堆积
光致发光
纳米技术
猝灭(荧光)
材料科学
结构刚度
金属有机骨架
刚度(电磁)
计算机科学
费斯特共振能量转移
荧光
工作(物理)
超分子化学
化学
生化工程
作者
Binhao Yang,Yixuan Wang,Jiaju Liang,Kaiyan Yuan,R. Qiao,Tao Zhang,Xinyi Yang,Bo Zou
标识
DOI:10.1038/s41467-026-68381-9
摘要
Full-visible-spectrum piezochromism is vital for advanced anti-counterfeiting and storage device applications, yet remains challenging. Polycyclic aromatic hydrocarbons represent a promising class of piezochromic materials. However, pressure-induced structural disorder severely limits their performance by causing photoluminescence (PL) quenching through energy dissipation. In framework materials, host-guest modes offer a promising avenue to overcome the limitations. Herein, we demonstrate that the halogen-bonded organic framework host incorporating acridine guests (denoted as XOF@AD) enables full-visible-spectrum piezochromism modulation with the PL red-shift of 237 nm during compression. Both experiments and calculations reveal that strengthened π-hole···π interactions lower its interaction energy to preserve the structural rigidity of XOF host. This suppresses the structural disorder of AD guests and maintains their enhanced π-π stacking interactions, which leads to a decreased band gap. This work establishes host-guest 3D-XOF as a superior platform that achieves full-visible-spectrum piezochromism and presents promising potential for pressure-responsive sensing.
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