
Jing Li,Jie Tang,Jinshi Yuan,Kun Zhang,Qingguo Shao,Yige Sun,L. C. Qin
标识
DOI:10.1016/j.electacta.2016.03.036
摘要
The graphene material prepared by the chemical reduction method usually has oxygenic functional groups in it and such functional groups often result in interactions between the graphene electrode and the electrolyte in supercapacitors. We have examined the existential form of interactions between graphene as the electrode and three kinds of ionic liquid, 1-ethyl-3-methylimidazolium bis (trifluoromethylsulfonyl) imide (EMI-TFSI), 1-ethyl-3-methylimidazolium tetrafluoroborate (EMI-BF4), and 1-methyl-1-propylpiperidinium bis (trifluoromethyl sulfonyl) imide (MPPp-TFSI), as the electrolyte of a supercapacitor. Mass spectroscopy (MS) and Fourier transform infrared spectroscopy (FT-IR) analyses confirmed that the residual hydroxyl groups in graphene were transferred to EMI+ and TFSI− lost oxygen atoms to graphene, while little reaction took place in BF4− or MPPp+, during the process of charging. The chemical reactions are suggested to contribute to the device capacitance while it is also one of the reasons for the decreased electrochemical stability window. In this study the highest energy density achieved using the graphene electrode is 169 Wh kg−1 in MPPp-TFSI electrolyte charged to 4.4 V.
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