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Synthesis of hybrid graphene-porphyrin microanofiber structures by ionic self-assembly

机译:离子自组装合成石墨烯-卟啉微/纳米纤维结构

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Cationic mesa-tetra(4-pyridyl) porphine (TPyP)-graphene oxide (GO) hybrid structures have been synthesized-by ionic self-assembly. The different aggregated structures shape were obtained through electrostatic and pi-pi stacking interactions, as indicated by redshift of porphyrin Soret band throughout the pH range of 1.5-9.1, fluorescence quenching, Raman spectra and Energy dispersive X-ray spectroscopy. A strong fluorescence quenching of the cationic porphyrin in the presence of graphene indicated that efficient electron or energy transfer occurred from the excited state of the cationic porphyrin to graphene. The investigation revealed a three-dimensional fiber structures formation under the acid conditions and leaf-like structures of the TPyP/GO assemblies under the alkaline conditions of the solution. The fibers morphology and cross-section was determined quantitatively by Scanning force microscopy; this revealed a diameter of the fibers up to hundreds of nanometers and the lengh up to hundreds of micrometers. The electrical properties of the fibers were investigated by spreading resistance and current-voltage characteristics measurements using Atomic Force Microscopy (AFM) with conductive cantilevers. The current-voltage characteristics fit to the Poole-Frenkel emission mechanism in the case of TPyP/GO sheets and Schottky emission dominate in the nanofibers case. This new graphene material shows a potential for energy, sensing and photonic applications. (C) 2015 Elsevier B.V. All rights reserved.
机译:阳离子台面-四(4-吡啶基)卟啉(TPyP)-氧化石墨烯(GO)杂化结构已通过离子自组装法合成。通过静电和pi-pi堆积相互作用获得了不同的聚集结构形状,如卟啉Soret带在1.5-9.1的整个pH范围内的红移,荧光猝灭,拉曼光谱和能量色散X射线光谱学所表明。在石墨烯存在下阳离子卟啉的强荧光猝灭表明,从阳离子卟啉的激发态到石墨烯发生了有效的电子或能量转移。研究表明,在酸性条件下,三维纤维结构形成,在碱性条件下,TPyP / GO组件的叶状结构形成。通过扫描力显微镜定量测定纤维的形态和横截面。这表明纤维的直径可达数百纳米,而长度则高达数百微米。使用带有导电悬臂的原子力显微镜(AFM),通过散布电阻和电流-电压特性测量来研究纤维的电性能。在TPyP / GO片的情况下,电流-电压特性符合Poole-Frenkel发射机理,而在纳米纤维的情况下,肖特基发射占主导地位。这种新的石墨烯材料显示出在能源,传感和光子应用方面的潜力。 (C)2015 Elsevier B.V.保留所有权利。

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