沸石咪唑盐骨架
材料科学
平版印刷术
纳米技术
共价键
咪唑酯
光子学
金属有机骨架
化学
光电子学
有机化学
吸附
作者
Xiaoli Tian,Wenjun Li,Fu Li,Mingfeng Cai,Yilong Si,Hao Tang,Haifang Li,Hao Zhang
标识
DOI:10.1002/anie.202500476
摘要
Precise and effective patterning strategies are essential for integrating metal‐organic frameworks (MOFs) into microelectronics, photonics, sensors, and other solid‐state devices. Direct lithography of MOFs with light and other irradiation sources has emerged as a promising patterning strategy. However, existing direct lithography methods often rely on the irradiation‐induced amorphization of the MOFs structures and the breaking of strong covalent bonds in their organic linkers. High‐energy sources (such as X‐rays or electron beams) and large irradiation doses—conditions unfavorable for scalable patterning—are thus required. Here, we report a photoinduced fluorination chemistry for patterning various zeolitic imidazolate frameworks (ZIFs) under mild UV irradiation. Using UV doses as low as 10 mJ cm–2, light‐sensitive fluorine‐containing molecules covalently bond to ZIFs and enhance their stability in water. This creates a water‐stability contrast between ZIFs in exposed and unexposed regions, enabling scalable direct photolithography of ZIFs with high resolution (2 μm) on 4‐inch wafers and flexible substrates. The patterned ZIFs preserve their original crystallinity and porous properties while gaining increased hydrophobicity. This allows for the demonstration of a water‐responsive fluorescent MOFs array with implications in sensing and multicolor information encryption.
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