Standard

Long-Lived Photocatalysis Centers Created in ZnO via Resonant Exciton Excitation. / Titov, V. V.; Lisachenko, A. A.; Akopyan, I. Kh; Labzovskaya, M.E.; Novikov, B. V.

в: Physics of the Solid State, Том 61, № 11, 01.11.2019, стр. 2134-2138.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

APA

Vancouver

Author

Titov, V. V. ; Lisachenko, A. A. ; Akopyan, I. Kh ; Labzovskaya, M.E. ; Novikov, B. V. / Long-Lived Photocatalysis Centers Created in ZnO via Resonant Exciton Excitation. в: Physics of the Solid State. 2019 ; Том 61, № 11. стр. 2134-2138.

BibTeX

@article{118b546315214493871c5b576db2a707,
title = "Long-Lived Photocatalysis Centers Created in ZnO via Resonant Exciton Excitation",
abstract = "Abstract: ZnO together with TiO2 is a main photocatalyst for various redox reactions to convert light energy into a chemical one and to purify the environment. Intrinsic surface defects in ZnO—the vacancies in anionic and cationic sublattices (F-type and V-type centers)—allow creation of long-lived (up to 103 s) photocatalysis centers and, therefore, tenfold increase in quantum yield of reactions. Slow surface states—the photocatalysis centers—appear via diffusion of electrons and holes generated during the interband transitions in the bulk of a photoactivated sample. The transfer efficiency, however, decreases sharply because of recombination of charge carriers and losses during overcoming the surface Schottky barrier. Neutral energy carriers—excitons—were used in this work to decrease these losses during the energy transfer to a surface. High exciton binding energy in ZnO (60 meV) allows it to move at room temperature without decay. The exciton energy loss for radiation is effectively decreased in our experiments via formation of a 2D surface structure. The results confirm high efficiency of exciton channel to form surface long-lived photocatalysis F-centers and V‑centers during the photoadsorption and photodesorption processes of oxygen, which simulate full cycle of a redox photocatalytic reaction.",
keywords = "2D structure, excitons, oxygen, photoadsorption, photodesorption, surface long-lived centers, ZnO",
author = "Titov, {V. V.} and Lisachenko, {A. A.} and Akopyan, {I. Kh} and M.E. Labzovskaya and Novikov, {B. V.}",
year = "2019",
month = nov,
day = "1",
doi = "10.1134/S1063783419110398",
language = "English",
volume = "61",
pages = "2134--2138",
journal = "Physics of the Solid State",
issn = "1063-7834",
publisher = "МАИК {"}Наука/Интерпериодика{"}",
number = "11",

}

RIS

TY - JOUR

T1 - Long-Lived Photocatalysis Centers Created in ZnO via Resonant Exciton Excitation

AU - Titov, V. V.

AU - Lisachenko, A. A.

AU - Akopyan, I. Kh

AU - Labzovskaya, M.E.

AU - Novikov, B. V.

PY - 2019/11/1

Y1 - 2019/11/1

N2 - Abstract: ZnO together with TiO2 is a main photocatalyst for various redox reactions to convert light energy into a chemical one and to purify the environment. Intrinsic surface defects in ZnO—the vacancies in anionic and cationic sublattices (F-type and V-type centers)—allow creation of long-lived (up to 103 s) photocatalysis centers and, therefore, tenfold increase in quantum yield of reactions. Slow surface states—the photocatalysis centers—appear via diffusion of electrons and holes generated during the interband transitions in the bulk of a photoactivated sample. The transfer efficiency, however, decreases sharply because of recombination of charge carriers and losses during overcoming the surface Schottky barrier. Neutral energy carriers—excitons—were used in this work to decrease these losses during the energy transfer to a surface. High exciton binding energy in ZnO (60 meV) allows it to move at room temperature without decay. The exciton energy loss for radiation is effectively decreased in our experiments via formation of a 2D surface structure. The results confirm high efficiency of exciton channel to form surface long-lived photocatalysis F-centers and V‑centers during the photoadsorption and photodesorption processes of oxygen, which simulate full cycle of a redox photocatalytic reaction.

AB - Abstract: ZnO together with TiO2 is a main photocatalyst for various redox reactions to convert light energy into a chemical one and to purify the environment. Intrinsic surface defects in ZnO—the vacancies in anionic and cationic sublattices (F-type and V-type centers)—allow creation of long-lived (up to 103 s) photocatalysis centers and, therefore, tenfold increase in quantum yield of reactions. Slow surface states—the photocatalysis centers—appear via diffusion of electrons and holes generated during the interband transitions in the bulk of a photoactivated sample. The transfer efficiency, however, decreases sharply because of recombination of charge carriers and losses during overcoming the surface Schottky barrier. Neutral energy carriers—excitons—were used in this work to decrease these losses during the energy transfer to a surface. High exciton binding energy in ZnO (60 meV) allows it to move at room temperature without decay. The exciton energy loss for radiation is effectively decreased in our experiments via formation of a 2D surface structure. The results confirm high efficiency of exciton channel to form surface long-lived photocatalysis F-centers and V‑centers during the photoadsorption and photodesorption processes of oxygen, which simulate full cycle of a redox photocatalytic reaction.

KW - 2D structure

KW - excitons

KW - oxygen

KW - photoadsorption

KW - photodesorption

KW - surface long-lived centers

KW - ZnO

UR - http://www.scopus.com/inward/record.url?scp=85074688730&partnerID=8YFLogxK

U2 - 10.1134/S1063783419110398

DO - 10.1134/S1063783419110398

M3 - Article

AN - SCOPUS:85074688730

VL - 61

SP - 2134

EP - 2138

JO - Physics of the Solid State

JF - Physics of the Solid State

SN - 1063-7834

IS - 11

ER -

ID: 51178115