128 0

Full metadata record

DC FieldValueLanguage
dc.contributor.author지텐드라 쿠마 싱-
dc.date.accessioned2022-08-11T01:42:31Z-
dc.date.available2022-08-11T01:42:31Z-
dc.date.issued2021-01-
dc.identifier.citationELECTROCHIMICA ACTA, v. 372, Page. 1-11en_US
dc.identifier.issn0013-4686-
dc.identifier.urihttps://www.sciencedirect.com/science/article/pii/S0013468621000438-
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/172302-
dc.description.abstractBismuth molybdates are considered the essential photocatalysts due to their mesoporous structure, low energy gap, suitable ion conductions, acousto-optics, photo-conduction, and sensing properties. The present report describes a cost-effective route for developing stable and efficient photocatalysts for optical to chemical energy conversion and environmental purification. In this work, we have developed nanostructured mixed bismuth molybdates with different thicknesses in the presence of TX-100 as the surfactant through drop-cast route taking bismuth nitrate and ammonium molybdate as the precursors. Final products were subsequently dried and annealed in air at 600 degrees C for 3 h. The semiconductors' photoelectrochemical performance was measured under periodic illumination in the presence of Na2SO4 (0.1 M) solution and (0.1 M) Na2SO3 with 0.1 M Na2SO4 for water and sacrificial oxidation, respectively. These materials exhibit noticeable photocatalytic activity even after successive runs, indicating stable behavior. The materials are composed of Bi2Mo2O9-Bi2MoO6 heterostructures and the film with optimized thickness yields a photocurrent of 220 mu A/cm(2) at 1.3 V. This value is exceptionally higher in magnitude than the literature reports employing conventionally prepared bismuth molybdates (1.8 mu A/cm(2)). Electrochemical impedance and photocurrent action spectra support a noticeable photon to current conversion efficiencies of the materials under illumination. (C) 2021 Elsevier Ltd. All rights reserved.en_US
dc.description.sponsorshipSB gratefully acknowledges the Institute Fellowship of IIEST, Shibpur. The present work was financially supported by CSIR (File no. 01(2876)/17/EMR-II, 02.05.2017) to the Department of Chem- istry, IIESTS. SG sincerely acknowledge Department of Science & Technology, Government of India for financial support (vide ref- erence no. SR/WOS-A/CS-10/2018, dated 02.01.2019) under DST- Women Scientist Scheme (DST-WOS-A). The authors also gratefully acknowledge the basic science research program through the Na- tional Research Foundation (NRF) of Korea funded by the Ministry of Science, ICT and Future Planning (No. 2015R1A5A1037548).en_US
dc.language.isoenen_US
dc.publisherPERGAMON-ELSEVIER SCIENCE LTDen_US
dc.subjectPhotoelectrochemical water oxidationen_US
dc.subjectHeterojunction bismuth molybdatesen_US
dc.subjectFavorable electron mobilityen_US
dc.subjectElectrochemical action spectraen_US
dc.subjectStable photocatalysten_US
dc.titleOptimization of semiconductor-electrolyte interfacial phenomena for stable and efficient photoelectrochemical water oxidation behavior of Bi2Mo2O9-Bi2MoO6 heterojunctionen_US
dc.typeArticleen_US
dc.relation.volume372-
dc.identifier.doi10.1016/j.electacta.2021.137754-
dc.relation.page1-11-
dc.relation.journalELECTROCHIMICA ACTA-
dc.contributor.googleauthorBaduri, Swarnendu-
dc.contributor.googleauthorSariket, Debasis-
dc.contributor.googleauthorRay, Debasish-
dc.contributor.googleauthorGhosh, Sangeeta-
dc.contributor.googleauthorSingh, Jitendra Kumar-
dc.contributor.googleauthorLee, Han-Seung-
dc.contributor.googleauthorBhattacharya, Chinmoy-
dc.relation.code2021004730-
dc.sector.campusE-
dc.sector.daehakOFFICE OF ACADEMIC AFFAIRS[E]-
dc.sector.departmentCENTER FOR CREATIVE CONVERGENCE EDUCATION-
dc.identifier.pidjk200386-
Appears in Collections:
OFFICE OF ACADEMIC AFFAIRS[E](교무처) > Center for Creative Convergence Education(창의융합교육원) > 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