Full metadata record
DC Field | Value | Language |
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dc.contributor.author | Gayathri, Rajalapati Durga | - |
dc.contributor.author | Gokulnath, Thavamani | - |
dc.contributor.author | Park, Ho-Yeol | - |
dc.contributor.author | Kim, Jeonghyeon | - |
dc.contributor.author | Kim, Hyerin | - |
dc.contributor.author | Kim, Jongyoun | - |
dc.contributor.author | Kim, BongSoo | - |
dc.contributor.author | Lee, Youngu | - |
dc.contributor.author | Yoon, Jinhwan | - |
dc.contributor.author | Jin, Sung-Ho | - |
dc.date.accessioned | 2022-03-23T05:00:18Z | - |
dc.date.available | 2022-03-23T05:00:18Z | - |
dc.date.created | 2022-03-03 | - |
dc.date.issued | 2022-03 | - |
dc.identifier.issn | 1944-8244 | - |
dc.identifier.uri | http://hdl.handle.net/20.500.11750/16392 | - |
dc.description.abstract | End group engineering on the side chain of pi-conjugated donor polymers is explored as an effective way to develop efficient photovoltaic devices. In this work, we designed and synthesized three new pi-conjugated polymers (PBDT-BZ-1, PBDT-S-BZ, and PBDT-BZ-F) with terminal aryl end groups on the side chain of chlorine-substituted benzo[1,2-b:4,5b ']dithiophene (BDT). End group modifications showed notable changes in energy levels, dipole moments, exciton lifetimes, energy losses, and charge transport properties. Remarkably, the three new polymers paired with IT-4F (halogen-free solvent processed/ toluene:DPE) displayed high power conversion efficiencies (PCEs) compared to a polymer (PBDT-Al-5) without a terminal end group (PCE of 7.32%). Interestingly, PBDT-S-BZ:IT-4F (PCE of 13.73%) showed a higher PCE than the benchmark PM7:IT-4F. The improved performance of PBDT-S-BZ well correlates with its improved charge mobility, well-interdigitated surface morphology, and high miscibility with a low Flory-Huggins interaction parameter (1.253). Thus, we successfully established a correlation between the end group engineering and bulk properties of the new polymers for realizing the high performance of halogen-free nonfullerene organic solar cells. © 2022 American Chemical Society. All rights reserved. | - |
dc.language | English | - |
dc.publisher | American Chemical Society | - |
dc.title | Impact of Aryl End Group Engineering of Donor Polymers on the Morphology and Efficiency of Halogen-Free Solvent-Processed Nonfullerene Organic Solar Cells | - |
dc.type | Article | - |
dc.identifier.doi | 10.1021/acsami.1c22784 | - |
dc.identifier.wosid | 000757908500001 | - |
dc.identifier.scopusid | 2-s2.0-85125366160 | - |
dc.identifier.bibliographicCitation | ACS Applied Materials & Interfaces, v.14, no.8, pp.10616 - 10626 | - |
dc.description.isOpenAccess | FALSE | - |
dc.subject.keywordAuthor | miscibility | - |
dc.subject.keywordAuthor | Flory-Huggins interaction parameter | - |
dc.subject.keywordAuthor | halogen-free solvent-processed nonfullerene organic solar cells | - |
dc.subject.keywordAuthor | end group | - |
dc.subject.keywordAuthor | morphology | - |
dc.subject.keywordPlus | CONJUGATED POLYMERS | - |
dc.subject.keywordPlus | RING ACCEPTOR | - |
dc.subject.keywordPlus | PERFORMANCE | - |
dc.subject.keywordPlus | FLUORINATION | - |
dc.subject.keywordPlus | SEPARATION | - |
dc.subject.keywordPlus | ALKYLTHIO | - |
dc.subject.keywordPlus | SINGLE | - |
dc.subject.keywordPlus | DRIVEN | - |
dc.citation.endPage | 10626 | - |
dc.citation.number | 8 | - |
dc.citation.startPage | 10616 | - |
dc.citation.title | ACS Applied Materials & Interfaces | - |
dc.citation.volume | 14 | - |
dc.description.journalRegisteredClass | scie | - |
dc.description.journalRegisteredClass | scopus | - |
dc.relation.journalResearchArea | Science & Technology - Other Topics; Materials Science | - |
dc.relation.journalWebOfScienceCategory | Nanoscience & Nanotechnology; Materials Science, Multidisciplinary | - |
dc.type.docType | Article | - |
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