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Photo-electrochemical characterization of a new lead-free relaxor ceramic and its application to degradation of Bezacryl under sunlight
The perovskite structure Ba 0.975 Ho 0.017 (Zr 0.20 Ti 0.75 )Sn 0.05 O 3 (BHZ20TS) underwent crystallization through a solid-state reaction, as indicated by X-ray diffractometry. The analysis revealed that the oxide crystallizes in a cubic symmetry. Upon substituting Ba 2+ with Ho 3+ , scanning elec...
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Published in: | Journal of the Iranian Chemical Society 2023-10, Vol.20 (10), p.2471-2479 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The perovskite structure Ba
0.975
Ho
0.017
(Zr
0.20
Ti
0.75
)Sn
0.05
O
3
(BHZ20TS) underwent crystallization through a solid-state reaction, as indicated by X-ray diffractometry. The analysis revealed that the oxide crystallizes in a cubic symmetry. Upon substituting Ba
2+
with Ho
3+
, scanning electron microscopy (SEM) revealed a dense microstructure with a decreased grain size. The thermal dependence of the dielectric constant at various frequencies exhibits characteristic behavior of a relaxor ferroelectric, in accordance with the Vogel–Fulcher and Curie–Weiss laws. The photo-electrochemical and photo-catalytic properties of the material were examined. The capacitance (
C
−2
)—potential (
E
) relationship exhibited n-type behavior, with an electron concentration (
N
A
) of 2.2 × 1016 cm
−3
and a flat band potential (
E
fb
) of − 0.60
V
SCE
. The synthesized compound was evaluated for its ability to induce the photo-degradation of Bezacryl (BEZ) under sunlight. The oxidation of BEZ was achieved by the radicals
·
OH and O
2
·−
. A significant reduction in color intensity, reaching approximately 60%, was reached within 100 min in a BEZ solution (10 mg L
−1
) under a flux intensity of 97 mW cm
−2
. The photo-oxidation process followed a pseudo-first-order kinetic model, with a half-life (
t
1/2
) of 57 min. |
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ISSN: | 1735-207X 1735-2428 |
DOI: | 10.1007/s13738-023-02841-7 |