Synthesis of all-conjugated poly(3-hexylthiophene)-block- poly(3-(4′-(3″,7″-dimethyloctyloxy)-3′-pyridinyl)thiophene) and its blend for photovoltaic applications
New all-conjugated block copolythiophene, poly(3-hexylthiophene)-block-poly(3-(4′-(3″,7″-dimethyloctyloxy)-3′-pyridinyl)thiophene) (P3HT-b-P3PyT) was successfully prepared by Grignard metathesis polymerization. The supramolecular interaction between [6,6]-phenyl-C₆₁-butyric acid methyl ester (PCBM)...
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Veröffentlicht in: | Journal of polymer science. Part A, Polymer chemistry Polymer chemistry, 2011-06, Vol.49 (12), p.2577-2587 |
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container_title | Journal of polymer science. Part A, Polymer chemistry |
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creator | Lai, Yi-Cang Ohshimizu, Kaoru Takahashi, Ayumi Hsu, Jung-Ching Higashihara, Tomoya Ueda, Mitsuru Chen, Wen-Chang |
description | New all-conjugated block copolythiophene, poly(3-hexylthiophene)-block-poly(3-(4′-(3″,7″-dimethyloctyloxy)-3′-pyridinyl)thiophene) (P3HT-b-P3PyT) was successfully prepared by Grignard metathesis polymerization. The supramolecular interaction between [6,6]-phenyl-C₆₁-butyric acid methyl ester (PCBM) and P3PyT was proposed to control the aggregated size of PCBM and long-term thermal stability of the photovoltaic cell, as evidenced by differential scanning calorimetry (DSC), transmission electron microscopy (TEM), and optical microscopy. The effect of different solvents on the electronic and optoelectronic properties was studied, including chloroform (CL), dichlorobenzene (DCB), and mixed solvent of CL/DCB. The optimized bulk heterojunction solar cell devices using the P3HT-b-P3PyT/PCBM blend showed a power conversion efficiency of 2.12%, comparable to that of P3HT/PCBM device despite the fact that former had a lower crystallinity or absorption coefficient. Furthermore, P3HT-b-P3PyT could be also used as a surfactant to enhance the long-term thermal stability of P3HT/PCBM-based solar cells by limiting the aggregated size of PCBM. This study represents a new supramolecular approach to design all-conjugated block copolymers for high-performance photovoltaic devices. |
doi_str_mv | 10.1002/pola.24689 |
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The supramolecular interaction between [6,6]-phenyl-C₆₁-butyric acid methyl ester (PCBM) and P3PyT was proposed to control the aggregated size of PCBM and long-term thermal stability of the photovoltaic cell, as evidenced by differential scanning calorimetry (DSC), transmission electron microscopy (TEM), and optical microscopy. The effect of different solvents on the electronic and optoelectronic properties was studied, including chloroform (CL), dichlorobenzene (DCB), and mixed solvent of CL/DCB. The optimized bulk heterojunction solar cell devices using the P3HT-b-P3PyT/PCBM blend showed a power conversion efficiency of 2.12%, comparable to that of P3HT/PCBM device despite the fact that former had a lower crystallinity or absorption coefficient. Furthermore, P3HT-b-P3PyT could be also used as a surfactant to enhance the long-term thermal stability of P3HT/PCBM-based solar cells by limiting the aggregated size of PCBM. This study represents a new supramolecular approach to design all-conjugated block copolymers for high-performance photovoltaic devices.</description><identifier>ISSN: 0887-624X</identifier><identifier>ISSN: 1099-0518</identifier><identifier>EISSN: 1099-0518</identifier><identifier>DOI: 10.1002/pola.24689</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>absorption ; Blends ; block copolymers ; chloroform ; compatibility ; composite polymers ; conjugated polymer ; crystal structure ; Devices ; Differential scanning calorimetry ; GRIM polymerization ; photovoltaic cell ; Photovoltaic cells ; Polymerization ; Solar cells ; Solvents ; surfactants ; Thermal stability ; transmission electron microscopy</subject><ispartof>Journal of polymer science. Part A, Polymer chemistry, 2011-06, Vol.49 (12), p.2577-2587</ispartof><rights>Copyright © 2011 Wiley Periodicals, Inc.