{"title":"Efficient CsPbBr3 sky-blue perovskite light-emitting diodes with enhanced stability via dual passivation using sodium sulfamate","authors":"Ganlu Fan, Chang Tan, Zhibo Ge, Li Song","doi":"10.1016/j.jlumin.2025.121319","DOIUrl":null,"url":null,"abstract":"<div><div>Perovskite light-emitting diodes (PeLEDs) have demonstrated considerable potential for application in next-generation display technologies, owing to their exceptional light-emitting properties and cost-effectiveness. However, the performance of perovskite-based blue PeLEDs remains inferior to that of green and red light-emitting devices. A primary factor contributing to this disparity is the substantial non-radiative losses, which result in a reduced photoluminescence quantum yield (PLQY) in the films. Here, we employ an additive strategy by incorporating sodium sulfamate (SAS) into the perovskite layer to passivate film defects and enhance the performance of blue PeLEDs. The results reveal that coordination between sulfamate ions and unsaturated Pb<sup>2+</sup> ions significantly mitigates non-radiative recombination losses in the bulk-phase perovskites. Moreover, the amino group forms hydrogen bonds with adjacent halogen ions, thereby inhibiting their migration and further improving the passivation effect. Consequently, the SAS-modified blue PeLED devices achieved an external quantum efficiency of 5.47 % and an operational lifetime of 19.8 min, approximately double that of the control. Our findings provide valuable insights and effective strategies for realizing high-performance blue PeLEDs.</div></div>","PeriodicalId":16159,"journal":{"name":"Journal of Luminescence","volume":"285 ","pages":"Article 121319"},"PeriodicalIF":3.3000,"publicationDate":"2025-05-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Luminescence","FirstCategoryId":"101","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S0022231325002595","RegionNum":3,"RegionCategory":"物理与天体物理","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"OPTICS","Score":null,"Total":0}
引用次数: 0
Abstract
Perovskite light-emitting diodes (PeLEDs) have demonstrated considerable potential for application in next-generation display technologies, owing to their exceptional light-emitting properties and cost-effectiveness. However, the performance of perovskite-based blue PeLEDs remains inferior to that of green and red light-emitting devices. A primary factor contributing to this disparity is the substantial non-radiative losses, which result in a reduced photoluminescence quantum yield (PLQY) in the films. Here, we employ an additive strategy by incorporating sodium sulfamate (SAS) into the perovskite layer to passivate film defects and enhance the performance of blue PeLEDs. The results reveal that coordination between sulfamate ions and unsaturated Pb2+ ions significantly mitigates non-radiative recombination losses in the bulk-phase perovskites. Moreover, the amino group forms hydrogen bonds with adjacent halogen ions, thereby inhibiting their migration and further improving the passivation effect. Consequently, the SAS-modified blue PeLED devices achieved an external quantum efficiency of 5.47 % and an operational lifetime of 19.8 min, approximately double that of the control. Our findings provide valuable insights and effective strategies for realizing high-performance blue PeLEDs.
期刊介绍:
The purpose of the Journal of Luminescence is to provide a means of communication between scientists in different disciplines who share a common interest in the electronic excited states of molecular, ionic and covalent systems, whether crystalline, amorphous, or liquid.
We invite original papers and reviews on such subjects as: exciton and polariton dynamics, dynamics of localized excited states, energy and charge transport in ordered and disordered systems, radiative and non-radiative recombination, relaxation processes, vibronic interactions in electronic excited states, photochemistry in condensed systems, excited state resonance, double resonance, spin dynamics, selective excitation spectroscopy, hole burning, coherent processes in excited states, (e.g. coherent optical transients, photon echoes, transient gratings), multiphoton processes, optical bistability, photochromism, and new techniques for the study of excited states. This list is not intended to be exhaustive. Papers in the traditional areas of optical spectroscopy (absorption, MCD, luminescence, Raman scattering) are welcome. Papers on applications (phosphors, scintillators, electro- and cathodo-luminescence, radiography, bioimaging, solar energy, energy conversion, etc.) are also welcome if they present results of scientific, rather than only technological interest. However, papers containing purely theoretical results, not related to phenomena in the excited states, as well as papers using luminescence spectroscopy to perform routine analytical chemistry or biochemistry procedures, are outside the scope of the journal. Some exceptions will be possible at the discretion of the editors.