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REVIEW article

Front. Carbon
Sec. Carbon-Based Heterostructures
Volume 3 - 2024 | doi: 10.3389/frcrb.2024.1393077
This article is part of the Research Topic Women in Carbon Science and Technology View all 8 articles

Functionalization of Graphene Oxide via Epoxide Groups: A Comprehensive Look at Synthetic Routes and Challenges

Provisionally accepted

The final, formatted version of the article will be published soon.

    Graphene oxide (GO) has attracted significant attention from the scientific community due to its mechanical, optical, electrical, and chemical properties. This review outlines synthetic methods for GO functionalization, including methods involving covalent and noncovalent bonds with organic molecules. In a novel contribution to this field, particular emphasis is placed on the functionalization via epoxy ring opening, an area that is still poorly studied and understood. First, we provide an overview of the basic structure and properties of graphene oxide. Subsequently, we explore the various methods employed to functionalize graphene oxide, noting the complexity of these reactions, which sometimes occur in a non-specific manner. However, there are some strategies for targeted functionalization. Furthermore, we present a critical analysis of the covalent functionalization through epoxy groups, demonstrating important aspects to be considered when choosing the reaction medium. The alkaline environment seems to favor this reaction, and this is a point of no consensus regarding the advantages and disadvantages of using basic pH in functionalization reactions. We also demonstrate some challenges involving the characterization and confirmation of the functionalization, mainly in the basal plane, and we show advances in the characterization techniques that can be further explored in future studies. Finally, some current challenges and future research directions are presented to contribute to the advancement in this field.

    Keywords: Functionalized graphene, Epoxy groups, Covalent derivatization, Epoxide opening, nucleophilic reactions. (Min.5-Max. 8

    Received: 28 Feb 2024; Accepted: 23 May 2024.

    Copyright: © 2024 Gonçalves, Costa, Martinez, Régnier, Gomes, Zarbin and Orth. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

    * Correspondence: Elisa S. Orth, Federal University of Paraná, Curitiba, 80060-000, Paraná, Brazil

    Disclaimer: All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.