Benzochalcogenodiazole-Based Donor-Acceptor-Acceptor Molecular Donors for Organic Solar Cells
Four new molecules with a donor–acceptor–acceptor (D‐A‐A) configuration, in which 2,1,3‐benzoxadiazole or 2,1,3‐benzoselenodiazole were adopted as the central bridging acceptor, were synthesized as electron donors for small‐molecule organic solar cells. In conjunction with two previously reported 2,...
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Veröffentlicht in: | ChemSusChem 2014-02, Vol.7 (2), p.457-465 |
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description | Four new molecules with a donor–acceptor–acceptor (D‐A‐A) configuration, in which 2,1,3‐benzoxadiazole or 2,1,3‐benzoselenodiazole were adopted as the central bridging acceptor, were synthesized as electron donors for small‐molecule organic solar cells. In conjunction with two previously reported 2,1,3‐benzothiadiazole‐based compounds, the influences of the benzochalcogenodiazole acceptor unit and the ditolylarylamine donor moiety on the molecular structure, electrochemical behavior, and optical properties of the materials were investigated systematically to obtain a clear structure–property relationship. Vacuum‐deposited hybrid planar mixed‐heterojunction devices fabricated with the new donors and C70 as the acceptor showed power conversion efficiencies in the range of 2.9–4.3 % under 1 sun (100 mW cm−2) AM 1.5 G simulated solar illumination. The current density–voltage characteristics of solar cells at various light intensities were measured, which revealed a high bimolecular recombination.
Put a chalcogen in it: Four new molecules with a donor–acceptor–acceptor configuration in which 2,1,3‐benzoxadiazole or 2,1,3‐benzoselenodiazole are adopted as the central bridging acceptor are synthesized as electron donors for small‐molecule organic solar cells. |
doi_str_mv | 10.1002/cssc.201301090 |
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Put a chalcogen in it: Four new molecules with a donor–acceptor–acceptor configuration in which 2,1,3‐benzoxadiazole or 2,1,3‐benzoselenodiazole are adopted as the central bridging acceptor are synthesized as electron donors for small‐molecule organic solar cells.</description><identifier>ISSN: 1864-5631</identifier><identifier>EISSN: 1864-564X</identifier><identifier>DOI: 10.1002/cssc.201301090</identifier><identifier>PMID: 24488678</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>chalcogens ; Electric Power Supplies ; electrochemistry ; electron transfer ; Models, Molecular ; Molecular Conformation ; Nitriles - chemistry ; Oxadiazoles - chemistry ; photochemistry ; Photovoltaic cells ; Selenium - chemistry ; Solar energy ; structure-property relationships ; Sunlight</subject><ispartof>ChemSusChem, 2014-02, Vol.7 (2), p.457-465</ispartof><rights>Copyright © 2014 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><rights>Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.</rights><rights>Copyright © 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c5140-7d48d3ee290b4de483e23d88e5841e1247772ba174eeb2b5746090b52fc7b32d3</citedby><cites>FETCH-LOGICAL-c5140-7d48d3ee290b4de483e23d88e5841e1247772ba174eeb2b5746090b52fc7b32d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcssc.201301090$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcssc.201301090$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27915,27916,45565,45566</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24488678$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ting, Hao-Chun</creatorcontrib><creatorcontrib>Chen, Yi-Hong</creatorcontrib><creatorcontrib>Lin, Li-Yen</creatorcontrib><creatorcontrib>Chou, Shu-Hua</creatorcontrib><creatorcontrib>Liu, Yi-Hung</creatorcontrib><creatorcontrib>Lin, Hao-Wu</creatorcontrib><creatorcontrib>Wong, Ken-Tsung</creatorcontrib><title>Benzochalcogenodiazole-Based Donor-Acceptor-Acceptor Molecular Donors for Organic Solar Cells</title><title>ChemSusChem</title><addtitle>ChemSusChem</addtitle><description>Four new molecules with a donor–acceptor–acceptor (D‐A‐A) configuration, in which 2,1,3‐benzoxadiazole or 2,1,3‐benzoselenodiazole were adopted as the central bridging acceptor, were synthesized as electron donors for small‐molecule organic solar cells. In conjunction with two previously reported 2,1,3‐benzothiadiazole‐based compounds, the influences of the benzochalcogenodiazole acceptor unit and the ditolylarylamine donor moiety on the molecular structure, electrochemical behavior, and optical properties of the materials were investigated systematically to obtain a clear structure–property relationship. Vacuum‐deposited hybrid planar mixed‐heterojunction devices fabricated with the new donors and C70 as the acceptor showed power conversion efficiencies in the range of 2.9–4.3 % under 1 sun (100 mW cm−2) AM 1.5 G simulated solar illumination. The current density–voltage characteristics of solar cells at various light intensities were measured, which revealed a high bimolecular recombination.
