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共价等离子体辅助功能化石墨烯上的丙烯酸酯聚合:一种合成杂化功能材料的途径。

Acrylates Polymerization on Covalent Plasma-Assisted Functionalized Graphene: A Route to Synthesize Hybrid Functional Materials.

作者信息

Muñoz Roberto, León-Boigues Laia, López-Elvira Elena, Munuera Carmen, Vázquez Luis, Mompeán Federico, Martín-Gago José Ángel, Palacio Irene, García-Hernández Mar

机构信息

Instituto de Ciencia de Materiales de Madrid (ICMM), CSIC, Sor Juana Inés de la Cruz 3, Madrid E-28049, Spain.

Universidad Complutense de Madrid, Madrid E-28040, Spain.

出版信息

ACS Appl Mater Interfaces. 2023 Oct 4;15(39):46171-46180. doi: 10.1021/acsami.3c07200. Epub 2023 Sep 22.

Abstract

The modification of the surface properties of graphene with polymers provides a method for expanding its scope into new applications as a hybrid material. Unfortunately, the chemical inertness of graphene hinders the covalent functionalization required to build them up. Developing new strategies to enhance the graphene chemical activity for efficient and stable functionalization, while preserving its electronic properties, is a major challenge. We here devise a covalent functionalization method that is clean, reproducible, scalable, and technologically relevant for the synthesis of a large-scale, substrate-supported graphene-polymer hybrid material. In a first step, hydrogen-assisted plasma activation of -aminophenol (-AP) linker molecules produces their stable and covalent attachment to large-area graphene. Second, an in situ radical polymerization reaction of 2-hydroxyethyl acrylate (HEA) is carried out on the functionalized surface, leading to a graphene-polymer hybrid functional material. The functionalization with a hydrophilic and soft polymer modifies the hydrophobicity of graphene and might enhance its biocompatibility. We have characterized these hybrid materials by atomic force microscopy (AFM), X-Ray photoelectron spectroscopy (XPS) and Raman spectroscopy and studied their electrical response, confirming that the graphene/-AP/PHEA architecture is anchored covalently by the sp hybridization and controlled polymerization reaction on graphene, retaining its suitable electronic properties. Among all the possibilities, we assess the proof of concept of this graphene-based hybrid platform as a humidity sensor. An enhanced sensitivity is obtained in comparison with pristine graphene and related materials. This functional nanoarchitecture and the two-step strategy open up future potential applications in sensors, biomaterials, or biotechnology fields.

摘要

用聚合物对石墨烯的表面性质进行改性,为将其作为一种混合材料拓展到新的应用领域提供了一种方法。不幸的是,石墨烯的化学惰性阻碍了构建它们所需的共价功能化。开发新的策略来提高石墨烯的化学活性以实现高效且稳定的功能化,同时保留其电子性质,是一项重大挑战。我们在此设计了一种共价功能化方法,该方法清洁、可重复、可扩展,并且在合成大规模、基底支撑的石墨烯 - 聚合物混合材料方面具有技术相关性。第一步,对氨基苯酚(-AP)连接分子的氢辅助等离子体活化使其稳定且共价地附着在大面积石墨烯上。第二步,在功能化表面上进行丙烯酸2 - 羟乙酯(HEA)的原位自由基聚合反应,从而得到石墨烯 - 聚合物混合功能材料。用亲水性和柔软的聚合物进行功能化改变了石墨烯的疏水性,并可能增强其生物相容性。我们通过原子力显微镜(AFM)、X射线光电子能谱(XPS)和拉曼光谱对这些混合材料进行了表征,并研究了它们的电响应,证实了石墨烯/-AP/PHEA结构通过sp杂化和石墨烯上的可控聚合反应共价锚定,保留了其合适的电子性质。在所有可能性中,我们评估了这种基于石墨烯的混合平台作为湿度传感器的概念验证。与原始石墨烯及相关材料相比,获得了更高的灵敏度。这种功能纳米结构和两步策略为传感器、生物材料或生物技术领域开辟了未来潜在的应用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2cbc/10561134/ae35f8a975f3/am3c07200_0001.jpg

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