Systematically Controlling Acceptor Fluorination Optimizes Hierarchical Morphology, Vertical Phase Separation, and Efficiency in Non‐Fullerene Organic Solar Cells
Non‐fullerene acceptor (NFA) end group (EG) functionalization, especially by fluorination, affects not only the energetics but also the morphology of bulk‐heterojunction (BHJ) organic solar cell (OSC) active layers, thereby influencing the power conversion efficiency (PCE) and other metrics of NFA‐b...
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creator | Zhang, Xiaohua Li, Guoping Mukherjee, Subhrangsu Huang, Wei Zheng, Ding Feng, Liang‐Wen Chen, Yao Wu, Jianglin Sangwan, Vinod K. Hersam, Mark C. DeLongchamp, Dean M. Yu, Junsheng Facchetti, Antonio Marks, Tobin J. |
description | Non‐fullerene acceptor (NFA) end group (EG) functionalization, especially by fluorination, affects not only the energetics but also the morphology of bulk‐heterojunction (BHJ) organic solar cell (OSC) active layers, thereby influencing the power conversion efficiency (PCE) and other metrics of NFA‐based OSCs. However, a quantitative understanding of how varying the degrees of NFA fluorination influence the blend morphological and photovoltaic properties remains elusive. Here a series of three A‐DAD‐A type NFAs (D = π‐donor group and A = π‐acceptor EG) which systematically increase the degree of EG fluorination and comprehensively investigate the resulting blends with the polymer donor PM6 in terms of optical properties, electronic structure, film crystallinity, charge carrier transport, and OSC performance is reported. The results indicate that the most highly fluorinated NFA, BT‐BO‐L4F, achieves an optimal BHJ hierarchical morphology where enhanced NFA molecule intermolecular π–π stacking and optimal vertical phase gradation are achieved in the BHJ blend. These factors also promote optimum NFA‐cathode contact, more balanced electron and hole mobility, and suppress both monomolecular and bimolecular recombination. As a result, both the short‐circuit current density and fill factor in this OSC series progressively increase with increasing EG fluorine density, and the resulting PCEs increase from 9 to 16.8%.
Organic solar cell active layers with A‐DAD‐A (A = acceptor; D = donor) non‐fullerene acceptors (NFAs) having different extents of end group fluorination are systematically characterized in terms of film crystallinity, donor‐acceptor depth distribution, charge carrier transport, and cell performance. The most fluorinated NFA, BT‐BO‐L4F, has optimal hierarchical morphology and vertical phase gradation, affording a power conversion efficiency of 16.81%. |
doi_str_mv | 10.1002/aenm.202102172 |
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Organic solar cell active layers with A‐DAD‐A (A = acceptor; D = donor) non‐fullerene acceptors (NFAs) having different extents of end group fluorination are systematically characterized in terms of film crystallinity, donor‐acceptor depth distribution, charge carrier transport, and cell performance. The most fluorinated NFA, BT‐BO‐L4F, has optimal hierarchical morphology and vertical phase gradation, affording a power conversion efficiency of 16.81%.</description><identifier>ISSN: 1614-6832</identifier><identifier>EISSN: 1614-6840</identifier><identifier>DOI: 10.1002/aenm.202102172</identifier><language>eng</language><publisher>Weinheim: Wiley Subscription Services, Inc</publisher><subject>bulk heterojunctions ; Carrier transport ; Circuits ; Current carriers ; Electronic structure ; Energy conversion efficiency ; Fluorination ; Fluorine ; Fullerenes ; Heterojunctions ; Hole mobility ; Morphology ; morphology control ; non‐fullerene solar cells ; Optical properties ; Optimization ; Phase separation ; Photovoltaic cells ; Polymer blends ; Solar cells ; Vertical separation</subject><ispartof>Advanced