On the controlled electrochemical preparation of R4N+ graphite intercalation compounds and their host structural deformation effects

被引:25
|
作者
Cooper, Adam J. [1 ]
Velicky, Matej [1 ]
Kinloch, Ian A. [2 ]
Dryfe, Robert A. W. [1 ]
机构
[1] Univ Manchester, Sch Chem, Manchester M13 9PL, Lancs, England
[2] Univ Manchester, Sch Mat, Manchester M13 9PL, Lancs, England
基金
英国工程与自然科学研究理事会;
关键词
Tetraalkylammonium; Intercalation; Graphite intercalation complex; LIQUID-PHASE EXFOLIATION; TETRAALKYLAMMONIUM CATIONS; ELECTRICAL-CONDUCTIVITY; CATHODIC BEHAVIOR; ALKALI-METAL; ION TRANSFER; GRAPHENE; TERNARY; ELECTROLYTES; REDUCTION;
D O I
10.1016/j.jelechem.2014.07.025
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
We present electrochemical studies of tetraalkylammonium (R4N+) reduction chemistry at Highly Orientated Pyrolytic Graphite (HOPG) and glassy carbon (GC) electrodes. We show that by electrochemically controlled intercalation and formation of a graphite intercalation complex (GIC) into layered HOPG, the irreversible reduction of the tetraalkylammonium cation can be prevented and subsequent de-intercalation of the GIC via the use of potentiostatic control is achievable. R4N+ cations with varying alkyl chain lengths (methyl, ethyl and butyl) have been shown to exhibit excellent charge recovery effects during charge/discharge studies. Finally the effects of electrode expansion on the degree of recovered charge have been investigated and the observed effects of R4N+ intercalation on the graphite cathode have been probed by scanning electron microscopy (SEM) and X-ray diffraction (XRD). (C) 2014 The Authors. Published by Elsevier B.V.
引用
收藏
页码:34 / 40
页数:7
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