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Low temperature fabrication of Fe2O3 nanorod film coated with ultra-thin g-C3N4 for a direct z-scheme exerting photocatalytic activitiesopen access

Authors
Kang, SuheeJang, JoonyoungPawar, Rajendra C.Ahn, Sung-HoonLee, Sunyong Caroline
Issue Date
Oct-2018
Publisher
Royal Society of Chemistry
Keywords
VISIBLE-LIGHT IRRADIATION; ENHANCED PHOTOELECTROCHEMICAL PERFORMANCE; HYDROGEN-PRODUCTION; FACILE SYNTHESIS; HYBRID PHOTOCATALYSTS; WATER; ALPHA-FE2O3; EFFICIENT; DEGRADATION; TIO2
Citation
RSC Advances, v.8, no.59, pp.33600 - 33613
Indexed
SCIE
SCOPUS
Journal Title
RSC Advances
Volume
8
Number
59
Start Page
33600
End Page
33613
URI
https://scholarworks.bwise.kr/erica/handle/2021.sw.erica/8029
DOI
10.1039/c8ra04499f
ISSN
2046-2069
Abstract
We engineered high aspect ratio Fe2O3 nanorods (with an aspect ratio of 17 : 1) coated with g-C3N4 using a sequential solvothermal method at very low temperature followed by a thermal evaporation method. Here, the high aspect ratio Fe2O3 nanorods were directly grown onto the FTO substrate under relatively low pressure conditions. The g-C3N4 was coated onto a uniform Fe2O3 nanorod film as the heterostructure, exhibiting rational band conduction and a valence band that engaged in surface photoredox reactions by a direct z-scheme mechanism. The heterostructures, particularly 0.75g-C3N4@Fe2O3 nanorods, exhibited outstanding photocatalytic activities compared to those of bare Fe2O3 nanorods. In terms of 4-nitrophenol degradation, 0.75g-C3N4@Fe2O3 nanorods degraded all of the organic pollutant within 6 h under visible irradiation at a kinetic constant of 12.71 x 10(-3) min(-1), about 15-fold more rapidly than bare Fe2O3. Further, the hydrogen evolution rate was 37.06 mmol h(-1) g(-1), 39-fold higher than that of bare Fe2O3. We suggest that electron and hole pairs are efficiently separated in g-C3N4@Fe2O3 nanorods, thus accelerating surface photoreaction via a direct z-scheme under visible illumination.
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ERICA 공학대학 (DEPARTMENT OF MATERIALS SCIENCE AND CHEMICAL ENGINEERING)
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