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dc.contributor.author장재영-
dc.date.accessioned2022-10-27T02:18:27Z-
dc.date.available2022-10-27T02:18:27Z-
dc.date.issued2021-02-
dc.identifier.citationACS APPLIED MATERIALS & INTERFACES, v. 13, no. 5, page. 6208-6218en_US
dc.identifier.issn1944-8244; 1944-8252en_US
dc.identifier.urihttps://pubs.acs.org/doi/10.1021/acsami.0c19352en_US
dc.identifier.urihttps://repository.hanyang.ac.kr/handle/20.500.11754/175868-
dc.description.abstractMetal oxide semiconductor/chalcogenide quantum dot (QD) heterostructured photoanodes show photocurrent densities ˃30 mA/cm(2) with ZnO, approaching the theoretical limits in photovoltaic (PV) cells. However, comparative performance has not been achieved with TiO2. Here, we applied a TiO2(B) surface passivation layer (SPL) on TiO2/QD (PbS and CdS) and achieved a photocurrent density of 34.59 mA/cm(2) under AM 1.5G illumination for PV cells, the highest recorded to date. The SPL improves electron conductivity by increasing the density of surface states, facilitating multiple trapping/detrapping transport, and increasing the coordination number of TiO2 nanoparticles. This, along with impeded electron recombination, led to enhanced collection efficiency, which is a major factor for performance. Furthermore, SPL-treated TiO2/QD photoanodes were successfully exploited in photo-electrochemical water splitting cells, showing an excellent photocurrent density of 14.43 mA/cm(2) at 0.82 V versus the Reversible Hydrogen Electrode (RHE). These results suggest a new promising strategy for the development of high-performance photoelectrochemical devices.en_US
dc.description.sponsorshipThis work was supported by the Korea Center for Artificial Photosynthesis (KCAP) of Sogang University, funded by the Ministry of Science, ICT, and Future Planning (MSIP) through a National Research Foundation of Korea (Grant no. 2009-0093883). This work also was supported by a grant from the Basic Science Research Program through the National Research Foundation (NRF) of Korea funded by the Ministry of Science and ICT (NRF-2019R1A2C1003429) and by the Ministry of Education (NRF-2018R1A6A1A03024231). Also, this work was supported by the Ministerio de Ciencia, Innovacio'n y Universidades of Spain through the project ENE2017-85087-C3-1-R. Therefore, the authors acknowledge and thank the Korean and Spanish governments for technical and financial support. S. D. G.en_US
dc.language.isoenen_US
dc.publisherAMER CHEMICAL SOCen_US
dc.subjectTiO2/QD; photoanode; photoelectrochemical cells; surface passivation layer; surface state; charge collection; photocurrent densityen_US
dc.titleInterfacial Engineering at Quantum Dot-Sensitized TiO2 Photoelectrodes for Ultrahigh Photocurrent Generationen_US
dc.typeArticleen_US
dc.relation.no5-
dc.relation.volume13-
dc.identifier.doi10.1021/acsami.0c19352en_US
dc.relation.page6208-6218-
dc.relation.journalACS APPLIED MATERIALS & INTERFACES-
dc.contributor.googleauthorKim, Tea-Yon-
dc.contributor.googleauthorKim, Byung Su-
dc.contributor.googleauthorOh, Jong Gyu-
dc.contributor.googleauthorPark, Seul Chan-
dc.contributor.googleauthorJang, Jaeyoung-
dc.contributor.googleauthorHamann, Thomas W.-
dc.contributor.googleauthorKang, Young Soo-
dc.contributor.googleauthorBang, Jin Ho-
dc.contributor.googleauthorGimenez, Sixto-
dc.contributor.googleauthorKang, Yong Soo-
dc.relation.code2021009211-
dc.sector.campusS-
dc.sector.daehakCOLLEGE OF ENGINEERING[S]-
dc.sector.departmentDEPARTMENT OF ENERGY ENGINEERING-
dc.identifier.pidjyjang15-
dc.identifier.orcidhttps://orcid.org/0000-0002-5548-8563-
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COLLEGE OF ENGINEERING[S](공과대학) > ENERGY ENGINEERING(에너지공학과) > Articles
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