Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/106884
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dc.contributorDepartment of Electrical and Electronic Engineering-
dc.creatorLi, Yen_US
dc.creatorZhou, Sen_US
dc.creatorXiong, Zen_US
dc.creatorQin, Men_US
dc.creatorLiu, Ken_US
dc.creatorCai, Gen_US
dc.creatorWang, Hen_US
dc.creatorZhao, Sen_US
dc.creatorLi, Gen_US
dc.creatorHsu, YJen_US
dc.creatorXu, Jen_US
dc.creatorLu, Xen_US
dc.date.accessioned2024-06-07T00:58:37Z-
dc.date.available2024-06-07T00:58:37Z-
dc.identifier.urihttp://hdl.handle.net/10397/106884-
dc.language.isoenen_US
dc.publisherAmerican Chemical Societyen_US
dc.rights© 2020 American Chemical Societyen_US
dc.rightsThis document is the Accepted Manuscript version of a Published Work that appeared in final form in ACS Applied Energy Materials, copyright © American Chemical Society after peer review and technical editing by the publisher. To access the final edited and published work see https://doi.org/10.1021/acsaem.0c02292.en_US
dc.subjectCharge transferen_US
dc.subjectHeterovalent dopingen_US
dc.subjectHybrid organic and perovskite solar cellsen_US
dc.subjectPerovskite quantum doten_US
dc.subjectSize modulationen_US
dc.titleSize modulation and heterovalent doping facilitated hybrid organic and perovskite quantum dot bulk heterojunction solar cellsen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage11359en_US
dc.identifier.epage11367en_US
dc.identifier.volume3en_US
dc.identifier.issue11en_US
dc.identifier.doi10.1021/acsaem.0c02292en_US
dcterms.abstractOrganic photovoltaics and halide perovskite solar cells are both solution-processable third-generation photovoltaic devices (PVs) attracting enormous research attention. In this study, we demonstrate a hybrid organic and perovskite PV device by mixing all-inorganic CsPbI3 quantum dots (QDs) into the conventional organic bulk heterojunction active layer of PBDB-T:IT-M. It is found that the charge transfer properties between QDs and organic donor/acceptor interfaces can be fine-tuned with the size modulation and the heterovalent bismuth (Bi) doping of perovskite QDs, leading to an increase in open-circuit voltage. In addition, the incorporation of perovskite QDs with different sizes could effectively modify the nanoscale bulk heterojunction morphology toward more efficient charge collection and thus a higher fill factor. The photocurrent of the devices can also be improved through Rayleigh scattering and light absorption of the QDs. As a result, a noticeable enhancement in device performance has been achieved by the PBDB-T:IT-M with 10 nm Bi-doped CsPbI3 QD device. This work provides one feasible route to fine-tune the energy level alignment and nanophase separation by integrating these two promising PV materials.-
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationACS applied energy materials, 23 Nov. 2020, v. 3, no. 11, p. 11359-11367en_US
dcterms.isPartOfACS applied energy materialsen_US
dcterms.issued2020-11-23-
dc.identifier.scopus2-s2.0-85095988991-
dc.identifier.eissn2574-0962en_US
dc.description.validate202405 bcch-
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberEIE-0122-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextCUHK Direct Granten_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS53155077-
dc.description.oaCategoryGreen (AAM)en_US
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