Yingya Liu

Prof. Yingya Liu

School of Chemical Engineering, Dalian University of Technology, Dalian 116023, China
orcid

Research Focus & Metrics

Academic Career Length

20Years (2007-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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16 January 2013 in Dalton Transactions
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Journal Article
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SBShyam Biswas
Shyam Biswas
JZJian Zhang
Jian Zhang
ZLZhibao Li
Zhibao Li
Yingya LiuYingya Liu
Yingya Liu
MGMaciej Grzywa
Maciej Grzywa
Pascal Van Der VoortPascal Van Der Voort
Pascal Van Der Voort
Three new functionalized UiO-66-X (X = –SO3H, 1; –CO2H, 2; –I; 3) frameworks incorporating BDC-X (BDC: 1,4-benzenedicarboxylate) linkers have been synthesized by a solvothermal method using conventional electric heating. The as-synthesized (AS) as well as the thermally activated compounds were characterized by X-ray powder diffraction (XRPD), diffuse reflectance infrared Fourier transform (DRIFT) spectroscopy, thermogravimetric (TG), and elemental analysis. The occluded H2BDC-X molecules can be removed by exchange with polar solvent molecules followed by thermal treatment under vacuum leading to the empty-pore forms of the title compounds. Thermogravimetric analysis (TGA) and temperature-dependent XRPD (TDXRPD) experiments indicate that 1, 2 and 3 are stable up to 260, 340 and 360 °C, respectively. The compounds maintain their structural integrity in water, acetic acid and 1 M HCl, as verified by XRPD analysis of the samples recovered after suspending them in the respective liquids. As confirmed by N2, CO2 and CH4 sorption analyses, all of the thermally activated compounds exhibit significant microporosity (SLangmuir: 769–842 m2 g−1), which are comparable to that of the parent UiO-66 compound. Compared to the unfunctionalized UiO-66 compound, all the three functionalized solids possess higher ideal selectivity in adsorption of CO2 over CH4 at 33 °C.

1 November 2007 in International Journal of Hydrogen Energy
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Journal Article
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Yingya LiuYingya Liu
Yingya Liu
JZJ Zeng
J Zeng
JZJ Zhang
J Zhang
FXF Xu
F Xu
LSL Sun
L Sun

1 June 2019 in Applied Catalysis B: Environment and Energy
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Journal Article
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ZSZhichao Sun
Zhichao Sun
Mingshan ZhuMingshan Zhu
Mingshan Zhu
XLXingshuai Lv
Xingshuai Lv
Yingya LiuYingya Liu
Yingya Liu
CSChuan Shi
Chuan Shi
TMTetsuro Majima
Tetsuro Majima

4 April 2017 in Advanced Functional Materials
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Anna M. KaczmarekAnna M. Kaczmarek
Anna M. Kaczmarek
Yingya LiuYingya Liu
Yingya Liu
CWChunhua Wang
Chunhua Wang
BLBrecht Laforce
Brecht Laforce
LVLaszlo Vincze
Laszlo Vincze
Rik Van DeunRik Van Deun
Rik Van Deun

21 May 2020 in Catalysts
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JSJiamin Sun
Jiamin Sun
Sara AbednatanziSara Abednatanzi
Sara Abednatanzi
Pascal Van Der VoortPascal Van Der Voort
Pascal Van Der Voort
Yingya LiuYingya Liu
Yingya Liu
Karen LeusKaren Leus
Karen Leus
The hybrid materials that are created by supporting or incorporating polyoxometalates (POMs) into/onto metal–organic frameworks (MOFs) have a unique set of properties. They combine the strong acidity, oxygen-rich surface, and redox capability of POMs, while overcoming their drawbacks, such as difficult handling, a low surface area, and a high solubility. MOFs are ideal hosts because of their high surface area, long-range ordered structure, and high tunability in terms of the pore size and channels. In some cases, MOFs add an extra dimension to the functionality of hybrids. This review summarizes the recent developments in the field of POM@MOF hybrids. The most common applied synthesis strategies are discussed, together with major applications, such as their use in catalysis (organocatalysis, electrocatalysis, and photocatalysis). The more than 100 papers on this topic have been systematically summarized in a handy table, which covers almost all of the work conducted in this field up to now.

31 January 2012 in Journal of Catalysis
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Karen LeusKaren Leus
Karen Leus
Matthias VandichelMatthias Vandichel
Matthias Vandichel
Yingya LiuYingya Liu
Yingya Liu
IMIlke Muylaert
Ilke Muylaert
JMJan Musschoot
Jan Musschoot
Pascal Van Der VoortPascal Van Der Voort
Pascal Van Der Voort