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Highly Porous SnO2/TiO2 Heterojunction Thin-Film Photocatalyst Using Gas-Flow Thermal Evaporation and Atomic Layer Depositionopen access

Authors
Kim, SungjinChang, Hyeon-KyungKim, Kwang BokKim, Hyun-JongLee, Ho-NyunPark, Tae JooPark, Young Min
Issue Date
Oct-2021
Publisher
Multidisciplinary Digital Publishing Institute (MDPI)
Keywords
photocatalyst; heterojunction; thermal evaporation deposition; atomic layer deposition; porous tin dioxide; titanium dioxide; core-shell structure
Citation
Catalysts, v.11, no.10, pp 1 - 11
Pages
11
Indexed
SCIE
SCOPUS
Journal Title
Catalysts
Volume
11
Number
10
Start Page
1
End Page
11
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/108163
DOI
10.3390/catal11101144
ISSN
2073-4344
2073-4344
Abstract
Highly porous heterojunction films of SnO2/TiO2 were prepared using gas-flow thermal evaporation followed by atomic layer deposition (ALD). Highly porous SnO2 was fabricated by introducing an inert gas, Ar, during thermal evaporation. To build heterogeneous structures, the TiO2 layers were conformally deposited on porous SnO2 with a range of 10 to 100 cycles by means of ALD. The photocatalytic properties for different TiO2 thicknesses on the porous SnO2 were compared using the degradation of methylene blue (MB) under UV irradiation. The comparisons showed that the SnO2/TiO2-50 heterostructures had the highest photocatalytic efficiency. It removed 99% of the MB concentration, and the decomposition rate constant (K) was 0.013 min(-1), which was approximately ten times that of the porous SnO2. On the other hand, SnO2/TiO2-100 exhibited a lower photocatalytic efficiency despite having a TiO2 layer thicker than SnO2/TiO2-50. After 100 cycles of TiO2 ALD deposition, the structure was transferred from the heterojunction to the core-sell structure covered with TiO2 on the porous SnO2, which was confirmed by TEM analysis. Since the electrons photogenerated by light irradiation were separated into SnO2 and produced reactive oxygen, O-2(-), the heterojunction structure, in which SnO2 was exposed to the surface, contributed to the high performance of the photocatalyst.</p>
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ERICA 공학대학 (DEPARTMENT OF MATERIALS SCIENCE AND CHEMICAL ENGINEERING)
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