Weiqiang Wei, Luyan Huang, Zihan Wang, Ya Xu, Zhou Fang, Yan He, Lisheng Zhang and Huifang Li*,
{"title":"电致发光用典型蓝色磷光发光体 FIrpic 在氧化还原状态下的化学稳定性机理研究","authors":"Weiqiang Wei, Luyan Huang, Zihan Wang, Ya Xu, Zhou Fang, Yan He, Lisheng Zhang and Huifang Li*, ","doi":"10.1021/acs.organomet.4c0030310.1021/acs.organomet.4c00303","DOIUrl":null,"url":null,"abstract":"<p >Iridium(III)bis[2-(4,6-difluorophenyl)pyridyl-N,C<sup>2′</sup>]picolinate (FIrpic) is a widely used light-blue phosphorescent material known for its favorable redox activity. However, the operational lifetime of FIrpic-based phosphorescent organic light-emitting diodes (PhOLEDs) remains unsatisfactory. To gain a deeper understanding of the chemical stability of FIrpic in various redox states, we explored its degradation mechanisms in the ground (<i>S</i><sub>0</sub>), one-electron oxidized (Ox.), and one-electron reduced (Re.) states using theoretical methods. Density functional theory (DFT) static calculations, combined with atomic center density matrix propagation (ADMP) simulations at temperatures of 500, 600, and 700 K, revealed that the cleavage of the Ir–N<sub>1</sub> bond is a crucial step in the chemical degradation process of FIrpic in both the ground and redox states. This bond breakage leads to a nonemissive five-coordinated trigonal bipyramidal intermediate. The degradation process is notably more facile in the redox states, particularly in the <i>Re</i>. Charge analysis indicates a decreasing trend in electronic delocalization between the LP<sub>N</sub> electron donor natural bond orbital (NBO) and the d*<sub>N–Ir(pic.)</sub> electron acceptor NBO, with the order S<sub>0</sub> > Ox. > Re. Our findings provide a deeper insight into the degradation mechanisms of FIrpic under different redox conditions. This understanding is crucial for the design of more stable materials in FIrpic-based PhOLEDs.</p>","PeriodicalId":56,"journal":{"name":"Organometallics","volume":null,"pages":null},"PeriodicalIF":2.5000,"publicationDate":"2024-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Mechanism Studies on the Chemical Stability of FIrpic, a Typical Blue Phosphorescent Emitter for Electroluminescence, in the Redox States\",\"authors\":\"Weiqiang Wei, Luyan Huang, Zihan Wang, Ya Xu, Zhou Fang, Yan He, Lisheng Zhang and Huifang Li*, \",\"doi\":\"10.1021/acs.organomet.4c0030310.1021/acs.organomet.4c00303\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Iridium(III)bis[2-(4,6-difluorophenyl)pyridyl-N,C<sup>2′</sup>]picolinate (FIrpic) is a widely used light-blue phosphorescent material known for its favorable redox activity. However, the operational lifetime of FIrpic-based phosphorescent organic light-emitting diodes (PhOLEDs) remains unsatisfactory. To gain a deeper understanding of the chemical stability of FIrpic in various redox states, we explored its degradation mechanisms in the ground (<i>S</i><sub>0</sub>), one-electron oxidized (Ox.), and one-electron reduced (Re.) states using theoretical methods. Density functional theory (DFT) static calculations, combined with atomic center density matrix propagation (ADMP) simulations at temperatures of 500, 600, and 700 K, revealed that the cleavage of the Ir–N<sub>1</sub> bond is a crucial step in the chemical degradation process of FIrpic in both the ground and redox states. This bond breakage leads to a nonemissive five-coordinated trigonal bipyramidal intermediate. The degradation process is notably more facile in the redox states, particularly in the <i>Re</i>. Charge analysis indicates a decreasing trend in electronic delocalization between the LP<sub>N</sub> electron donor natural bond orbital (NBO) and the d*<sub>N–Ir(pic.)</sub> electron acceptor NBO, with the order S<sub>0</sub> > Ox. > Re. Our findings provide a deeper insight into the degradation mechanisms of FIrpic under different redox conditions. This understanding is crucial for the design of more stable materials in FIrpic-based PhOLEDs.</p>\",\"PeriodicalId\":56,\"journal\":{\"name\":\"Organometallics\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":2.5000,\"publicationDate\":\"2024-09-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Organometallics\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acs.organomet.4c00303\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, INORGANIC & NUCLEAR\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Organometallics","FirstCategoryId":"92","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acs.organomet.4c00303","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
Mechanism Studies on the Chemical Stability of FIrpic, a Typical Blue Phosphorescent Emitter for Electroluminescence, in the Redox States
Iridium(III)bis[2-(4,6-difluorophenyl)pyridyl-N,C2′]picolinate (FIrpic) is a widely used light-blue phosphorescent material known for its favorable redox activity. However, the operational lifetime of FIrpic-based phosphorescent organic light-emitting diodes (PhOLEDs) remains unsatisfactory. To gain a deeper understanding of the chemical stability of FIrpic in various redox states, we explored its degradation mechanisms in the ground (S0), one-electron oxidized (Ox.), and one-electron reduced (Re.) states using theoretical methods. Density functional theory (DFT) static calculations, combined with atomic center density matrix propagation (ADMP) simulations at temperatures of 500, 600, and 700 K, revealed that the cleavage of the Ir–N1 bond is a crucial step in the chemical degradation process of FIrpic in both the ground and redox states. This bond breakage leads to a nonemissive five-coordinated trigonal bipyramidal intermediate. The degradation process is notably more facile in the redox states, particularly in the Re. Charge analysis indicates a decreasing trend in electronic delocalization between the LPN electron donor natural bond orbital (NBO) and the d*N–Ir(pic.) electron acceptor NBO, with the order S0 > Ox. > Re. Our findings provide a deeper insight into the degradation mechanisms of FIrpic under different redox conditions. This understanding is crucial for the design of more stable materials in FIrpic-based PhOLEDs.
期刊介绍:
Organometallics is the flagship journal of organometallic chemistry and records progress in one of the most active fields of science, bridging organic and inorganic chemistry. The journal publishes Articles, Communications, Reviews, and Tutorials (instructional overviews) that depict research on the synthesis, structure, bonding, chemical reactivity, and reaction mechanisms for a variety of applications, including catalyst design and catalytic processes; main-group, transition-metal, and lanthanide and actinide metal chemistry; synthetic aspects of polymer science and materials science; and bioorganometallic chemistry.