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Photostimulated generation of defects and surface reactions on a series of wide band gap metal-oxide solids. / Emeline, A. V.; Kataeva, G. V.; Ryabchuk, V. K.; Serpone, N.

In: Journal of Physical Chemistry B, Vol. 103, No. 43, 28.10.1999, p. 9190-9199.

Research output: Contribution to journalArticlepeer-review

Harvard

Emeline, AV, Kataeva, GV, Ryabchuk, VK & Serpone, N 1999, 'Photostimulated generation of defects and surface reactions on a series of wide band gap metal-oxide solids', Journal of Physical Chemistry B, vol. 103, no. 43, pp. 9190-9199.

APA

Emeline, A. V., Kataeva, G. V., Ryabchuk, V. K., & Serpone, N. (1999). Photostimulated generation of defects and surface reactions on a series of wide band gap metal-oxide solids. Journal of Physical Chemistry B, 103(43), 9190-9199.

Vancouver

Emeline AV, Kataeva GV, Ryabchuk VK, Serpone N. Photostimulated generation of defects and surface reactions on a series of wide band gap metal-oxide solids. Journal of Physical Chemistry B. 1999 Oct 28;103(43):9190-9199.

Author

Emeline, A. V. ; Kataeva, G. V. ; Ryabchuk, V. K. ; Serpone, N. / Photostimulated generation of defects and surface reactions on a series of wide band gap metal-oxide solids. In: Journal of Physical Chemistry B. 1999 ; Vol. 103, No. 43. pp. 9190-9199.

BibTeX

@article{17331d0354b74ddb88cd78483cdd4582,
title = "Photostimulated generation of defects and surface reactions on a series of wide band gap metal-oxide solids",
abstract = "The interconnection between photostimulated formation and destruction of defect centers (F- and V-type color centers) and surface photochemical reactions taking place on the surface has been examined for a series of 21 wide band gap metal-oxide specimens, which comprise insulators and semiconductors whose band-gap energies span the range from ca. 3 eV (ZnO, TiO2) to ca. 11 eV (BeO). Photostimulated post-adsorption of O2 was seen for 9 of the 21 metal oxides tested. Three of these specimens, namely scandia (Sc2O3), zirconia (ZrO2), and normal spinel (MgAl2O4), were chosen for detailed study to establish that spectral sensitization of metal oxides by UV illumination is a generally occurring phenomenon which is carried over to photostimulated adsorption of molecules and to surface photochemical reactions. Results demonstrate that irradiation into the absorption bands of the color centers of the photocolored metal oxides leads to a red shift of the spectral limit of surface photoreactions. A simple mechanism is described quantitatively for the photocoloration and surface reactions. Quantum yields of photobleaching of color centers in vacuo and in the presence of H2 and O2 are reported for scandia and zirconia, together with the quantum yields of photoadsorption of H2 and O2 molecules.",
author = "Emeline, {A. V.} and Kataeva, {G. V.} and Ryabchuk, {V. K.} and N. Serpone",
year = "1999",
month = oct,
day = "28",
language = "English",
volume = "103",
pages = "9190--9199",
journal = "Journal of Physical Chemistry B",
issn = "1520-6106",
publisher = "American Chemical Society",
number = "43",

}

RIS

TY - JOUR

T1 - Photostimulated generation of defects and surface reactions on a series of wide band gap metal-oxide solids

AU - Emeline, A. V.

AU - Kataeva, G. V.

AU - Ryabchuk, V. K.

AU - Serpone, N.

PY - 1999/10/28

Y1 - 1999/10/28

N2 - The interconnection between photostimulated formation and destruction of defect centers (F- and V-type color centers) and surface photochemical reactions taking place on the surface has been examined for a series of 21 wide band gap metal-oxide specimens, which comprise insulators and semiconductors whose band-gap energies span the range from ca. 3 eV (ZnO, TiO2) to ca. 11 eV (BeO). Photostimulated post-adsorption of O2 was seen for 9 of the 21 metal oxides tested. Three of these specimens, namely scandia (Sc2O3), zirconia (ZrO2), and normal spinel (MgAl2O4), were chosen for detailed study to establish that spectral sensitization of metal oxides by UV illumination is a generally occurring phenomenon which is carried over to photostimulated adsorption of molecules and to surface photochemical reactions. Results demonstrate that irradiation into the absorption bands of the color centers of the photocolored metal oxides leads to a red shift of the spectral limit of surface photoreactions. A simple mechanism is described quantitatively for the photocoloration and surface reactions. Quantum yields of photobleaching of color centers in vacuo and in the presence of H2 and O2 are reported for scandia and zirconia, together with the quantum yields of photoadsorption of H2 and O2 molecules.

AB - The interconnection between photostimulated formation and destruction of defect centers (F- and V-type color centers) and surface photochemical reactions taking place on the surface has been examined for a series of 21 wide band gap metal-oxide specimens, which comprise insulators and semiconductors whose band-gap energies span the range from ca. 3 eV (ZnO, TiO2) to ca. 11 eV (BeO). Photostimulated post-adsorption of O2 was seen for 9 of the 21 metal oxides tested. Three of these specimens, namely scandia (Sc2O3), zirconia (ZrO2), and normal spinel (MgAl2O4), were chosen for detailed study to establish that spectral sensitization of metal oxides by UV illumination is a generally occurring phenomenon which is carried over to photostimulated adsorption of molecules and to surface photochemical reactions. Results demonstrate that irradiation into the absorption bands of the color centers of the photocolored metal oxides leads to a red shift of the spectral limit of surface photoreactions. A simple mechanism is described quantitatively for the photocoloration and surface reactions. Quantum yields of photobleaching of color centers in vacuo and in the presence of H2 and O2 are reported for scandia and zirconia, together with the quantum yields of photoadsorption of H2 and O2 molecules.

UR - http://www.scopus.com/inward/record.url?scp=0000484039&partnerID=8YFLogxK

M3 - Article

AN - SCOPUS:0000484039

VL - 103

SP - 9190

EP - 9199

JO - Journal of Physical Chemistry B

JF - Journal of Physical Chemistry B

SN - 1520-6106

IS - 43

ER -

ID: 35144516