Asymmetric Polymer Additive for Morphological Regulation and Thermally Stable Organic Solar Cells
High thermal stability is crucial for the commercialization of organic solar cells (OSCs). The thermal stability of OSCs has been improved using the tailoring blend morphology of bulk heterojunctions (BHJs). Herein, we demonstrated thermally stable OSCs in a ternary blended system containing low-cry...
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Veröffentlicht in: | ACS applied materials & interfaces 2023-06, Vol.15 (22), p.27026-27033 |
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creator | Park, Sang Ah Kim, Do Hui Chung, Dasol Kim, Jeongsu Park, Taiho Cho, Shinuk Kim, Minjun |
description | High thermal stability is crucial for the commercialization of organic solar cells (OSCs). The thermal stability of OSCs has been improved using the tailoring blend morphology of bulk heterojunctions (BHJs). Herein, we demonstrated thermally stable OSCs in a ternary blended system containing low-crystalline semiconducting polymers (asy-PNDI1FTVT and PTB7-Th) and a non-fullerene acceptor (Y6). The asymmetric n-type semiconducting polymer (asy-PNDI1FTVT) differed from general symmetric semiconducting polymers as it randomly substituted fluorine atoms at the donor moiety (TVT), resulting in significantly lower crystallinity. asy-PNDI1FTVT in PTB7-Th:Y6 exhibited a well-mixed morphology at the BHJ and efficiently facilitated the charge dissociation process with an enhanced fill factor and power conversion efficiency. Furthermore, the ternary system of PTB7-Th:Y6:asy-PNDI1FTVT suppressed phase separation with negligible burn-in loss and performance degradation under thermal stress. The experiments showed that our devices without encapsulation retained over 90% of their initial efficiencies after 100 h at 65 °C. These results show significant potential for the development of thermally stable OSCs with reasonable efficiency. |
doi_str_mv | 10.1021/acsami.3c04804 |
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The thermal stability of OSCs has been improved using the tailoring blend morphology of bulk heterojunctions (BHJs). Herein, we demonstrated thermally stable OSCs in a ternary blended system containing low-crystalline semiconducting polymers (asy-PNDI1FTVT and PTB7-Th) and a non-fullerene acceptor (Y6). The asymmetric n-type semiconducting polymer (asy-PNDI1FTVT) differed from general symmetric semiconducting polymers as it randomly substituted fluorine atoms at the donor moiety (TVT), resulting in significantly lower crystallinity. asy-PNDI1FTVT in PTB7-Th:Y6 exhibited a well-mixed morphology at the BHJ and efficiently facilitated the charge dissociation process with an enhanced fill factor and power conversion efficiency. Furthermore, the ternary system of PTB7-Th:Y6:asy-PNDI1FTVT suppressed phase separation with negligible burn-in loss and performance degradation under thermal stress. The experiments showed that our devices without encapsulation retained over 90% of their initial efficiencies after 100 h at 65 °C. These results show significant potential for the development of thermally stable OSCs with reasonable efficiency.</description><identifier>ISSN: 1944-8244</identifier><identifier>EISSN: 1944-8252</identifier><identifier>DOI: 10.1021/acsami.3c04804</identifier><identifier>PMID: 37220162</identifier><language>eng</language><publisher>United States: American Chemical Society</publisher><subject>Organic Electronic Devices</subject><ispartof>ACS applied materials & interfaces, 2023-06, Vol.15 (22), p.27026-27033</ispartof><rights>2023 American Chemical Society</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-a2811-e8fae403cc1cc6a7d87e5bf66df5d4b93eb5b27b00ef0f9eacf7a52117a37af3</citedby><cites>FETCH-LOGICAL-a2811-e8fae403cc1cc6a7d87e5bf66df5d4b93eb5b27b00ef0f9eacf7a52117a37af3</cites><orcidid>0000-0002-6855-833X ; 0000-0002-5867-4679</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://pubs.acs.org/doi/pdf/10.1021/acsami.3c04804$$EPDF$$P50$$Gacs$$H</linktopdf><linktohtml>$$Uhttps://pubs.acs.org/doi/10.1021/acsami.3c04804$$EHTML$$P50$$Gacs$$H</linktohtml><link.rule.ids>314,780,784,2765,27076,27924,27925,56738,56788</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37220162$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Park, Sang Ah</creatorcontrib><creatorcontrib>Kim, Do Hui</creatorcontrib><creatorcontrib>Chung, Dasol</creatorcontrib><creatorcontrib>Kim, Jeongsu</creatorcontrib><creatorcontrib>Park, Taiho</creatorcontrib><creatorcontrib>Cho, Shinuk</creatorcontrib><creatorcontrib>Kim, Minjun</creatorcontrib><title>Asymmetric Polymer Additive for Morphological Regulation and Thermally Stable Organic Solar Cells</title><title>ACS applied materials & interfaces</title><addtitle>ACS Appl. Mater. Interfaces</addtitle><description>High thermal stability is crucial for the commercialization of organic solar cells (OSCs). The thermal stability of OSCs has been improved using the tailoring blend morphology of bulk heterojunctions (BHJs). Herein, we demonstrated thermally stable OSCs in a ternary blended system containing low-crystalline semiconducting polymers (asy-PNDI1FTVT