Jong-Hyung Kim

Long-Range π-Conjugation in Phenothiazine-containing Donor-Acceptor Dyes for Application in Dye-Sensitized Solar Cells

Four organic donor-π-bridge-acceptor dyes containing phenothiazine as a spacer and cyanoacrylic acid as an acceptor were synthesized and tested as sensitizers in dye-sensitized solar cells (DSCs). The influence of iodide- and cobalt-based redox electrolytes on the photovoltaic device performance was investigated. In these new dyes, systematic π-conjugation was extended by inserting one or two phenothiazine moieties and investigated within the context of the resulting photoinduced charge-transfer properties. A detailed investigation, including transient absorption spectroscopy and quantum chemical methods, provided important information on the role of extended π-conjugation on the photophysical properties and photovoltaic device performance. Overall, the results showed that the extension of π-conjugation by one phenothiazine unit resulted in the best device performance owing to reduced recombination rates, whereas extension by two phenothiazine units reduced dye adsorption on TiO2 probably owing to the increase in molecular size. The performance of the dyes in DSCs was found to be a complex interaction between dye structure and size.

Silicon phthalocyanine-azobenzene-[60]fullerene light harvesting pentad: synthesis, characterization and electron transfer reaction studied by laser flash photolysis

Electron-transfer reaction of the newly synthesized light harvesting pentad composed of silicon phthalocyanine (SiPc) that is connected with two fullerene C60 and two azobenzene units to form SiPc-(azobenzene)2-(C60)2 pentad has been studied by laser flash photolysis and other complementary techniques. This combination between SiPc, azobenzene and C60 in the examined SiPc-(azobenzene)2-(C60)2 pentad leads to strong light absorption over the whole visible spectrum. Photoexcitation of the pentad results in rapid formation of the charge-separated state by photoinduced electron transfer from the singlet-excited state of the SiPc moiety to the C60 moiety. The charge-separated state has a lifetime of 2.50 ns in benzonitrile.

Synthesis and electroluminescence property of new hexaphenylbenzene derivatives including amine group for blue emitters.

Three new blue-emitting compounds of 5P-VA, 5P-VTPA, and 5P-DVTPA for organic light-emitting diode (OLED) based on hexaphenylbenzene moiety were demonstrated. Physical properties by the change of the substitution groups of the synthesized materials were systematically examined. Photoluminescence spectrum of the synthesized materials showed maximum emitting wavelengths of about 400 to 447 nm in solution state and 451 to 461 nm in film state, indicating deep blue emission color. OLED devices were fabricated by the synthesized compounds using vacuum deposit process as an emitting layer. The device structure was ITO/2-TNATA 60 nm/ NPB 15 nm/ EML 35 nm/ TPBi 20 nm/ LiF 1 nm/ Al 200 nm. External quantum efficiencies and CIE values of 5P-VA, 5P-VTPA, and 5P-DVTPA were 1.89%, 3.59%, 3.34%, and (0.154, 0.196), (0.150, 0.076), (0.148, 0.120), respectively. 5P-VTPA and 5P-DVTPA exhibited superior highly blue quality and thermal property such as high Td of 448°C and 449°C.

Synthesis and Electroluminescence Property of New Hexaphenyl Benzene Derivatives Including Emitting Materials for OLED

Three new emitting compounds of 5P-VCB, 5P-VAn and 5P-VPy for OLED based on hexaphenylbenzene moiety were synthesized. Physical properties by the change of the substitution groups of the synthesized materials were systematically examined. Photoluminescence spectrum of the synthesized materials showed maximum emitting wavelengths of about 420∼487 nm in solution state and 452∼488 nm in film state, indicating blue emission color. OLED devices were fabricated by the synthesized compounds using vacuum deposition process as an emitting layer. Current efficiencies and CIE values of 5P-VCB, 5P-VAn and 5P-VPy were 1.76, 0.38 and 7.91 cd/A and (0.15, 0.07), (0.20, 0.31) and (0.20, 0.36), respectively.