Please use this identifier to cite or link to this item: https://doi.org/10.1016/j.solmat.2010.07.017
DC FieldValue
dc.titleOrganic molecules based on dithienyl-2,1,3-benzothiadiazole as new donor materials for solution-processed organic photovoltaic cells
dc.contributor.authorWu, Z.
dc.contributor.authorFan, B.
dc.contributor.authorXue, F.
dc.contributor.authorAdachi, C.
dc.contributor.authorOuyang, J.
dc.date.accessioned2014-10-07T09:52:48Z
dc.date.available2014-10-07T09:52:48Z
dc.date.issued2010-12
dc.identifier.citationWu, Z., Fan, B., Xue, F., Adachi, C., Ouyang, J. (2010-12). Organic molecules based on dithienyl-2,1,3-benzothiadiazole as new donor materials for solution-processed organic photovoltaic cells. Solar Energy Materials and Solar Cells 94 (12) : 2230-2237. ScholarBank@NUS Repository. https://doi.org/10.1016/j.solmat.2010.07.017
dc.identifier.issn09270248
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/86617
dc.description.abstractPolymers based on dithienyl-2,1,3-benzothiadiazole (TBT) have received strong attention as the donor materials of polymer photovoltaic cells (PVs), since they can have a low band gap. But soluble small organic molecules based on TBT have been rarely studied. This paper reports the synthesis of two small organic molecules based on TBT and their application as the donor materials of solution-processed bulk heterojunction organic photovoltaic cells (OPVs). These compounds were soluble in common organic solvents, such as chloroform, chlorobenzene and tetrahydrofuran. They have band gaps comparable to poly(3-hexylthiophene) (P3HT) and lower HOMO and LUMO (HOMO: highest occupied molecular orbital, LUMO: lowest unoccupied molecular orbital) levels than P3HT. These molecules and [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) were used as the donors and acceptor to fabricate bulk heterojunction OPVs through solution processing. After optimization of the experimental conditions, power conversion efficiency (PCE) of 0.66% was achieved on the solution-processed OPVs under AM 1.5G, 100 mW cm-2 illumination. © 2010 Elsevier B.V. All rights reserved.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1016/j.solmat.2010.07.017
dc.sourceScopus
dc.subjectBulk heterojunction
dc.subjectDithienyl-2,1,3-benzothiadiazole (TBT)
dc.subjectOrganic solar cells
dc.subjectSolution processing
dc.subjectSonogashira coupling reaction
dc.typeArticle
dc.contributor.departmentMATERIALS SCIENCE AND ENGINEERING
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1016/j.solmat.2010.07.017
dc.description.sourcetitleSolar Energy Materials and Solar Cells
dc.description.volume94
dc.description.issue12
dc.description.page2230-2237
dc.description.codenSEMCE
dc.identifier.isiut000283959500041
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