energy materials, 2022-01, Vol.12 (1), p.n/a</ispartof><rights>2021 Wiley‐VCH GmbH</rights><rights>2022 Wiley‐VCH GmbH</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3572-505a8b225e0774a673df92700e79e62360b8cd6ac1255d35dc542fd2fb57e1573</citedby><cites>FETCH-LOGICAL-c3572-505a8b225e0774a673df92700e79e62360b8cd6ac1255d35dc542fd2fb57e1573</cites><orcidid>0000-0001-8771-0141</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Faenm.202102172$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Faenm.202102172$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1416,27915,27916,45565,45566</link.rule.ids></links><search><creatorcontrib>Zhang, Xiaohua</creatorcontrib><creatorcontrib>Li, Guoping</creatorcontrib><creatorcontrib>Mukherjee, Subhrangsu</creatorcontrib><creatorcontrib>Huang, Wei</creatorcontrib><creatorcontrib>Zheng, Ding</creatorcontrib><creatorcontrib>Feng, Liang‐Wen</creatorcontrib><creatorcontrib>Chen, Yao</creatorcontrib><creatorcontrib>Wu, Jianglin</creatorcontrib><creatorcontrib>Sangwan, Vinod K.</creatorcontrib><creatorcontrib>Hersam, Mark C.</creatorcontrib><creatorcontrib>DeLongchamp, Dean M.</creatorcontrib><creatorcontrib>Yu, Junsheng</creatorcontrib><creatorcontrib>Facchetti, Antonio</creatorcontrib><creatorcontrib>Marks, Tobin J.</creatorcontrib><title>Systematically Controlling Acceptor Fluorination Optimizes Hierarchical Morphology, Vertical Phase Separation, and Efficiency in Non‐Fullerene Organic Solar Cells</title><title>Advanced energy materials</title><description>Non‐fullerene acceptor (NFA) end group (EG) functionalization, especially by fluorination, affects not only the energetics but also the morphology of bulk‐heterojunction (BHJ) organic solar cell (OSC) active layers, thereby influencing the power conversion efficiency (PCE) and other metrics of NFA‐based OSCs. However, a quantitative understanding of how varying the degrees of NFA fluorination influence the blend morphological and photovoltaic properties remains elusive. Here a series of three A‐DAD‐A type NFAs (D = π‐donor group and A = π‐acceptor EG) which systematically increase the degree of EG fluorination and comprehensively investigate the resulting blends with the polymer donor PM6 in terms of optical properties, electronic structure, film crystallinity, charge carrier transport, and OSC performance is reported. The results indicate that the most highly fluorinated NFA, BT‐BO‐L4F, achieves an optimal BHJ hierarchical morphology where enhanced NFA molecule intermolecular π–π stacking and optimal vertical phase gradation are achieved in the BHJ blend. These factors also promote optimum NFA‐cathode contact, more balanced electron and hole mobility, and suppress both monomolecular and bimolecular recombination. As a result, both the short‐circuit current density and fill factor in this OSC series progressively increase with increasing EG fluorine density, and the resulting PCEs increase from 9 to 16.8%.
Organic solar cell active layers with A‐DAD‐A (A = acceptor; D = donor) non‐fullerene acceptors (NFAs) having different extents of end group fluorination are systematically characterized in terms of film crystallinity, donor‐acceptor depth distribution, charge carrier transport, and cell performance. The most fluorinated NFA, BT‐BO‐L4F, has optimal hierarchical morphology and vertical phase gradation, affording a power conversion efficiency of 16.81%.