Light-Induced Self-Assembled Polydiacetylene/Carbon Dot Functional "Honeycomb"
- Authors
- Kadamannil, Nila Nandha; Shames, Alexander I.; Bisht, Rajesh; Biswas, Sudipta; Shauloff, Nitzan; Lee, Haksu; Kim, Jong-Man; Jelinek, Raz
- Issue Date
- Apr-2024
- Publisher
- American Chemical Society
- Keywords
- honeycomb; polydiacetylene; carbon-dots; composite nanostructures; light-induced self-assembly; photocatalysis; organic supercapacitor
- Citation
- ACS Applied Materials & Interfaces, v.16, no.17, pp 22593 - 22603
- Pages
- 11
- Indexed
- SCIE
SCOPUS
- Journal Title
- ACS Applied Materials & Interfaces
- Volume
- 16
- Number
- 17
- Start Page
- 22593
- End Page
- 22603
- URI
- https://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/197995
- DOI
- 10.1021/acsami.4c03368
- ISSN
- 1944-8244
1944-8252
- Abstract
- The design of functional supramolecular assemblies from individual molecular building blocks is a fundamental challenge in chemistry and material science. We report on the fabrication of "honeycomb" films by light-induced coassembly of diacetylene derivatives and carbon dots. Specifically, modulating noncovalent interactions between the carbon dots, macrocyclic diacetylene, and anthraquinone diacetylene facilitates formation of thin films exhibiting a long-range, uniform pore structure. We show that light irradiation at distinct wavelengths plays a key role in the assembly process and generation of unique macro-porous morphology, by both initiating interactions between the carbon dots and the anthraquinone moieties and giving rise to the topotactic polymerization of the polydiacetylene network. We further demonstrate utilization of the macro-porous film as a photocatalytic platform for water pollutant degradation and as potential supercapacitor electrodes, both applications taking advantage of the high surface area, hydrophobicity, and pore structure of the film.
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