Kyung Hee University · Engineering
Professor Jongwook Park's research lab specializes in the design, synthesis, and application of novel organic semiconductors for optoelectronic devices, with a primary focus on high-performance blue organic light-emitting diodes (OLEDs). The lab develops advanced emitter materials featuring tailored molecular architectures—such as anthracene, pyrene, and indenopyrazine cores—engineered for enhanced thermal stability, high photoluminescence quantum yield, and narrow emission bandwidths. Key research directions include molecular engineering of dendritic and dual-core architectures to improve device efficiency, color purity, and operational stability in non-doped and doped OLED configurations.
Figures are computed from collected data and may differ slightly.
9,10-Bis(3′,5′-diphenylphenyl)anthracene [MAM], 9-(3′,5′-diphenylphenyl)-10-(3‴,5‴-diphenylbiphenyl-4″-yl)anthracene [MAT], and 9,10-bis(3″,5″-diphenylbiphenyl-4′-yl)anthracene [TAT] were newly synthesized through boration and Suzuki aryl–aryl coupling reactions. We have demonstrated that the EL performance of blue-light emitters can be optimized and improved by varying the chemical structures of the side groups. In the thin film state, the three materials exhibit PLmax values in the range of 43
New blue fluorescent compounds containing tetra-substituted ethylene moieties have been designed and synthesized. These materials, 1,2-di(4′-tert-butylphenyl)-1,2-bis(4′-(anthracene-9-yl)phenyl)ethene [BPBAPE, 1A], 1,2-diphenyl-1,2-bis(4′-(anthracene-9-yl)phenyl)ethene [PBAPE, 1B], 9,10-bis(4-(1,2,2-tris(4-tert-butylphenyl)vinyl)phenyl)anthracene [BTBPPA, 2A], and 9,10-bis(4-(1,2,2-triphenylvinyl)phenyl)anthracene [BTPPA, 2B], were synthesized through Suzuki and McMurry reactions. By fabricating
We describe two novel blue emission materials based on a new type of dual core concept. 1-Phenyl-6-(10-phenyl-anthracen-9-yl)-pyrene (Ph-AP-Ph) and 1-[1,1′;3′,1′′]terphenyl-5′-yl-6-(10-[1,1′;3′,1′′]terphenyl-5′-yl-anthracen-9-yl)-pyrene (TP-AP-TP) were synthesized through boronylation and Suzuki coupling reactions. The Tg values of Ph-AP-Ph and TP-AP-TP were 228 °C and 243 °C, respectively, compared to values of 135 °C and 139 °C for the single core materials 9-(3′,5′-diphenylphenyl)-10-(3′′′,5′
In this study, four emitters of blue light are synthesized by selecting pyrene with its high photoluminescence quantum yield (PLQY) as the core group and variants of the electron-donating diphenylamine (DPA) as side groups. The four compounds have different numbers, sizes, and substitution positions of alkyl groups on the DPA. Each of the four compounds when doped in OLED devices shows a high current efficiency (CE) of over 7 cd A<sup>-1</sup> and a high external quantum efficiency (EQE) of over
Deep blue emitting materials with a new core structure containing indenopyrazine have been synthesized; a non-doped device using one of these materials as a blue emitter was found to exhibit high external quantumn efficiency of 4.6% and excellent color purity of (0.154, 0.078) as well as narrow emission band of 47 nm FWHM.
This study not only describes the synthesis and characterization of a novel indenofluorene derivative, 6,6,12,12-tetraethyl-2,8-bis-[1,1′;3′,1′]terphenyl-4′-yl-6,12-dihydro-indeno[1,2-b]fluorine (TP-EIF), for use as an emitting material in blue organic light emitting diodes (OLEDs), but also the comparison with 6,6,12,12-tetraethyl-2,8-bis-[1,1′;3′,1′]terphenyl-4′-yl-6,12-dihydro-diindeno[1,2-b;1′,2′-e]pyrazine (TP-EPY). UV-visible and PL spectra showed that the TP-EPY absorption and emission ba
Deep-blue emitters based on phenanthro[9,10-d]oxazole (PO) and anthracene moiety for non-doped fluorescenct OLEDs.
The chrysene group, with its large band gap and high stability, was selected as a central core structure for ultra-deep-blue emitters. The effects of different side groups on the intrinsic properties of the chrysene core were systematically investigated.
The wavelength of excimer formation and efficiency of an OLED device were controlled through the change of the center position of the triple-core chromophore.
White emission with two sharp strong peaks - a molecular emission peak at 455 nm and an excimer emission peak at 591 nm - was obtained by introducing a terphenyl group into a highly twisted core chromophore, which promoted a molecular orientation in the film state suitable for excimer formation.
We introduced phenyl and naphthyl groups onto various positions of dual cores. Of the synthesized compounds, Na-AP-Na was found to exhibit the highest EL device efficiency of 5.46 cd A<sup>−1</sup>.
Abstract Perovskite is a very promising material that is being extensively studied at the bulk and nanosize scales because it has outstanding optical properties, including high quantum efficiency and narrow emission spectra. However, perovskite has stability issues related to heat, air, and light. To overcome these, highly stable perovskite quantum dots (PeQDs) are developed using excess Zn precursor and trioctylphosphine‐oxide (TOPO). In particular, it is clarified that Zn and TOPO are combined
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