</description><subject>bulk heterojunctions</subject><subject>Carrier transport</subject><subject>Circuits</subject><subject>Current carriers</subject><subject>Electronic structure</subject><subject>Energy conversion efficiency</subject><subject>Fluorination</subject><subject>Fluorine</subject><subject>Fullerenes</subject><subject>Heterojunctions</subject><subject>Hole mobility</subject><subject>Morphology</subject><subject>morphology control</subject><subject>non‐fullerene solar cells</subject><subject>Optical properties</subject><subject>Optimization</subject><subject>Phase separation</subject><subject>Photovoltaic cells</subject><subject>Polymer blends</subject><subject>Solar cells</subject><subject>Vertical separation</subject><issn>1614-6832</issn><issn>1614-6840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><recordid>eNqFkc9OGzEQh1cVlYqAa8-WeiXBf9b27jGKEkACgpTCdeV4ZxMjx96ON0LLiUfoQ_TJ-iTdkAqOjEaaOXzfzOGXZd8ZHTNK-YWBsB1zytnQmn_Jjpli-UgVOT163wX_lp2l9ESHyktGhTjO_iz71MHWdM4a73syjaHD6L0LazKxFtouIpn7XUQXBigGsmg7t3UvkMiVAzRoN3uV3EZsN9HHdX9OHgHf7pH7jUlAltAafJPPiQk1mTWNsw6C7YkL5C6Gv6-_5zvvASEAWeDaBGfJMnqDZArep9Psa2N8grP_8yR7mM9-Tq9GN4vL6-nkZmSF1HwkqTTFinMJVOvcKC3qpuSaUtAlKC4UXRW2VsYyLmUtZG1lzpuaNyupgUktTrIfh7stxl87SF31FHcYhpcVV0wVhShVOVDjA2UxpoTQVC26rcG-YrTah1Htw6jewxiE8iA8Ow_9J3Q1md3dfrj_AMB2kXs</recordid><startdate>20220101</startdate><enddate>20220101</enddate><creator>Zhang, Xiaohua</creator><creator>Li, Guoping</creator><creator>Mukherjee, Subhrangsu</creator><creator>Huang, Wei</creator><creator>Zheng, Ding</creator><creator>Feng, Liang‐Wen</creator><creator>Chen, Yao</creator><creator>Wu, Jianglin</creator><creator>Sangwan, Vinod K.</creator><creator>Hersam, Mark C.</creator><creator>DeLongchamp, Dean M.</creator><creator>Yu, Junsheng</creator><creator>Facchetti, Antonio</creator><creator>Marks, Tobin J.</creator><general>Wiley Subscription Services, Inc</general><scope>AAYXX</scope><scope>CITATION</scope><scope>7SP</scope><scope>7TB</scope><scope>8FD</scope><scope>F28</scope><scope>FR3</scope><scope>H8D</scope><scope>L7M</scope><orcidid>https://orcid.org/0000-0001-8771-0141</orcidid></search><sort><creationdate>20220101</creationdate><title>Systematically Controlling Acceptor Fluorination Optimizes Hierarchical Morphology, Vertical Phase Separation, and Efficiency in Non‐Fullerene Organic Solar Cells</title><author>Zhang, Xiaohua ; Li, Guoping ; Mukherjee, Subhrangsu ; Huang, Wei ; Zheng, Ding ; Feng, Liang‐Wen ; Chen, Yao ; Wu, Jianglin ; Sangwan, Vinod K. ; Hersam, Mark C. ; DeLongchamp, Dean M. ; Yu, Junsheng ; Facchetti, Antonio ; Marks, Tobin J.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3572-505a8b225e0774a673df92700e79e62360b8cd6ac1255d35dc542fd2fb57e1573</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>bulk heterojunctions</topic><topic>Carrier transport</topic><topic>Circuits</topic><topic>Current carriers</topic><topic>Electronic structure</topic><topic>Energy conversion efficiency</topic><topic>Fluorination</topic><topic>Fluorine</topic><topic>Fullerenes</topic><topic>Heterojunctions</topic><topic>Hole mobility</topic><topic>Morphology</topic><topic>morphology control</topic><topic>non‐fullerene solar cells</topic><topic>Optical properties</topic><topic>Optimization</topic><topic>Phase separation</topic><topic>Photovoltaic cells</topic><topic>Polymer blends</topic><topic>Solar cells</topic><topic>Vertical separation</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Zhang, Xiaohua</creatorcontrib><creatorcontrib>Li, Guoping</creatorcontrib><creatorcontrib>Mukherjee, Subhrangsu</creatorcontrib><creatorcontrib>Huang, Wei</creatorcontrib><creatorcontrib>Zheng, Ding</creatorcontrib><creatorcontrib>Feng, Liang‐Wen</creatorcontrib><creatorcontrib>Chen, Yao</creatorcontrib><creatorcontrib>Wu, Jianglin</creatorcontrib><creatorcontrib>Sangwan, Vinod K.</creatorcontrib><creatorcontrib>Hersam, Mark C.</creatorcontrib><creatorcontrib>DeLongchamp, Dean M.</creatorcontrib><creatorcontrib>Yu, Junsheng</creatorcontrib><creatorcontrib>Facchetti, Antonio</creatorcontrib><creatorcontrib>Marks, Tobin J.