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Enhanced blue photoluminescence and new crystallinity of Ag/organic rubrene core-shell nanoparticles through hydrothermal treatment

Authors
Kim, Taek JoonKim, Dong IlLee, YongjunKim, JeongyongJoo, Jinsoo
Issue Date
11월-2020
Publisher
ELSEVIER
Keywords
Photoluminescence; Core-shell nanoparticle; Hydrothermal treatment; Rubrene; Surface plasmon; Ag nanoparticle
Citation
CURRENT APPLIED PHYSICS, v.20, no.11, pp.1201 - 1206
Indexed
SCIE
SCOPUS
KCI
Journal Title
CURRENT APPLIED PHYSICS
Volume
20
Number
11
Start Page
1201
End Page
1206
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/51992
DOI
10.1016/j.cap.2020.08.007
ISSN
1567-1739
Abstract
Light-emitting organic semiconductors have attracted considerable attention for the nanoscale fabrication of organic-based displays and their potential application in optoelectronics, plasmonics, and photonics. In this study, core-shell hybrid nanostructures of organic rubrene coated on Ag nanoparticles (NPs) have been synthesized using a chemical reduction method. The thickness of the rubrene shell was 2.6-6.0 nm and the diameter of the Ag core was 30-70 nm. The optical and structural properties of the Ag/rubrene core-shell NPs were tuned by hydrothermal (HT) treatment at 190 degrees C. The Ag/rubrene core-shell NPs were characterized by high-resolution transmission electron microscopy and energy-dispersive X-ray (EDX) spectroscopy before and after the HT treatment, and their structural properties were confirmed through X-ray diffraction (XRD) analysis. XRD peaks related to an orthorhombic phase were observed along with the original triclinic crystal structure of the rubrene shell, and the triclinic crystal domain size increased from 28.2 nm to 30.8 nm owing to the HT treatment. Interestingly, the green light emission (lambda(em) = 550 nm) of the Ag/rubrene core-shell NPs changed to blue light emission (lambda(em) = 425 nm), increasing in intensity through the HT treatment. This is caused by the crystal change with H-type aggregation and enhanced energy transfer from a surface plasmon resonance.
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