Loading…

Photo-Cross-Linkable Azide-Functionalized Polythiophene for Thermally Stable Bulk Heterojunction Solar Cells

We have synthesized photo-cross-linkable azide-functionalized poly(3-hexylthiophene) to explore improvements in the thermal stability of bulk heterojunction solar cells. Exposing blends of photo-cross-linkable polythiophene and [6,6]-phenyl-C61-butyric acid methyl ester to ultraviolet light preferen...

Full description

Saved in:
Bibliographic Details
Published in:Macromolecules 2012-03, Vol.45 (5), p.2338-2347
Main Authors: Nam, Chang-Yong, Qin, Yang, Park, Young S, Hlaing, Htay, Lu, Xinhui, Ocko, Benjamin M, Black, Charles T, Grubbs, Robert B
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-a382t-eab7435eee5a14c5ff390eb119b2eed3ddf652abe2d6fb104ce52942bcc1131d3
cites cdi_FETCH-LOGICAL-a382t-eab7435eee5a14c5ff390eb119b2eed3ddf652abe2d6fb104ce52942bcc1131d3
container_end_page 2347
container_issue 5
container_start_page 2338
container_title Macromolecules
container_volume 45
creator Nam, Chang-Yong
Qin, Yang
Park, Young S
Hlaing, Htay
Lu, Xinhui
Ocko, Benjamin M
Black, Charles T
Grubbs, Robert B
description We have synthesized photo-cross-linkable azide-functionalized poly(3-hexylthiophene) to explore improvements in the thermal stability of bulk heterojunction solar cells. Exposing blends of photo-cross-linkable polythiophene and [6,6]-phenyl-C61-butyric acid methyl ester to ultraviolet light preferentially cross-linked the polythiophene without degrading its optical or electrical properties. X-ray scattering measurements showed that cross-linking slightly compacted the polythiophene chain lamellar stacking while increasing the polymer crystal coherence length by 20%. Optimized solar cells having cross-linked active blend layers retained 65% of their initial photovoltaic power conversion efficiency after 40 h of thermal annealing at 110 °C, while devices using un-cross-linked commercial polythiophene underwent significant phase separation and retained less than 30% of their initial efficiency after annealing.
doi_str_mv 10.1021/ma3001725
format article
fullrecord <record><control><sourceid>acs_osti_</sourceid><recordid>TN_cdi_osti_scitechconnect_1109539</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>a066467763</sourcerecordid><originalsourceid>FETCH-LOGICAL-a382t-eab7435eee5a14c5ff390eb119b2eed3ddf652abe2d6fb104ce52942bcc1131d3</originalsourceid><addsrcrecordid>eNptkMFPwjAUhxujiYge_A8WEw8eqn3tytgRFxETEknA89J1b1mhrKQtB_jrBTF48fQu3_dL3kfIPbBnYBxe1kowBhmXF6QHkjMqh0Jekh5jPKU5z7NrchPC8sCATEWP2FnroqOFdyHQqelWqrKYjPamRjredjoa1ylr9lgnM2d3sTVu02KHSeN8smjRr5W1u2Qef7zXrV0lE4zo3fJXTubOKp8UaG24JVeNsgHvfm-ffI3fFsWETj_fP4rRlCox5JGiqrJUSESUClItm0bkDCuAvOKItajrZiC5qpDXg6YClmqUPE95pTWAgFr0ycNp14VoyqBNRN1q13WoYwnAcinyA_R0gvTxd49NufFmrfyuBFYeW5bnlgf28cRuVNDKNl512oSzwOUAsqFkf5zSoVy6rT-0C__sfQMinYEy</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Photo-Cross-Linkable Azide-Functionalized Polythiophene for Thermally Stable Bulk Heterojunction Solar Cells</title><source>American Chemical Society:Jisc Collections:American Chemical Society Read &amp; Publish Agreement 2022-2024 (Reading list)</source><creator>Nam, Chang-Yong ; Qin, Yang ; Park, Young S ; Hlaing, Htay ; Lu, Xinhui ; Ocko, Benjamin M ; Black, Charles T ; Grubbs, Robert B</creator><creatorcontrib>Nam, Chang-Yong ; Qin, Yang ; Park, Young S ; Hlaing, Htay ; Lu, Xinhui ; Ocko, Benjamin M ; Black, Charles T ; Grubbs, Robert B ; Brookhaven National Laboratory (BNL)</creatorcontrib><description>We have synthesized photo-cross-linkable azide-functionalized poly(3-hexylthiophene) to explore improvements in the thermal stability of bulk heterojunction solar cells. Exposing blends of photo-cross-linkable polythiophene and [6,6]-phenyl-C61-butyric acid methyl ester to ultraviolet light preferentially cross-linked the polythiophene without degrading its optical or electrical properties. X-ray scattering measurements showed that cross-linking slightly compacted the polythiophene chain lamellar stacking while increasing the polymer crystal coherence length by 20%. Optimized solar cells having cross-linked active blend layers retained 65% of their initial photovoltaic power conversion efficiency after 40 h of thermal annealing at 110 °C, while devices using un-cross-linked commercial polythiophene underwent significant phase separation and retained less than 30% of their initial efficiency after annealing.