</creatorcontrib><collection>CrossRef</collection><collection>Electronics & Communications Abstracts</collection><collection>Mechanical & Transportation Engineering Abstracts</collection><collection>Technology Research Database</collection><collection>ANTE: Abstracts in New Technology & Engineering</collection><collection>Engineering Research Database</collection><collection>Aerospace Database</collection><collection>Advanced Technologies Database with Aerospace</collection><jtitle>Advanced energy materials</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Zhang, Xiaohua</au><au>Li, Guoping</au><au>Mukherjee, Subhrangsu</au><au>Huang, Wei</au><au>Zheng, Ding</au><au>Feng, Liang‐Wen</au><au>Chen, Yao</au><au>Wu, Jianglin</au><au>Sangwan, Vinod K.</au><au>Hersam, Mark C.</au><au>DeLongchamp, Dean M.</au><au>Yu, Junsheng</au><au>Facchetti, Antonio</au><au>Marks, Tobin J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Systematically Controlling Acceptor Fluorination Optimizes Hierarchical Morphology, Vertical Phase Separation, and Efficiency in Non‐Fullerene Organic Solar Cells</atitle><jtitle>Advanced energy materials</jtitle><date>2022-01-01</date><risdate>2022</risdate><volume>12</volume><issue>1</issue><epage>n/a</epage><issn>1614-6832</issn><eissn>1614-6840</eissn><abstract>Non‐fullerene acceptor (NFA) end group (EG) functionalization, especially by fluorination, affects not only the energetics but also the morphology of bulk‐heterojunction (BHJ) organic solar cell (OSC) active layers, thereby influencing the power conversion efficiency (PCE) and other metrics of NFA‐based OSCs. However, a quantitative understanding of how varying the degrees of NFA fluorination influence the blend morphological and photovoltaic properties remains elusive. Here a series of three A‐DAD‐A type NFAs (D = π‐donor group and A = π‐acceptor EG) which systematically increase the degree of EG fluorination and comprehensively investigate the resulting blends with the polymer donor PM6 in terms of optical properties, electronic structure, film crystallinity, charge carrier transport, and OSC performance is reported. The results indicate that the most highly fluorinated NFA, BT‐BO‐L4F, achieves an optimal BHJ hierarchical morphology where enhanced NFA molecule intermolecular π–π stacking and optimal vertical phase gradation are achieved in the BHJ blend. These factors also promote optimum NFA‐cathode contact, more balanced electron and hole mobility, and suppress both monomolecular and bimolecular recombination. As a result, both the short‐circuit current density and fill factor in this OSC series progressively increase with increasing EG fluorine density, and the resulting PCEs increase from 9 to 16.8%.
Organic solar cell active layers with A‐DAD‐A (A = acceptor; D = donor) non‐fullerene acceptors (NFAs) having different extents of end group fluorination are systematically characterized in terms of film crystallinity, donor‐acceptor depth distribution, charge carrier transport, and cell performance. The most fluorinated NFA, BT‐BO‐L4F, has optimal hierarchical morphology and vertical phase gradation, affording a power conversion efficiency of 16.81%.</abstract><cop>Weinheim</cop><pub>Wiley Subscription Services, Inc</pub><doi>10.1002/aenm.202102172</doi><tpages>12</tpages><orcidid>https://orcid.org/0000-0001-8771-0141</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | bulk heterojunctions Carrier transport Circuits Current carriers Electronic structure Energy conversion efficiency Fluorination Fluorine Fullerenes Heterojunctions Hole mobility Morphology morphology control non‐fullerene solar cells Optical properties Optimization Phase separation Photovoltaic cells Polymer blends Solar cells Vertical separation |
title | Systematically Controlling Acceptor Fluorination Optimizes Hierarchical Morphology, Vertical Phase Separation, and Efficiency in Non‐Fullerene Organic Solar Cells |
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