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In-situ synthesis and characterization of electrically conductive polypyrrole/graphene nanocomposites

机译:导电聚吡咯/石墨烯纳米复合材料的原位合成与表征

摘要

Polypyrrole (PPy)/graphene (GR) nanocomposites were successfully prepared via in-situ polymerization of graphite oxide (GO) and pyrrole monomer followed by chemical reduction using hydrazine monohydrate. The large surface area and high aspect ratio of the in-situ generated graphene played an important role in justifying the noticeable improvements in electrical conductivity of the prepared composites via chemical reduction. X-ray photoelectron spectroscopy (XPS) analysis revealed theudremoval of oxygen functionality from the GO surface after reduction and the bonding structure of the reduced composites were further determined from FTIR and Raman spectroscopic analysis. For PPy/GR composite, intensity ratio between D band and G band was high (w1.17), indicating an increased number of c-sp2 domains that were formed during the reduction process. A reasonable improvement in thermal stability of the reduced composite was also observed. Transmission electron microscopy (TEM) observations indicated the dispersion of the graphene nanosheets within the PPy matrix.
机译:通过氧化石墨(GO)和吡咯单体的原位聚合,然后使用肼一水合物进行化学还原,成功制备了聚吡咯(PPy)/石墨烯(GR)纳米复合材料。原位生成的石墨烯的大表面积和高纵横比在证明通过化学还原制得的复合材料的电导率显着提高中起着重要作用。 X射线光电子能谱(XPS)分析显示还原后GO表面上的氧官能团的脱除,并通过FTIR和拉曼光谱分析进一步确定了还原复合物的键合结构。对于PPy / GR复合材料,D带和G带之间的强度比很高(w1.17),表明在还原过程中形成的c-sp2域数量增加。还观察到了还原的复合材料的热稳定性的合理改善。透射电子显微镜(TEM)观察表明,石墨烯纳米片在PPy基质中的分散。

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