In a groundbreaking advancement poised to redefine the future of display technologies, researchers at the Korea Advanced Institute of Science and Technology (KAIST) have unveiled a novel in-situ molecular passivation strategy that markedly elevates the performance and spectral stability of pure-blue perovskite light-emitting diodes (PeLEDs). This breakthrough hinges on the precise coordination of under-coordinated lead(II) ions during the vacuum thermal evaporation process, utilizing a phenanthroline-based small molecule ligand named BUPH1. The innovation addresses long-standing challenges that have hampered the efficiency and color stability of vacuum-processed blue PeLEDs, charting a promising trajectory for next-generation wide-gamut displays.
Metal halide perovskites have emerged over recent years as front-runners in optoelectronic applications, especially in light-emitting devices, due to their suite of exceptional optoelectronic properties. These include narrow emission linewidths, tunable bandgaps, high photoluminescence quantum yields, and compatibility with scalable manufacturing techniques. Notably, unlike many solution-processed perovskites that often struggle with film uniformity and thickness control, vacuum thermal evaporation seamlessly integrates into existing OLED fabrication lines. This manufacturing synergy enables atomic-level precision, enabling uniform films with superior morphological quality—a fundamental requirement for the industrial realization of perovskite LEDs.
Achieving pure-blue emission within the spectral window of approximately 460 to 475 nanometers is essential for adhering to international display standards like Rec.2020, which demands vivid, energy-efficient, and eye-friendly blue pixels. The human eye’s sensitivity and visual comfort are optimized within this pure-blue spectrum, avoiding the drawbacks seen in deeper hues below 460 nm that cause eye fatigue and lighter tones above 475 nm that appear washed out. Nonetheless, engineering perovskite materials to fluoresce stably and efficiently at these wavelengths has been fraught with the challenges of phase segregation, spectral drift, and intrinsic defects associated with halide composition.
Early vacuum-evaporated perovskite films have suffered from the prevalence of unsaturated Pb(II) centers formed under halide-deficient conditions, which act as potent non-radiative recombination sites. These defects undermine the photoluminescence quantum efficiency and lead to rapid spectral shifts under operational bias, destabilizing color purity over time. The complex ion migration dynamics within mixed halide perovskites further exacerbate this instability, severely limiting device performance and longevity.
The research team led by Professor Byungha Shin innovatively integrates a phenanthroline-based ligand, BUPH1 (4,7-di(9H-carbazol-9-yl)-1,10-phenanthroline), directly into the evaporation process. By co-evaporating BUPH1 concomitantly with the perovskite precursors, the nitrogen lone pairs within BUPH1 effectively coordinate to the under-coordinated Pb(II) ions as the film crystallizes. This in-situ molecular passivation method significantly mitigates halide-vacancy defects without necessitating post-deposition treatments, curbing non-radiative losses and suppressing ion migration pathways responsible for detrimental spectral drift.
Simultaneously, the careful tuning of the halide composition via co-evaporation of lead(II) bromide (PbBr₂), cesium chloride (CsCl), and cesium bromide (CsBr) facilitates precise bandgap control to target the pure-blue emission window. This co-deposition strategy overcomes the challenges posed by phase segregation that often plagues mixed-halide perovskites, ensuring spectral homogeneity and stability.
The devices fabricated through this approach achieve a narrow full-width at half maximum (FWHM) of 19 nm and peak electroluminescence emission centered at 472 nm, squarely aligning with the Rec.2020 blue primary standard. Impressively, the external quantum efficiency (EQE) reaches 3.1%, setting a new benchmark among thermally evaporated pure-blue PeLEDs. Beyond high efficiency, these devices demonstrate remarkable spectral stability under continuous electrical bias, a crucial attribute for practical display applications where color consistency is paramount.
This work exemplifies the materials science community’s ongoing pursuit to reconcile the high efficiency of solution-processed perovskites with the manufacturing advantages of vacuum-deposited devices. By embedding passivation agents directly within the thermal evaporation process, the researchers circumvent the complexities of multi-step surface treatments, maintaining compatibility with established vacuum-tool fabrication lines ubiquitous in OLED production.
Looking ahead, the research team aims to further elevate device metrics such as luminance and operational lifetime by investigating additional passivation chemistries and engineering fully thermally evaporated device stacks optimized for commercial fabrication. This prospective enhancement will be vital to transitioning perovskite-based pure-blue emitters from laboratory demonstrations into robust components for ultra-high definition displays and solid-state lighting.
This advancement not only bridges a critical gap in perovskite LED technology but also opens avenues for widespread industrial adoption, potentially catalyzing the next wave of display innovation characterized by vibrant, energy-efficient, and durable blue pixels. The synergy of precise vacuum deposition techniques with intelligent molecular design presents a scalable blueprint for future photonic devices beyond displays, including lasers and sensors.
The research team, including Jiyoung Kwon, Yunna Kim, Nakyung Kim, Jinu Park, Sukki Lee, Seoyeon Park, and Byungha Shin of KAIST along with Sunwoo Kang from Dankook University, underscores the importance of multidisciplinary collaboration in tackling complex materials challenges. Their work received support from the National Research Foundation of Korea, reflecting strategic governmental investment fostering innovation in next-generation electronics.
Such progress reinforces the position of metal halide perovskites at the frontier of materials research, emphasizing their versatility in addressing industry-critical performance goals while adhering to scalable and industry-compatible manufacturing modes. As the field moves forward, the principled combination of chemistry, physics, and process engineering showcased in this study will undoubtedly serve as a template for translating emergent materials into impactful technologies.
Subject of Research: Not applicable
Article Title: In situ molecular passivation for improved performance and spectral stability in thermally evaporated pure blue perovskite light-emitting diodes
News Publication Date: 25-Aug-2025
Web References:
Industrial Chemistry & Materials Journal
DOI: 10.1039/D5IM00134J
References: Not provided
Image Credits: Byungha Shin, Korea Advanced Institute of Science and Technology (KAIST), Republic of Korea
Keywords
Perovskite LEDs, pure-blue emission, spectral stability, molecular passivation, vacuum thermal evaporation, phenanthroline ligand, BUPH1, wide-gamut display, electroluminescence, halide vacancy, ion migration suppression, metal halide perovskites
Tags: atomic-level precision in film fabricationchallenges in blue PeLED efficiencyhigh photoluminescence quantum yieldsin-situ molecular passivationlead(II) ions coordinationoptoelectronic applications of perovskitesphenanthroline-based ligand BUPH1pure-blue perovskite LEDsscalable manufacturing techniques for LEDsspectral stability of PeLEDsvacuum thermal evaporation processwide-gamut display technologies
