光致发光
发光
量子产额
荧光
材料科学
纳米技术
氢键
光电子学
多孔性
光化学
结构稳定性
化学工程
化学物理
聚集诱导发射
辐射传输
量子效率
纳米晶
氢
结构变化
自发辐射
格子(音乐)
产量(工程)
多孔介质
化学
量子
分子
生物成像
波长
合理设计
金属有机骨架
半导体
压缩性
热稳定性
纳米-
化学稳定性
作者
Ting Zhang,Shuo Shan,Yunjia Bai,Yixuan Wang,Yang Shou,Xinyi Yang,Bo Zou
出处
期刊:Nano Letters
[American Chemical Society]
日期:2026-02-16
卷期号:26 (8): 2971-2977
被引量:1
标识
DOI:10.1021/acs.nanolett.6c00163
摘要
Luminescent metal-organic frameworks (MOFs), featuring tunable porous architectures and unique optical properties, hold great promise for applications in bioimaging, fluorescent sensing, and environmental monitoring. However, balancing structural stability, active site density, and emission efficiency in photofunctional MOFs remains highly challenging. Herein, we present a pressure treatment strategy to precisely regulate the local structural environment of MIL-116(Al), thereby enabling efficient blue emission. MIL-116(Al) inherently possesses excellent structural stability and abundant active sites; however, its weak luminescence limits practical applications. Pressure-induced negative linear compressibility results in strengthened hydrogen bonds between uncoordinated carboxyl groups and lattice water molecules. The resulting rigidification suppresses vibrational and rotational motions of aromatic linkers, thereby promoting radiative recombination in MIL-116(Al). Consequently, pressure-treated MIL-116(Al) displays bright-blue emission, with its photoluminescence quantum yield increasing from 4.5% to 60.7%. These results establish a new paradigm for optimizing the performance of photofunctional MOFs with broad implications for optoelectronic applications.
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