贵金属
纳米材料
亚甲蓝
4-硝基苯酚
催化作用
共价键
共价有机骨架
纳米颗粒
金属
化学
选择性催化还原
纳米复合材料
材料科学
化学工程
硝基苯酚
纳米技术
有机化学
光催化
冶金
工程类
作者
Yulong Xu,Xiaofei Shi,Rui Hua,Rui Zhang,Youjin Yao,Bo Zhao,Tong Liu,Jianzhong Zheng,Guang Lü
标识
DOI:10.1016/j.apcatb.2019.118142
摘要
Noble metal nanoparticles (NPs) and covalent organic frameworks (COFs) represent two types of the most studied nanomaterials due to their excellent properties and broad applications. Herein, Fe3O4@COF (TAPB-DMTP) core-shell structure was constructed and used as a support for the immobilization of ultrafine Au NPs for the first time. Au NPs (4.0 nm) were in situ synthesized via the post-reduction method with NaBH4 and immobilized homogeneously in shells of Fe3O4@COF. The resultant core-shell structured Fe3O4@COF-Au exhibits remarkably catalytic activities, good thermal and chemical stabilities, and convenient magnetic separability in reduction of 4-nitrophenol (4-NP) and methylene blue (MB) with NaBH4. More importantly, this synthesis strategy is also applicable to other noble metal NPs (for example, Pt and Pd) to construct such multifunctional hybrid nanomaterials for catalysis application.
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