Put a chalcogen in it: Four new molecules with a donor–acceptor–acceptor configuration in which 2,1,3‐benzoxadiazole or 2,1,3‐benzoselenodiazole are adopted as the central bridging acceptor are synthesized as electron donors for small‐molecule organic solar cells.</description><subject>chalcogens</subject><subject>Electric Power Supplies</subject><subject>electrochemistry</subject><subject>electron transfer</subject><subject>Models, Molecular</subject><subject>Molecular Conformation</subject><subject>Nitriles - chemistry</subject><subject>Oxadiazoles - chemistry</subject><subject>photochemistry</subject><subject>Photovoltaic cells</subject><subject>Selenium - chemistry</subject><subject>Solar energy</subject><subject>structure-property relationships</subject><subject>Sunlight</subject><issn>1864-5631</issn><issn>1864-564X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkM1P20AQxVcVqHy0V44oEhcuDvsx9q6PwYG0UiiHFNFLtVqvJ9Sp4w27sWjy13cj0whx6WlGM7_3NPMIOWN0yCjlVzYEO-SUCcpoTj-QY6YySNIMfhzse8GOyEkIC0ozmmfZR3LEAZTKpDomP6-x3Tr7yzTWPWHrqtpsXYPJtQlYDcaudT4ZWYur9ZtmcBcR2zXG90QYzOPw3j-ZtraDmdstCmya8Ikczk0T8PNrPSUPtzffiy_J9H7ytRhNE5syoImsQFUCkee0hApBCeSiUgpTBQwZByklLw2TgFjyMpUQH6FlyudWloJX4pRc9r4r7547DGu9rIONF5gWXRc0gxwETVmuInrxDl24zrfxuh0lQPIcaKSGPWW9C8HjXK98vTR-oxnVu-D1Lni9Dz4Kzl9tu3KJ1R7_l3QE8h54qRvc_MdOF7NZ8dY86bV1WOOfvdb43zqTQqb68dtEAwCbTNOxzsVfe4qdnA</recordid><startdate>201402</startdate><enddate>201402</enddate><creator>Ting, Hao-Chun</creator><creator>Chen, Yi-Hong</creator><creator>Lin, Li-Yen</creator><creator>Chou, Shu-Hua</creator><creator>Liu, Yi-Hung</creator><creator>Lin, Hao-Wu</creator><creator>Wong, Ken-Tsung</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><general>Wiley Subscription Services, Inc</general><scope>BSCLL</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201402</creationdate><title>Benzochalcogenodiazole-Based Donor-Acceptor-Acceptor Molecular Donors for Organic Solar Cells</title><author>Ting, Hao-Chun ; Chen, Yi-Hong ; Lin, Li-Yen ; Chou, Shu-Hua ; Liu, Yi-Hung ; Lin, Hao-Wu ; Wong, Ken-Tsung</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c5140-7d48d3ee290b4de483e23d88e5841e1247772ba174eeb2b5746090b52fc7b32d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>chalcogens</topic><topic>Electric Power Supplies</topic><topic>electrochemistry</topic><topic>electron transfer</topic><topic>Models, Molecular</topic><topic>Molecular Conformation</topic><topic>Nitriles - chemistry</topic><topic>Oxadiazoles - chemistry</topic><topic>photochemistry</topic><topic>Photovoltaic cells</topic><topic>Selenium - chemistry</topic><topic>Solar energy</topic><topic>structure-property relationships</topic><topic>Sunlight</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ting, Hao-Chun</creatorcontrib><creatorcontrib>Chen, Yi-Hong</creatorcontrib><creatorcontrib>Lin, Li-Yen</creatorcontrib><creatorcontrib>Chou, Shu-Hua</creatorcontrib><creatorcontrib>Liu, Yi-Hung</creatorcontrib><creatorcontrib>Lin, Hao-Wu</creatorcontrib><creatorcontrib>Wong, Ken-Tsung</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>ChemSusChem</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ting, Hao-Chun</au><au>Chen, Yi-Hong</au><au>Lin, Li-Yen</au><au>Chou, Shu-Hua</au><au>Liu, Yi-Hung</au><au>Lin, Hao-Wu</au><au>Wong, Ken-Tsung</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Benzochalcogenodiazole-Based Donor-Acceptor-Acceptor Molecular Donors for Organic Solar Cells</atitle><jtitle>ChemSusChem</jtitle><addtitle>ChemSusChem</addtitle><date>2014-02</date><risdate>2014</risdate><volume>7</volume><issue>2</issue><spage>457</spage><epage>465</epage><pages>457-465</pages><issn>1864-5631</issn><eissn>1864-564X</eissn><abstract>Four new molecules with a donor–acceptor–acceptor (D‐A‐A) configuration, in which 2,1,3‐benzoxadiazole or 2,1,3‐benzoselenodiazole were adopted as the central bridging acceptor, were synthesized as electron donors for small‐molecule organic solar cells. In conjunction with two previously reported 2,1,3‐benzothiadiazole‐based compounds, the influences of the benzochalcogenodiazole acceptor unit and the ditolylarylamine donor moiety on the molecular structure, electrochemical behavior, and optical properties of the materials were investigated systematically to obtain a clear structure–property relationship. Vacuum‐deposited hybrid planar mixed‐heterojunction devices fabricated with the new donors and C70 as the acceptor showed power conversion efficiencies in the range of 2.9–4.3 % under 1 sun (100 mW cm−2) AM 1.5 G simulated solar illumination. The current density–voltage characteristics of solar cells at various light intensities were measured, which revealed a high bimolecular recombination.
Put a chalcogen in it: Four new molecules with a donor–acceptor–acceptor configuration in which 2,1,3‐benzoxadiazole or 2,1,3‐benzoselenodiazole are adopted as the central bridging acceptor are synthesized as electron donors for small‐molecule organic solar cells.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><pmid>24488678</pmid><doi>10.1002/cssc.201301090</doi><tpages>9</tpages></addata></record> |
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subjects | chalcogens Electric Power Supplies electrochemistry electron transfer Models, Molecular Molecular Conformation Nitriles - chemistry Oxadiazoles - chemistry photochemistry Photovoltaic cells Selenium - chemistry Solar energy structure-property relationships Sunlight |
title | Benzochalcogenodiazole-Based Donor-Acceptor-Acceptor Molecular Donors for Organic Solar Cells |
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