Microwave-assisted synthesis of 2D Zr-MOF nanosheets supported gold nanocomposites as efficient catalysts for the reduction of 4-nitrophenol

硼氢化钠 催化作用 贵金属 纳米复合材料 纳米颗粒 4-硝基苯酚 材料科学 X射线光电子能谱 化学工程 硼氢化 还原剂 选择性催化还原 纳米技术 无机化学 化学 有机化学 工程类
作者
Xiangyue Liu,Li Ye,Yijun Liu,Sijun Li,Li Feng,Jinliang Zhuang,Jing Tang
出处
期刊:Journal of Alloys and Compounds [Elsevier BV]
卷期号:922: 165939-165939 被引量:14
标识
DOI:10.1016/j.jallcom.2022.165939
摘要

Two-dimensional metal-organic framework nanosheets (2D MONs) are excellent heterogeneous catalysts owing to their high density and accessible catalytic sites, reduced diffusion pathways for reactants/products, and fast electron transport. Moreover, the employment of 2D MONs as supports to encapsulate noble nanoparticles can not only stabilize the noble nanoparticles, but also significantly improve their catalytic activity through the synergetic effect between 2D MONs and noble nanoparticles. Herein, we reported a microwave-assisted method for the rapid preparation of 2D UiO-67 metal-organic framework nanosheets (named UiO-67 NS). The Au nanoparticles modified UiO-67 nanocomposites (denoted as Au/UiO-67 NS nanocomposites) are formed by the in situ reduction of HAuCl4 in the pores of UiO-67 NS. The Au/UiO-67 NS nanocomposites show excellent catalytic activity for the reduction of 4-nitrophenol to 4-aminophenol, and only 20 equivalent sodium borohydride can completely reduce 10 mM 4-NP in 100 s, thanks to highly exposed Au NPs and reduced diffusion distance. In addition, XPS characterizations showed that the binding energy of Au 4 f in Au/UiO-67 NS nanocomposites displays a 0.48 eV less than that of Au nanoparticles on UiO-67 octahedral microcrystals (denoted as [email protected] OM), which is believed to be responsible for the enhanced catalytic activity toward the reduction of 4-nitrophenol.
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