1998
DOI: 10.1006/jssc.1998.7816
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Electronic State Characterization of TiO2Ultrafine Particles by Luminescence Spectroscopy

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Cited by 78 publications
(49 citation statements)
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“…Excitation is made using 359 nm wavelength. The emission peak at 425 nm could be assigned to the bandto-band transition of free excitons (self-trapped excitons) localized on octahedral TiO 2 nanoparticles [26][27][28][29]. Peak at 402 nm could be associated with free exciton emission of anatase TiO 2 nanoparticles.…”
Section: Resultsmentioning
confidence: 96%
“…Excitation is made using 359 nm wavelength. The emission peak at 425 nm could be assigned to the bandto-band transition of free excitons (self-trapped excitons) localized on octahedral TiO 2 nanoparticles [26][27][28][29]. Peak at 402 nm could be associated with free exciton emission of anatase TiO 2 nanoparticles.…”
Section: Resultsmentioning
confidence: 96%
“…Ultrafine metal and oxide particles find wide applications because they exhibit novel physical and chemical properties that markedly differ from those of bulk materials [1][2][3][4].…”
Section: Introductionmentioning
confidence: 99%
“…Since the resolution of our time resolved spectroscopic system was 5 ns, the lifetime of broad emission centered at 435 nm was assumed to be sub-nano second. It was reported that the broad band centered at 435 nm is due to the free excitons of the titania nanoparticles [13,14], and the broad emission bands at 535 and 650 nm are attributed to oxygen vacancy levels [12]. Since the emissions radiated by the recombination of free excitons disappear within several nanoseconds, these signals cannot be detected by photon-counting system (PC mode).…”
Section: Resultsmentioning
confidence: 98%