Microstructural analysis of undoped and moderately Sc-doped TiO<inf>2</inf>anatase nanoparticles using Scherrer equation and Debye function analysis
The result's identifiers
Result code in IS VaVaI
<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F61388980%3A_____%2F18%3A00491938" target="_blank" >RIV/61388980:_____/18:00491938 - isvavai.cz</a>
Result on the web
<a href="http://dx.doi.org/10.1016/j.matchar.2018.07.022" target="_blank" >http://dx.doi.org/10.1016/j.matchar.2018.07.022</a>
DOI - Digital Object Identifier
<a href="http://dx.doi.org/10.1016/j.matchar.2018.07.022" target="_blank" >10.1016/j.matchar.2018.07.022</a>
Alternative languages
Result language
angličtina
Original language name
Microstructural analysis of undoped and moderately Sc-doped TiO<inf>2</inf>anatase nanoparticles using Scherrer equation and Debye function analysis
Original language description
UV light sensitive undoped and moderate (4 at.%) Sc-doped anatase nanocrystallites were prepared by an efficient and environmentally benign method based on homogeneous hydrolysis of TiOSO4and Sc2(C2O4)3.5H2O aqueous solutions using urea as a precipitation agent, without post-synthesis calcination or annealing. X-ray diffraction study of the obtained powders revealed single phase anatase in both samples. Two different methods were applied to estimate the anatase crystallite size and shape from the X-ray diffraction data. The first one is based on the more conventional Scherrer equation (as implanted in GSAS-II program) while the second one is based on Debye function analysis (as implanted in DUBUSSY suite version 2.2), which is considered to be more adequate for nanocrystallites. Although each program has its own shape models, both methods indicated similar results of elongated nanocrystallite geometry for Sc-doped TiO2: (i) GSAS-II confirmed ellipsoid shape with equatorial size of 5.1(0) nm and axial size of 6.8(0), (ii) DEBUSSY suite 2.2 showed cylinder shape with diameter of equivalent circle in the ab-plane, Dab= 4.9(1.0) nm and crystallite length along the c-axis, Lc= 5.4(3.2) nm. For the undoped TiO2sample, equatorial size of 5.5(0) nm and axial size of 7.3(0) nm for the ellipsoid shape was determined according to GSAS-II, while Dab= 5.5(1.3) nm and Lc= 6.0(2.2) nm for the cylinder shape was determined by DEBUSSY suite 2.2. These outcomes were found to corroborate with HRTEM analysis. Doping with 4 at.% Sc caused ~0.3% growth of lattice parameters from a = 3.7979 [4] Å, c = 9.4995 [9] Å for the undoped sample to a = 3.8110 [7] Å, c = 9.5274 [16] Å for the moderately Sc doped sample, while reduction in the Ti vacancies by half was confirmed by both methods. The introducing of Sc as electronically active secondary species into the crystal lattice of TiO2can greatly alter its optical absorption. The incorporation of Sc into the crystal lattice of TiO2favors the substitution of Ti, as both have approximately the same ionic size, and generates surface oxygen vacancies which can act as trapping center for the photogenerated electrons and reduce the recombination of electron–hole pairs. We can expect Sc doped TiO2nanomaterials to have applications as effective photocatalysts for selective photocatalytic oxidation of various environmental organic pollutants.
Czech name
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Czech description
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Classification
Type
J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database
CEP classification
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OECD FORD branch
10402 - Inorganic and nuclear chemistry
Result continuities
Project
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Continuities
I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace
Others
Publication year
2018
Confidentiality
S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů
Data specific for result type
Name of the periodical
Materials Characterization
ISSN
1044-5803
e-ISSN
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Volume of the periodical
144
Issue of the periodical within the volume
OCT
Country of publishing house
US - UNITED STATES
Number of pages
10
Pages from-to
287-296
UT code for WoS article
000447477300029
EID of the result in the Scopus database
2-s2.0-85050130836