Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/100290
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dc.contributorDepartment of Applied Physicsen_US
dc.creatorLiu, Sen_US
dc.creatorLi, Cen_US
dc.creatorXu, Xen_US
dc.creatorYou, Pen_US
dc.creatorWang, Nen_US
dc.creatorWang, Jen_US
dc.creatorMiao, Qen_US
dc.creatorYan, Fen_US
dc.date.accessioned2023-08-08T01:54:40Z-
dc.date.available2023-08-08T01:54:40Z-
dc.identifier.issn2050-7488en_US
dc.identifier.urihttp://hdl.handle.net/10397/100290-
dc.language.isoenen_US
dc.publisherRoyal Society of Chemistryen_US
dc.rightsThis journal is © The Royal Society of Chemistry 2019en_US
dc.rightsThe following publication Liu, S., Li, C., Xu, X., You, P., Wang, N., Wang, J., ... & Yan, F. (2019). Efficiency enhancement of organic photovoltaics by introducing high-mobility curved small-molecule semiconductors as additives. Journal of Materials Chemistry A, 7(20), 12740-12750 is available at https://doi.org/10.1039/c9ta02636c.en_US
dc.titleEfficiency enhancement of organic photovoltaics by introducing high-mobility curved small-molecule semiconductors as additivesen_US
dc.typeJournal/Magazine Articleen_US
dc.identifier.spage12740en_US
dc.identifier.epage12750en_US
dc.identifier.volume7en_US
dc.identifier.issue20en_US
dc.identifier.doi10.1039/c9ta02636cen_US
dcterms.abstractOwing to their unique molecular geometry and packing modes in the solid state, curved organic semiconductor molecules such as hexabenzoperylenes and dibenzo[a,m]rubicene exhibit high hole mobilities of ∼1 cm2 V-1 s-1, which are much higher than the hole mobilities of the active layers in organic photovoltaics (OPVs). The efficiencies of OPVs based on a fullerene acceptor are relatively improved by over 20% by introducing high-mobility curved p-type organic semiconductors into the active layers as additives in only a few weight percentage. This can be attributed to the increased hole mobilities in the devices. In comparison, the significant efficiency enhancement cannot be observed when high-mobility planar molecules are introduced into the active layers. In view of the curved p-type semiconductors being more compatible with a fullerene acceptor in their molecular shape than a planar one, we consider that the intimate interaction between the curved molecule and the fullerene acceptor can enhance exciton dissociation and hole transfer and thus boost the power conversion efficiencies of the devices.en_US
dcterms.accessRightsopen accessen_US
dcterms.bibliographicCitationJournal of materials chemistry A, 28 May 2019, v. 7, no. 20, p. 12740-12750en_US
dcterms.isPartOfJournal of materials chemistry Aen_US
dcterms.issued2019-05-28-
dc.identifier.scopus2-s2.0-85065907883-
dc.identifier.eissn2050-7496en_US
dc.description.validate202308 bcvcen_US
dc.description.oaAccepted Manuscripten_US
dc.identifier.FolderNumberAP-0337-
dc.description.fundingSourceRGCen_US
dc.description.fundingSourceOthersen_US
dc.description.fundingTextThe Hong Kong Polytechnic Universityen_US
dc.description.pubStatusPublisheden_US
dc.identifier.OPUS25769020-
dc.description.oaCategoryGreen (AAM)en_US
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