光致发光
系统间交叉
量子产额
材料科学
激发态
发光
表征(材料科学)
天线效应
光电子学
光化学
能量转移
化学物理
量子效率
氢键
产量(工程)
配体(生物化学)
纳米技术
键能
量子
过程(计算)
氢
能量(信号处理)
能量转换
光发射
自发辐射
作者
Zhihao Xiao,Xiao Yu,Rui-dong Qiao,Jiaju Liang,Yixuan Wang,Jiajia Ning,Yongming Sui,Xinyi Yang,Bo Zou,Zhihao Xiao,Xiao Yu,Rui-dong Qiao,Jiaju Liang,Yixuan Wang,Jiajia Ning,Yongming Sui,Xinyi Yang,Bo Zou
出处
期刊:Nano Letters
[American Chemical Society]
日期:2025-11-14
卷期号:25 (47): 16780-16787
标识
DOI:10.1021/acs.nanolett.5c04986
摘要
Europium-based metal-organic frameworks offer a unique platform for photoluminescent materials due to the tunable ligand structures and the inherent properties of lanthanides. However, their practical applications are limited by low luminescence efficiency due to inefficient ligand-to-metal energy transfer (LMET). Herein, we introduce a pressure-induced hydrogen bond enhancement strategy to promote the LMET process, triggering the bright red light behavior in the initially weakly emitting Eu(BTC)(H2O)6 (H3BTC: benzene-1,3,5-tricarboxylic acid). As the pressure approaches 9.2 GPa, the photoluminescence quantum yield of the sample increases from an initial value of 19.2% to 69.1%. Furthermore, the red-light emission corresponds to CIE coordinates of (0.66, 0.31) at 9.2 GPa, which meets the requirements of the Rec. 2020 display standard. Systematic photophysical characterization results reveal that the enhanced hydrogen bonds effectively optimize intersystem crossing and improve the efficiency of the sensitization process from the ligand antenna to the excited state of Eu3+ ions.
科研通智能强力驱动
Strongly Powered by AbleSci AI