Self-Assembly of 2D Gold Nanoparticle Superlattice in a Polymer Vesicle Layer Driven by Hydrophobic Interaction
- Authors
- Jang, Jong Dae; Bae, Moongi; Do, Changwoo; Choi, Soo-Hyung; Bang, Joona; Han, Young Soo; Kim, Tae-Hwan
- Issue Date
- 22-7월-2021
- Publisher
- AMER CHEMICAL SOC
- Citation
- JOURNAL OF PHYSICAL CHEMISTRY LETTERS, v.12, no.28, pp.6736 - 6743
- Indexed
- SCIE
SCOPUS
- Journal Title
- JOURNAL OF PHYSICAL CHEMISTRY LETTERS
- Volume
- 12
- Number
- 28
- Start Page
- 6736
- End Page
- 6743
- URI
- https://scholar.korea.ac.kr/handle/2021.sw.korea/137110
- DOI
- 10.1021/acs.jpclett.1c01684
- ISSN
- 1948-7185
- Abstract
- Self-assembly of gold nanoparticles (AuNPs) into highly ordered superstructures provides a promising route toward fabricating materials with new functionalities or enhanced physical properties. Although self-assembly of AuNPs has garnered significant research attention recently, a highly ordered superlattice of AuNPs under a low concentration in a confined geometry formed by nonfunctionalized materials has not been reported. Herein, we investigate the self-assembly of a 2D AuNPs superlattice in a polymer vesicle layer using hydrophobic interactions, which exhibits centered rectangular lattice symmetry. To create the highly ordered AuNPs superlattice, the P(EG(x)-b-iPGE(y)) block copolymers that form the thickness of the hydrophobic vesicle layer comparable to the size of the AuNP are used as a template to control the AuNP degree of freedom. To the best of our knowledge, this study provides the first demonstration of a centered rectangular structure formation of AuNPs at the vesicle layer in 2D confined geometry.
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