453 0

Full metadata record

DC FieldValueLanguage
dc.contributor.author이선영-
dc.date.accessioned2018-12-19T07:25:11Z-
dc.date.available2018-12-19T07:25:11Z-
dc.date.issued2018-01-
dc.identifier.citationMATERIALS CHEMISTRY AND PHYSICS, v. 203, Page. 118-124en_US
dc.identifier.issn0254-0584-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0254058417307666-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/80953-
dc.description.abstractAntimony-doped tin oxide (ATO), titanium dioxide (TiO2) and ATO/TiO2 mixtures (30:70, 50:50, 70:30 vol%) powders were deposited using a nanoparticle deposition system (NPDS). X-ray diffraction (XRD) data and field-emission scanning electron microscope (FE-SEM) images confirmed that the phases and morphologies of the deposited ATO and TiO2 were similar to those of their pristine structures. Photoelectrochemical (PEC) measurements showed the highest photocurrent of 1.5 mA for the 50:50 vol% ATO/TiO2 film, which compared with 1.2 mA for the other (30:70 and 70:30 vol% ATO/TiO2) hybrid samples, and 0.35 and 0.04 mA for pure TiO2 and ATO, respectively. Methylene blue (MB) dye was degraded in the presence of the 50:50 vol% ATO/TiO2 film, which had the best photocatalytic activity after 7 h of ultraviolet (UV) irradiation. The kinetic rate constant of this film was 0.15 h−1, which was double that of the TiO2 film (0.06 h−1). The photoluminescence intensity of the 50:50 vol% ATO/TiO2 film was low over a wide range of wavelengths, which indicated that its recombination rate was less than that of the ATO and TiO2 films. Finally, the recycle results demonstrated that the 50:50 vol% ATO/TiO2 film was stable to photodegradation for up to six cycles. These heterojunction films containing ATO and TiO2 thus had better photocatalytic properties than the pure TiO2 and ATO films due to the reduction in recombination. Our facile method of preparing heterojunction films by a dry deposition method provided films with good photocatalytic properties.en_US
dc.description.sponsorshipThis work was supported by Nano-material Technology Development Program through the National Research Foundation of Korea (NRF) funded by the ministry of Science, ICT and Future Planning (2009-0082580). This work was also supported by the National Research Foundation of Korea (NRF) grant funded by the Korea government (Ministry of education) (No. NPF-2016R1D1A1A02936936) and by the Industrial Technology Innovation Program of the Korea Evaluation Institute of Industrial Technology (KEIT) granted financial resource from the Ministry of Trade, Industry & Energy, Republic of Korea (No. 10062510).en_US
dc.language.isoen_USen_US
dc.publisherELSEVIER SCIENCE SAen_US
dc.subjectPhotocatalysisen_US
dc.subjectTiO2en_US
dc.subjectATOen_US
dc.subjectHeterojunctionen_US
dc.subjectNanoparticle depositionen_US
dc.subjectVISIBLE-LIGHT IRRADIATIONen_US
dc.subjectWATER OXIDATIONen_US
dc.subjectCOLD SPRAYen_US
dc.subjectZNOen_US
dc.subjectDECOMPOSITIONen_US
dc.subjectPHOTOANODESen_US
dc.subjectPERFORMANCEen_US
dc.subjectALPHA-FE2O3en_US
dc.subjectG-C3N4en_US
dc.subjectOXIDEen_US
dc.titlePhotocatalytic evaluation of ATO/TiO2 heterojunction films fabricated by a nanoparticle deposition systemen_US
dc.typeArticleen_US
dc.relation.volume203-
dc.identifier.doi10.1016/j.matchemphys.2017.09.065-
dc.relation.page118-124-
dc.relation.journalMATERIALS CHEMISTRY AND PHYSICS-
dc.contributor.googleauthorPark, Yunchan-
dc.contributor.googleauthorKim, Hyungsub-
dc.contributor.googleauthorPawar, Rajendra C.-
dc.contributor.googleauthorKang, Suhee-
dc.contributor.googleauthorLee, Caroline Sunyong-
dc.relation.code2018001257-
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