Loading…
Difluorinated Oligothiophenes for High‐Efficiency All‐Small‐Molecule Organic Solar Cells: Positional Isomeric Effect of Fluorine Substitution on Performance Variations
Three symmetrically difluorinated organic semiconductors (namely D5T2F‐P, D5T2F‐S, and D5T2F‐T) containing rhodanine‐flanked pentathiophene structures are synthesized and used as donors in all‐small‐molecule organic solar cells (ASM‐OSCs) prepared with the small‐molecule acceptor 2,2′‐((2Z,2′Z)‐((4,...
Saved in:
Published in: | Solar RRL 2020-03, Vol.4 (3), p.n/a |
---|---|
Main Authors: | , , , , , , , , , |
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-c2892-ed54024c299665483069a69ce593b12d8d0084cf183aba21fe7393016cab0f213 |
---|---|
cites | cdi_FETCH-LOGICAL-c2892-ed54024c299665483069a69ce593b12d8d0084cf183aba21fe7393016cab0f213 |
container_end_page | n/a |
container_issue | 3 |
container_start_page | |
container_title | Solar RRL |
container_volume | 4 |
creator | Duan, Tainan Gao, Jie Babics, Maxime Kan, Zhipeng Zhong, Cheng Singh, Ranbir Yu, Donghong Lee, Jaewon Xiao, Zeyun Lu, Shirong |
description | Three symmetrically difluorinated organic semiconductors (namely D5T2F‐P, D5T2F‐S, and D5T2F‐T) containing rhodanine‐flanked pentathiophene structures are synthesized and used as donors in all‐small‐molecule organic solar cells (ASM‐OSCs) prepared with the small‐molecule acceptor 2,2′‐((2Z,2′Z)‐((4,4,9,9‐tetrahexyl‐4,9‐dihydro‐s‐indaceno[1,2‐b:5,6‐b′]dithiophene‐2,7‐diyl)bis(methanylylidene))bis(5,6‐difluoro‐3‐oxo‐2,3‐dihydro‐1H‐indene‐2,1‐diylidene))dimalononitrile (IDIC‐4F). The different substitutional positions of fluorine atoms (–F) in the conjugated backbone of the donor molecule lead to various material and photovoltaic properties being exhibited. Among the three isomers, the centrally fluorinated D5T2F‐P exhibits a redshifted absorption spectrum, downshifted highest occupied molecular orbital (HOMO) energy level, and improved miscibility with IDIC‐4F in the blend films, all of which result in superior device performance. The power conversion efficiency (PCE) of the ASM‐OSCs based on D5T2F‐P:IDIC‐4F reaches an impressive value of 9.36% with an open‐circuit voltage (VOC) value of 0.86 V and a short‐circuit current density (JSC) value of 16.94 mA cm−2, whereas those of D5T2F‐S (6.11%) and D5T2F‐T (5.42%) are much lower. In comparison, an ASM‐OSC based on the nonfluorinated analogue DRCN5T fabricated under the same conditions exhibits poorer performance (8.03% with IDIC‐4F), revealing 16% enhancement in the PCE achieved through backbone fluorination. The PCE of 9.36% may be one of the highest efficiencies of oligothiophene‐based ASM‐OSCs reported in the literature to date.
