光热治疗
材料科学
纳米技术
堆积
催化作用
共轭体系
纳米材料
胶体
纳米颗粒
光热效应
胶束
纳米尺度
多相催化
吸收(声学)
产量(工程)
化学工程
纳米器件
聚合物
混合材料
动力学
一步到位
化学合成
纳米结构
作者
Chang Lv,Xiaokuang Xue,Jiechao Ge,Yong‐Chao Zheng,Xu‐Bing Li,Tierui Zhang,Li‐Zhu Wu,Huaping Wang
标识
DOI:10.1002/anie.202525678
摘要
Micelle-confined synthesis is a well-established bottom-up strategy for nanomaterials synthesis, offering precise synthetic control and inherent dispersibility in solution. Herein, we pioneer a reverse micelle-confined growth strategy for synthesizing two-dimensional conjugated metal-organic frameworks (2D c-MOFs) colloids, including Cu/Zn/Mn-HHTP. And scalable synthesis under mild conditions is also achieved. The confined space of micelle microenvironment effectively regulates the growth kinetics and stacking morphology, yielding nanoscale 2D c-MOFs in minutes that form stable colloids in various solvents for over 20 days. Considering the efficient visible-near infrared absorption in addition to the strong light-matter interactions of the 2D c-MOF colloids, an exceptional photothermal conversion efficiency of 80.3% is achieved under 880 nm laser irradiation, which outperforms most other 2D photothermal materials. Leveraging this, the material served as an efficient catalyst toward the selective oxidation of a chemical warfare agent simulant (i.e., 2-chloroethyl ethyl sulfide, CEES) under visible light, reaching near 100% yield to non-toxic sulfoxide with extremely low 2D c-MOFs usage. Our work highlights that micelle-confined synthesis serves as an efficient, energy-saving, and green strategy for fabricating 2D c-MOF colloids, paving the way for their applications in catalysis and beyond.
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