Dual interfacial H-bonding-enhanced deep-blue hybrid copper-iodide LEDs

• 成果类型: Article
• 署名作者: Zhu, Kun; Reid, Obadiah; Rangan, Sylvie; Wang, Li; Li, Jingbai; Durai, Kevin Antony Jesu; Zhou, Kang; Javed, Nasir; Kasaei, Leila; Yang, Chongqing; Li, Mingxing; Sun, Yue; Tan, Kui; Cotlet, Mircea; Liu, Yi; Feldman, Leonard C.; O'Carroll, Deirdre M.; Zhu, Kai; Li, Jing
• 署名单位: Rutgers University System; Rutgers University New Brunswick; Rutgers University System; Rutgers University New Brunswick; United States Department of Energy (DOE); National Renewable Energy Laboratory - USA; Shenzhen Polytechnic University; University of North Texas System; University of North Texas Denton; Rutgers University System; Rutgers University New Brunswick; United States Department of Energy (DOE); Lawrence Berkeley National Laboratory; United States Department of Energy (DOE); Brookhaven National Laboratory
• 刊物名称: Nature
• ISSN/ISSBN: 0028-3188
• DOI: 10.1038/s41586-025-09257-8
• 发表日期: 2025-07-31
• 关键词: light-emitting-diodes; highly efficient; quantum; FAMILY; robust

摘要

Solution-processed light-emitting diodes based on non-toxic copper-iodide hybrids1 are a compelling solution for efficient and stable deep-blue lighting, owing to their tunability, high photoluminescence efficiency and environmental sustainability2. Here we present a hybrid copper-iodide that shows near-unity photoluminescence quantum yield (99.6%) with an emission wavelength of 449 nm and colour coordinates (0.147, 0.087), alongside its emission mechanism and charge transport characteristics. We use the thin film of this hybrid as the sole active emissive layer to fabricate deep-blue light-emitting diodes and subsequently enhance the device performance through a dual interfacial hydrogen-bond passivation strategy. This synergetic surface modification approach, integrating a hydrogen-bond-acceptor self-assembled monolayer with an ultrathin polymethyl methacrylate capping layer, effectively passivates both heterojunctions of the copper-iodide hybrid emissive layer and optimizes charge injections. We achieve a maximum external quantum efficiency of 12.57%, a maximum luminance of 3,970.30 cd m-2 with colour coordinates (0.147, 0.091) and an excellent operational stability (half-lifetime) of 204 hours under ambient conditions. We further showcase a large-area device of 4 cm2 that maintains high efficiency. Our findings reveal the potential of copper-iodide-based hybrid materials for applications in solid-state lighting3 and display technologies4, offering a versatile strategy for enhancing device performances.