<HashMap><database>biostudies-literature</database><scores/><additional><submitter>He Q</submitter><funding>U.S. Department of Energy</funding><funding>King Abdullah University of Science and Technology</funding><funding>EPSRC</funding><funding>Office of Naval Research</funding><funding>Engineering and Physical Sciences Research Council</funding><pagination>e2414042</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11923974</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>12(11)</volume><pubmed_abstract>Most current highly efficient organic solar cells utilize small molecules like Y6 and its derivatives as electron acceptors in the photoactive layer. In this work, a small molecule acceptor, SC8-IT4F, is developed through outer side chain engineering on the terminal thiophene of a conjugated 6,12-dihydro-dithienoindeno[2,3-d:2',3'-d']-s-indaceno[1,2-b:5,6-b']dithiophene (IDTT) central core. Compared to the reference molecule C8-IT4F, which lacks outer side chains, SC8-IT4F displays notable differences in molecule geometry (as shown by simulations), thermal behavior, single-crystal packing, and film morphology. Blend films of SC8-IT4F and the polymer donor PM6 exhibit larger carrier mobilities, longer carrier lifetimes, and reduced recombination compared to C8-IT4F, resulting in improved de</pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pubmed_title>Significant Efficiency Enhancements in Non-Y Series Acceptors by the Addition of Outer Side Chains.</pubmed_title><pmcid>PMC11923974</pmcid><funding_grant_id>DE‐AC02‐05CH11231</funding_grant_id><funding_grant_id>EP/VO48686/1</funding_grant_id><funding_grant_id>DE-AC02-05CH11231</funding_grant_id><funding_grant_id>N000142412104</funding_grant_id><funding_grant_id>ORFS-CRG11-2022-5045</funding_grant_id><funding_grant_id>ORFS‐CRG11‐2022‐5045</funding_grant_id><pubmed_authors>Laquai F</pubmed_authors><pubmed_authors>Ding B</pubmed_authors><pubmed_authors>Heeney M</pubmed_authors><pubmed_authors>Hu X</pubmed_authors><pubmed_authors>Ade H</pubmed_authors><pubmed_authors>Glocklhofer F</pubmed_authors><pubmed_authors>White AJP</pubmed_authors><pubmed_authors>He Q</pubmed_authors><pubmed_authors>Kafourou P</pubmed_authors><pubmed_authors>Fei Z</pubmed_authors><pubmed_authors>Anthopoulos TD</pubmed_authors><pubmed_authors>Hadmojo WT</pubmed_authors><pubmed_authors>Lee B</pubmed_authors><pubmed_authors>De Castro CSP</pubmed_authors><pubmed_authors>Althobaiti W</pubmed_authors><pubmed_authors>Mukherjee S</pubmed_authors><pubmed_authors>Alqurashi M</pubmed_authors><pubmed_authors>Luke J</pubmed_authors><pubmed_authors>Gorenflot J</pubmed_authors></additional><is_claimable>false</is_claimable><name>Significant Efficiency Enhancements in Non-Y Series Acceptors by the Addition of Outer Side Chains.</name><description>Most current highly efficient organic solar cells utilize small molecules like Y6 and its derivatives as electron acceptors in the photoactive layer. In this work, a small molecule acceptor, SC8-IT4F, is developed through outer side chain engineering on the terminal thiophene of a conjugated 6,12-dihydro-dithienoindeno[2,3-d:2',3'-d']-s-indaceno[1,2-b:5,6-b']dithiophene (IDTT) central core. Compared to the reference molecule C8-IT4F, which lacks outer side chains, SC8-IT4F displays notable differences in molecule geometry (as shown by simulations), thermal behavior, single-crystal packing, and film morphology. Blend films of SC8-IT4F and the polymer donor PM6 exhibit larger carrier mobilities, longer carrier lifetimes, and reduced recombination compared to C8-IT4F, resulting in improved de</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Mar</publication><modification>2025-04-04T00:06:29.129Z</modification><creation>2025-04-04T00:06:29.129Z</creation></dates><accession>S-EPMC11923974</accession><cross_references><pubmed>39840615</pubmed><doi>10.1002/advs.202414042</doi></cross_references></HashMap>