Standard

Effect of Sc3+/V5+ Co-Doping on Photocatalytic Activity of TiO2. / Murzin, Petr D.; Murashkina, A. A.; Emeline, A. V.; Bahnemann, D. W.

In: Topics in Catalysis, Vol. 64, No. 13-16, 11.2021, p. 817 - 823.

Research output: Contribution to journalArticlepeer-review

Harvard

APA

Vancouver

Author

Murzin, Petr D. ; Murashkina, A. A. ; Emeline, A. V. ; Bahnemann, D. W. / Effect of Sc3+/V5+ Co-Doping on Photocatalytic Activity of TiO2. In: Topics in Catalysis. 2021 ; Vol. 64, No. 13-16. pp. 817 - 823.

BibTeX

@article{034f22aff26c490694ae571f93be2a35,
title = "Effect of Sc3+/V5+ Co-Doping on Photocatalytic Activity of TiO2",
abstract = "Series of Sc/V co-doped rutile TiO2 with different Sc/V ratio was synthesized. Samples were characterized by XRD, SEM, XPS, BET, EPR, diffuse reflectance spectroscopy and Kelvin probe methods. EPR spectroscopy reveals a simultaneous increase of V4+ and Ti3+ as vanadium content grows. At the same time, an increase of vanadium concentration in co-doped samples results in stronger absorption in visible light range. However, a photocatalytic activity dependence on the co-dopant ratio demonstrates “volcano” plot behavior with maximum at 75/25 Sc/V ratio, while the work function dependence on Sc/V ratio demonstrates a negative correlation with photocatalytic activity resulting in a minimal value of work function at the same optimal ratio of co-dopant content. The analysis of the experimental results infers that alteration of Sc/V co-doping ratio leads to redistribution between shallow traps, which are not effective in charge carrier recombination, and deep traps, which act as effective recombination centers, with maximal shallow traps concentration corresponding to the optimal Sc/V ratio equal to 75/25, yielding the lowest recombination efficiency and therefore, the highest photocatalytic activity. Redistribution of defect states induced by co-doping should be distinguished as a primary factor of alteration of photocatalytic activity in co-doped TiO2. Presented results demonstrate that photoactivity of co-doped titania cannot be considered as result of either independent action of dopants or their additive effect.",
keywords = "Co-doping, Intrinsic defects, Phenol photodegradation, Photocatalysis, Shallow traps, TiO, Work function, ELECTRON, EPR, IONS, NANOPARTICLES, PHOTODEGRADATION, ABSORPTION, TITANIUM-DIOXIDE, TiO2",
author = "Murzin, {Petr D.} and Murashkina, {A. A.} and Emeline, {A. V.} and Bahnemann, {D. W.}",
year = "2021",
month = nov,
doi = "10.1007/s11244-020-01292-1",
language = "English",
volume = "64",
pages = "817 -- 823",
journal = "Topics in Catalysis",
issn = "1022-5528",
publisher = "Springer Nature",
number = "13-16",

}

RIS

TY - JOUR

T1 - Effect of Sc3+/V5+ Co-Doping on Photocatalytic Activity of TiO2

AU - Murzin, Petr D.

AU - Murashkina, A. A.

AU - Emeline, A. V.

AU - Bahnemann, D. W.

PY - 2021/11

Y1 - 2021/11

N2 - Series of Sc/V co-doped rutile TiO2 with different Sc/V ratio was synthesized. Samples were characterized by XRD, SEM, XPS, BET, EPR, diffuse reflectance spectroscopy and Kelvin probe methods. EPR spectroscopy reveals a simultaneous increase of V4+ and Ti3+ as vanadium content grows. At the same time, an increase of vanadium concentration in co-doped samples results in stronger absorption in visible light range. However, a photocatalytic activity dependence on the co-dopant ratio demonstrates “volcano” plot behavior with maximum at 75/25 Sc/V ratio, while the work function dependence on Sc/V ratio demonstrates a negative correlation with photocatalytic activity resulting in a minimal value of work function at the same optimal ratio of co-dopant content. The analysis of the experimental results infers that alteration of Sc/V co-doping ratio leads to redistribution between shallow traps, which are not effective in charge carrier recombination, and deep traps, which act as effective recombination centers, with maximal shallow traps concentration corresponding to the optimal Sc/V ratio equal to 75/25, yielding the lowest recombination efficiency and therefore, the highest photocatalytic activity. Redistribution of defect states induced by co-doping should be distinguished as a primary factor of alteration of photocatalytic activity in co-doped TiO2. Presented results demonstrate that photoactivity of co-doped titania cannot be considered as result of either independent action of dopants or their additive effect.

AB - Series of Sc/V co-doped rutile TiO2 with different Sc/V ratio was synthesized. Samples were characterized by XRD, SEM, XPS, BET, EPR, diffuse reflectance spectroscopy and Kelvin probe methods. EPR spectroscopy reveals a simultaneous increase of V4+ and Ti3+ as vanadium content grows. At the same time, an increase of vanadium concentration in co-doped samples results in stronger absorption in visible light range. However, a photocatalytic activity dependence on the co-dopant ratio demonstrates “volcano” plot behavior with maximum at 75/25 Sc/V ratio, while the work function dependence on Sc/V ratio demonstrates a negative correlation with photocatalytic activity resulting in a minimal value of work function at the same optimal ratio of co-dopant content. The analysis of the experimental results infers that alteration of Sc/V co-doping ratio leads to redistribution between shallow traps, which are not effective in charge carrier recombination, and deep traps, which act as effective recombination centers, with maximal shallow traps concentration corresponding to the optimal Sc/V ratio equal to 75/25, yielding the lowest recombination efficiency and therefore, the highest photocatalytic activity. Redistribution of defect states induced by co-doping should be distinguished as a primary factor of alteration of photocatalytic activity in co-doped TiO2. Presented results demonstrate that photoactivity of co-doped titania cannot be considered as result of either independent action of dopants or their additive effect.

KW - Co-doping

KW - Intrinsic defects

KW - Phenol photodegradation

KW - Photocatalysis

KW - Shallow traps

KW - TiO

KW - Work function

KW - ELECTRON

KW - EPR

KW - IONS

KW - NANOPARTICLES

KW - PHOTODEGRADATION

KW - ABSORPTION

KW - TITANIUM-DIOXIDE

KW - TiO2

UR - http://www.scopus.com/inward/record.url?scp=85086389248&partnerID=8YFLogxK

UR - https://www.mendeley.com/catalogue/797e84fc-20e2-37ac-a087-410ab70426d5/

U2 - 10.1007/s11244-020-01292-1

DO - 10.1007/s11244-020-01292-1

M3 - Article

AN - SCOPUS:85086389248

VL - 64

SP - 817

EP - 823

JO - Topics in Catalysis

JF - Topics in Catalysis

SN - 1022-5528

IS - 13-16

ER -

ID: 60422378