1990
DOI: 10.1021/ma00212a018
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Singlet oxygen formation in a solid organic polymer upon irradiation of the oxygen-polymer charge-transfer band

Abstract: Singlet molecular oxygen (1 02) phosphorescence has been observed at 1270 nm in a timeresolved experiment subsequent to pulsed UV laser photolysis of the oxygen (3Eg-02)-polymer chargetransfer (CT) absorption band of solid polystyrene samples. These data indicate that the polymer-oxygen CT potential surface (polymer,+02*-) is coupled to the potential surface of the polymer-1Ag02 complex. Continued photolysis into the CT absorption band results in the formation of products that act as 1 02 photosensitizers, thu… Show more

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Cited by 36 publications
(42 citation statements)
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“…38,39 Longer illumination time can transform the CTC into irreversible oxidation products. 40,41 The latter can be intensified by irradiation of the solar cell with UV light, because this wavelength range is known to excite semiconductor oxides, producing oxygen-rich species. 27,[42][43][44] Thus, analyses of the HSC under inert atmosphere conditions could, in principle, prevent the reaction of atmospheric oxygen with the MEH-PPV polymer improving device lifetime.…”
Section: Resultsmentioning
confidence: 99%
“…38,39 Longer illumination time can transform the CTC into irreversible oxidation products. 40,41 The latter can be intensified by irradiation of the solar cell with UV light, because this wavelength range is known to excite semiconductor oxides, producing oxygen-rich species. 27,[42][43][44] Thus, analyses of the HSC under inert atmosphere conditions could, in principle, prevent the reaction of atmospheric oxygen with the MEH-PPV polymer improving device lifetime.…”
Section: Resultsmentioning
confidence: 99%
“…The mechanisms of organic dye photobleaching in polymer matrices are often complex, sensitive to environmental and excitation conditions and specific to each class of dyes, but photodegradation has generally been found to occur via (1) reactive radical intermediates ( e.g. peroxy radicals) formed by the photoexcitation of dyes upon excitation to higher excited electronic states in a polar environment (26–28) or (2) degradation by reaction with 1 O 2 , produced by sensitization of ground state triplet oxygen via an organic dye or other absorber (26–28). Several teams of researchers have investigated the lifetimes, mechanisms of generation, physical quenching and chemical quenching of singlet molecular oxygen in homogeneous polymer matrices (29), as well as cyanine (30) and merocyanine (31) dye‐doped in thin films.…”
Section: Resultsmentioning
confidence: 99%
“…Under oxygen-containing atmosphere the polymer by itself can undergo the formation of an oxygen-anion doping, or charge transfer complex (CTC), between the polymer and oxygen from the environment, [MEH-PPV· + /O 2 · -] (32, 33, 13, 45, 7). Longer irradiation time can transform the CTC into irreversible oxidation products (34,35). The later can be intensified by irradiation of the solar cell with UV-light since this wavelength range is known to excite semiconductor oxides producing oxygen-rich species (23,44,48).…”
Section: Resultsmentioning
confidence: 99%