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Spectral Dependencies of the Quantum Yield of Photochemical Processes on the Surface of Wide Band Gap Solids. 3. Gas/Solid Systems. / Emeline, A. V.; Kuzmin, G. N.; Purevdorj, D.; Ryabchuk, V. K.; Serpone, N.

в: Journal of Physical Chemistry B, Том 104, № 14, 13.04.2000, стр. 2989-2999.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

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Emeline, A. V. ; Kuzmin, G. N. ; Purevdorj, D. ; Ryabchuk, V. K. ; Serpone, N. / Spectral Dependencies of the Quantum Yield of Photochemical Processes on the Surface of Wide Band Gap Solids. 3. Gas/Solid Systems. в: Journal of Physical Chemistry B. 2000 ; Том 104, № 14. стр. 2989-2999.

BibTeX

@article{e9d18e29051641be984f35af169629d1,
title = "Spectral Dependencies of the Quantum Yield of Photochemical Processes on the Surface of Wide Band Gap Solids. 3. Gas/Solid Systems",
abstract = "The spectral dependencies of quantum yields of photostimulated adsorption of oxygen on KBr and ZrO2 specimens were assessed during photoexcitation into the F centers produced by preirradiation with UV light. The spectral limits of this adsorption were shifted to wavelengths longer than the absorption band edge of the specimens. However, of great import are the spectral dependencies of the quantum yields of photochemical processes for the original state(s) of metal oxides irradiated in the intrinsic and extrinsic absorption bands. Such dependencies for the photoadsorption of donor (H2 and CH4) and acceptor (O2) molecules in gas/solid systems are reported for a variety of metal oxides of varying band gaps (Eg), namely TiO2 (rutile form, Eg = 3.0 eV), ZnO (3.0 eV), ZrO2 (5.0), Sc2 O3 (5.4 eV), MgO (8.7 eV), and CaO (7.5 eV) as well as for Bi2 O3 (3.2 eV), CeO2 (3.4 eV), Ga2 O3 (4.4 eV), In2 O3 (3.1 eV), Nb2 O5 (3.3 eV), and Y2 O3 (5.5 eV). The approach taken to model and compare with experimental results was reported earlier (ref 4). For the first six metal oxides, the dependencies are rationalized on the basis of the absorption spectra of the specimens for which the origins of the extrinsic light absorption are known. The corresponding dependencies for the remaining oxides in the series are nonetheless also reported albeit they await characterization of the origins of the spectral features for a complete understanding to be achieved.",
author = "Emeline, {A. V.} and Kuzmin, {G. N.} and D. Purevdorj and Ryabchuk, {V. K.} and N. Serpone",
year = "2000",
month = apr,
day = "13",
doi = "10.1021/jp9926589",
language = "English",
volume = "104",
pages = "2989--2999",
journal = "Journal of Physical Chemistry B",
issn = "1520-6106",
publisher = "American Chemical Society",
number = "14",

}

RIS

TY - JOUR

T1 - Spectral Dependencies of the Quantum Yield of Photochemical Processes on the Surface of Wide Band Gap Solids. 3. Gas/Solid Systems

AU - Emeline, A. V.

AU - Kuzmin, G. N.

AU - Purevdorj, D.

AU - Ryabchuk, V. K.

AU - Serpone, N.

PY - 2000/4/13

Y1 - 2000/4/13

N2 - The spectral dependencies of quantum yields of photostimulated adsorption of oxygen on KBr and ZrO2 specimens were assessed during photoexcitation into the F centers produced by preirradiation with UV light. The spectral limits of this adsorption were shifted to wavelengths longer than the absorption band edge of the specimens. However, of great import are the spectral dependencies of the quantum yields of photochemical processes for the original state(s) of metal oxides irradiated in the intrinsic and extrinsic absorption bands. Such dependencies for the photoadsorption of donor (H2 and CH4) and acceptor (O2) molecules in gas/solid systems are reported for a variety of metal oxides of varying band gaps (Eg), namely TiO2 (rutile form, Eg = 3.0 eV), ZnO (3.0 eV), ZrO2 (5.0), Sc2 O3 (5.4 eV), MgO (8.7 eV), and CaO (7.5 eV) as well as for Bi2 O3 (3.2 eV), CeO2 (3.4 eV), Ga2 O3 (4.4 eV), In2 O3 (3.1 eV), Nb2 O5 (3.3 eV), and Y2 O3 (5.5 eV). The approach taken to model and compare with experimental results was reported earlier (ref 4). For the first six metal oxides, the dependencies are rationalized on the basis of the absorption spectra of the specimens for which the origins of the extrinsic light absorption are known. The corresponding dependencies for the remaining oxides in the series are nonetheless also reported albeit they await characterization of the origins of the spectral features for a complete understanding to be achieved.

AB - The spectral dependencies of quantum yields of photostimulated adsorption of oxygen on KBr and ZrO2 specimens were assessed during photoexcitation into the F centers produced by preirradiation with UV light. The spectral limits of this adsorption were shifted to wavelengths longer than the absorption band edge of the specimens. However, of great import are the spectral dependencies of the quantum yields of photochemical processes for the original state(s) of metal oxides irradiated in the intrinsic and extrinsic absorption bands. Such dependencies for the photoadsorption of donor (H2 and CH4) and acceptor (O2) molecules in gas/solid systems are reported for a variety of metal oxides of varying band gaps (Eg), namely TiO2 (rutile form, Eg = 3.0 eV), ZnO (3.0 eV), ZrO2 (5.0), Sc2 O3 (5.4 eV), MgO (8.7 eV), and CaO (7.5 eV) as well as for Bi2 O3 (3.2 eV), CeO2 (3.4 eV), Ga2 O3 (4.4 eV), In2 O3 (3.1 eV), Nb2 O5 (3.3 eV), and Y2 O3 (5.5 eV). The approach taken to model and compare with experimental results was reported earlier (ref 4). For the first six metal oxides, the dependencies are rationalized on the basis of the absorption spectra of the specimens for which the origins of the extrinsic light absorption are known. The corresponding dependencies for the remaining oxides in the series are nonetheless also reported albeit they await characterization of the origins of the spectral features for a complete understanding to be achieved.

UR - http://www.scopus.com/inward/record.url?scp=0034643503&partnerID=8YFLogxK

U2 - 10.1021/jp9926589

DO - 10.1021/jp9926589

M3 - Article

AN - SCOPUS:0034643503

VL - 104

SP - 2989

EP - 2999

JO - Journal of Physical Chemistry B

JF - Journal of Physical Chemistry B

SN - 1520-6106

IS - 14

ER -

ID: 35144247