Difluorinated pentathiophene derivatives are synthesized and used as electron donors in all‐small‐molecule organic solar cells. The different substitutional positions of the fluorine atoms in the conjugated backbone of the donor molecules lead to various material and photovoltaic properties. A champion power conversion efficiency of 9.36% is obtained with central fluorinated isomer‐based device. |
doi_str_mv | 10.1002/solr.201900472 |
format | article |
fullrecord | <record><control><sourceid>wiley_cross</sourceid><recordid>TN_cdi_crossref_primary_10_1002_solr_201900472</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>SOLR201900472</sourcerecordid><originalsourceid>FETCH-LOGICAL-c2892-ed54024c299665483069a69ce593b12d8d0084cf183aba21fe7393016cab0f213</originalsourceid><addsrcrecordid>eNqFUM1Kw0AQDqJg0V497wuk7m7SJOut1NYWKilGxVvYbGbblU227CZIbz6CL-JL-SQmVtSbMDDDzPfDfJ53QfCIYEwvndF2RDFhGIcxPfIGNIhin7Dk6fjPfOoNnXvGHSEM4yQiA-_9WkndGqtq3kCJUq02ptkqs9tCDQ5JY9FCbbYfr28zKZVQUIs9mmjdLbKKf_Vbo0G0GlBqN7xWAmVGc4umoLW7QmvjVKNMzTVaOlOB7QCdFIgGGYnmB29AWVu4RjVtD0VdrcF23hWvBaBHbhXvD-7cO5FcOxh-9zPvYT67ny78VXqznE5WvqAJoz6U47B7UVDGomgcJgGOGI-YgDELCkLLpMQ4CYUkScALTomEOGABJpHgBZaUBGfe6KArrHHOgsx3VlXc7nOC8z7vvM87_8m7I7AD4UVp2P-DzrN0dffL_QR-lYvW</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype></control><display><type>article</type><title>Difluorinated Oligothiophenes for High‐Efficiency All‐Small‐Molecule Organic Solar Cells: Positional Isomeric Effect of Fluorine Substitution on Performance Variations</title><source>Wiley</source><creator>Duan, Tainan ; Gao, Jie ; Babics, Maxime ; Kan, Zhipeng ; Zhong, Cheng ; Singh, Ranbir ; Yu, Donghong ; Lee, Jaewon ; Xiao, Zeyun ; Lu, Shirong</creator><creatorcontrib>Duan, Tainan ; Gao, Jie ; Babics, Maxime ; Kan, Zhipeng ; Zhong, Cheng ; Singh, Ranbir ; Yu, Donghong ; Lee, Jaewon ; Xiao, Zeyun ; Lu, Shirong</creatorcontrib><description>Three symmetrically difluorinated organic semiconductors (namely D5T2F‐P, D5T2F‐S, and D5T2F‐T) containing rhodanine‐flanked pentathiophene structures are synthesized and used as donors in all‐small‐molecule organic solar cells (ASM‐OSCs) prepared with the small‐molecule acceptor 2,2′‐((2Z,2′Z)‐((4,4,9,9‐tetrahexyl‐4,9‐dihydro‐s‐indaceno[1,2‐b:5,6‐b′]dithiophene‐2,7‐diyl)bis(methanylylidene))bis(5,6‐difluoro‐3‐oxo‐2,3‐dihydro‐1H‐indene‐2,1‐diylidene))dimalononitrile (IDIC‐4F). The different substitutional positions of fluorine atoms (–F) in the conjugated backbone of the donor molecule lead to various material and photovoltaic properties being exhibited. Among the three isomers, the centrally fluorinated D5T2F‐P exhibits a redshifted absorption spectrum, downshifted highest occupied molecular orbital (HOMO) energy level, and improved miscibility with IDIC‐4F in the blend films, all of which result in superior device performance. The power conversion efficiency (PCE) of the ASM‐OSCs based on D5T2F‐P:IDIC‐4F reaches an impressive value of 9.36% with an open‐circuit voltage (VOC) value of 0.86 V and a short‐circuit current density (JSC) value of 16.94 mA cm−2, whereas those of D5T2F‐S (6.11%) and D5T2F‐T (5.42%) are much lower. In comparison, an ASM‐OSC based on the nonfluorinated analogue DRCN5T fabricated under the same conditions exhibits poorer performance (8.03% with IDIC‐4F), revealing 16% enhancement in the PCE achieved through backbone fluorination. The PCE of 9.36% may be one of the highest efficiencies of oligothiophene‐based ASM‐OSCs reported in the literature to date.
