Skip to main content
U.S. Department of Energy
Office of Scientific and Technical Information

Triplet photophysical properties of poly(2-vinylnaphthalene) and poly(N-vinylcarbazole) solid films in a low-temperature regime

Journal Article · · Journal of Physical Chemistry; (USA)
DOI:https://doi.org/10.1021/j100349a023· OSTI ID:6752263
The delayed fluorescence intensity from solid films of poly(2-vinylnaphthalene) (P2VN) and poly(N-vinylcarbazole) (PVCA) both yield maxima below 77 K when plotted as a function of temperature. For PVCA, earlier work had already established the existence of one maximum at 200 K along with a minimum at 145 K. Thus, the new maximum observed here near 40 K is the third extremum found for this polymer verifying earlier predictions of its existence. For P2VN a maximum in the delayed fluorescence-temperature profile is found near 55 K but no others are observed up to ambient temperature. The major source of delayed fluorescence intensity in both polymers is thought to arise from triplet-triplet hetero annihilations involving a mobile triplet exciton, T{sub m}, and a shallow-trapped one, T{sub s}. The increase in DF intensity from the lowest temperature up to the low-temperature maximum is due to an increasing rate of T{sub m} mobility. The maximum occurs at a temperature such that the rate of thermally induced detrapping of T{sub s} approaches that of competing processes for its relaxation to the ground state. A similar mechanism is proposed for PVCA. This mechanism is consistent with the observation that the low-temperature maxima disappear at long times after the excitation pulse and that the temperature corresponding to the maximum increases as the delay time decreases.
OSTI ID:
6752263
Journal Information:
Journal of Physical Chemistry; (USA), Journal Name: Journal of Physical Chemistry; (USA) Vol. 93:12; ISSN 0022-3654; ISSN JPCHA
Country of Publication:
United States
Language:
English