Title :
Radiative transition from even-parity state in conjugated polymer
Author :
Kobayashi, T. ; Hamazaki, J. ; Arakawa, M. ; Kunugita, H. ; Ema, K. ; Endo, K. ; Ochiai, K. ; Rikukawa, M. ; Sanui, K.
Author_Institution :
Dept. of Phys., Sophia Univ., Tokyo, Japan
Abstract :
Summary form only given. In nonfluorescent /spl pi/ conjugated polymers, e.g. polydiacetylene (PDA), the dipole forbidden 2A/sub g/ state lies below the allowed 1B/sub u/ state. On the other hand, in the fluorescent polymers such as poly-(p-phenylenvinylene) (PPV) and polythiophene (PT), the 2A/sub g/ state is considered to be above the 1B/sub u/ state. Whether the polymer shows fluorescence or not is determined by the order of the 1B/sub u/ and the 2A/sub g/ states. However, the electron-phonon coupling relaxes the selection rule. Moreover, in the case where the 1B/sub u/ and 2A/sub g/ states lie close to each other, the radiative transition from the 2A/sub g/ state can be enhanced. In the research, we confirm that photoluminescence in a PT derivative contains the contribution from the 2A/sub g/ state, and conclude that the 2A/sub g/ state lies slightly below the 1B/sub u/ state in this material.
Keywords :
Langmuir-Blodgett films; electron-phonon interactions; fluorescence; optical polymers; photoluminescence; polymer films; time resolved spectra; 1B/sub u/ state; 2A/sub g/ state; conjugated polymer; dipole forbidden state; electron-phonon coupling; even-parity state; fluorescence; fluorescent polymers; nonfluorescent /spl pi/ conjugated polymers; photoluminescence; poly-(p-phenylenvinylene); polydiacetylene; polythiophene; radiative transition; selection rule; Absorption; Chemical technology; Fluorescence; Laser theory; Laser transitions; Phonons; Photoluminescence; Polymers; Solid lasers; Solid state circuits;
Conference_Titel :
Lasers and Electro-Optics, 2001. CLEO '01. Technical Digest. Summaries of papers presented at the Conference on
Conference_Location :
Baltimore, MD, USA
Print_ISBN :
1-55752-662-1
DOI :
10.1109/CLEO.2001.947827