Highly efficient orange OLEDs with narrow-emitting symmetric tetradentate platinum (II) complexes based on rigid steric hinderance aza-triptycene pyridazine ligands
{"title":"Highly efficient orange OLEDs with narrow-emitting symmetric tetradentate platinum (II) complexes based on rigid steric hinderance aza-triptycene pyridazine ligands","authors":"Qunbo Mei, Xueyan Ma, Beibei Qiu, You Zhai, Lanlan Zhao, Nianshu Li, Bihai Tong","doi":"10.1039/d5qi01049g","DOIUrl":null,"url":null,"abstract":"A series of symmetric tetradentate platinum (II) complexes with rigid steric hinderance aza-triptycene pyridazine ligands Pt-DPM, Pt-PIP and Pt-DPT were synthesized and fully characterized. These complexes exhibited excellent thermal stability with Td of 407-462 °C. All these complexes showed orange emission with emission maxima at 580-593 nm and short lifetimes of 3.37-3.82 μs. Most importantly, these complexes have narrow full width at half maximum of 38-45 nm in thin films. The phosphorescence spectra of Pt-DPM, Pt-PIP and Pt-DPT showed orange emission peak at 585 nm, 588nm and 580nm in PMMA film at a concentration of 1 wt % at room temperature. Furthermore, introduction of aza-triptycene skeleton with rigid steric hindrance reduced bimolecular interactions, then lead to a significant increase in the PLQYs (>88%) compared with the reference platinum (II) complex Pt-D. Solution-processed organic light-emitting diodes using three new platinum (II) complexes as emitters show excellent performance. The device based on the reference platinum complex Pt-D shows a peak external quantum efficiency, current efficiency, and brightness of 4.35 %, 1.97 cd A-1, and 16926 cd m-2, respectively. The efficiencies are dramatically improved to 9.67%, 23.67 cd A-1, and 26670 cd m-2 for the OLED based on the sterically hindered aza-triptycene tetradentate platinum (II) complex Pt-DPM with methyl substituted, and to 16.94%, 44.66 cd A-1, and 54918 cd m-2 for the OLED based on the sterically hindered aza-triptycene tetradentate platinum (II) complex Pt-DPT with isopropyl group substituted, respectively. Due to the introduction of aza-triptycene unit and isopropyl group with steric hindrance, the device has good properties even at high doping concentration. When neat device based on Pt-DPT was adopted as the emitting layer, the non-doped orange device gives a high-brightness of 10873 cd m-2 and luminous efficiency of 9.56 cd A-1 along with CIE coordinates of (0.59, 0.40). These results suggest that these materials have potential application in OLEDs.","PeriodicalId":79,"journal":{"name":"Inorganic Chemistry Frontiers","volume":"81 1","pages":""},"PeriodicalIF":6.1000,"publicationDate":"2025-05-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Inorganic Chemistry Frontiers","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1039/d5qi01049g","RegionNum":1,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, INORGANIC & NUCLEAR","Score":null,"Total":0}
引用次数: 0
Abstract
A series of symmetric tetradentate platinum (II) complexes with rigid steric hinderance aza-triptycene pyridazine ligands Pt-DPM, Pt-PIP and Pt-DPT were synthesized and fully characterized. These complexes exhibited excellent thermal stability with Td of 407-462 °C. All these complexes showed orange emission with emission maxima at 580-593 nm and short lifetimes of 3.37-3.82 μs. Most importantly, these complexes have narrow full width at half maximum of 38-45 nm in thin films. The phosphorescence spectra of Pt-DPM, Pt-PIP and Pt-DPT showed orange emission peak at 585 nm, 588nm and 580nm in PMMA film at a concentration of 1 wt % at room temperature. Furthermore, introduction of aza-triptycene skeleton with rigid steric hindrance reduced bimolecular interactions, then lead to a significant increase in the PLQYs (>88%) compared with the reference platinum (II) complex Pt-D. Solution-processed organic light-emitting diodes using three new platinum (II) complexes as emitters show excellent performance. The device based on the reference platinum complex Pt-D shows a peak external quantum efficiency, current efficiency, and brightness of 4.35 %, 1.97 cd A-1, and 16926 cd m-2, respectively. The efficiencies are dramatically improved to 9.67%, 23.67 cd A-1, and 26670 cd m-2 for the OLED based on the sterically hindered aza-triptycene tetradentate platinum (II) complex Pt-DPM with methyl substituted, and to 16.94%, 44.66 cd A-1, and 54918 cd m-2 for the OLED based on the sterically hindered aza-triptycene tetradentate platinum (II) complex Pt-DPT with isopropyl group substituted, respectively. Due to the introduction of aza-triptycene unit and isopropyl group with steric hindrance, the device has good properties even at high doping concentration. When neat device based on Pt-DPT was adopted as the emitting layer, the non-doped orange device gives a high-brightness of 10873 cd m-2 and luminous efficiency of 9.56 cd A-1 along with CIE coordinates of (0.59, 0.40). These results suggest that these materials have potential application in OLEDs.
合成了一系列具有刚性位阻的氮杂三烯吡啶配体Pt-DPM、Pt-PIP和Pt-DPT的对称四齿铂配合物,并对其进行了表征。这些配合物具有良好的热稳定性,Td为407 ~ 462℃。所有配合物均呈橙色发光,最大发光波长为580 ~ 593 nm,寿命短,为3.37 ~ 3.82 μs。最重要的是,这些配合物在薄膜中具有窄的全宽,最大半宽为38-45 nm。Pt-DPM、Pt-PIP和Pt-DPT在室温浓度为1wt %的PMMA薄膜中的磷光光谱在585 nm、588nm和580nm处呈现橙色发射峰。此外,引入具有刚性位阻的氮杂三甲烯骨架减少了双分子相互作用,与参考铂(II)配合物Pt-D相比,PLQYs显著增加(>88%)。以三种新型铂(II)配合物为发光体的溶液处理有机发光二极管表现出优异的性能。该器件基于参考铂配合物Pt-D,其外部量子效率、电流效率和亮度峰值分别为4.35%、1.97 cd a -1和16926 cd m-2。甲基取代的位阻氮杂三烯四齿铂(II)配合物Pt-DPM的发光效率分别为9.67%、23.67 cd A-1和26670 cd m-2,异丙基取代的位阻氮杂三烯四齿铂(II)配合物Pt-DPT的发光效率分别为16.94%、44.66 cd A-1和54918 cd m-2。由于引入了具有位阻的叠氮三烯单元和异丙基,该器件在高掺杂浓度下仍具有良好的性能。当采用基于Pt-DPT的整齐器件作为发射层时,未掺杂的橙色器件的高亮度为10873 cd m-2,发光效率为9.56 cd a -1, CIE坐标为(0.59,0.40)。这些结果表明这些材料在oled中具有潜在的应用前景。