Fe3O4 encapsulated mesoporous silica nanospheres with tunable size and large void pore

Magnetic Fe3O4 and mesoporous silica core-shell nanospheres with tunable size from 110–800 nm were synthesized via a one step self-assembly method. The morphological, structural, textural, and magnetic properties were well-characterized by scanning electron microscopy, transmission electron microsco...

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Main Authors: Liu, T., Liu, L., Liu, Jian, Liu, Shaomin, Qiao, S.
Format: Journal Article
Published: Gaodeng Jiaoyu Chubanshe 2014
Online Access:http://hdl.handle.net/20.500.11937/40311
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author Liu, T.
Liu, L.
Liu, Jian
Liu, Shaomin
Qiao, S.
author_facet Liu, T.
Liu, L.
Liu, Jian
Liu, Shaomin
Qiao, S.
author_sort Liu, T.
building Curtin Institutional Repository
collection Online Access
description Magnetic Fe3O4 and mesoporous silica core-shell nanospheres with tunable size from 110–800 nm were synthesized via a one step self-assembly method. The morphological, structural, textural, and magnetic properties were well-characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, N2 adsorption-desorption and magnetometer. These nanocomposites, which possess high surface area, large pore volume and well-defined pore size, exhibit two dimensional hexagonal (P6mm) mesostructures. Interestingly, magnetic core and mesoporous silica shell nanocomposites with large void pore (20 nm) on the shell were generated by increasing the ratio of ethanol/water. Additionally, the obtained nanocomposites combined magnetization response and large void pore, implying the possibility of applications in drug/gene targeting delivery. The cell internalization capacity of NH2-functionalized nanocomposites in the case of cancer cells (HeLa cells) was exemplified to demonstrate their nano-medicine application.
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institution Curtin University Malaysia
institution_category Local University
last_indexed 2025-11-14T09:02:37Z
publishDate 2014
publisher Gaodeng Jiaoyu Chubanshe
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spelling curtin-20.500.11937-403112017-09-13T13:38:55Z Fe3O4 encapsulated mesoporous silica nanospheres with tunable size and large void pore Liu, T. Liu, L. Liu, Jian Liu, Shaomin Qiao, S. Magnetic Fe3O4 and mesoporous silica core-shell nanospheres with tunable size from 110–800 nm were synthesized via a one step self-assembly method. The morphological, structural, textural, and magnetic properties were well-characterized by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, N2 adsorption-desorption and magnetometer. These nanocomposites, which possess high surface area, large pore volume and well-defined pore size, exhibit two dimensional hexagonal (P6mm) mesostructures. Interestingly, magnetic core and mesoporous silica shell nanocomposites with large void pore (20 nm) on the shell were generated by increasing the ratio of ethanol/water. Additionally, the obtained nanocomposites combined magnetization response and large void pore, implying the possibility of applications in drug/gene targeting delivery. The cell internalization capacity of NH2-functionalized nanocomposites in the case of cancer cells (HeLa cells) was exemplified to demonstrate their nano-medicine application. 2014 Journal Article http://hdl.handle.net/20.500.11937/40311 10.1007/s11705-014-1413-2 Gaodeng Jiaoyu Chubanshe restricted
spellingShingle Liu, T.
Liu, L.
Liu, Jian
Liu, Shaomin
Qiao, S.
Fe3O4 encapsulated mesoporous silica nanospheres with tunable size and large void pore
title Fe3O4 encapsulated mesoporous silica nanospheres with tunable size and large void pore
title_full Fe3O4 encapsulated mesoporous silica nanospheres with tunable size and large void pore
title_fullStr Fe3O4 encapsulated mesoporous silica nanospheres with tunable size and large void pore
title_full_unstemmed Fe3O4 encapsulated mesoporous silica nanospheres with tunable size and large void pore
title_short Fe3O4 encapsulated mesoporous silica nanospheres with tunable size and large void pore
title_sort fe3o4 encapsulated mesoporous silica nanospheres with tunable size and large void pore
url http://hdl.handle.net/20.500.11937/40311