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Dithienobenzodithiophene-Based Small Molecule Organic Solar Cells with over 7% Efficiency via Additive- and Thermal-Annealing-Free Processing
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| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Song, Hyeng Gun | - |
| dc.contributor.author | Kim, Yu Jin | - |
| dc.contributor.author | Lee, Ji Sang | - |
| dc.contributor.author | Kim, Yun-Hi | - |
| dc.contributor.author | Park, Chan Eon | - |
| dc.contributor.author | Kwon, Soon-Ki | - |
| dc.date.accessioned | 2022-12-26T19:49:02Z | - |
| dc.date.available | 2022-12-26T19:49:02Z | - |
| dc.date.issued | 2016-12 | - |
| dc.identifier.issn | 1944-8244 | - |
| dc.identifier.issn | 1944-8252 | - |
| dc.identifier.uri | https://scholarworks.gnu.ac.kr/handle/sw.gnu/15066 | - |
| dc.description.abstract | Here we introduce a novel small molecule based on dithienobenzodithiophene and rhodanine, DTBDT-Rho, developed to study the effect of the rhodanine substitutuent on small molecule bulk heterojunction (BHJ) solar cells. DTBDT-Rho possesses distinct crystalline characteristics, sufficient solubility in chlorinated solvents, and broad absorption properties. Therefore, solution-processed BHJ photovoltaic cells made with DTBDT-Rho:PC71BM blends showed an extremely high power conversion efficiency (PCE; 7.10%); notably, this PCE value was obtained without the use of additives or thermal treatments. To our knowledge, the PCE over 7% is a significantly powerful value among rhodanine-based small molecule BHJ solar cells without additives or thermal treatments. | - |
| dc.format.extent | 7 | - |
| dc.language | 영어 | - |
| dc.language.iso | ENG | - |
| dc.publisher | American Chemical Society | - |
| dc.title | Dithienobenzodithiophene-Based Small Molecule Organic Solar Cells with over 7% Efficiency via Additive- and Thermal-Annealing-Free Processing | - |
| dc.type | Article | - |
| dc.publisher.location | 미국 | - |
| dc.identifier.doi | 10.1021/acsami.6b11297 | - |
| dc.identifier.scopusid | 2-s2.0-85006874589 | - |
| dc.identifier.wosid | 000390728900022 | - |
| dc.identifier.bibliographicCitation | ACS Applied Materials & Interfaces, v.8, no.50, pp 34353 - 34359 | - |
| dc.citation.title | ACS Applied Materials & Interfaces | - |
| dc.citation.volume | 8 | - |
| dc.citation.number | 50 | - |
| dc.citation.startPage | 34353 | - |
| dc.citation.endPage | 34359 | - |
| dc.type.docType | Article | - |
| dc.description.isOpenAccess | N | - |
| dc.description.journalRegisteredClass | sci | - |
| dc.description.journalRegisteredClass | scie | - |
| dc.description.journalRegisteredClass | scopus | - |
| dc.relation.journalResearchArea | Science & Technology - Other Topics | - |
| dc.relation.journalResearchArea | Materials Science | - |
| dc.relation.journalWebOfScienceCategory | Nanoscience & Nanotechnology | - |
| dc.relation.journalWebOfScienceCategory | Materials Science, Multidisciplinary | - |
| dc.subject.keywordPlus | PHOTOVOLTAIC DEVICES | - |
| dc.subject.keywordPlus | CONJUGATED POLYMER | - |
| dc.subject.keywordPlus | BANDGAP POLYMER | - |
| dc.subject.keywordPlus | ENERGY-LOSSES | - |
| dc.subject.keywordPlus | PERFORMANCE | - |
| dc.subject.keywordPlus | MORPHOLOGY | - |
| dc.subject.keywordPlus | CRYSTALLIZATION | - |
| dc.subject.keywordPlus | ACCEPTOR | - |
| dc.subject.keywordPlus | COPLANARITY | - |
| dc.subject.keywordPlus | STRATEGIES | - |
| dc.subject.keywordAuthor | dithienobenzodithiophene | - |
| dc.subject.keywordAuthor | rhodanine | - |
| dc.subject.keywordAuthor | small molecule solar cell | - |
| dc.subject.keywordAuthor | power conversion efficiency | - |
| dc.subject.keywordAuthor | without additives or thermal treatments | - |
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