and PTB7-Th) and a non-fullerene acceptor (Y6). The asymmetric n-type semiconducting polymer (asy-PNDI1FTVT) differed from general symmetric semiconducting polymers as it randomly substituted fluorine atoms at the donor moiety (TVT), resulting in significantly lower crystallinity. asy-PNDI1FTVT in PTB7-Th:Y6 exhibited a well-mixed morphology at the BHJ and efficiently facilitated the charge dissociation process with an enhanced fill factor and power conversion efficiency. Furthermore, the ternary system of PTB7-Th:Y6:asy-PNDI1FTVT suppressed phase separation with negligible burn-in loss and performance degradation under thermal stress. The experiments showed that our devices without encapsulation retained over 90% of their initial efficiencies after 100 h at 65 °C. These results show significant potential for the development of thermally stable OSCs with reasonable efficiency.</description><subject>Organic Electronic Devices</subject><issn>1944-8244</issn><issn>1944-8252</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp1kE1PwzAMhiMEYmNw5YhyREgdSZp-HaeJL2loiO1euamzdUqbkbRI_fcUbezGyT48fm0_hNxyNuVM8EdQHupqGiomUybPyJhnUgapiMT5qZdyRK683zEWh4JFl2QUJkIwHosxgZnv6xpbVyn6YU1fo6Ozsqza6hupto6-W7ffWmM3lQJDP3HTGWgr21BoSrreoqvBmJ6uWigM0qXbQDNErawBR-dojL8mFxqMx5tjnZD189N6_hosli9v89kiAJFyHmCqASULleJKxZCUaYJRoeO41FEpiyzEIipEUjCGmukMQekEIsF5AmECOpyQ-0Ps3tmvDn2b15VXwwHQoO18PixJE5mFWTyg0wOqnPXeoc73rqrB9Tln-a_V_GA1P1odBu6O2V1RY3nC_zQOwMMBGAbzne1cM3z6X9oPJWyD7Q</recordid><startdate>20230607</startdate><enddate>20230607</enddate><creator>Park, Sang Ah</creator><creator>Kim, Do Hui</creator><creator>Chung, Dasol</creator><creator>Kim, Jeongsu</creator><creator>Park, Taiho</creator><creator>Cho, Shinuk</creator><creator>Kim, Minjun</creator><general>American Chemical Society</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-6855-833X</orcidid><orcidid>https://orcid.org/0000-0002-5867-4679</orcidid></search><sort><creationdate>20230607</creationdate><title>Asymmetric Polymer Additive for Morphological Regulation and Thermally Stable Organic Solar Cells</title><author>Park, Sang Ah ; Kim, Do Hui ; Chung, Dasol ; Kim, Jeongsu ; Park, Taiho ; Cho, Shinuk ; Kim, Minjun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-a2811-e8fae403cc1cc6a7d87e5bf66df5d4b93eb5b27b00ef0f9eacf7a52117a37af3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Organic Electronic Devices</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Park, Sang Ah</creatorcontrib><creatorcontrib>Kim, Do Hui</creatorcontrib><creatorcontrib>Chung, Dasol</creatorcontrib><creatorcontrib>Kim, Jeongsu</creatorcontrib><creatorcontrib>Park, Taiho</creatorcontrib><creatorcontrib>Cho, Shinuk</creatorcontrib><creatorcontrib>Kim, Minjun</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>ACS applied materials & interfaces</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Park, Sang Ah</au><au>Kim, Do Hui</au><au>Chung, Dasol</au><au>Kim, Jeongsu</au><au>Park, Taiho</au><au>Cho, Shinuk</au><au>Kim, Minjun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Asymmetric Polymer Additive for Morphological Regulation and Thermally Stable Organic Solar Cells</atitle><jtitle>ACS applied materials & interfaces</jtitle><addtitle>ACS Appl. Mater. Interfaces</addtitle><date>2023-06-07</date><risdate>2023</risdate><volume>15</volume><issue>22</issue><spage>27026</spage><epage>27033</epage><pages>27026-27033</pages><issn>1944-8244</issn><eissn>1944-8252</eissn><abstract>High thermal stability is crucial for the commercialization of organic solar cells (OSCs). The thermal stability of OSCs has been improved using the tailoring blend morphology of bulk heterojunctions (BHJs). Herein, we demonstrated thermally stable OSCs in a ternary blended system containing low-crystalline semiconducting polymers (asy-PNDI1FTVT and PTB7-Th) and a non-fullerene acceptor (Y6). The asymmetric n-type semiconducting polymer (asy-PNDI1FTVT) differed from general symmetric semiconducting polymers as it randomly substituted fluorine atoms at the donor moiety (TVT), resulting in significantly lower crystallinity. asy-PNDI1FTVT in PTB7-Th:Y6 exhibited a well-mixed morphology at the BHJ and efficiently facilitated the charge dissociation process with an enhanced fill factor and power conversion efficiency. Furthermore, the ternary system of PTB7-Th:Y6:asy-PNDI1FTVT suppressed phase separation with negligible burn-in loss and performance degradation under thermal stress. The experiments showed that our devices without encapsulation retained over 90% of their initial efficiencies after 100 h at 65 °C. These results show significant potential for the development of thermally stable OSCs with reasonable efficiency.</abstract><cop>United States</cop><pub>American Chemical Society</pub><pmid>37220162</pmid><doi>10.1021/acsami.3c04804</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-6855-833X</orcidid><orcidid>https://orcid.org/0000-0002-5867-4679</orcidid></addata></record> |
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title | Asymmetric Polymer Additive for Morphological Regulation and Thermally Stable Organic Solar Cells |
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