Martina Rimmele, Zhuoran Qiao, Filip Aniés, Adam V Marsh, Aren Yazmaciyan, George Harrison, Shadi Fatayer, Nicola Gasparini, Martin Heeney
{"title":"Energy Level Tuning in Conjugated Donor Polymers by Chalcogen Exchange for Low Dark Current Organic Photodetectors.","authors":"Martina Rimmele, Zhuoran Qiao, Filip Aniés, Adam V Marsh, Aren Yazmaciyan, George Harrison, Shadi Fatayer, Nicola Gasparini, Martin Heeney","doi":"10.1021/acsmaterialslett.4c01899","DOIUrl":null,"url":null,"abstract":"<p><p>The performance of organic photodetectors (OPDs) using conjugated polymer donors and molecular acceptors has improved rapidly, but many polymers are difficult to upscale due to their complex structures. This study examines two low-complexity thiophene copolymers with substituted benzooxadiazole (<b>FO6-BO-T</b>) or benzothiadiazole (<b>FO6-T</b>). Substituting sulfur with oxygen in <b>FO6-BO-T</b> increased its ionization energy without affecting the optical gap. When blended with the nonfullerene acceptor IDSe, <b>FO6-BO-T</b> showed a significantly lower dark current density (2.06·10<sup>-9</sup> A cm<sup>-2</sup> at -2 V) compared to <b>FO6-T</b>. Grazing incidence wide-angle X-ray scattering (GIWAXS) measurements demonstrated that pristine <b>FO6-BO-T</b> exhibited a more ordered morphology than <b>FO6-T</b>. However, blending resulted in a significant disruption to the ordered domains in both cases, with a loss of orientational order, suggesting that <b>FO6-BO-T</b>'s improved performance is largely related to its increased ionization energy. This study demonstrates the potential of chalcogen atom engineering to enhance the performance of the OPD in scalable polymers.</p>","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":null,"pages":null},"PeriodicalIF":11.3000,"publicationDate":"2024-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11539101/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Catalysis ","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acsmaterialslett.4c01899","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/4 0:00:00","PubModel":"eCollection","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
The performance of organic photodetectors (OPDs) using conjugated polymer donors and molecular acceptors has improved rapidly, but many polymers are difficult to upscale due to their complex structures. This study examines two low-complexity thiophene copolymers with substituted benzooxadiazole (FO6-BO-T) or benzothiadiazole (FO6-T). Substituting sulfur with oxygen in FO6-BO-T increased its ionization energy without affecting the optical gap. When blended with the nonfullerene acceptor IDSe, FO6-BO-T showed a significantly lower dark current density (2.06·10-9 A cm-2 at -2 V) compared to FO6-T. Grazing incidence wide-angle X-ray scattering (GIWAXS) measurements demonstrated that pristine FO6-BO-T exhibited a more ordered morphology than FO6-T. However, blending resulted in a significant disruption to the ordered domains in both cases, with a loss of orientational order, suggesting that FO6-BO-T's improved performance is largely related to its increased ionization energy. This study demonstrates the potential of chalcogen atom engineering to enhance the performance of the OPD in scalable polymers.
期刊介绍:
ACS Catalysis is an esteemed journal that publishes original research in the fields of heterogeneous catalysis, molecular catalysis, and biocatalysis. It offers broad coverage across diverse areas such as life sciences, organometallics and synthesis, photochemistry and electrochemistry, drug discovery and synthesis, materials science, environmental protection, polymer discovery and synthesis, and energy and fuels.
The scope of the journal is to showcase innovative work in various aspects of catalysis. This includes new reactions and novel synthetic approaches utilizing known catalysts, the discovery or modification of new catalysts, elucidation of catalytic mechanisms through cutting-edge investigations, practical enhancements of existing processes, as well as conceptual advances in the field. Contributions to ACS Catalysis can encompass both experimental and theoretical research focused on catalytic molecules, macromolecules, and materials that exhibit catalytic turnover.