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Facile synthesis of morphology and size-controlled zirconium metal-organic framework UiO-66: the role of hydrofluoric acid in crystallization

发表时间:2019-03-09
点击次数:
论文类型:
期刊论文
第一作者:
Han, Yitong
通讯作者:
Han, YT (reprint author), Dalian Univ Technol, Sch Chem Engn, PSU DUT Joint Ctr Energy Res, State Key Lab Fine Chem, Dalian 116024, Peoples R China.
合写作者:
Guo, Xinwen,Liu, Min,Li, Keyan,Zuo, Yi,Wei, Yingxu,Xu, Shutao,Zhang, Guoliang,Song, Chunshan,Zhang, Zongchao
发表时间:
2015-01-01
发表刊物:
CRYSTENGCOMM
收录刊物:
SCIE、Scopus
文献类型:
J
卷号:
17
期号:
33
页面范围:
6434-6440
ISSN号:
1466-8033
摘要:
UiO-66 with crystal size ranging from hundreds of nanometers to a few micrometers and with cubic and cuboctahedral morphologies were synthesized. Crystal size and morphology varied with the additive amount of hydrofluoric acid and the concentration of reactants (ZrCl4 and H2BDC) during solvothermal synthesis. According to energy dispersive spectrometry (EDS) and F-19 MAS NMR measurements, the fluorine ions directly bonded to Zr in the SBUs (secondary building units) in the MOF framework due to their strongest electronegativity. The bonding of the fluorine ions and Zr not only compensated for the charge imbalance of the framework caused by missing linkers but also competed with the linkers to coordinate with the Zr metal centers, thereby controlling the processes of nucleation and growth of the UiO-66 crystals. The samples were further characterized by scanning electron microscopy (SEM), powder X-ray diffraction (XRD), Fourier transform-infrared (FT-IR) spectroscopy, thermogravimetric analysis (TGA) and Ar sorption isotherms, showing that the introduction of fluorine enhanced the thermostability and porosity of UiO-66.
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