</description><identifier>ISSN: 0024-9297</identifier><identifier>EISSN: 1520-5835</identifier><identifier>DOI: 10.1021/ma3001725</identifier><identifier>CODEN: MAMOBX</identifier><language>eng</language><publisher>Washington, DC: American Chemical Society</publisher><subject>Applied sciences ; Energy ; Exact sciences and technology ; Natural energy ; Organic polymers ; Photovoltaic conversion ; Physicochemistry of polymers ; Polymers with particular properties ; Preparation, kinetics, thermodynamics, mechanism and catalysts ; Solar cells. Photoelectrochemical cells ; Solar energy</subject><ispartof>Macromolecules, 2012-03, Vol.45 (5), p.2338-2347</ispartof><rights>Copyright © 2012 American Chemical Society</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a382t-eab7435eee5a14c5ff390eb119b2eed3ddf652abe2d6fb104ce52942bcc1131d3</citedby><cites>FETCH-LOGICAL-a382t-eab7435eee5a14c5ff390eb119b2eed3ddf652abe2d6fb104ce52942bcc1131d3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=25617850$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.osti.gov/biblio/1109539$$D View this record in Osti.gov$$Hfree_for_read</backlink></links><search><creatorcontrib>Nam, Chang-Yong</creatorcontrib><creatorcontrib>Qin, Yang</creatorcontrib><creatorcontrib>Park, Young S</creatorcontrib><creatorcontrib>Hlaing, Htay</creatorcontrib><creatorcontrib>Lu, Xinhui</creatorcontrib><creatorcontrib>Ocko, Benjamin M</creatorcontrib><creatorcontrib>Black, Charles T</creatorcontrib><creatorcontrib>Grubbs, Robert B</creatorcontrib><creatorcontrib>Brookhaven National Laboratory (BNL)</creatorcontrib><title>Photo-Cross-Linkable Azide-Functionalized Polythiophene for Thermally Stable Bulk Heterojunction Solar Cells</title><title>Macromolecules</title><addtitle>Macromolecules</addtitle><description>We have synthesized photo-cross-linkable azide-functionalized poly(3-hexylthiophene) to explore improvements in the thermal stability of bulk heterojunction solar cells. Exposing blends of photo-cross-linkable polythiophene and [6,6]-phenyl-C61-butyric acid methyl ester to ultraviolet light preferentially cross-linked the polythiophene without degrading its optical or electrical properties. X-ray scattering measurements showed that cross-linking slightly compacted the polythiophene chain lamellar stacking while increasing the polymer crystal coherence length by 20%. Optimized solar cells having cross-linked active blend layers retained 65% of their initial photovoltaic power conversion efficiency after 40 h of thermal annealing at 110 °C, while devices using un-cross-linked commercial polythiophene underwent significant phase separation and retained less than 30% of their initial efficiency after annealing.</description><subject>Applied sciences</subject><subject>Energy</subject><subject>Exact sciences and technology</subject><subject>Natural energy</subject><subject>Organic polymers</subject><subject>Photovoltaic conversion</subject><subject>Physicochemistry of polymers</subject><subject>Polymers with particular properties</subject><subject>Preparation, kinetics, thermodynamics, mechanism and catalysts</subject><subject>Solar cells. Photoelectrochemical cells</subject><subject>Solar energy</subject><issn>0024-9297</issn><issn>1520-5835</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNptkMFPwjAUhxujiYge_A8WEw8eqn3tytgRFxETEknA89J1b1mhrKQtB_jrBTF48fQu3_dL3kfIPbBnYBxe1kowBhmXF6QHkjMqh0Jekh5jPKU5z7NrchPC8sCATEWP2FnroqOFdyHQqelWqrKYjPamRjredjoa1ylr9lgnM2d3sTVu02KHSeN8smjRr5W1u2Qef7zXrV0lE4zo3fJXTubOKp8UaG24JVeNsgHvfm-ffI3fFsWETj_fP4rRlCox5JGiqrJUSESUClItm0bkDCuAvOKItajrZiC5qpDXg6YClmqUPE95pTWAgFr0ycNp14VoyqBNRN1q13WoYwnAcinyA_R0gvTxd49NufFmrfyuBFYeW5bnlgf28cRuVNDKNl512oSzwOUAsqFkf5zSoVy6rT-0C__sfQMinYEy</recordid><startdate>20120313</startdate><enddate>20120313</enddate><creator>Nam, Chang-Yong</creator><creator>Qin, Yang</creator><creator>Park, Young S</creator><creator>Hlaing, Htay</creator><creator>Lu, Xinhui</creator><creator>Ocko, Benjamin M</creator><creator>Black, Charles T</creator><creator>Grubbs, Robert B</creator><general>American Chemical Society</general><scope>IQODW</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>OTOTI</scope></search><sort><creationdate>20120313</creationdate><title>Photo-Cross-Linkable Azide-Functionalized Polythiophene for Thermally Stable Bulk Heterojunction Solar Cells</title><author>Nam, Chang-Yong ; Qin, Yang ; Park, Young S ; Hlaing, Htay ; Lu, Xinhui ; Ocko, Benjamin M ; Black, Charles T ; Grubbs, Robert