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  • 【論文受理】D2 渡邊雄一郎君と M2 吉岡良君のビスターピリジン電子輸送材料の論文が J Mater Chem C (IF: 5.066) に受理!
2016年08月29日
【論文受理】D2 渡邊雄一郎君と M2 吉岡良君のビスターピリジン電子輸送材料の論文が J Mater Chem C (IF: 5.066) に受理!

D2 渡邊雄一郎君 (Yuichiro Watanabe) と M2 吉岡良君 (Ryo Yoshioka) のビスターピリジン電子輸送材料に関する「Fundamental Functions of Peripheral and Core Pyridine Rings in a Series of Bis-terpyridine Derivatives for High-Performance Organic Light-Emitting Devices」と題するの論文が、英国王立化学会(RSC) の J. Mater. Chem. C (IF: 5.066) にアクセプトされました。雄一郎、吉岡、おめでとうございます!

 

Title: Fundamental Functions of Peripheral and Core Pyridine Rings in a Series of Bis-terpyridine Derivatives for High-Performance Organic Light-Emitting Devices

 

By Y. Watanabe, R. Yoshioka, H. Sasabe*, T. Kamata, H. Katagiri, D. Yokoyama, J. Kido*, J. Mater. Chem. C, accepted.

 

Abstract: In this study, we comprehensively investigated a series of bis-terpyridine isomers, n-TerPyB as optoelectronic materials. As a result, we have revealed that the fundamental roles of the peripheral and core pyridine rings of TerPyB. The peripheral four pyridines deepen the ionization potential because of their electron-withdrawing property, and form intramolecular hydrogen bonds (H-bonds) for 2-TerPyB and intermolecular H-bonds for 3-TerPyB and 4-TerPyB. Intermolecular H-bonds in the solid state were observed to play critical roles in determining the molecular aggregation behavior and in enhancing the horizontal molecular orientation and the electron mobility. Further, we have revealed that the two fundamental roles of the core pyridines are (i) to render the molecular structure planar via intramolecular H-bonds and (ii) to increase the Ea to enhance electron injection without sacrificing electron mobility. Finally, we successfully fabricated proof-of-concept organic light-emitting devices (OLEDs) using TerPyB as an electron-transporter. An OLED with 3-TerPyB exhibited an extremely low operating voltage of 2.2 V at a luminance of 1 cd m–2; the power efficiency and the external quantum efficiency of the device were 104 lm W–1, and 23.5% at 100 cd m–2, respectively. We believe that these results open new possibilities in terpyridine chemistry and materials science.

 

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