<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Kim HK</submitter><funding>Hong Kong Innovation and Technology Commission</funding><funding>Basic and Applied Research Major Program of Guangdong Province</funding><funding>Fundamental Research Funds for the Central University</funding><funding>National Natural Science Foundation of China</funding><funding>Hong Kong Research Grants Council</funding><funding>Foshan-HKUST</funding><funding>National Key Research and Development Program of China</funding><funding>Shen Zhen Technology and Innovation Commission</funding><pagination>e2202223</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC9443469</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>9(25)</volume><pubmed_abstract>A group of regioregular polymer acceptors is synthesized by polymerizing Y6 moieties with different linker units including thiophene, vinylene, 2,2'-bithiophene, and thieno[3,2-b]thiophene, and their optoelectrical properties and photovoltaic performances are studied systematically. It is found that the linker units have significant impacts on the backbone planarity, conjugation, and hence optoelectrical properties of polymer acceptors. The vinylene-based PYF-V-o polymer shows a smaller dihedral angle between the end groups and vinylene units and a more rigid polymer backbone, thus affording bathochromic absorption and better electron-transporting capacity. As a result, the PM6:PYF-V-o based all-polymer solar cells (all-PSCs) are able to achieve the highest power conversion efficiency of 1</pubmed_abstract><journal>Advanced science (Weinheim, Baden-Wurttemberg, Germany)</journal><pubmed_title>Linker Unit Modulation of Polymer Acceptors Enables Highly Efficient Air-Processed All-Polymer Solar Cells.</pubmed_title><pmcid>PMC9443469</pmcid><funding_grant_id>FSUST19-CAT0202</funding_grant_id><funding_grant_id>16310019</funding_grant_id><funding_grant_id>2019YFA0705900</funding_grant_id><funding_grant_id>020514380274</funding_grant_id><funding_grant_id>ITC-CNERC14SC01</funding_grant_id><funding_grant_id>C6023-19G</funding_grant_id><funding_grant_id>16309221</funding_grant_id><funding_grant_id>16310020</funding_grant_id><funding_grant_id>JCYJ20200109140801751</funding_grant_id><funding_grant_id>2019B030302007</funding_grant_id><funding_grant_id>22075057</funding_grant_id><pubmed_authors>Kim HK</pubmed_authors><pubmed_authors>Qi Z</pubmed_authors><pubmed_authors>Chen S</pubmed_authors><pubmed_authors>Yan H</pubmed_authors><pubmed_authors>Yu H</pubmed_authors><pubmed_authors>Shi X</pubmed_authors><pubmed_authors>Pan M</pubmed_authors><pubmed_authors>Zhao H</pubmed_authors><pubmed_authors>Liu W</pubmed_authors><pubmed_authors>Ma W</pubmed_authors></additional><is_claimable>false</is_claimable><name>Linker Unit Modulation of Polymer Acceptors Enables Highly Efficient Air-Processed All-Polymer Solar Cells.</name><description>A group of regioregular polymer acceptors is synthesized by polymerizing Y6 moieties with different linker units including thiophene, vinylene, 2,2'-bithiophene, and thieno[3,2-b]thiophene, and their optoelectrical properties and photovoltaic performances are studied systematically. It is found that the linker units have significant impacts on the backbone planarity, conjugation, and hence optoelectrical properties of polymer acceptors. The vinylene-based PYF-V-o polymer shows a smaller dihedral angle between the end groups and vinylene units and a more rigid polymer backbone, thus affording bathochromic absorption and better electron-transporting capacity. As a result, the PM6:PYF-V-o based all-polymer solar cells (all-PSCs) are able to achieve the highest power conversion efficiency of 1</description><dates><release>2022-01-01T00:00:00Z</release><publication>2022 Sep</publication><modification>2025-04-04T12:26:46.347Z</modification><creation>2025-04-04T12:26:46.347Z</creation></dates><accession>S-EPMC9443469</accession><cross_references><pubmed>35811305</pubmed><doi>10.1002/advs.202202223</doi></cross_references></HashMap>