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The Nanoscale Structure and Stability of Organic Photovoltaic Blends Processed with Solvent Additives
Controlling the nanomorphology in bulk heterojunction photoactive blends is crucial for optimizing the performance and stability of organic photovoltaic (OPV) technologies. A promising approach is to alter the drying dynamics and consequently, the nanostructure of the blend film using solvent additi...
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creator | Kilbride, Rachel C. Spooner, Emma L. K. Burg, Stephanie L. Oliveira, Bárbara L. Charas, Ana Bernardo, Gabriel Dalgliesh, Robert King, Stephen Lidzey, David G. Jones, Richard A. L. Parnell, Andrew J. |
description | Controlling the nanomorphology in bulk heterojunction photoactive blends is crucial for optimizing the performance and stability of organic photovoltaic (OPV) technologies. A promising approach is to alter the drying dynamics and consequently, the nanostructure of the blend film using solvent additives such as 1,8‐diiodooctane (DIO). Although this approach is demonstrated extensively for OPV systems incorporating fullerene‐based acceptors, it is unclear how solvent additive processing influences the morphology and stability of nonfullerene acceptor (NFA) systems. Here, small angle neutron scattering (SANS) is used to probe the nanomorphology of two model OPV systems processed with DIO: a fullerene‐based system (PBDB‐T:PC71BM) and an NFA‐based system (PBDB‐T:ITIC). To overcome the low intrinsic neutron scattering length density contrast in polymer:NFA blend films, the synthesis of a deuterated NFA analog (ITIC‐d52) is reported. Using SANS, new insights into the nanoscale evolution of fullerene and NFA‐based systems are provided by characterizing films immediately after fabrication, after thermal annealing, and after aging for 1 year. It is found that DIO processing influences fullerene and NFA‐based systems differently with NFA‐based systems characterized by more phase‐separated domains. After long‐term aging, SANS reveals both systems demonstrate some level of thermodynamic induced domain coarsening.
Using small angle neutron scattering (SANS), the influence of solvent additives on the nanoscale structure and stability of organic photovoltaic blend films is explored. Distinct differences in the morphological evolution of fullerene and non‐fullerene acceptor systems are revealed, providing new insights into the relationships between film processing, structure, and stability. |
doi_str_mv | 10.1002/smll.202311109 |
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Using small angle neutron scattering (SANS), the influence of solvent additives on the nanoscale structure and stability of organic photovoltaic blend films is explored. Distinct differences in the morphological evolution of fullerene and non‐fullerene acceptor systems are revealed, providing new insights into the relationships between film processing, structure, and stability.</description><identifier>ISSN: 1613-6810</identifier><identifier>ISSN: 1613-6829</identifier><identifier>EISSN: 1613-6829</identifier><identifier>DOI: 10.1002/smll.202311109</identifier><identifier>PMID: 38597752</identifier><language>eng</language><publisher>Germany: Wiley Subscription Services, Inc</publisher><subject>1,8‐diiodooctane ; Additives ; Aging (artificial) ; Chemical synthesis ; Deuteration ; Fullerenes ; Heterojunctions ; Mixtures ; Neutron scattering ; Neutrons ; nonfullerene acceptors ; organic photovoltaics ; Polymer films ; small angle neutron scattering ; solvent additives ; Solvents ; Stability</subject><ispartof>Small (Weinheim an der Bergstrasse, Germany), 2024-08, Vol.20 (33), p.e2311109-n/a</ispartof><rights>2024 The Authors. Small published by Wiley‐VCH GmbH</rights><rights>2024 The Authors. Small published by Wiley‐VCH GmbH.</rights><rights>2024. This article is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c3689-2be50d6d9aad0ee2172e48cff0642b1f9cb372da0621d2cb96ccc7e24130e7553</cites><orcidid>0000-0001-7392-4915 ; 0000-0002-6814-679X ; 0000-0001-6717-6826 ; 0000-0001-5400-6369 ; 0000-0001-7870-9843 ; 0000-0003-3386-9151 ; 0000-0001-8858-0625 ; 0000-0002-8558-1160 ; 0000-0002-3985-923X ; 0000-0001-9575-550X ; 0000-0001-8606-8644</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38597752$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kilbride, Rachel C.</creatorcontrib><creatorcontrib>Spooner, Emma L. K.</creatorcontrib><creatorcontrib>Burg, Stephanie L.</creatorcontrib><creatorcontrib>Oliveira, Bárbara L.</creatorcontrib><creatorcontrib>Charas, Ana</creatorcontrib><creatorcontrib>Bernardo, Gabriel</creatorcontrib><creatorcontrib>Dalgliesh, Robert</creatorcontrib><creatorcontrib>King, Stephen</creatorcontrib><creatorcontrib>Lidzey, David G.</creatorcontrib><creatorcontrib>Jones, Richard A. L.</creatorcontrib><creatorcontrib>Parnell, Andrew J.</creatorcontrib><title>The Nanoscale Structure and Stability of Organic Photovoltaic Blends Processed with Solvent Additives</title><title>Small (Weinheim an der Bergstrasse, Germany)</title><addtitle>Small</addtitle><description>Controlling the nanomorphology in bulk heterojunction photoactive blends is crucial for optimizing the performance and stability of organic photovoltaic (OPV) technologies. A promising approach is to alter the drying dynamics and consequently, the nanostructure of the blend film using solvent additives such as 1,8‐diiodooctane (DIO). Although this approach is demonstrated extensively for OPV systems incorporating fullerene‐based acceptors, it is unclear how solvent additive processing influences the morphology and stability of nonfullerene acceptor (NFA) systems. Here, small angle neutron scattering (SANS) is used to probe the nanomorphology of two model OPV systems processed with DIO: a fullerene‐based system (PBDB‐T:PC71BM) and an NFA‐based system (PBDB‐T:ITIC). To overcome the low intrinsic neutron scattering length density contrast in polymer:NFA blend films, the synthesis of a deuterated NFA analog (ITIC‐d52) is reported. Using SANS, new insights into the nanoscale evolution of fullerene and NFA‐based systems are provided by characterizing films immediately after fabrication, after thermal annealing, and after aging for 1 year. It is found that DIO processing influences fullerene and NFA‐based systems differently with NFA‐based systems characterized by more phase‐separated domains. After long‐term aging, SANS reveals both systems demonstrate some level of thermodynamic induced domain coarsening.
