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Bioluminescence-induced photocatalysis on semiconducting oxide nanosheetsopen access

Authors
Kamada, KaiSano, HideakiNakagoe, OsamuTanabe, ShujiOh, Jae-Min
Issue Date
Jan-2024
Publisher
Taylor & Francis
Keywords
Photocatalyst; bioluminescence; oxide nanosheet; enzyme
Citation
Journal of Asian Ceramic Societies, v.12, no.1, pp 86 - 92
Pages
7
Indexed
SCIE
SCOPUS
Journal Title
Journal of Asian Ceramic Societies
Volume
12
Number
1
Start Page
86
End Page
92
URI
https://scholarworks.dongguk.edu/handle/sw.dongguk/26259
DOI
10.1080/21870764.2023.2301239
ISSN
2187-0764
2187-0764
Abstract
A novel semiconductor photocatalytic reaction system employing a photo-emitting enzyme as an internal light source is pro-posed in the present study. The system completely overturns common sense that conventional photocatalytic reactions must require irradiation from an external light source. A horseradish peroxidase (HRP) catalyzing oxidative bioluminescence reaction of luminol in the presence of H2O2 and manganate nanosheets (MNSs) with a narrow bandgap were utilized for an internal light source and semiconductor photocatalysts, respectively, and both of them coexisted in a same reactant solution. In other words, nano-sized light sources were highly dispersed in the solution, resulting in photo-excitation of MNSs over the entire solution. Photo-activated MNSs simultaneously caused oxidation and reduction, where platinum hexachloride anions (PtCl62-) were utilized as a model substance to be reacted photocatalytically. According to X-ray absorption near edge spectroscopy (XANES) of MNSs after the photocatalytic reaction, the anions were mainly transformed into solid phases of PtO2 and/or Pt(OH)(4) by reacting with holes in MNSs. In contrast, a control experiment without HRP, i.e. a dark experiment, did not leave any evidence for photocatalytic reaction of PtCl62-. The detailed mechanism and the advantages/disadvantages of the proposed unique system are explained.
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