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Optimization of coupled plasmonic effects for viable phosphorescence of metal-free purely organic phosphor
- Optimization of coupled plasmonic effects for viable phosphorescence of metal-free purely organic phosphor
- Wang H.; Jung J.; Chung K.; Lim J.W.; You Y.; Kim J.; Kim D.H.
- Ewha Authors
- 김동하; 유영민
- SCOPUS Author ID
- 김동하; 유영민
- Issue Date
- Journal Title
- Journal of Applied Physics
- vol. 122, no. 15
- American Institute of Physics Inc.
- SCI; SCIE; SCOPUS
- Metal-free purely organic phosphorescent molecules are attractive alternatives to organometallic and inorganic counterparts because of their low cost and readily tunable optical properties through a wide chemical design window. However, their weak phosphorescent intensity due to inefficient spin-orbit coupling and, consequently, prevailing non-radiative decay processes limit their practical applicability. Here, we systematically studied phosphorescence emission enhancement of a purely organic phosphor system via plasmon resonance energy transfer. By precisely tuning the distance between purely organic phosphor crystals and plasmonic nanostructures using layer-by-layer assembled polyelectrolyte multilayers as a dielectric spacer, maximum 2.8 and 2.5 times enhancement in photoluminescence intensity was observed when the phosphor crystals were coupled with ∼55 nm AuNPs and ∼7 nm AgNPs, respectively, at the distance of 9.6 nm. When the distance is within the range of 3 nm, a dramatic decrease in phosphorescence intensity was observed, while at a larger distance, the plasmonic effect diminished rapidly. The distance-dependent plasmon-induced phosphorescence enhancement mechanism was further investigated by time-resolved photoluminescence measurements. Our results reveal the correlation between the amplification efficiency and plasmonic band, spatial factor, and spectral characteristics of the purely organic phosphor, which may provide an insightful picture to extend the utility of organic phosphors by using surface plasmon-induced emission enhancement scheme. © 2017 Author(s).
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- 자연과학대학 > 화학·나노과학전공 > Journal papers
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