摘要
Structurally well-defined graphene nanoribbons (GNRs) have attracted great interest because of their unique optical, electronic, and magnetic properties. However, strong π–π interactions within GNRs result in poor liquid-phase dispersibility, which impedes further investigation of these materials in numerous research areas, including supramolecular self-assembly. Structurally defined GNRs were synthesized by a bottom-up strategy, involving grafting of hydrophilic poly(ethylene oxide) (PEO) chains of different lengths (GNR-PEO). PEO grafting of 42–51 % percent produces GNR-PEO materials with excellent dispersibility in water with high GNR concentrations of up to 0.5 mg mL−1. The “rod–coil” brush-like architecture of GNR-PEO resulted in 1D hierarchical self-assembly behavior in the aqueous phase, leading to the formation of ultralong nanobelts, or spring-like helices, with tunable mean diameters and pitches. In aqueous dispersions the superstructures absorbed in the near-infrared range, which enabled highly efficient conversion of photon energy into thermal energy.
| 源语言 | 英语 |
|---|---|
| 页(从-至) | 3366-3371 |
| 页数 | 6 |
| 期刊 | Angewandte Chemie - International Edition |
| 卷 | 57 |
| 期 | 13 |
| DOI | |
| 出版状态 | 已出版 - 19 3月 2018 |
| 已对外发布 | 是 |
指纹
探究 'Supramolecular Nanostructures of Structurally Defined Graphene Nanoribbons in the Aqueous Phase' 的科研主题。它们共同构成独一无二的指纹。引用此
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