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Functionalized graphene oxide-reinforced electrospun carbon nanofibers as ultrathin supercapacitor electrode

机译:官能化的石墨烯氧化物增强电纺碳纳米纤维作为超超级电容器

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摘要

Graphene oxide has been used widely as a starting precursor for applications that cater to the needs of tunable graphene. However, the hydrophilic characteristic limits their application, especially in a hydrophobic condition. Herein, a novel non-covalent surface modification approach towards graphene oxide was conducted via a UV-induced photo-polymerization technique that involves two major routes; a UV-sensitive initiator embedded via pi-pi interactions on the graphene planar rings, and the polymerization of hydrophobic polymeric chains along the surface. The functionalized graphene oxide successfully achieved the desired hydrophobicity as it displayed the characteristic of being readily dissolved in organic solvent. Upon its addition into a polymeric solution and subjected to an electrospinning process, non-woven random nanofibers embedded with graphene oxide sheets were obtained. The prepared polymeric nanofibers were subjected to two-step thermal treatments that eventually converted the polymeric chains into a carbon-rich conductive structure. A unique morphology was observed upon the addition of the functionalized graphene oxide, whereby the sheets were embedded and intercalated within the carbon nanofibers and formed a continuous structure. This reinforcement effectively enhanced the electrochemical performance of the carbon nanofibers by recording a specific capacitance of up to 140.10. F/g at the current density of 1. A/g, which was approximately three folds more than that of pristine nanofibers. It also retained the capacitance up to 96.2% after 1000 vigorous charge/discharge cycles. This functionalization technique opens up a new pathway in tuning the solubility nature of graphene oxide towards the synthesis of a graphene oxide-reinforced polymeric structure.
机译:石墨烯氧化物已被广泛用于作为迎合可调谐石墨烯需求的应用的起始前体。然而,亲水性的特征限制了它们的应用,尤其是在疏水性条件下。在此,通过UV诱导的光聚合技术进行了一种朝向氧化石墨烯的非共价表面改性方法,涉及两个主要途径;通过石墨烯平面环上通过PI-PI相互作用嵌入的紫外敏感引发剂,以及沿着表面的疏水性聚合物链的聚合。官能化的石墨烯氧化物成功地实现了所需的疏水性,因为它显示出易于溶解在有机溶剂中的特性。在添加到聚合物溶液中并进行静电纺丝工艺后,获得嵌入具有石墨烯片的非织造随机纳米纤维。对制备的聚合物纳米纤维进行两步热处理,最终将聚合物链转化为富含碳的导电结构。在加入官能化的石墨烯氧化物时观察到一种独特的形态,由此嵌入和嵌入碳纳米纤维内并形成连续结构。这种加强件通过记录高达140.10的特定电容而有效地增强了碳纳米纤维的电化学性能。 F / g的电流密度为1.a / g,比原始纳米纤维的大约三倍约为三倍。在1000次充气/放电循环后,它还保留了高达96.2%的电容。该官能化技术在调整石墨烯溶解性方面对石墨烯氧化物增强聚合物结构的合成进行了新的途径。

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