共价键
量子点
铀
纳米技术
氢
材料科学
化学
有机化学
冶金
作者
Zhimin Jia,Xiaofeng Li,Sidong Lei,Li Yang,Jie Zhang,Yingdi Zou,Ziqian Han,Ningning He,Feng Zhao,Lijian Ma
出处
期刊:ACS materials letters
[American Chemical Society]
日期:2024-03-06
卷期号:6 (4): 1297-1303
被引量:1
标识
DOI:10.1021/acsmaterialslett.3c01401
摘要
The preparation of low-dimensional covalent–organic frameworks (COFs) is currently a hot and challenging research topic, especially for zero-dimensional (0D) COF quantum dots (COQDs). Herein, for the first time we introduce a facile and efficient approach to fabricating COQDs by selectively disassembling hydrogen-covalent hybridized organic frameworks (H–COFs). By taking advantage of the disparate stabilities between noncovalent and covalent bonds within the periodic lamellar structures of H–COFs, we disrupt the hydrogen bonds through ultrasonic treatment, resulting in the decomposition of H–COFs into COQDs with abundant functional groups, uniform size, high yield, and good stability. Notably, the as-prepared COQD-1 exhibits excellent fluorescence properties, enabling its application in the detection of low-concentration UO22+ with high sensitivity, high selectivity, and good visuality. This study not only presents a novel strategy for preparing COQDs but also highlights their potential in fluorescence-based metal ion detection.
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