Optoelectronic Properties and Charge Transfer in Donor–Acceptor All-Conjugated Diblock Copolymers
All-conjugated block copolymers, which can self-assemble into well-ordered morphologies, provide exciting opportunities to rationally design and control the nanoscale organization of electron–donor and electron–acceptor moieties in optoelectronic active layers. Here we report on the steady-state and...
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Veröffentlicht in: | J. Phys. Chem. C 2011-05, Vol.115 (18), p.9260-9266 |
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creator | Botiz, Ioan Schaller, Richard D Verduzco, Rafael Darling, Seth B |
description | All-conjugated block copolymers, which can self-assemble into well-ordered morphologies, provide exciting opportunities to rationally design and control the nanoscale organization of electron–donor and electron–acceptor moieties in optoelectronic active layers. Here we report on the steady-state and time-resolved optical characterization of block copolymer films and solutions containing poly(3-hexylthiophene) as the donor block and poly(9,9-dioctylfluorene) with and without copolymerization with benzothiadiazole as the acceptor block. Transient absorption measurements suggest rapid charge transfer occurs in both systems, with higher efficiency observed in the latter composition. These results indicate that this class of materials has promise in preparing highly ordered bulk heterojunction all-polymer organic photovoltaic devices. |
doi_str_mv | 10.1021/jp201344p |
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(ANL), Argonne, IL (United States)</creatorcontrib><description>All-conjugated block copolymers, which can self-assemble into well-ordered morphologies, provide exciting opportunities to rationally design and control the nanoscale organization of electron–donor and electron–acceptor moieties in optoelectronic active layers. Here we report on the steady-state and time-resolved optical characterization of block copolymer films and solutions containing poly(3-hexylthiophene) as the donor block and poly(9,9-dioctylfluorene) with and without copolymerization with benzothiadiazole as the acceptor block. Transient absorption measurements suggest rapid charge transfer occurs in both systems, with higher efficiency observed in the latter composition. These results indicate that this class of materials has promise in preparing highly ordered bulk heterojunction all-polymer organic photovoltaic devices.</description><identifier>ISSN: 1932-7447</identifier><identifier>EISSN: 1932-7455</identifier><identifier>DOI: 10.1021/jp201344p</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>ABSORPTION ; BINDING ENERGY ; C: Energy Conversion and Storage ; COPOLYMERIZATION ; COPOLYMERS ; DESIGN ; EFFICIENCY ; ELECTRONS ; HETEROJUNCTIONS ; INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY ; TRANSIENTS ; VALENCE</subject><ispartof>J. Phys. Chem. 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(ANL), Argonne, IL (United States)</creatorcontrib><title>Optoelectronic Properties and Charge Transfer in Donor–Acceptor All-Conjugated Diblock Copolymers</title><title>J. Phys. Chem. C</title><addtitle>J. Phys. Chem. C</addtitle><description>All-conjugated block copolymers, which can self-assemble into well-ordered morphologies, provide exciting opportunities to rationally design and control the nanoscale organization of electron–donor and electron–acceptor moieties in optoelectronic active layers. Here we report on the steady-state and time-resolved optical characterization of block copolymer films and solutions containing poly(3-hexylthiophene) as the donor block and poly(9,9-dioctylfluorene) with and without copolymerization with benzothiadiazole as the acceptor block. Transient absorption measurements suggest rapid charge transfer occurs in both systems, with higher efficiency observed in the latter composition. These results indicate that this class of materials has promise in preparing highly ordered bulk heterojunction all-polymer organic photovoltaic devices.</description><subject>ABSORPTION</subject><subject>BINDING ENERGY</subject><subject>C: Energy Conversion and Storage</subject><subject>COPOLYMERIZATION</subject><subject>COPOLYMERS</subject><subject>DESIGN</subject><subject>EFFICIENCY</subject><subject>ELECTRONS</subject><subject>HETEROJUNCTIONS</subject><subject>INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY</subject><subject>TRANSIENTS</subject><subject>VALENCE</subject><issn>1932-7447</issn><issn>1932-7455</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNpt0L1OwzAQB3ALgUQpDLyBhcTAEPBnE49VypdUqQxljpyr0yakdmS7QzfegTfkSTAq6sR0N_zudPdH6JqSe0oYfegGRigXYjhBI6o4y3Ih5emxF_k5ugihI0Ty5EYIFkN0pjcQvbMt4DfvBuNjawLWdoXLjfZrg5de29AYj1uLZ846__35NQUwadbjad9npbPdbq2jWeFZW_cOPnDpBtfvt8aHS3TW6D6Yq786Ru9Pj8vyJZsvnl_L6TzTXLKY8ZxNckVNAUCprDmbFIXUUnFREFnkWqla1DRvhKwLxWTDFZXCgC5AUybIio_RzWGvC7GtArTRwAactem7ihIqlZAJ3R0QeBeCN001-Har_T6J6jfC6hhhsrcHqyFUndt5m87_x_0AwDhwTA</recordid><startdate>20110512</startdate><enddate>20110512</enddate><creator>Botiz, Ioan</creator><creator>Schaller, Richard D</creator><creator>Verduzco, Rafael</creator><creator>Darling, Seth B</creator><general>American Chemical Society</general><scope>AAYXX</scope><scope>CITATION</scope><scope>OTOTI</scope></search><sort><creationdate>20110512</creationdate><title>Optoelectronic Properties and Charge Transfer in Donor–Acceptor All-Conjugated Diblock Copolymers</title><author>Botiz, Ioan ; Schaller, Richard D ; Verduzco, Rafael ; Darling, Seth B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a352t-3726791e8cc115b326885a593480587a99b4b17f45b8925f39154eca8ca1240d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>ABSORPTION</topic><topic>BINDING ENERGY</topic><topic>C: Energy Conversion and Storage</topic><topic>COPOLYMERIZATION</topic><topic>COPOLYMERS</topic><topic>DESIGN</topic><topic>EFFICIENCY</topic><topic>ELECTRONS</topic><topic>HETEROJUNCTIONS</topic><topic>INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY</topic><topic>TRANSIENTS</topic><topic>VALENCE</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Botiz, Ioan</creatorcontrib><creatorcontrib>Schaller, Richard D</creatorcontrib><creatorcontrib>Verduzco, Rafael</creatorcontrib><creatorcontrib>Darling, Seth B</creatorcontrib><creatorcontrib>Argonne National Lab. 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C</addtitle><date>2011-05-12</date><risdate>2011</risdate><volume>115</volume><issue>18</issue><spage>9260</spage><epage>9266</epage><pages>9260-9266</pages><issn>1932-7447</issn><eissn>1932-7455</eissn><abstract>All-conjugated block copolymers, which can self-assemble into well-ordered morphologies, provide exciting opportunities to rationally design and control the nanoscale organization of electron–donor and electron–acceptor moieties in optoelectronic active layers. Here we report on the steady-state and time-resolved optical characterization of block copolymer films and solutions containing poly(3-hexylthiophene) as the donor block and poly(9,9-dioctylfluorene) with and without copolymerization with benzothiadiazole as the acceptor block. Transient absorption measurements suggest rapid charge transfer occurs in both systems, with higher efficiency observed in the latter composition. 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subjects | ABSORPTION BINDING ENERGY C: Energy Conversion and Storage COPOLYMERIZATION COPOLYMERS DESIGN EFFICIENCY ELECTRONS HETEROJUNCTIONS INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY TRANSIENTS VALENCE |
title | Optoelectronic Properties and Charge Transfer in Donor–Acceptor All-Conjugated Diblock Copolymers |
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