材料科学
兴奋剂
漏斗
量子效率
二极管
光电子学
红外线的
发光二极管
分析化学(期刊)
原子物理学
光学
物理
色谱法
有机化学
化学
作者
Wei Li,Donglei Zhou,Yuhang Fang,Yanrun Jia,Tianyuan Wang,Yuqi Wang,Yue Wang,Ruixin Song,Enhui Wang,Xue Bai,Wen Xu,Hongwei Song
标识
DOI:10.1002/adfm.202510052
摘要
Abstract Quasi‐two‐dimensional (quasi‐2D) perovskites exhibit efficient visible‐light emission, but have remained challenging for near‐infrared (NIR) electroluminescence. Here, a breakthrough is reported in achieving NIR emissions at 986 and 1540 nm through quantum cutting in ytterbium/erbium (Yb 3+ /Er 3+ )‐doped quasi‐2D perovskite films. Atomic‐scale transmission electron microscopy reveals that Yb 3+ ions substitute Pb 2+ sites, establishing robust halide coordination that stabilizes the lattice and enables efficient energy transfer. The synergistic combination of Yb 3+ doping and phosphatidylethanolamine (PE) modulates perovskite domain phase distribution, driving the photoluminescence quantum yield (PLQY) to an exceptional 170%—a notable enhancement for NIR emitters. Transient absorption spectroscopy uncovers a cascaded energy transfer mechanism: photoexcited carriers in low‐n‐phases funnel into the n = ∞ phase, enabling sequential energy transfer to Yb 3+ ions and subsequent NIR emission. NIR light‐emitting diodes are fabricated with record‐high external quantum efficiencies (EQEs) of 9.32% at 986 nm and 1.96% at 1540 nm. This work provides atomic‐scale insights into lanthanide ion integration in perovskites and establishes a universal strategy for quantum‐cutting sensitization in optoelectronic materials, paving the way for next‐generation NIR optoelectronic technologies.
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