Zhenye Wang, Di Zhang, Lvpeng Yang, Meichen Xu, Junfeng Liu, Zhi Wang, Yerun Gao, Li-Yuan Zhang, Lianbin Niu, Ming Shao
{"title":"Realization of Evaporated Electrode-Based Intrinsically Stretchable Ternary Organic Solar Cells through Encapsulation Strategy","authors":"Zhenye Wang, Di Zhang, Lvpeng Yang, Meichen Xu, Junfeng Liu, Zhi Wang, Yerun Gao, Li-Yuan Zhang, Lianbin Niu, Ming Shao","doi":"10.1021/acsmaterialslett.4c01548","DOIUrl":null,"url":null,"abstract":"The mechanical properties of organic solar cells are of great importance to ensure their application in wearable or stretchable electronics. Here, we introduce polymer acceptor (N2200) into the active layer blend, and realize intrinsically stretchable organic solar cells (<i>is</i>-OSCs) with evaporated electrode via encapsulation strategy. The incorporation of N2200 simultaneously enhances the mechanical stretchability and PCE of <i>is</i>-OSCs, attributed to the enhanced polymer chain entanglement, and N2200 can act as tie molecules to provide electric connection among small molecule domains. More importantly, encapsulating the evaporated electrode-based <i>is</i>-OSCs leads to significant improvement in its mechanical stretchability, with 80% PCE retention under a large strain of 20%, compared to <2.5% strain for the unencapsulated ones. Additionally, encapsulated <i>is</i>-OSCs retained 67% PCE after 1000 test cycles at a stretch strain of 15%, whereas unencapsulated devices can only retain 33% PCE after 200 test cycles under a small strain of 5%.","PeriodicalId":9,"journal":{"name":"ACS Catalysis ","volume":null,"pages":null},"PeriodicalIF":11.3000,"publicationDate":"2024-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Catalysis ","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acsmaterialslett.4c01548","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 0
Abstract
The mechanical properties of organic solar cells are of great importance to ensure their application in wearable or stretchable electronics. Here, we introduce polymer acceptor (N2200) into the active layer blend, and realize intrinsically stretchable organic solar cells (is-OSCs) with evaporated electrode via encapsulation strategy. The incorporation of N2200 simultaneously enhances the mechanical stretchability and PCE of is-OSCs, attributed to the enhanced polymer chain entanglement, and N2200 can act as tie molecules to provide electric connection among small molecule domains. More importantly, encapsulating the evaporated electrode-based is-OSCs leads to significant improvement in its mechanical stretchability, with 80% PCE retention under a large strain of 20%, compared to <2.5% strain for the unencapsulated ones. Additionally, encapsulated is-OSCs retained 67% PCE after 1000 test cycles at a stretch strain of 15%, whereas unencapsulated devices can only retain 33% PCE after 200 test cycles under a small strain of 5%.
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.