B</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a382t-eab7435eee5a14c5ff390eb119b2eed3ddf652abe2d6fb104ce52942bcc1131d3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Applied sciences</topic><topic>Energy</topic><topic>Exact sciences and technology</topic><topic>Natural energy</topic><topic>Organic polymers</topic><topic>Photovoltaic conversion</topic><topic>Physicochemistry of polymers</topic><topic>Polymers with particular properties</topic><topic>Preparation, kinetics, thermodynamics, mechanism and catalysts</topic><topic>Solar cells. Photoelectrochemical cells</topic><topic>Solar energy</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Nam, Chang-Yong</creatorcontrib><creatorcontrib>Qin, Yang</creatorcontrib><creatorcontrib>Park, Young S</creatorcontrib><creatorcontrib>Hlaing, Htay</creatorcontrib><creatorcontrib>Lu, Xinhui</creatorcontrib><creatorcontrib>Ocko, Benjamin M</creatorcontrib><creatorcontrib>Black, Charles T</creatorcontrib><creatorcontrib>Grubbs, Robert B</creatorcontrib><creatorcontrib>Brookhaven National Laboratory (BNL)</creatorcontrib><collection>Pascal-Francis</collection><collection>CrossRef</collection><collection>OSTI.GOV</collection><jtitle>Macromolecules</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Nam, Chang-Yong</au><au>Qin, Yang</au><au>Park, Young S</au><au>Hlaing, Htay</au><au>Lu, Xinhui</au><au>Ocko, Benjamin M</au><au>Black, Charles T</au><au>Grubbs, Robert B</au><aucorp>Brookhaven National Laboratory (BNL)</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Photo-Cross-Linkable Azide-Functionalized Polythiophene for Thermally Stable Bulk Heterojunction Solar Cells</atitle><jtitle>Macromolecules</jtitle><addtitle>Macromolecules</addtitle><date>2012-03-13</date><risdate>2012</risdate><volume>45</volume><issue>5</issue><spage>2338</spage><epage>2347</epage><pages>2338-2347</pages><issn>0024-9297</issn><eissn>1520-5835</eissn><coden>MAMOBX</coden><abstract>We have synthesized photo-cross-linkable azide-functionalized poly(3-hexylthiophene) to explore improvements in the thermal stability of bulk heterojunction solar cells. Exposing blends of photo-cross-linkable polythiophene and [6,6]-phenyl-C61-butyric acid methyl ester to ultraviolet light preferentially cross-linked the polythiophene without degrading its optical or electrical properties. X-ray scattering measurements showed that cross-linking slightly compacted the polythiophene chain lamellar stacking while increasing the polymer crystal coherence length by 20%. Optimized solar cells having cross-linked active blend layers retained 65% of their initial photovoltaic power conversion efficiency after 40 h of thermal annealing at 110 °C, while devices using un-cross-linked commercial polythiophene underwent significant phase separation and retained less than 30% of their initial efficiency after annealing.</abstract><cop>Washington, DC</cop><pub>American Chemical Society</pub><doi>10.1021/ma3001725</doi><tpages>10</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0024-9297
ispartof Macromolecules, 2012-03, Vol.45 (5), p.2338-2347
issn 0024-9297
1520-5835
language eng
recordid cdi_osti_scitechconnect_1109539
source American Chemical Society:Jisc Collections:American Chemical Society Read & Publish Agreement 2022-2024 (Reading list)
subjects Applied sciences
Energy
Exact sciences and technology
Natural energy
Organic polymers
Photovoltaic conversion
Physicochemistry of polymers
Polymers with particular properties
Preparation, kinetics, thermodynamics, mechanism and catalysts
Solar cells. Photoelectrochemical cells
Solar energy
title Photo-Cross-Linkable Azide-Functionalized Polythiophene for Thermally Stable Bulk Heterojunction Solar Cells
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-04T01%3A59%3A08IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-acs_osti_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Photo-Cross-Linkable%20Azide-Functionalized%20Polythiophene%20for%20Thermally%20Stable%20Bulk%20Heterojunction%20Solar%20Cells&rft.jtitle=Macromolecules&rft.au=Nam,%20Chang-Yong&rft.aucorp=Brookhaven%20National%20Laboratory%20(BNL)&rft.date=2012-03-13&rft.volume=45&rft.issue=5&rft.spage=2338&rft.epage=2347&rft.pages=2338-2347&rft.issn=0024-9297&rft.eissn=1520-5835&rft.coden=MAMOBX&rft_id=info:doi/10.1021/ma3001725&rft_dat=%3Cacs_osti_%3Ea066467763%3C/acs_osti_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-a382t-eab7435eee5a14c5ff390eb119b2eed3ddf652abe2d6fb104ce52942bcc1131d3%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_id=info:pmid/&rfr_iscdi=true