Mayara G. Gonçalves, Vinícius O. Costa, André H. G. Martinez, Bernardo M. Régnier, Gabriel C. B. Gomes, Aldo Zarbin, Elisa S. Orth
{"title":"Functionalization of graphene oxide via epoxide groups: a comprehensive review of synthetic routes and challenges","authors":"Mayara G. Gonçalves, Vinícius O. Costa, André H. G. Martinez, Bernardo M. Régnier, Gabriel C. B. Gomes, Aldo Zarbin, Elisa S. Orth","doi":"10.3389/frcrb.2024.1393077","DOIUrl":null,"url":null,"abstract":"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 those involving covalent and noncovalent bonds with organic molecules. In a novel contribution to this field, particular emphasis is placed on functionalization via epoxy ring opening, a poorly studied and understood topic. We first provide an overview of the basic structure and properties of graphene oxide. We then 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. An alkaline environment seems to favor this reaction, and there is 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 characterization techniques that can be explored in future studies. Finally, some current challenges and future research directions are presented to contribute to the advancement of the field.","PeriodicalId":502487,"journal":{"name":"Frontiers in Carbon","volume":"13 2","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Frontiers in Carbon","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.3389/frcrb.2024.1393077","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
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 those involving covalent and noncovalent bonds with organic molecules. In a novel contribution to this field, particular emphasis is placed on functionalization via epoxy ring opening, a poorly studied and understood topic. We first provide an overview of the basic structure and properties of graphene oxide. We then 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. An alkaline environment seems to favor this reaction, and there is 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 characterization techniques that can be explored in future studies. Finally, some current challenges and future research directions are presented to contribute to the advancement of the field.
氧化石墨烯(GO)因其机械、光学、电学和化学特性而备受科学界关注。本综述概述了 GO 功能化的合成方法,包括与有机分子共价键和非共价键的合成方法。作为对这一领域的新贡献,本综述特别强调了通过环氧树脂开环进行功能化的方法,这是一个研究和理解不多的课题。我们首先概述了氧化石墨烯的基本结构和特性。然后,我们探讨了对氧化石墨烯进行功能化的各种方法,并指出了这些反应的复杂性,这些反应有时会以非特异性的方式发生。不过,也有一些有针对性的功能化策略。此外,我们还对通过环氧基团进行共价官能化进行了批判性分析,展示了在选择反应介质时需要考虑的重要方面。碱性环境似乎更有利于这种反应,而在官能化反应中使用碱性 pH 值的利弊尚未达成共识。我们还展示了涉及表征和确认功能化的一些挑战,主要是在基底面上,我们还展示了表征技术的进步,这些都可以在未来的研究中进行探索。最后,我们提出了一些当前面临的挑战和未来的研究方向,以促进该领域的发展。