Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 3366-3371 |
| Number of pages | 6 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 57 |
| Issue number | 13 |
| DOIs | |
| State | Published - 19 Mar 2018 |
| Externally published | Yes |
Keywords
- graphene nanoribbons
- helices
- photothermal conversion
- self-assembly
- water-dispersible