343 0

Full metadata record

DC FieldValueLanguage
dc.contributor.author이선영-
dc.date.accessioned2018-04-19T01:29:22Z-
dc.date.available2018-04-19T01:29:22Z-
dc.date.issued2016-09-
dc.identifier.citationMATERIALS CHEMISTRY AND PHYSICS, v. 181, Page. 241-247en_US
dc.identifier.issn0254-0584-
dc.identifier.issn1879-3312-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0254058416304692-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/69317-
dc.description.abstractFerric oxide powder in the alpha phase (alpha-Fe2O3) was deposited on an aluminum oxide (Al2O3) substrate by a nanoparticle deposition system using the dry deposition method. X-ray diffraction (XRD) images confirmed that the phase of the deposited alpha-Fe2O3 did not change. The deposited alpha-Fe2O3 was characterized in terms of its microstructure using scanning electron microscopy (SEM). A porous network microstructure formed when small agglomerates of Fe2O3 (SAF) were deposited. The deposition and formation mechanism of the microstructure were investigated using SEM and three-dimensional (3D) profile analysis. First, a dense coating layer formed when the film was thinner than the particle size. After that, as the film thickness increased to over 5 mu m, the porous network structure formed by excavating the surface of the coating layer as it was bombarded by particles. Rhodamine B (RhB) was degraded after 6 h of exposure to the Fe2O3 coating layer with SAF, which has good photocatalytic activity and a high porous network structure. The kinetic rate constants of the SAF and large agglomerates of Fe2O3 (LAF) were calculated to be 0.197(h(-1)) and 0.128(h(-1)), respectively, based on the absorbance results. Using linear sweep voltammetry, we confirmed that the photoelectric effect occurred in the coating layer by measuring the resulting current under illuminated and dark conditions. (C) 2016 Elsevier B.V. All rights reserved.en_US
dc.description.sponsorshipThis work was supported by the Energy Efficiency of Resources Core Technology Program (No.20142020103730) of the Korea Institute of Energy Technology Evaluation and Planning, granted financial resource from the Ministry of Trade, Industry & Energy, Republic of Korea. This research was also supported by the Basic Science Research Program of the National Research Foundation of Korea, funded by the Ministry of Education, Science and Technology (No.2013R1A1A2074605) and was supported by the Human Resources Development program(No. 20154030200680) of the Korea Institute of Energy Technology Evaluation and Planning(KETEP) grant funded by the Korea government Ministry of Trade, Industry and Energy.en_US
dc.language.isoen_USen_US
dc.publisherELSEVIER SCIENCE SAen_US
dc.subjectCeramicen_US
dc.subjectCoatingen_US
dc.subjectPorous materialsen_US
dc.subjectElectrochemical propertiesen_US
dc.subjectHEMATITE PHOTOANODEen_US
dc.subjectTHIN-FILMSen_US
dc.subjectWATERen_US
dc.subjectALPHA-FE2O3en_US
dc.subjectSYSTEMen_US
dc.subjectMETALen_US
dc.subjectTIO2en_US
dc.titlePhotocatalytic evaluation of self-assembled porous network structure of ferric oxide film fabricated by dry deposition processen_US
dc.typeArticleen_US
dc.relation.volume181-
dc.identifier.doi10.1016/j.matchemphys.2016.06.055-
dc.relation.page241-247-
dc.relation.journalMATERIALS CHEMISTRY AND PHYSICS-
dc.contributor.googleauthorPark, Y-
dc.contributor.googleauthorKim, H-
dc.contributor.googleauthorLee, GY-
dc.contributor.googleauthorPawar, RC-
dc.contributor.googleauthorLee, JS-
dc.contributor.googleauthorLee, CS-
dc.relation.code2016001297-
dc.sector.campusE-
dc.sector.daehakCOLLEGE OF ENGINEERING SCIENCES[E]-
dc.sector.departmentDEPARTMENT OF MATERIALS SCIENCE AND CHEMICAL ENGINEERING-
dc.identifier.pidsunyonglee-
Appears in Collections:
COLLEGE OF ENGINEERING SCIENCES[E](공학대학) > MATERIALS SCIENCE AND CHEMICAL ENGINEERING(재료화학공학과) > Articles
Files in This Item:
There are no files associated with this item.
Export
RIS (EndNote)
XLS (Excel)
XML


qrcode

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.

BROWSE