Standard

Bismuth-doped gadolinium oxide films for UV-Vis multicolor conversion: Combined XPS, DFT and photoluminescence study. / Zatsepin, Anatoly F.; Kuznetsova, Yulia A.; Zatsepin, Dmitry A. и др.
в: Journal of Alloys and Compounds, Том 949, 169815, 01.07.2023.

Результаты исследований: Вклад в журналСтатьяРецензирование

Harvard

APA

Vancouver

Zatsepin AF, Kuznetsova YA, Zatsepin DA, Wong C-H, Law W, Tang C-Y и др. Bismuth-doped gadolinium oxide films for UV-Vis multicolor conversion: Combined XPS, DFT and photoluminescence study. Journal of Alloys and Compounds. 2023 июль 1;949:169815. doi: 10.1016/j.jallcom.2023.169815

Author

BibTeX

@article{687059762d45480ca8c31626c3658793,
title = "Bismuth-doped gadolinium oxide films for UV-Vis multicolor conversion: Combined XPS, DFT and photoluminescence study",
abstract = "Results of XPS characterization, theoretical modeling and photoluminescence study of bismuth-implanted gadolinium oxide (Gd2O3:Bi) films are presented. Scenarios for the introduction of bismuth ions into amorphous-crystalline Gd2O3 host and mechanisms for the formation of optically active centers are considered. It has been demonstrated that the optical properties of Gd2O3:Bi films are guided by the interplay of a quite complex system of single Bi2+ ions, (Bi3+–Bi3+) pairs and single Bi3+-ions, oxygen vacancies and {"}defective{"} gadolinium ions. Photoinduced excitation-relaxation processes involving various Bi-related centers and defect states of the host are observed. Due to the multicolor emission (red, green and blue) of single Bi2+ ions, (Bi3+- Bi3+) pairs and single Bi3+ ions excited in the ultraviolet spectral range, the UV–VIS energy conversion in a wide spectral range is realized. The advantage of Gd2O3:Bi as a material for energy conversion lies in the fact that due to the polyvalence of bismuth and the variety of different optical centers, a wide range of both absorbed UV light and emitted VIS light is involved in the conversion. This indicates the prospects for practical use of Gd2O3:Bi films as multifunctional material for energy conversion and photo-detection systems.",
author = "Zatsepin, {Anatoly F.} and Kuznetsova, {Yulia A.} and Zatsepin, {Dmitry A.} and Chi-Ho Wong and Wing-cheung Law and Chak-Yin Tang and Gavrilov, {Nikolay V.} and Boukhwalov, {Danil V.}",
note = "This work was supported by the Russian Science Foundation (Project No. 21-12-00392 ).",
year = "2023",
month = jul,
day = "1",
doi = "10.1016/j.jallcom.2023.169815",
language = "English",
volume = "949",
journal = "Journal of Alloys and Compounds",
issn = "0925-8388",
publisher = "Elsevier Inc.",

}

RIS

TY - JOUR

T1 - Bismuth-doped gadolinium oxide films for UV-Vis multicolor conversion: Combined XPS, DFT and photoluminescence study

AU - Zatsepin, Anatoly F.

AU - Kuznetsova, Yulia A.

AU - Zatsepin, Dmitry A.

AU - Wong, Chi-Ho

AU - Law, Wing-cheung

AU - Tang, Chak-Yin

AU - Gavrilov, Nikolay V.

AU - Boukhwalov, Danil V.

N1 - This work was supported by the Russian Science Foundation (Project No. 21-12-00392 ).

PY - 2023/7/1

Y1 - 2023/7/1

N2 - Results of XPS characterization, theoretical modeling and photoluminescence study of bismuth-implanted gadolinium oxide (Gd2O3:Bi) films are presented. Scenarios for the introduction of bismuth ions into amorphous-crystalline Gd2O3 host and mechanisms for the formation of optically active centers are considered. It has been demonstrated that the optical properties of Gd2O3:Bi films are guided by the interplay of a quite complex system of single Bi2+ ions, (Bi3+–Bi3+) pairs and single Bi3+-ions, oxygen vacancies and "defective" gadolinium ions. Photoinduced excitation-relaxation processes involving various Bi-related centers and defect states of the host are observed. Due to the multicolor emission (red, green and blue) of single Bi2+ ions, (Bi3+- Bi3+) pairs and single Bi3+ ions excited in the ultraviolet spectral range, the UV–VIS energy conversion in a wide spectral range is realized. The advantage of Gd2O3:Bi as a material for energy conversion lies in the fact that due to the polyvalence of bismuth and the variety of different optical centers, a wide range of both absorbed UV light and emitted VIS light is involved in the conversion. This indicates the prospects for practical use of Gd2O3:Bi films as multifunctional material for energy conversion and photo-detection systems.

AB - Results of XPS characterization, theoretical modeling and photoluminescence study of bismuth-implanted gadolinium oxide (Gd2O3:Bi) films are presented. Scenarios for the introduction of bismuth ions into amorphous-crystalline Gd2O3 host and mechanisms for the formation of optically active centers are considered. It has been demonstrated that the optical properties of Gd2O3:Bi films are guided by the interplay of a quite complex system of single Bi2+ ions, (Bi3+–Bi3+) pairs and single Bi3+-ions, oxygen vacancies and "defective" gadolinium ions. Photoinduced excitation-relaxation processes involving various Bi-related centers and defect states of the host are observed. Due to the multicolor emission (red, green and blue) of single Bi2+ ions, (Bi3+- Bi3+) pairs and single Bi3+ ions excited in the ultraviolet spectral range, the UV–VIS energy conversion in a wide spectral range is realized. The advantage of Gd2O3:Bi as a material for energy conversion lies in the fact that due to the polyvalence of bismuth and the variety of different optical centers, a wide range of both absorbed UV light and emitted VIS light is involved in the conversion. This indicates the prospects for practical use of Gd2O3:Bi films as multifunctional material for energy conversion and photo-detection systems.

UR - http://www.scopus.com/inward/record.url?partnerID=8YFLogxK&scp=85151299521

UR - https://gateway.webofknowledge.com/gateway/Gateway.cgi?GWVersion=2&SrcAuth=tsmetrics&SrcApp=tsm_test&DestApp=WOS_CPL&DestLinkType=FullRecord&KeyUT=000966486300001

U2 - 10.1016/j.jallcom.2023.169815

DO - 10.1016/j.jallcom.2023.169815

M3 - Article

VL - 949

JO - Journal of Alloys and Compounds

JF - Journal of Alloys and Compounds

SN - 0925-8388

M1 - 169815

ER -

ID: 37146466