Difluorinated pentathiophene derivatives are synthesized and used as electron donors in all‐small‐molecule organic solar cells. The different substitutional positions of the fluorine atoms in the conjugated backbone of the donor molecules lead to various material and photovoltaic properties. A champion power conversion efficiency of 9.36% is obtained with central fluorinated isomer‐based device.</description><identifier>ISSN: 2367-198X</identifier><identifier>EISSN: 2367-198X</identifier><identifier>DOI: 10.1002/solr.201900472</identifier><language>eng</language><subject>binding energies ; fluorination ; nonfullerene ; organic solar cells ; small-molecule donors</subject><ispartof>Solar RRL, 2020-03, Vol.4 (3), p.n/a</ispartof><rights>2020 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c2892-ed54024c299665483069a69ce593b12d8d0084cf183aba21fe7393016cab0f213</citedby><cites>FETCH-LOGICAL-c2892-ed54024c299665483069a69ce593b12d8d0084cf183aba21fe7393016cab0f213</cites><orcidid>0000-0001-6438-1082</orcidid></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>Duan, Tainan</creatorcontrib><creatorcontrib>Gao, Jie</creatorcontrib><creatorcontrib>Babics, Maxime</creatorcontrib><creatorcontrib>Kan, Zhipeng</creatorcontrib><creatorcontrib>Zhong, Cheng</creatorcontrib><creatorcontrib>Singh, Ranbir</creatorcontrib><creatorcontrib>Yu, Donghong</creatorcontrib><creatorcontrib>Lee, Jaewon</creatorcontrib><creatorcontrib>Xiao, Zeyun</creatorcontrib><creatorcontrib>Lu, Shirong</creatorcontrib><title>Difluorinated Oligothiophenes for High‐Efficiency All‐Small‐Molecule Organic Solar Cells: Positional Isomeric Effect of Fluorine Substitution on Performance Variations</title><title>Solar RRL</title><description>Three symmetrically difluorinated organic semiconductors (namely D5T2F‐P, D5T2F‐S, and D5T2F‐T) containing rhodanine‐flanked pentathiophene structures are synthesized and used as donors in all‐small‐molecule organic solar cells (ASM‐OSCs) prepared with the small‐molecule acceptor 2,2′‐((2Z,2′Z)‐((4,4,9,9‐tetrahexyl‐4,9‐dihydro‐s‐indaceno[1,2‐b:5,6‐b′]dithiophene‐2,7‐diyl)bis(methanylylidene))bis(5,6‐difluoro‐3‐oxo‐2,3‐dihydro‐1H‐indene‐2,1‐diylidene))dimalononitrile (IDIC‐4F). The different substitutional positions of fluorine atoms (–F) in the conjugated backbone of the donor molecule lead to various material and photovoltaic properties being exhibited. Among the three isomers, the centrally fluorinated D5T2F‐P exhibits a redshifted absorption spectrum, downshifted highest occupied molecular orbital (HOMO) energy level, and improved miscibility with IDIC‐4F in the blend films, all of which result in superior device performance. The power conversion efficiency (PCE) of the ASM‐OSCs based on D5T2F‐P:IDIC‐4F reaches an impressive value of 9.36% with an open‐circuit voltage (VOC) value of 0.86 V and a short‐circuit current density (JSC) value of 16.94 mA cm−2, whereas those of D5T2F‐S (6.11%) and D5T2F‐T (5.42%) are much lower. In comparison, an ASM‐OSC based on the nonfluorinated analogue DRCN5T fabricated under the same conditions exhibits poorer performance (8.03% with IDIC‐4F), revealing 16% enhancement in the PCE achieved through backbone fluorination. The PCE of 9.36% may be one of the highest efficiencies of oligothiophene‐based ASM‐OSCs reported in the literature to date.
