Low band-gap donor–acceptor copolymers based on dioxocyclopenta[c]thiophene derivatives as acceptor units: synthesis, properties, and photovoltaic performances
New donor-acceptor type copolymers containing dihexyldioxocyclopenta[c]thiophene or (dihexylmethylidene)dioxocyclopenta[c]thiophene as acceptor units have been designed and synthesized for the application as hole-transporting (p-type) organic semiconducting materials in organic photovoltaics (OPVs)....
Gespeichert in:
Veröffentlicht in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2013-01, Vol.1 (47), p.15000-15009 |
---|---|
Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 15009 |
---|---|
container_issue | 47 |
container_start_page | 15000 |
container_title | Journal of materials chemistry. A, Materials for energy and sustainability |
container_volume | 1 |
creator | Huang, Jianming Ie, Yutaka Karakawa, Makoto Aso, Yoshio |
description | New donor-acceptor type copolymers containing dihexyldioxocyclopenta[c]thiophene or (dihexylmethylidene)dioxocyclopenta[c]thiophene as acceptor units have been designed and synthesized for the application as hole-transporting (p-type) organic semiconducting materials in organic photovoltaics (OPVs). The investigation of photophysical and physicochemical properties revealed that these copolymers featured low optical band gaps (1.56-1.73 eV) and low-lying HOMO energy levels (-5.40 to -5.02 eV). Bulk heterojunction OPV devices based on these copolymers and [6,6]-phenyl-C sub(61)-butyric acid methyl ester as active layers showed moderate power conversion efficiencies (PCEs) of between 1.36 and 2.68% under air mass 1.5 simulated solar illumination. Space-charge-limited current measurements and atomic force microscopy measurements of the blend films revealed that both charge-transporting characteristics and film morphologies have significant influences on the photovoltaic performances. OPV devices based on the copolymers with [6,6]-phenyl-C sub(71)-butyric acid methyl ester showed a PCE of up to 5.17% with a short circuit current of 10.1 mA cm super(-2), an open circuit voltage of 0.80 V and a fill factor of 0.64. |
doi_str_mv | 10.1039/c3ta13504g |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1671518991</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>1671518991</sourcerecordid><originalsourceid>FETCH-LOGICAL-c363t-4d6a2510bdfe2c25ea7e8302a2f103be0b96f0fa9c248ac5c61e94583e3c4e523</originalsourceid><addsrcrecordid>eNqFUc2KFEEMbkTBZXcvPkEdRWytn66aLm-y-AcDXtyTSJNJp3dKeiptVc2sc_Md9gl8tX0SS1bdoyGQD_LlS8jXNE-UfKGk8S_RFFDGyu7qQXOipZXtqvPu4T_c94-b85y_yhq9lM77k-bnmq_FBuLYXsEiRo6cbn_cACIthZNAXng-7ijlSso0Co5iDPyd8YgzLxQLfMYvZRt42VIkMVIKByjhQFlAzb86-xhKfiXyMZYt5ZCfiyXV8VQCVVzXi2XLhQ88FwgoamfitIOIlM-aRxPMmc7_1NPm8u2bTxfv2_XHdx8uXq9bNM6UthsdaKvkZpxIo7YEK-qN1KCn-pwNyY13k5zAo-56QItOke9sb8hgR1ab0-bpnW697Nuechl2ISPNM0TifR6UWymreu_V_6nWabcyXrpKfXZHxcQ5J5qGJYUdpOOg5PDbteHeNfML3g-Qew</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1562673906</pqid></control><display><type>article</type><title>Low band-gap donor–acceptor copolymers based on dioxocyclopenta[c]thiophene derivatives as acceptor units: synthesis, properties, and photovoltaic performances</title><source>Alma/SFX Local Collection</source><source>Royal Society of Chemistry E-Journals</source><creator>Huang, Jianming ; Ie, Yutaka ; Karakawa, Makoto ; Aso, Yoshio</creator><creatorcontrib>Huang, Jianming ; Ie, Yutaka ; Karakawa, Makoto ; Aso, Yoshio</creatorcontrib><description>New donor-acceptor type copolymers containing dihexyldioxocyclopenta[c]thiophene or (dihexylmethylidene)dioxocyclopenta[c]thiophene as acceptor units have been designed and synthesized for the application as hole-transporting (p-type) organic semiconducting materials in organic photovoltaics (OPVs). The investigation of photophysical and physicochemical properties revealed that these copolymers featured low optical band gaps (1.56-1.73 eV) and low-lying HOMO energy levels (-5.40 to -5.02 eV). Bulk heterojunction OPV devices based on these copolymers and [6,6]-phenyl-C sub(61)-butyric acid methyl ester as active layers showed moderate power conversion efficiencies (PCEs) of between 1.36 and 2.68% under air mass 1.5 simulated solar illumination. Space-charge-limited current measurements and atomic force microscopy measurements of the blend films revealed that both charge-transporting characteristics and film morphologies have significant influences on the photovoltaic performances. OPV devices based on the copolymers with [6,6]-phenyl-C sub(71)-butyric acid methyl ester showed a PCE of up to 5.17% with a short circuit current of 10.1 mA cm super(-2), an open circuit voltage of 0.80 V and a fill factor of 0.64.