</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3859-62b6f401c2d9400bfed330da23b9472c601ffc25be58af11795c982bf2ae0603</citedby><cites>FETCH-LOGICAL-c3859-62b6f401c2d9400bfed330da23b9472c601ffc25be58af11795c982bf2ae0603</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%2Fpola.24689$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fpola.24689$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,27924,27925,45574,45575</link.rule.ids></links><search><creatorcontrib>Lai, Yi-Cang</creatorcontrib><creatorcontrib>Ohshimizu, Kaoru</creatorcontrib><creatorcontrib>Takahashi, Ayumi</creatorcontrib><creatorcontrib>Hsu, Jung-Ching</creatorcontrib><creatorcontrib>Higashihara, Tomoya</creatorcontrib><creatorcontrib>Ueda, Mitsuru</creatorcontrib><creatorcontrib>Chen, Wen-Chang</creatorcontrib><title>Synthesis of all-conjugated poly(3-hexylthiophene)-block- poly(3-(4′-(3″,7″-dimethyloctyloxy)-3′-pyridinyl)thiophene) and its blend for photovoltaic applications</title><title>Journal of polymer science. Part A, Polymer chemistry</title><addtitle>J. Polym. Sci. A Polym. Chem</addtitle><description>New all-conjugated block copolythiophene, poly(3-hexylthiophene)-block-poly(3-(4′-(3″,7″-dimethyloctyloxy)-3′-pyridinyl)thiophene) (P3HT-b-P3PyT) was successfully prepared by Grignard metathesis polymerization. The supramolecular interaction between [6,6]-phenyl-C₆₁-butyric acid methyl ester (PCBM) and P3PyT was proposed to control the aggregated size of PCBM and long-term thermal stability of the photovoltaic cell, as evidenced by differential scanning calorimetry (DSC), transmission electron microscopy (TEM), and optical microscopy. The effect of different solvents on the electronic and optoelectronic properties was studied, including chloroform (CL), dichlorobenzene (DCB), and mixed solvent of CL/DCB. The optimized bulk heterojunction solar cell devices using the P3HT-b-P3PyT/PCBM blend showed a power conversion efficiency of 2.12%, comparable to that of P3HT/PCBM device despite the fact that former had a lower crystallinity or absorption coefficient. Furthermore, P3HT-b-P3PyT could be also used as a surfactant to enhance the long-term thermal stability of P3HT/PCBM-based solar cells by limiting the aggregated size of PCBM. This study represents a new supramolecular approach to design all-conjugated block copolymers for high-performance photovoltaic devices.</description><subject>absorption</subject><subject>Blends</subject><subject>block copolymers</subject><subject>chloroform</subject><subject>compatibility</subject><subject>composite polymers</subject><subject>conjugated polymer</subject><subject>crystal structure</subject><subject>Devices</subject><subject>Differential scanning calorimetry</subject><subject>GRIM polymerization</subject><subject>photovoltaic cell</subject><subject>Photovoltaic cells</subject><subject>Polymerization</subject><subject>Solar cells</subject><subject>Solvents</subject><subject>surfactants</subject><subject>Thermal stability</subject><subject>transmission electron microscopy</subject><issn>0887-624X</issn><issn>1099-0518</issn><issn>1099-0518</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp9kc9u1DAQxiMEEkvLhRcgN3YrXPwnTuJjW0GpuqIrdYG9WY5jN269cYi9ZXPr63CFN-qT1Eso3LjMjDS_79OMviR5heAhghC_65wVhzjLS_YkmSDIGIAUlU-TCSzLAuQ4Wz1PXnh_DWHc0XKS_Lgc2tAob3zqdCqsBdK115srEVSdRrdhSkCjtoMNjXFdo1o1A5V18gY8bqfZ_d1PMCX3d7_eFrGA2qxVaIYIhVi2wwyQHdENvalNO9jZP6tUtHVqgk8rq-KkXZ92jQvu1tkgjExF11kjRTCu9fvJMy2sVy__9L1k-eH98uQjmF-cnp0czYEkJWXxxyrXGUQS1yyDsNKqJgTWApOKZQWWOURaS0wrRUuhESoYlazElcZCwRySveTNaNv17ttG-cDXxktlrWiV23jOIMopLSGN5MFIyt553yvNu96sRT9wBPkuDb5Lg_9OI8JohL8bq4b_kHxxMT961IBRY3xQ278a0d_wvCAF5V8_nfLF-WqxOs6_8GXkX4-8Fo6Lq954_vkSx3tj2gQTxMgDFJ-sZg</recordid><startdate>20110615</startdate><enddate>20110615</enddate><creator>Lai, Yi-Cang</creator><creator>Ohshimizu, Kaoru</creator><creator>Takahashi, Ayumi</creator><creator>Hsu, Jung-Ching</creator><creator>Higashihara, Tomoya</creator><creator>Ueda, Mitsuru</creator><creator>Chen, Wen-Chang</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><scope>FBQ</scope><scope>BSCLL</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7SR</scope><scope>8FD</scope><scope>JG9</scope></search><sort><creationdate>20110615</creationdate><title>Synthesis of all-conjugated poly(3-hexylthiophene)-block- poly(3-(4′-(3″,7″-dimethyloctyloxy)-3′-pyridinyl)thiophene) and its blend for photovoltaic applications</title><author>Lai, Yi-Cang ; Ohshimizu, Kaoru ; Takahashi, Ayumi ; Hsu, Jung-Ching ; Higashihara, Tomoya ; Ueda, Mitsuru ; Chen, Wen-Chang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3859-62b6f401c2d9400bfed330da23b9472c601ffc25be58af11795c982bf2ae0603</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>absorption</topic><topic>Blends</topic><topic>block copolymers</topic><topic>chloroform</topic><topic>compatibility</topic><topic>composite polymers</topic><topic>conjugated polymer</topic><topic>crystal structure</topic><topic>Devices</topic><topic>Differential scanning calorimetry</topic><topic>GRIM polymerization</topic><topic>photovoltaic cell</topic><topic>Photovoltaic cells</topic><topic>Polymerization</topic><topic>Solar cells</topic><topic>Solvents</topic><topic>surfactants</topic><topic>Thermal stability</topic><topic>transmission electron microscopy</topic><toplevel>online_resources</toplevel><creatorcontrib>Lai, Yi-Cang</creatorcontrib><creatorcontrib>Ohshimizu, Kaoru</creatorcontrib><creatorcontrib>Takahashi, Ayumi</creatorcontrib><creatorcontrib>Hsu, Jung-Ching</creatorcontrib><creatorcontrib>Higashihara, Tomoya</creatorcontrib><creatorcontrib>Ueda, Mitsuru</creatorcontrib><creatorcontrib>Chen, Wen-Chang</creatorcontrib><collection>AGRIS</collection><collection>Istex</collection><collection>CrossRef</collection><collection>Engineered Materials Abstracts</collection><collection>Technology Research Database</collection><collection>Materials Research Database</collection><jtitle>Journal of polymer science. Part A, Polymer chemistry</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lai, Yi-Cang</au><au>Ohshimizu, Kaoru</au><au>Takahashi, Ayumi</au><au>Hsu, Jung-Ching</au><au>Higashihara, Tomoya</au><au>Ueda, Mitsuru</au><au>Chen, Wen-Chang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Synthesis of all-conjugated poly(3-hexylthiophene)-block- poly(3-(4′-(3″,7″-dimethyloctyloxy)-3′-pyridinyl)thiophene) and its blend for photovoltaic applications</atitle><jtitle>Journal of polymer science. Part A, Polymer chemistry</jtitle><addtitle>J. Polym. Sci. A Polym. Chem</addtitle><date>2011-06-15</date><risdate>2011</risdate><volume>49</volume><issue>12</issue><spage>2577</spage><epage>2587</epage><pages>2577-2587</pages><issn>0887-624X</issn><issn>1099-0518</issn><eissn>1099-0518</eissn><abstract>New all-conjugated block copolythiophene, poly(3-hexylthiophene)-block-poly(3-(4′-(3″,7″-dimethyloctyloxy)-3′-pyridinyl)thiophene) (P3HT-b-P3PyT) was successfully prepared by Grignard metathesis polymerization. The supramolecular interaction between [6,6]-phenyl-C₆₁-butyric acid methyl ester (PCBM) and P3PyT was proposed to control the aggregated size of PCBM and long-term thermal stability of the photovoltaic cell, as evidenced by differential scanning calorimetry (DSC), transmission electron microscopy (TEM), and optical microscopy. The effect of different solvents on the electronic and optoelectronic properties was studied, including chloroform (CL), dichlorobenzene (DCB), and mixed solvent of CL/DCB. The optimized bulk heterojunction solar cell devices using the P3HT-b-P3PyT/PCBM blend showed a power conversion efficiency of 2.12%, comparable to that of P3HT/PCBM device despite the fact that former had a lower crystallinity or absorption coefficient. Furthermore, P3HT-b-P3PyT could be also used as a surfactant to enhance the long-term thermal stability of P3HT/PCBM-based solar cells by limiting the aggregated size of PCBM. This study represents a new supramolecular approach to design all-conjugated block copolymers for high-performance photovoltaic devices.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><doi>10.1002/pola.24689</doi><tpages>11</tpages></addata></record> |
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subjects | absorption Blends block copolymers chloroform compatibility composite polymers conjugated polymer crystal structure Devices Differential scanning calorimetry GRIM polymerization photovoltaic cell Photovoltaic cells Polymerization Solar cells Solvents surfactants Thermal stability transmission electron microscopy |
title | Synthesis of all-conjugated poly(3-hexylthiophene)-block- poly(3-(4′-(3″,7″-dimethyloctyloxy)-3′-pyridinyl)thiophene) and its blend for photovoltaic applications |
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