Microphase-Separated Donor-Acceptor Diblock Copolymers: Influence of HOMO Energy Levels and Morphology on Polymer Solar Cells

The synthesis of novel semiconducting donor–acceptor (D–A) diblock copolymers by means of nitroxide‐mediated polymerization (NMP) is reported. The copolymers contain functional moieties for hole transport, electron transport, and light absorption. The first block, representing the donor, is made up...

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Veröffentlicht in:Advanced functional materials 2007-06, Vol.17 (9), p.1493-1500
Hauptverfasser: Sommer, M., Lindner, S. M., Thelakkat, M.
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Lindner, S. M.
Thelakkat, M.
description The synthesis of novel semiconducting donor–acceptor (D–A) diblock copolymers by means of nitroxide‐mediated polymerization (NMP) is reported. The copolymers contain functional moieties for hole transport, electron transport, and light absorption. The first block, representing the donor, is made up of either substituted triphenylamines (poly(bis(4‐methoxyphenyl)‐4′‐vinylphenylamine), PvDMTPA) or substituted tetraphenylbenzidines (poly(N,N′‐bis(4‐methoxyphenyl)‐N‐phenyl‐N′‐4‐vinylphenyl‐(1,1′‐biphenyl)‐4,4′‐diamine), PvDMTPD). The second block consists of perylene diimide side groups attached to a polyacrylate backbone (PPerAcr) via a flexible spacer. This block is responsible for absorption in the visible range and for electron‐transport properties. The electrochemical properties of these fully functionalized diblock copolymers, PvDMTPA‐b‐PPerAcr and PvDMTPD‐b‐PPerAcr, are investigated by cyclic voltammetry (CV), and their morphology is investigated by transmission electron microscopy (TEM). All diblock copolymers exhibit microphase‐separated domains in the form of either wire‐ or wormlike structures made of perylene diimide embedded in a hole‐conductor matrix. In single‐active‐layer organic solar cells, PvDMTPD‐b‐PPerAcr reveals a fourfold improvement in power conversion efficiency (η = 0.26 %, short‐circuit current (ISC) 1.21 mA cm–2), and PvDMTPA‐b‐PPerAcr a fivefold increased efficiency (η = 0.32 %, ISC = 1.14 mA cm–2) compared with its unsubstituted analogue PvTPA‐b‐PPerAcr (η = 0.065 %, ISC = 0.23 mA cm–2). A series of novel semiconducting donor–acceptor block copolymers that contain substituted triphenylamines as donors and perylene diimide as the acceptor (see figure) are synthesized by means of nitroxide‐mediated polymerization, and the influence of morphology and the highest occupied molecular orbital (HOMO) level of the donor on block‐copolymer solar‐cell characteristics is studied.
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All diblock copolymers exhibit microphase‐separated domains in the form of either wire‐ or wormlike structures made of perylene diimide embedded in a hole‐conductor matrix. In single‐active‐layer organic solar cells, PvDMTPD‐b‐PPerAcr reveals a fourfold improvement in power conversion efficiency (η = 0.26 %, short‐circuit current (ISC) 1.21 mA cm–2), and PvDMTPA‐b‐PPerAcr a fivefold increased efficiency (η = 0.32 %, ISC = 1.14 mA cm–2) compared with its unsubstituted analogue PvTPA‐b‐PPerAcr (η = 0.065 %, ISC = 0.23 mA cm–2). A series of novel semiconducting donor–acceptor block copolymers that contain substituted triphenylamines as donors and perylene diimide as the acceptor (see figure) are synthesized by means of nitroxide‐mediated polymerization, and the influence of morphology and the highest occupied molecular orbital (HOMO) level of the donor on block‐copolymer solar‐cell characteristics is studied.