Munehiro Hasegawa
Kyoto University
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Publication
Featured researches published by Munehiro Hasegawa.
Applied Physics Express | 2014
Hirohiko Fukagawa; Katsuyuki Morii; Munehiro Hasegawa; Yoichi Arimoto; Taisuke Kamada; Takahisa Shimizu; Toshihiro Yamamoto
The feasibility of a highly efficient and air-stable organic light-emitting diode (OLED) was examined. A phosphorescent OLED not containing an air-sensitive material was fabricated by employing an inverted structure with an air-stable electron injection layer. Efficient electron injection from the bottom cathode to the emitting layer was demonstrated from the fact that the device characteristics of the inverted OLED were almost the same as those of a conventional OLED. No dark spot formation was observed after 250 days in the inverted OLED encapsulated by a barrier film with a water vapor transmission rate of 10−4 g m−2 day−1.
Scientific Reports | 2015
Hirohiko Fukagawa; Takahisa Shimizu; Taisuke Kamada; Shota Yui; Munehiro Hasegawa; Katsuyuki Morii; Toshihiro Yamamoto
Organic light-emitting diodes (OLEDs) have been intensively studied as a key technology for next-generation displays and lighting. The efficiency of OLEDs has improved markedly in the last 15 years by employing phosphorescent emitters. However, there are two main issues in the practical application of phosphorescent OLEDs (PHOLEDs): the relatively short operational lifetime and the relatively high cost owing to the costly emitter with a concentration of about 10% in the emitting layer. Here, we report on our success in resolving these issues by the utilization of thermally activated delayed fluorescent materials, which have been developed in the past few years, as the host material for the phosphorescent emitter. Our newly developed PHOLED employing only 1 wt% phosphorescent emitter exhibits an external quantum efficiency of over 20% and a long operational lifetime of about 20 times that of an OLED consisting of a conventional host material and 1 wt% phosphorescent emitter.
Pure and Applied Chemistry | 2006
Masahiro Murakami; Yasufumi Miyamoto; Munehiro Hasegawa; Ippei Usui; Takanori Matsuda
The silyl substituent of 3-silylcyclobutene prefers inward rotation rather than outward rotation during a thermal ring-opening reaction, giving the Z-isomer predominantly. This intriguing behavior was explained by assuming electron-accepting interactions between the low-lying σ*-orbital of the silicon-carbon linkage and the highest occupied molecular orbital (HOMO) of the opening cyclobutene system, which are possible only in the inward transition state. On the basis of this finding, a novel method for the stereoselective synthesis of functionalized 1,3-butadiene derivatives from cyclobutenones was developed. Boryl substituents exhibit even stronger preference for inward rotation than silyl substituents as a result of electron delocalization from the cyclobutene HOMO into the vacant p-orbital of boron at the inward transition state.
Advanced Materials | 2018
Hirohiko Fukagawa; Tsubasa Sasaki; Toshimitsu Tsuzuki; Yoshiki Nakajima; Tatsuya Takei; Genichi Motomura; Munehiro Hasegawa; Katsuyuki Morii; Takahisa Shimizu
Although organic light-emitting diodes (OLEDs) are promising for use in applications such as in flexible displays, reports of long-lived flexible OLED-based devices are limited due to the poor environmental stability of OLEDs. Flexible substrates such as plastic allow ambient oxygen and moisture to permeate into devices, which degrades the alkali metals used for the electron-injection layer in conventional OLEDs (cOLEDs). Here, the fabrication of a long-lived flexible display is reported using efficient and stable inverted OLEDs (iOLEDs), in which electrons can be effectively injected without the use of alkali metals. The flexible display employing iOLEDs can emit light for over 1 year with simplified encapsulation, whereas a flexible display employing cOLEDs exhibits almost no luminescence after only 21 d with the same encapsulation. These results demonstrate the great potential of iOLEDs to replace cOLEDs employing alkali metals for use in a wide variety of flexible organic optoelectronic devices.
Organic Light Emitting Materials and Devices XIX | 2015
Hirohiko Fukagawa; Katsuyuki Morii; Munehiro Hasegawa; Shun Gouda; Toshimitsu Tsuzuki; Takahisa Shimizu; Toshihiro Yamamoto
The OLED is one of the key devices for realizing future flexible displays and lightings. One of the biggest challenges left for the OLED fabricated on a flexible substrate is the improvement of its resistance to oxygen and moisture. A high barrier layer [a water vapor transmission rate (WVTR) of about 10-6 g/m2/day] is proposed to be necessary for the encapsulation of conventional OLEDs. Some flexible high barrier layers have recently been demonstrated; however, such high barrier layers require a complex process, which makes flexible OLEDs expensive. If an OLED is prepared without using air-sensitive materials such as alkali metals, no stringent encapsulation is necessary for such an OLED. In this presentation, we will discuss our continuing efforts to develop an inverted OLED (iOLED) prepared without using alkali metals. iOLEDs with a bottom cathode are considered to be effective for realizing air-stable OLEDs since the electron injection layer (EIL) can be prepared by fabrication processes that might damage the organic layers, resulting in the enhanced range of materials suitable for EILs. We have demonstrated that a highly efficient and relatively air-stable iOLED can be realized by employing poly(ethyleneimine) as an EIL. Dark spot formation was not observed after 250 days in the poly(ethyleneimine)-based iOLED encapsulated by a barrier film with a WVTR of 10-4 g/m2/day. In addition, we have demonstrated the fabrication of a highly operational stable iOLED utilizing a newly developed EIL. The iOLED exhibits an expected half-lifetime of over 10,000 h from an initial luminance of 1,000 cd/m2.
Journal of the American Chemical Society | 1994
Norimichi Kojima; Munehiro Hasegawa; Hiroshi Kitagawa; Takumi Kikegawa; O. Shimomura
Journal of the American Chemical Society | 2005
Masahiro Murakami; Ippei Usui; Munehiro Hasegawa; Takanori Matsuda
Journal of Organic Chemistry | 2004
Masahiro Murakami; Munehiro Hasegawa; Hideyuki Igawa
Angewandte Chemie | 2004
Masahiro Murakami; Munehiro Hasegawa
Journal of Organic Chemistry | 2007
Munehiro Hasegawa; Masahiro Murakami