Difluorinated pentathiophene derivatives are synthesized and used as electron donors in all‐small‐molecule organic solar cells. The different substitutional positions of the fluorine atoms in the conjugated backbone of the donor molecules lead to various material and photovoltaic properties. A champion power conversion efficiency of 9.36% is obtained with central fluorinated isomer‐based device.</description><subject>binding energies</subject><subject>fluorination</subject><subject>nonfullerene</subject><subject>organic solar cells</subject><subject>small-molecule donors</subject><issn>2367-198X</issn><issn>2367-198X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNqFUM1Kw0AQDqJg0V497wuk7m7SJOut1NYWKilGxVvYbGbblU227CZIbz6CL-JL-SQmVtSbMDDDzPfDfJ53QfCIYEwvndF2RDFhGIcxPfIGNIhin7Dk6fjPfOoNnXvGHSEM4yQiA-_9WkndGqtq3kCJUq02ptkqs9tCDQ5JY9FCbbYfr28zKZVQUIs9mmjdLbKKf_Vbo0G0GlBqN7xWAmVGc4umoLW7QmvjVKNMzTVaOlOB7QCdFIgGGYnmB29AWVu4RjVtD0VdrcF23hWvBaBHbhXvD-7cO5FcOxh-9zPvYT67ny78VXqznE5WvqAJoz6U47B7UVDGomgcJgGOGI-YgDELCkLLpMQ4CYUkScALTomEOGABJpHgBZaUBGfe6KArrHHOgsx3VlXc7nOC8z7vvM87_8m7I7AD4UVp2P-DzrN0dffL_QR-lYvW</recordid><startdate>202003</startdate><enddate>202003</enddate><creator>Duan, Tainan</creator><creator>Gao, Jie</creator><creator>Babics, Maxime</creator><creator>Kan, Zhipeng</creator><creator>Zhong, Cheng</creator><creator>Singh, Ranbir</creator><creator>Yu, Donghong</creator><creator>Lee, Jaewon</creator><creator>Xiao, Zeyun</creator><creator>Lu, Shirong</creator><scope>AAYXX</scope><scope>CITATION</scope><orcidid>https://orcid.org/0000-0001-6438-1082</orcidid></search><sort><creationdate>202003</creationdate><title>Difluorinated Oligothiophenes for High‐Efficiency All‐Small‐Molecule Organic Solar Cells: Positional Isomeric Effect of Fluorine Substitution on Performance Variations</title><author>Duan, Tainan ; Gao, Jie ; Babics, Maxime ; Kan, Zhipeng ; Zhong, Cheng ; Singh, Ranbir ; Yu, Donghong ; Lee, Jaewon ; Xiao, Zeyun ; Lu, Shirong</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c2892-ed54024c299665483069a69ce593b12d8d0084cf183aba21fe7393016cab0f213</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>binding energies</topic><topic>fluorination</topic><topic>nonfullerene</topic><topic>organic solar cells</topic><topic>small-molecule donors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Duan, Tainan</creatorcontrib><creatorcontrib>Gao, Jie</creatorcontrib><creatorcontrib>Babics, Maxime</creatorcontrib><creatorcontrib>Kan, Zhipeng</creatorcontrib><creatorcontrib>Zhong, Cheng</creatorcontrib><creatorcontrib>Singh, Ranbir</creatorcontrib><creatorcontrib>Yu, Donghong</creatorcontrib><creatorcontrib>Lee, Jaewon</creatorcontrib><creatorcontrib>Xiao, Zeyun</creatorcontrib><creatorcontrib>Lu, Shirong</creatorcontrib><collection>CrossRef</collection><jtitle>Solar RRL</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Duan, Tainan</au><au>Gao, Jie</au><au>Babics, Maxime</au><au>Kan, Zhipeng</au><au>Zhong, Cheng</au><au>Singh, Ranbir</au><au>Yu, Donghong</au><au>Lee, Jaewon</au><au>Xiao, Zeyun</au><au>Lu, Shirong</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Difluorinated Oligothiophenes for High‐Efficiency All‐Small‐Molecule Organic Solar Cells: Positional Isomeric Effect of Fluorine Substitution on Performance Variations</atitle><jtitle>Solar RRL</jtitle><date>2020-03</date><risdate>2020</risdate><volume>4</volume><issue>3</issue><epage>n/a</epage><issn>2367-198X</issn><eissn>2367-198X</eissn><abstract>Three