{"title":"Understanding and engineering spontaneous orientation polarization in organic light-emitting devices","authors":"E. Pakhomenko, Siliang He, R. Holmes","doi":"10.1063/5.0141588","DOIUrl":null,"url":null,"abstract":"Organic light-emitting devices (OLEDs) are a ubiquitous technology for displays with growing application in a variety of other spaces. The future success of this technology depends on further improvements in device efficiency and stability. One pathway for improvement relies on engineering molecular orientation in the organic thin films comprising an OLED. This review is focused on the subsequent spontaneous alignment of molecular electric dipole moments, known as spontaneous orientation polarization (SOP), a phenomenon observed for many common OLED materials. The magnitude of polarization fields associated with SOP rival what is experienced in an OLED under high injection and can significantly impact electronic and excitonic behavior. Here, we first review current work describing the mechanism for the formation of SOP, reflecting an interplay between several factors, such as molecular shape, intermolecular interactions, and processing conditions. We also consider several strategies to tune the polarization sign and magnitude, with emphasis on connecting observations to quantitative models of SOP formation. Building on this discussion of SOP in organic thin films, we review how polarization in OLED active layers impacts key aspects of device performance, including charge injection, luminescence efficiency, and stability. Finally, this review concludes with an outlook on areas of future development needed to realize broad control over SOP for a variety of applications, highlighting gaps in our current understanding of this phenomenon.","PeriodicalId":72559,"journal":{"name":"Chemical physics reviews","volume":" ","pages":""},"PeriodicalIF":6.1000,"publicationDate":"2023-05-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chemical physics reviews","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1063/5.0141588","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, PHYSICAL","Score":null,"Total":0}
引用次数: 3
Abstract
Organic light-emitting devices (OLEDs) are a ubiquitous technology for displays with growing application in a variety of other spaces. The future success of this technology depends on further improvements in device efficiency and stability. One pathway for improvement relies on engineering molecular orientation in the organic thin films comprising an OLED. This review is focused on the subsequent spontaneous alignment of molecular electric dipole moments, known as spontaneous orientation polarization (SOP), a phenomenon observed for many common OLED materials. The magnitude of polarization fields associated with SOP rival what is experienced in an OLED under high injection and can significantly impact electronic and excitonic behavior. Here, we first review current work describing the mechanism for the formation of SOP, reflecting an interplay between several factors, such as molecular shape, intermolecular interactions, and processing conditions. We also consider several strategies to tune the polarization sign and magnitude, with emphasis on connecting observations to quantitative models of SOP formation. Building on this discussion of SOP in organic thin films, we review how polarization in OLED active layers impacts key aspects of device performance, including charge injection, luminescence efficiency, and stability. Finally, this review concludes with an outlook on areas of future development needed to realize broad control over SOP for a variety of applications, highlighting gaps in our current understanding of this phenomenon.