Hironobu Iwawaki
Canon Inc.
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Featured researches published by Hironobu Iwawaki.
Dalton Transactions | 2005
Shinjiro Okada; Keiji Okinaka; Hironobu Iwawaki; Manabu Furugori; Masashi Hashimoto; Taihei Mukaide; Jun Kamatani; Satoshi Igawa; Akira Tsuboyama; Takao Takiguchi; Kazunori Ueno
This study reports substituent effects of iridium complexes with 1-phenylisoquinoline ligands. The emission spectra and phosphorescence quantum yields of the complexes differ from that of tris(1-phenylisoquinolinato-C2,N)iridium(iii)(Irpiq) depending on the substituents. The maximum emission peak, quantum yield and lifetime of those complexes ranged from 598-635 nm, 0.17-0.32 and 1.07-2.34 micros, respectively. This indicates the nature of the substituents has a significant influence on the kinetics of the excited-state decay. The substituents attached to phenyl ring have an influence on a stability of the HOMO. Furthermore, those substituents have effect on the contribution to a mixing between 3pi-pi* and (3)MLCT for the lowest excited states. Some of the complexes display the larger quantum yield than Irpiq, which has the quantum yield of 0.22. The organic light emitting diode (OLED) device based on tris [1-(4-fluoro-5-methylphenyl)isoquinolinato-C2,N]iridium(iii)(Ir4F5Mpiq) yielded high external quantum efficiency of 15.5% and a power efficiency of 12.4 lm W(-1) at a luminance of 218 cd m(-2). An emission color of the device was close to an NTSC specification with CIE chromaticity characteristics of (0.66, 0.34).
SID Symposium Digest of Technical Papers | 2002
Shinjiro Okada; Hironobu Iwawaki; Manabu Furugori; Jun Kamatani; Satoru Igawa; Takashi Moriyama; Seishi Miura; Akira Tsuboyama; Takao Takiguchi; Hidemasa Mizutani
We studied red emissive materials of Ir-complex. We demonstrate high efficiency red OLED devices employing phosphorescent dopant. Ir(piq)3 [Iridium(III)tris(1-phenyl-isoquinolinato-N, C2)] shows maximum emission peak of 623nm and excellent Q.Y with 0.66 compared to Ir(ppy)3 as a unit. Efficiency of the EL device is 8.0 lm/W, 9.3 cd/A at 100cd/m2, 623 lm/W, 8.4 cd/A at 300cd/m2. CIE- coordinate is (0.68,0.33) and it meets NTSC specification.
Journal of the American Chemical Society | 2003
Akira Tsuboyama; Hironobu Iwawaki; Manabu Furugori; Taihei Mukaide; Jun Kamatani; Satoshi Igawa; Takashi Moriyama; Seishi Miura; Takao Takiguchi; Shinjiro Okada; Mikio Hoshino; Kazunori Ueno
Archive | 2003
Takashi Moriyama; Shinjiro Okada; Akira Tsuboyama; Takao Takiguchi; Seishi Miura; Satoshi Igawa; Jun Kamatani; Hironobu Iwawaki
Archive | 2007
Satoshi Igawa; Hironobu Iwawaki; Atsushi Kamatani; Manabu Kogori; Kiyoshi Miura; Takashi Moriyama; Shinjiro Okada; Takao Takiguchi; Akira Tsuboyama; 聖志 三浦; 悟史 井川; 学 古郡; 明 坪山; 伸二郎 岡田; 洋伸 岩脇; 孝志 森山; 隆雄 滝口; 淳 鎌谷
Archive | 2003
Akira Tsuboyama; Shinjiro Okada; Takao Takiguchi; Kazunori Ueno; Satoshi Igawa; Jun Kamatani; Manabu Furugori; Hironobu Iwawaki
Archive | 2004
Kengo Kishino; Shinjiro Okada; Akira Tsuboyama; Satoshi Igawa; Manabu Furugori; Hironobu Iwawaki
Archive | 2003
Akira Tsuboyama; Shinjiro Okada; Takao Takiguchi; Koichi Suzuki; Seishi Miura; Takashi Moriyama; Satoshi Igawa; Jun Kamatani; Manabu Furugori; Hironobu Iwawaki
Archive | 2008
Hiroki Ohrui; Akihito Saitoh; Chika Negishi; Hironobu Iwawaki; Masanori Muratsubaki; Shinjiro Okada
Archive | 2004
Manabu Furugori; Shinjiro Okada; Akira Tsuboyama; Takao Takiguchi; Seishi Miura; Takashi Moriyama; Satoshi Igawa; Jun Kamatani; Hironobu Iwawaki