symmetrically difluorinated organic semiconductors (namely D5T2F‐P, D5T2F‐S, and D5T2F‐T) containing rhodanine‐flanked pentathiophene structures are synthesized and used as donors in all‐small‐molecule organic solar cells (ASM‐OSCs) prepared with the small‐molecule acceptor 2,2′‐((2Z,2′Z)‐((4,4,9,9‐tetrahexyl‐4,9‐dihydro‐s‐indaceno[1,2‐b:5,6‐b′]dithiophene‐2,7‐diyl)bis(methanylylidene))bis(5,6‐difluoro‐3‐oxo‐2,3‐dihydro‐1H‐indene‐2,1‐diylidene))dimalononitrile (IDIC‐4F). The different substitutional positions of fluorine atoms (–F) in the conjugated backbone of the donor molecule lead to various material and photovoltaic properties being exhibited. Among the three isomers, the centrally fluorinated D5T2F‐P exhibits a redshifted absorption spectrum, downshifted highest occupied molecular orbital (HOMO) energy level, and improved miscibility with IDIC‐4F in the blend films, all of which result in superior device performance. The power conversion efficiency (PCE) of the ASM‐OSCs based on D5T2F‐P:IDIC‐4F reaches an impressive value of 9.36% with an open‐circuit voltage (VOC) value of 0.86 V and a short‐circuit current density (JSC) value of 16.94 mA cm−2, whereas those of D5T2F‐S (6.11%) and D5T2F‐T (5.42%) are much lower. In comparison, an ASM‐OSC based on the nonfluorinated analogue DRCN5T fabricated under the same conditions exhibits poorer performance (8.03% with IDIC‐4F), revealing 16% enhancement in the PCE achieved through backbone fluorination. The PCE of 9.36% may be one of the highest efficiencies of oligothiophene‐based ASM‐OSCs reported in the literature to date.
Difluorinated pentathiophene derivatives are synthesized and used as electron donors in all‐small‐molecule organic solar cells. The different substitutional positions of the fluorine atoms in the conjugated backbone of the donor molecules lead to various material and photovoltaic properties. A champion power conversion efficiency of 9.36% is obtained with central fluorinated isomer‐based device.</abstract><doi>10.1002/solr.201900472</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0001-6438-1082</orcidid></addata></record> |
fulltext | fulltext |
identifier | ISSN: 2367-198X |
ispartof | Solar RRL, 2020-03, Vol.4 (3), p.n/a |
issn | 2367-198X 2367-198X |
language | eng |
recordid | cdi_crossref_primary_10_1002_solr_201900472 |
source | Wiley |
subjects | binding energies fluorination nonfullerene organic solar cells small-molecule donors |
title | Difluorinated Oligothiophenes for High‐Efficiency All‐Small‐Molecule Organic Solar Cells: Positional Isomeric Effect of Fluorine Substitution on Performance Variations |
url | http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-24T17%3A01%3A47IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-wiley_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Difluorinated%20Oligothiophenes%20for%20High%E2%80%90Efficiency%20All%E2%80%90Small%E2%80%90Molecule%20Organic%20Solar%20Cells:%20Positional%20Isomeric%20Effect%20of%20Fluorine%20Substitution%20on%20Performance%20Variations&rft.jtitle=Solar%20RRL&rft.au=Duan,%20Tainan&rft.date=2020-03&rft.volume=4&rft.issue=3&rft.epage=n/a&rft.issn=2367-198X&rft.eissn=2367-198X&rft_id=info:doi/10.1002/solr.201900472&rft_dat=%3Cwiley_cross%3ESOLR201900472%3C/wiley_cross%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c2892-ed54024c299665483069a69ce593b12d8d0084cf183aba21fe7393016cab0f213%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 |