</description><identifier>ISSN: 1616-301X</identifier><identifier>EISSN: 1616-3028</identifier><identifier>DOI: 10.1002/adfm.200600634</identifier><language>eng</language><publisher>Weinheim: WILEY-VCH Verlag</publisher><subject>Copolymers ; Semiconductors ; Solar cells ; Structure-property relationships</subject><ispartof>Advanced functional materials, 2007-06, Vol.17 (9), p.1493-1500</ispartof><rights>Copyright © 2007 WILEY‐VCH Verlag GmbH &amp; Co. 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Funct. Mater</addtitle><description>The synthesis of novel semiconducting donor–acceptor (D–A) diblock copolymers by means of nitroxide‐mediated polymerization (NMP) is reported. The copolymers contain functional moieties for hole transport, electron transport, and light absorption. The first block, representing the donor, is made up of either substituted triphenylamines (poly(bis(4‐methoxyphenyl)‐4′‐vinylphenylamine), PvDMTPA) or substituted tetraphenylbenzidines (poly(N,N′‐bis(4‐methoxyphenyl)‐N‐phenyl‐N′‐4‐vinylphenyl‐(1,1′‐biphenyl)‐4,4′‐diamine), PvDMTPD). The second block consists of perylene diimide side groups attached to a polyacrylate backbone (PPerAcr) via a flexible spacer. This block is responsible for absorption in the visible range and for electron‐transport properties. The electrochemical properties of these fully functionalized diblock copolymers, PvDMTPA‐b‐PPerAcr and PvDMTPD‐b‐PPerAcr, are investigated by cyclic voltammetry (CV), and their morphology is investigated by transmission electron microscopy (TEM). All diblock copolymers exhibit microphase‐separated domains in the form of either wire‐ or wormlike structures made of perylene diimide embedded in a hole‐conductor matrix. In single‐active‐layer organic solar cells, PvDMTPD‐b‐PPerAcr reveals a fourfold improvement in power conversion efficiency (η = 0.26 %, short‐circuit current (ISC) 1.21 mA cm–2), and PvDMTPA‐b‐PPerAcr a fivefold increased efficiency (η = 0.32 %, ISC = 1.14 mA cm–2) compared with its unsubstituted analogue PvTPA‐b‐PPerAcr (η = 0.065 %, ISC = 0.23 mA cm–2). A series of novel semiconducting donor–acceptor block copolymers that contain substituted triphenylamines as donors and perylene diimide as the acceptor (see figure) are synthesized by means of nitroxide‐mediated polymerization, and the influence of morphology and the highest occupied molecular orbital (HOMO) level of the donor on block‐copolymer solar‐cell characteristics is studied.</description><subject>Copolymers</subject><subject>Semiconductors</subject><subject>Solar cells</subject><subject>Structure-property relationships</subject><issn>1616-301X</issn><issn>1616-3028</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2007</creationdate><recordtype>article</recordtype><recordid>eNqFkM9LwzAUx4soOKdXzzl560zTNG29zf3qYHPCJnoLWfrq6tKmJp26g_-7HZXhTXjwHsn383h8HOfawz0PY3Ir0qzoEYxZUz49cToe85jrYxKdHmfv5dy5sPYNYy8Mfdpxvue5NLraCAvuEiphRA0pGupSG7cvJVS1NmiYr5WWWzTQlVb7Aoy9Q9MyUzsoJSCdoWQxX6BRCeZ1j2bwAcoiUaZork210Uo3r7pEjy2LlloJgwaglL10zjKhLFz99q7zNB6tBok7W0ymg_7MlZRQ6qYkEkAgioVkTMR-RoiXUipBrFMiSRxRYOnhOySwjmQcpAKAhQSDCPwQMr_r3LR7K6Pfd2BrXuRWNheIEvTOchLHYRQEcRPstcFGirUGMl6ZvBBmzz3MD5b5wTI_Wm6AuAU-cwX7f9K8PxzP_7Juy-a2hq8jK8yWs9APA_78MOGrMYtoktzze_8HqCqScg</recordid><startdate>20070618</startdate><enddate>20070618</enddate><creator>Sommer, M.</creator><creator>Lindner, S. M.</creator><creator>Thelakkat, M.</creator><general>WILEY-VCH Verlag</general><general>WILEY‐VCH Verlag</general><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7SR</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20070618</creationdate><title>Microphase-Separated Donor-Acceptor Diblock Copolymers: Influence of HOMO Energy Levels and Morphology on Polymer Solar Cells</title><author>Sommer, M. ; Lindner, S. M. ; Thelakkat, M.