</description><identifier>ISSN: 2050-7488</identifier><identifier>EISSN: 2050-7496</identifier><identifier>DOI: 10.1039/c3ta13504g</identifier><language>eng</language><subject>Copolymers ; Devices ; Energy gaps (solid state) ; Esters ; Open circuit voltage ; Photovoltaic cells ; Solar cells ; Sustainability</subject><ispartof>Journal of materials chemistry. A, Materials for energy and sustainability, 2013-01, Vol.1 (47), p.15000-15009</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c363t-4d6a2510bdfe2c25ea7e8302a2f103be0b96f0fa9c248ac5c61e94583e3c4e523</citedby><cites>FETCH-LOGICAL-c363t-4d6a2510bdfe2c25ea7e8302a2f103be0b96f0fa9c248ac5c61e94583e3c4e523</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>Huang, Jianming</creatorcontrib><creatorcontrib>Ie, Yutaka</creatorcontrib><creatorcontrib>Karakawa, Makoto</creatorcontrib><creatorcontrib>Aso, Yoshio</creatorcontrib><title>Low band-gap donor–acceptor copolymers based on dioxocyclopenta[c]thiophene derivatives as acceptor units: synthesis, properties, and photovoltaic performances</title><title>Journal of materials chemistry. A, Materials for energy and sustainability</title><description>New donor-acceptor type copolymers containing dihexyldioxocyclopenta[c]thiophene or (dihexylmethylidene)dioxocyclopenta[c]thiophene as acceptor units have been designed and synthesized for the application as hole-transporting (p-type) organic semiconducting materials in organic photovoltaics (OPVs). The investigation of photophysical and physicochemical properties revealed that these copolymers featured low optical band gaps (1.56-1.73 eV) and low-lying HOMO energy levels (-5.40 to -5.02 eV). Bulk heterojunction OPV devices based on these copolymers and [6,6]-phenyl-C sub(61)-butyric acid methyl ester as active layers showed moderate power conversion efficiencies (PCEs) of between 1.36 and 2.68% under air mass 1.5 simulated solar illumination. Space-charge-limited current measurements and atomic force microscopy measurements of the blend films revealed that both charge-transporting characteristics and film morphologies have significant influences on the photovoltaic performances. OPV devices based on the copolymers with [6,6]-phenyl-C sub(71)-butyric acid methyl ester showed a PCE of up to 5.17% with a short circuit current of 10.1 mA cm super(-2), an open circuit voltage of 0.80 V and a fill factor of 0.64.</description><subject>Copolymers</subject><subject>Devices</subject><subject>Energy gaps (solid state)</subject><subject>Esters</subject><subject>Open circuit voltage</subject><subject>Photovoltaic cells</subject><subject>Solar cells</subject><subject>Sustainability</subject><issn>2050-7488</issn><issn>2050-7496</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><recordid>eNqFUc2KFEEMbkTBZXcvPkEdRWytn66aLm-y-AcDXtyTSJNJp3dKeiptVc2sc_Md9gl8tX0SS1bdoyGQD_LlS8jXNE-UfKGk8S_RFFDGyu7qQXOipZXtqvPu4T_c94-b85y_yhq9lM77k-bnmq_FBuLYXsEiRo6cbn_cACIthZNAXng-7ijlSso0Co5iDPyd8YgzLxQLfMYvZRt42VIkMVIKByjhQFlAzb86-xhKfiXyMZYt5ZCfiyXV8VQCVVzXi2XLhQ88FwgoamfitIOIlM-aRxPMmc7_1NPm8u2bTxfv2_XHdx8uXq9bNM6UthsdaKvkZpxIo7YEK-qN1KCn-pwNyY13k5zAo-56QItOke9sb8hgR1ab0-bpnW697Nuechl2ISPNM0TifR6UWymreu_V_6nWabcyXrpKfXZHxcQ5J5qGJYUdpOOg5PDbteHeNfML3g-Qew</recordid><startdate>20130101</startdate><enddate>20130101</enddate><creator>Huang, Jianming</creator><creator>Ie, Yutaka</creator><creator>Karakawa, Makoto</creator><creator>Aso, Yoshio</creator><scope>AAYXX</scope><scope>CITATION</scope><scope>7ST</scope><scope>7U6</scope><scope>C1K</scope><scope>7SP</scope><scope>7SR</scope><scope>7SU</scope><scope>7U5</scope><scope>8BQ</scope><scope>8FD</scope><scope>FR3</scope><scope>JG9</scope><scope>L7M</scope></search><sort><creationdate>20130101</creationdate><title>Low band-gap donor–acceptor copolymers based on dioxocyclopenta[c]thiophene derivatives as acceptor units: synthesis, properties, and photovoltaic performances</title><author>Huang, Jianming ; Ie, Yutaka ; Karakawa, Makoto ; Aso, Yoshio</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c363t-4d6a2510bdfe2c25ea7e8302a2f103be0b96f0fa9c248ac5c61e94583e3c4e523</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2013</creationdate><topic>Copolymers</topic><topic>Devices</topic><topic>Energy