Microplasma electrochemistry (MIPEC) strategy for accelerating the synthesis of metal organic frameworks at room temperature

A microplasma electrochemistry (MIPEC) strategy was developed for the fast and controllable synthesis of MOFs at room temperature with microplasma acting as cathode. The MIPEC method shows both high space-time yield and high current efficiency, thus has potential for the large-scale synthesis of MOF...

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Veröffentlicht in:Chinese chemical letters 2021-01, Vol.32 (1), p.497-500
Hauptverfasser: Wei, Guoyu, Lu, Yuexiang, Liu, Shuang, Li, Hongpeng, Liu, Xuegang, Ye, Gang, Chen, Jing
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Sprache:eng
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Zusammenfassung:A microplasma electrochemistry (MIPEC) strategy was developed for the fast and controllable synthesis of MOFs at room temperature with microplasma acting as cathode. The MIPEC method shows both high space-time yield and high current efficiency, thus has potential for the large-scale synthesis of MOFs and accelerating other organic materials synthesis process. [Display omitted] Metal organic frameworks (MOFs) are a kind of promising materials in many applications, while the fast and controllable synthesis of MOFs is still challenging. Here, taking HKUST-1 as illustration, a micro-plasma electrochemistry (MIPEC) strategy was developed to accelerate the synthesis process of MOFs with micro-plasma acting as cathode. Treating the HKUST-1 precursor solution with micro-plasma cathode could not only transfer the electrons into the solution leading to the deprotonation effect, but also generate radical species to trigger and accelerate the nucleation and growth of MOFs at the plasma-liquid interface. Thus, uniform and nanosize MOFs could be prepared within minutes. The obtained MOFs show similar excellent uranium adsorption properties compared with those obtained by other method, with a highly adsorption capability of uranium with 550 mg/g in minutes. The novel MIPEC strategy developed in this work provides an alternative for controllable synthesis of MOFs, and especially has potential application in accelerating traditional organic synthesis.
ISSN:1001-8417
1878-5964
DOI:10.1016/j.cclet.2020.04.019