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Unraveling the twin and tunability of the crystal domain sizes in the medium-pore zeolite zsm-57 by electron crystallography

文献类型:期刊论文

作者Wang, Lei1; Yan, Nana1,2; Liu, Xiaona1,2; Zhao, Xuebin1,2; Shen, Meikun3; Liu, Leifeng4; Tian, Peng1; Guo, Peng1; Liu, Zhongmin1
刊名Chemistry-a european journal
出版日期2019-01-18
卷号25期号:4页码:1029-1036
关键词Alkali metals Crystal growth Electron diffraction Transmission electron microscopy Twin structures Zeolites
ISSN号0947-6539
DOI10.1002/chem.201804269
通讯作者Guo, peng(pguo@dicp.ac.cn) ; Liu, zhongmin(zml@dicp.ac.cn)
英文摘要Tailoring the morphology of a specific crystalline material through distinct crystal growth mechanisms (classical and nonclassical) is challenging. herein, we report the two unique morphologies of a medium-pore (10x8-ring) zeolite, zsm-57, prepared by employing an identical organic structure-directing agent (osda) and different inorganic cations, namely na+ and k+, denoted as zsm-57-na (pentagonal nanoplates) and zsm-57-k (pentagonal nanoprisms), respectively. the tunable twin domain size and twin boundaries in both samples have been unraveled at the atomic level by electron crystallography. it is of significance to note that the 10-ring pore openings run perpendicular to the pentagonal nanoplates and nanoprisms. moreover, the distinct crystal growth mechanisms, which result in the different unique morphologies and tunable twin domains, were further determined by electron crystallography combined with other techniques. nonclassical growth involving the aggregation of amorphous aluminosilicate nanoparticles to the smooth zsm-57-na crystal surface dominates the zsm-57-na crystallization process. for the zsm-57-k sample, the classical layer-by-layer growth through the addition of silica molecules to advancing steps on the crystal surface dominates the zsm-57-k crystallization process. the different morphologies of both samples result in the distinct catalytic lifespan of the methanol conversion and selectivity of lower olefins.
WOS关键词HIGH-SILICA ZEOLITE ; INITIO STRUCTURE SOLUTION ; FRAMEWORK TOPOLOGY ; BOROSILICATE ZEOLITE ; CRYSTALLIZATION ; MORPHOLOGY ; INTERGROWTH ; GROWTH ; MESOCRYSTALS ; DISORDER
WOS研究方向Chemistry
WOS类目Chemistry, Multidisciplinary
语种英语
WOS记录号WOS:000456318800021
出版者WILEY-V C H VERLAG GMBH
URI标识http://www.irgrid.ac.cn/handle/1471x/2372903
专题大连化学物理研究所
通讯作者Guo, Peng; Liu, Zhongmin
作者单位1.Chinese Acad Sci, Dalian Inst Chem Phys, Natl Engn Lab Methanol Olefins, Dalian Natl Lab Clean Energy, Dalian 116023, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100049, Peoples R China
3.Washington Univ, Dept Chem, 1 Brookings Dr, St Louis, MO 63130 USA
4.Univ Birmingham, Sch Met & Mat, Birmingham B15 2TT, W Midlands, England
推荐引用方式
GB/T 7714
Wang, Lei,Yan, Nana,Liu, Xiaona,et al. Unraveling the twin and tunability of the crystal domain sizes in the medium-pore zeolite zsm-57 by electron crystallography[J]. Chemistry-a european journal,2019,25(4):1029-1036.
APA Wang, Lei.,Yan, Nana.,Liu, Xiaona.,Zhao, Xuebin.,Shen, Meikun.,...&Liu, Zhongmin.(2019).Unraveling the twin and tunability of the crystal domain sizes in the medium-pore zeolite zsm-57 by electron crystallography.Chemistry-a european journal,25(4),1029-1036.
MLA Wang, Lei,et al."Unraveling the twin and tunability of the crystal domain sizes in the medium-pore zeolite zsm-57 by electron crystallography".Chemistry-a european journal 25.4(2019):1029-1036.

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来源:大连化学物理研究所

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