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4244-d28ae2e89ac66a93f221d44ceabd2c2984e6de89a72eb8c95daee6720ea537ef3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2007</creationdate><topic>Copolymers</topic><topic>Semiconductors</topic><topic>Solar cells</topic><topic>Structure-property relationships</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sommer, M.</creatorcontrib><creatorcontrib>Lindner, S. M.</creatorcontrib><creatorcontrib>Thelakkat, M.</creatorcontrib><collection>Istex</collection><collection>CrossRef</collection><collection>Electronics &amp; Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Advanced functional materials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sommer, M.</au><au>Lindner, S. M.</au><au>Thelakkat, M.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Microphase-Separated Donor-Acceptor Diblock Copolymers: Influence of HOMO Energy Levels and Morphology on Polymer Solar Cells</atitle><jtitle>Advanced functional materials</jtitle><addtitle>Adv. Funct. Mater</addtitle><date>2007-06-18</date><risdate>2007</risdate><volume>17</volume><issue>9</issue><spage>1493</spage><epage>1500</epage><pages>1493-1500</pages><issn>1616-301X</issn><eissn>1616-3028</eissn><abstract>The synthesis of novel semiconducting donor–acceptor (D–A) diblock copolymers by means of nitroxide‐mediated polymerization (NMP) is reported. The copolymers contain functional moieties for hole transport, electron transport, and light absorption. The first block, representing the donor, is made up of either substituted triphenylamines (poly(bis(4‐methoxyphenyl)‐4′‐vinylphenylamine), PvDMTPA) or substituted tetraphenylbenzidines (poly(N,N′‐bis(4‐methoxyphenyl)‐N‐phenyl‐N′‐4‐vinylphenyl‐(1,1′‐biphenyl)‐4,4′‐diamine), PvDMTPD). The second block consists of perylene diimide side groups attached to a polyacrylate backbone (PPerAcr) via a flexible spacer. This block is responsible for absorption in the visible range and for electron‐transport properties. The electrochemical properties of these fully functionalized diblock copolymers, PvDMTPA‐b‐PPerAcr and PvDMTPD‐b‐PPerAcr, are investigated by cyclic voltammetry (CV), and their morphology is investigated by transmission electron microscopy (TEM). All diblock copolymers exhibit microphase‐separated domains in the form of either wire‐ or wormlike structures made of perylene diimide embedded in a hole‐conductor matrix. In single‐active‐layer organic solar cells, PvDMTPD‐b‐PPerAcr reveals a fourfold improvement in power conversion efficiency (η = 0.26 %, short‐circuit current (ISC) 1.21 mA cm–2), and PvDMTPA‐b‐PPerAcr a fivefold increased efficiency (η = 0.32 %, ISC = 1.14 mA cm–2) compared with its unsubstituted analogue PvTPA‐b‐PPerAcr (η = 0.065 %, ISC = 0.23 mA cm–2). A series of novel semiconducting donor–acceptor block copolymers that contain substituted triphenylamines as donors and perylene diimide as the acceptor (see figure) are synthesized by means of nitroxide‐mediated polymerization, and the influence of morphology and the highest occupied molecular orbital (HOMO) level of the donor on block‐copolymer solar‐cell characteristics is studied.</abstract><cop>Weinheim</cop><pub>WILEY-VCH Verlag</pub><doi>10.1002/adfm.200600634</doi><tpages>8</tpages></addata></record>
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subjects Copolymers
Semiconductors
Solar cells
Structure-property relationships
title Microphase-Separated Donor-Acceptor Diblock Copolymers: Influence of HOMO Energy Levels and Morphology on Polymer Solar Cells
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