Journal
CHEMPHYSCHEM
Volume 10, Issue 11, Pages 1789-1793Publisher
WILEY-BLACKWELL
DOI: 10.1002/cphc.200900155
Keywords
kinetics; photochemistry; singlet oxygen; tio(2); two-photon excitation
Funding
- NSF-PREM [DMR-0611539]
- NIH-RCMI [2G12RR073459]
- NSF-MRSEC [MRI-0421406]
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Singlet oxygen (O-1(2)) signals observed upon illumination at 532 nm are a consequence of TiO2 excitation in a two-photon process, and at 355 nm in a one-photon pathway. After corrections for light reflectance, the relative quantum yields of O-1(2), production are 0.23 +/- 0.01 and 0.22 +/- 0.02 for 532 and 355 nm excitation, respectively. Total quenching rate constants of O-1(2) removal by TiO2 particles are near the diffusion-controlled rate limit. By employing O-1(2) as a probe, we have established an efficient and simple method to elucidate the nature of TiO2 photoexcitation.
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