Photodeposition of Molybdenum Sulfide on Mtio3 (m: Ba, Sr) Perovskites for Photocatalytic Hydrogen Evolution
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Date
2023
Journal Title
Journal ISSN
Volume Title
Publisher
Elsevier Science Sa
Open Access Color
Green Open Access
No
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Publicly Funded
No
Abstract
Photocatalytic hydrogen evolution using by semiconductor materials have been studied effectively by converting solar energy into the chemical energy. Perovskite-based materials have been widely used as semiconductor catalysts for the photocatalytic hydrogen production. Herein, molybdenum sulfide photodeposited onto MTiO3 (M: Ba, Sr) perovskites (MTiO3/MoSx) have been investigated on the photocatalytic hydrogen evolution under solar light irradiation in the presence of triethanolamine (TEOA) and eosin Y (EY) as an electron donor and photosensitizer, respectively. Compared to pristine MTiO3, BaTiO3/MoSx and SrTiO3/MoSx show a remarkable improvement in the hydrogen production efficiency and stability. Photocatalytic hydrogen evolution activities found in the order of SrTiO3/MoSx > BaTiO3/MoSx > MoSx > SrTiO3 > BaTiO3. In addition, photocatalytic hydrogen activity of SrTiO3/Pt was evaluated for comparison with SrTiO3/MoSx under the same conditions and SrTiO3/MoSx produced higher hydrogen activity than SrTiO3/Pt due to the high active sites created by MoSx on the catalyst surface which is originated from Mo-S and S-S bonds.
Description
Keywords
Hydrogen evolution, Photocatalyst, Photodeposition, Perovskites, Titanates, Amorphous Mosx, H-2 Production, Nanoparticles, Cocatalyst, Eosin, Cds, Titanate, Srtio3, Fe, Ni
Turkish CoHE Thesis Center URL
Fields of Science
02 engineering and technology, 0210 nano-technology, 01 natural sciences, 0104 chemical sciences
Citation
WoS Q
Q2
Scopus Q
Q1

OpenCitations Citation Count
11
Source
Journal Of Photochemistry And Photobiology A-Chemistry
Volume
436
Issue
Start Page
114375
End Page
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Citations
CrossRef : 5
Scopus : 13
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Mendeley Readers : 7
SCOPUS™ Citations
13
checked on Feb 03, 2026
Web of Science™ Citations
12
checked on Feb 03, 2026
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1
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