Nitrogen functionalization of graphene offers new hybrid materials with improved performance for important technological applications. Despite studies highlighting the dependence of the performance of nitrogen-functionalized graphene on the types of nitrogen functional groups that are present, precise synthetic control over their ratio is challenging. Herein, the synthesis of nitrogen-functionalized graphene rich in amino groups by a Bucherer-type reaction under hydrothermal conditions is reported. The efficiency of the synthetic method under two hydrothermal conditions was examined for graphite oxide produced by Hummers and Hofmann oxidation routes. The morphological and structural properties of the amino-functionalized graphene were fully characterized. The use of a synthetic method with a well-known mechanism for derivatization of graphene will open new avenues for highly reproducible functionalization of graphene materials. Amino-functionalized graphene: Graphene functionalized with amino groups was obtained by a Bucherer-type reaction of graphite oxide with sodium hydrogensulfite/ammonia under hydrothermal conditions, which selectively converted hydroxyl to amino groups (see figure). The functionalization is only effective on graphite oxide produced by the Hummers oxidation method as opposed to the Hofmann oxidation method.
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All Science Journal Classification (ASJC) codes
- Organic Chemistry