gaps (solid state)</topic><topic>Esters</topic><topic>Open circuit voltage</topic><topic>Photovoltaic cells</topic><topic>Solar cells</topic><topic>Sustainability</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Huang, Jianming</creatorcontrib><creatorcontrib>Ie, Yutaka</creatorcontrib><creatorcontrib>Karakawa, Makoto</creatorcontrib><creatorcontrib>Aso, Yoshio</creatorcontrib><collection>CrossRef</collection><collection>Environment Abstracts</collection><collection>Sustainability Science Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Electronics & Communications Abstracts</collection><collection>Engineered Materials Abstracts</collection><collection>Environmental Engineering Abstracts</collection><collection>Solid State and Superconductivity Abstracts</collection><collection>METADEX</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Materials Research Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Journal of materials chemistry. A, Materials for energy and sustainability</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Huang, Jianming</au><au>Ie, Yutaka</au><au>Karakawa, Makoto</au><au>Aso, Yoshio</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Low band-gap donor–acceptor copolymers based on dioxocyclopenta[c]thiophene derivatives as acceptor units: synthesis, properties, and photovoltaic performances</atitle><jtitle>Journal of materials chemistry. A, Materials for energy and sustainability</jtitle><date>2013-01-01</date><risdate>2013</risdate><volume>1</volume><issue>47</issue><spage>15000</spage><epage>15009</epage><pages>15000-15009</pages><issn>2050-7488</issn><eissn>2050-7496</eissn><abstract>New donor-acceptor type copolymers containing dihexyldioxocyclopenta[c]thiophene or (dihexylmethylidene)dioxocyclopenta[c]thiophene as acceptor units have been designed and synthesized for the application as hole-transporting (p-type) organic semiconducting materials in organic photovoltaics (OPVs). The investigation of photophysical and physicochemical properties revealed that these copolymers featured low optical band gaps (1.56-1.73 eV) and low-lying HOMO energy levels (-5.40 to -5.02 eV). Bulk heterojunction OPV devices based on these copolymers and [6,6]-phenyl-C sub(61)-butyric acid methyl ester as active layers showed moderate power conversion efficiencies (PCEs) of between 1.36 and 2.68% under air mass 1.5 simulated solar illumination. Space-charge-limited current measurements and atomic force microscopy measurements of the blend films revealed that both charge-transporting characteristics and film morphologies have significant influences on the photovoltaic performances. OPV devices based on the copolymers with [6,6]-phenyl-C sub(71)-butyric acid methyl ester showed a PCE of up to 5.17% with a short circuit current of 10.1 mA cm super(-2), an open circuit voltage of 0.80 V and a fill factor of 0.64.</abstract><doi>10.1039/c3ta13504g</doi><tpages>10</tpages></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2050-7488 |
ispartof | Journal of materials chemistry. A, Materials for energy and sustainability, 2013-01, Vol.1 (47), p.15000-15009 |
issn | 2050-7488 2050-7496 |
language | eng |
recordid | cdi_proquest_miscellaneous_1671518991 |
source | Alma/SFX Local Collection; Royal Society of Chemistry E-Journals |
subjects | Copolymers Devices Energy gaps (solid state) Esters Open circuit voltage Photovoltaic cells Solar cells Sustainability |
title | Low band-gap donor–acceptor copolymers based on dioxocyclopenta[c]thiophene derivatives as acceptor units: synthesis, properties, and photovoltaic performances |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-22T16%3A48%3A39IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Low%20band-gap%20donor%E2%80%93acceptor%20copolymers%20based%20on%20dioxocyclopenta%5Bc%5Dthiophene%20derivatives%20as%20acceptor%20units:%20synthesis,%20properties,%20and%20photovoltaic%20performances&rft.jtitle=Journal%20of%20materials%20chemistry.%20A,%20Materials%20for%20energy%20and%20sustainability&rft.au=Huang,%20Jianming&rft.date=2013-01-01&rft.volume=1&rft.issue=47&rft.spage=15000&rft.epage=15009&rft.pages=15000-15009&rft.issn=2050-7488&rft.eissn=2050-7496&rft_id=info:doi/10.1039/c3ta13504g&rft_dat=%3Cproquest_cross%3E1671518991%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1562673906&rft_id=info:pmid/&rfr_iscdi=true |