Refinements to the structure of graphite oxide: absolute quantification of functional groups via selective labelling

被引:79
作者
Eng, Alex Yong Sheng [1 ]
Chua, Chun Kiang [1 ]
Pumera, Martin [1 ]
机构
[1] Nanyang Technol Univ, Sch Phys & Math Sci, Div Chem & Biol Chem, Singapore 637371, Singapore
关键词
ELECTRON-TRANSFER KINETICS; GRAPHENE OXIDE; CARBON NANOTUBES; INHERENT ELECTROCHEMISTRY; CHEMICAL-MODIFICATION; GLASSY-CARBON; SURFACE; COVALENT; PERMANGANATE; REDUCTION;
D O I
10.1039/c5nr05891k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Chemical modification and functionalization of inherent functional groups within graphite oxide ( GO) are essential aspects of graphene-based nano-materials used in wide-ranging applications. Despite extensive research, there remains some discrepancy in its structure, with current knowledge limited primarily to spectroscopic data from XPS, NMR and vibrational spectroscopies. We report herein an innovative electrochemistry-based approach. Four electroactive labels are chosen to selectively functionalize groups in GO, and quantification of each group is achieved by voltammetric analysis. This allows for the first time quantification of absolute amounts of each group, with a further advantage of distinguishing various carbonyl species: namely ortho-and para-quinones from aliphatic ketones. Intrinsic variations in the compositions of permanganate versus chlorate-oxidized GOs were thus observed. Principal differences include permanganate-GO exhibiting substantial quinonyl content, in comparison to chlorate-GO with the vast majority of its carbonyls as isolated ketones. The results confirm that carboxylic groups are rare in actuality, and are in fact entirely absent from chlorate-GO. These observations refine and advance our understanding of GO structure by addressing certain disparities in past models resulting from employment of different oxidation routes, with the vital implication that GO production methods cannot be used interchangeably in the manufacture of graphene-based devices.
引用
收藏
页码:20256 / 20266
页数:11
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