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界面络合驱动阳离子磷树枝状大分子与氧化石墨烯片的三维组装。

Interfacial complexation driven three-dimensional assembly of cationic phosphorus dendrimers and graphene oxide sheets.

作者信息

Katir Nadia, Benayad Anass, Rouchon Denis, Marcotte Nathalie, El Brahmi Nabil, Majoral Jean Pierre, Bousmina Mosto, El Kadib Abdelkrim

机构信息

Euromed Research Center, Engineering Division, Euro-Mediterranean University of Fez (UEMF) Route de Meknes 30000 Fès Morocco

CEA, LITEN, Department of Nanomaterials, MINATEC 17 rue des martyrs F-38054 Grenoble Cedex 09 France.

出版信息

Nanoscale Adv. 2018 Aug 17;1(1):314-321. doi: 10.1039/c8na00047f. eCollection 2019 Jan 15.

Abstract

High content nitrogen, sulfur and phosphorus heteroatoms assembled in tree-like dendrimers (DG ) are confined within the galleries of two-dimensional graphene oxide (GO). The presence of the ternary diethyl--ethyl-ammonium groups on the dendrimer peripheries ensures the exfoliation of graphene sheets thereby affording interfacially bridged, three-dimensional heteroatom-enriched graphene-based hybrid nanostructures (DG -GO). Dendrimer generation (from 1 to 4) that reflects the bulkiness of these conceived nano-trees impacts increasingly the degree of dispersion-exfoliation and sheet desordering. The long-term stability of these aqueous suspensions associated with their handling flexibility allows uniform accommodation of the resulting hybrid materials as flame-retardants in bioplastics.

摘要

组装在树枝状聚合物(DG )中的高含量氮、硫和磷杂原子被限制在二维氧化石墨烯(GO)的层间。树枝状聚合物外围的三元二乙 - 乙基铵基团的存在确保了石墨烯片的剥离,从而提供了界面桥接的、富含杂原子的三维石墨烯基杂化纳米结构(DG -GO)。反映这些设想的纳米树体积大小的树枝状聚合物代数(从1到4)对分散 - 剥离程度和片层无序度的影响越来越大。这些水性悬浮液的长期稳定性及其操作灵活性使得所得的杂化材料能够作为阻燃剂均匀地应用于生物塑料中。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/086e/9473195/2078f0bf06bf/c8na00047f-f1.jpg

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