Origin of Oxygen in Graphene Oxide Revealed by 17O and 18O Isotopic Labeling

被引:1
作者
Halbig, Christian E. [1 ,2 ]
Mukherjee, Bristy [3 ]
Eigler, Siegfried [1 ]
Garaj, Slaven [2 ,3 ,4 ]
机构
[1] Free Univ Berlin, Dept Chem Biol & Pharm, D-14195 Berlin, Germany
[2] Natl Univ Singapore, Fac Sci, Dept Phys, Singapore 117551, Singapore
[3] Natl Univ Singapore, Dept Mat Sci & Engn, Singapore 117575, Singapore
[4] Natl Univ Singapore, Dept Biomed Engn, Singapore 117583, Singapore
基金
新加坡国家研究基金会;
关键词
SOLID-STATE NMR; GRAPHITE OXIDE; SULFURIC-ACID; OXIDATION; MECHANISM; OLEFINS; PERMANGANATE; STABILITY; KINETICS; OZONE;
D O I
10.1021/jacs.3c12543
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Wet-chemical oxidation of graphite in a mixture of sulfuric acid with a strong oxidizer, such as potassium permanganate, leads to the formation of graphene oxide with hydroxyl and epoxide groups as the major functional groups. Nevertheless, the reaction mechanism remains unclear and the source of oxygen is a subject of debate. It could theoretically originate from the oxidizer, water, or sulfuric acid. In this study, we employed 18O and 17O labeled reagents to experimentally elucidate the reaction mechanism and, thus, determine the origin of oxo-functional groups. Our findings reveal the multifaceted roles of sulfuric acid, acting as a dispersion medium, a dehydrating agent for potassium permanganate, and an intercalant. Additionally, it significantly acts as a source of oxygen next to manganese oxides. Through 17O solid-state magic-angle spinning (MAS) NMR experiments, we exclude water as a direct reaction partner during oxygenation. With labeling experiments, we conclude on mechanistic insights, which may be exploited for the synthesis of novel graphene derivatives.
引用
收藏
页码:7431 / 7438
页数:8
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