Using small angle neutron scattering (SANS), the influence of solvent additives on the nanoscale structure and stability of organic photovoltaic blend films is explored. Distinct differences in the morphological evolution of fullerene and non‐fullerene acceptor systems are revealed, providing new insights into the relationships between film processing, structure, and stability.</description><subject>1,8‐diiodooctane</subject><subject>Additives</subject><subject>Aging (artificial)</subject><subject>Chemical synthesis</subject><subject>Deuteration</subject><subject>Fullerenes</subject><subject>Heterojunctions</subject><subject>Mixtures</subject><subject>Neutron scattering</subject><subject>Neutrons</subject><subject>nonfullerene acceptors</subject><subject>organic photovoltaics</subject><subject>Polymer films</subject><subject>small angle neutron scattering</subject><subject>solvent additives</subject><subject>Solvents</subject><subject>Stability</subject><issn>1613-6810</issn><issn>1613-6829</issn><issn>1613-6829</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><recordid>eNqFkctLAzEQh4Movq8eJeDFS2seu5vNUcUXVFuonpdsMmsj6UaTbKX_vVuqFbx4mhn45mOYH0InlAwpIewizp0bMsI4pZTILbRPC8oHRcnk9qanZA8dxPhGCKcsE7toj5e5FCJn-wieZ4CfVOujVg7wNIVOpy4AVq3pJ1VbZ9MS-waPw6tqrcaTmU9-4V1S_XDloDURT4LXECMY_GnTDE-9W0Cb8KUxNtkFxCO00ygX4fi7HqKX25vn6_vBaHz3cH05GmhelHLAasiJKYxUyhAARgWDrNRNQ4qM1bSRuuaCGUUKRg3TtSy01gJYRjkBkef8EJ2vve_Bf3QQUzW3UYNzqgXfxYoT3lMiE7JHz_6gb74LbX9dT0nOmSizlXC4pnTwMQZoqvdg5yosK0qqVQDVKoBqE0C_cPqt7eo5mA3-8_EekGvg0zpY_qOrpo-j0a_8C08PkuI</recordid><startdate>20240801</startdate><enddate>20240801</enddate><creator>Kilbride, Rachel C.</creator><creator>Spooner, Emma L. 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A promising approach is to alter the drying dynamics and consequently, the nanostructure of the blend film using solvent additives such as 1,8‐diiodooctane (DIO). Although this approach is demonstrated extensively for OPV systems incorporating fullerene‐based acceptors, it is unclear how solvent additive processing influences the morphology and stability of nonfullerene acceptor (NFA) systems. Here, small angle neutron scattering (SANS) is used to probe the nanomorphology of two model OPV systems processed with DIO: a fullerene‐based system (PBDB‐T:PC71BM) and an NFA‐based system (PBDB‐T:ITIC). To overcome the low intrinsic neutron scattering length density contrast in polymer:NFA blend films, the synthesis of a deuterated NFA analog (ITIC‐d52) is reported. Using SANS, new insights into the nanoscale evolution of fullerene and NFA‐based systems are provided by characterizing films immediately after fabrication, after thermal annealing, and after aging for 1 year. It is found that DIO processing influences fullerene and NFA‐based systems differently with NFA‐based systems characterized by more phase‐separated domains. After long‐term aging, SANS reveals both systems demonstrate some level of thermodynamic induced domain coarsening.
Using small angle neutron scattering (SANS), the influence of solvent additives on the nanoscale structure and stability of organic photovoltaic blend films is explored. Distinct differences in the morphological evolution of fullerene and non‐fullerene acceptor systems are revealed, providing new insights into the relationships between film processing, structure, and stability.</abstract><cop>Germany</cop><pub>Wiley Subscription Services, Inc</pub><pmid>38597752</pmid><doi>10.1002/smll.202311109</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-7392-4915</orcidid><orcidid>https://orcid.org/0000-0002-6814-679X</orcidid><orcidid>https://orcid.org/0000-0001-6717-6826</orcidid><orcidid>https://orcid.org/0000-0001-5400-6369</orcidid><orcidid>https://orcid.org/0000-0001-7870-9843</orcidid><orcidid>https://orcid.org/0000-0003-3386-9151</orcidid><orcidid>https://orcid.org/0000-0001-8858-0625</orcidid><orcidid>https://orcid.org/0000-0002-8558-1160</orcidid><orcidid>https://orcid.org/0000-0002-3985-923X</orcidid><orcidid>https://orcid.org/0000-0001-9575-550X</orcidid><orcidid>https://orcid.org/0000-0001-8606-8644</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | 1,8‐diiodooctane Additives Aging (artificial) Chemical synthesis Deuteration Fullerenes Heterojunctions Mixtures Neutron scattering Neutrons nonfullerene acceptors organic photovoltaics Polymer films small angle neutron scattering solvent additives Solvents Stability |
title | The Nanoscale Structure and Stability of Organic Photovoltaic Blends Processed with Solvent Additives |
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