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Cited by 218

The DOI matches its Crossref record; 4 of the 4 references it cites were found in a registry or an index.

Ni@SiO2yolk-shell nanoreactor catalysts: High temperature stability and recyclability

Park, Ji Chan, Bang, Jung Up, Lee, Joongoo, Ko, Chang Hyun, Song, Hyunjoon·2010·J. Mater. Chem.

Abstract

Nickel-based catalysts have been good candidates for steam reforming of methane, but their stability has been restricted due to the agglomeration among particles at high temperature. In the present work, a new type of Ni@SiO2 yolk-shell nanoreactor framework comprising Ni cores inside hollow silica shells has been prepared through direct silica coating and subsequent selective etching of the metal cores. This nanoreactor framework is remarkably stable at high temperatures up to 973 K, because the silica hollow shells around the nickel cores essentially block particle sintering. The Ni@SiO2 nanoreactor structure is employed as a model catalyst for the steam methane reforming reaction. The catalysts exhibit a continuous conversion rate of methane and hydrogen, and significantly enhanced stability at high temperatures, leading to high recyclability without loss of catalytic activity. These reaction properties are superior to Ni/MCF catalysts, and comparable with state-of-the-art commercial catalysts. This catalyst design can be generalized for other bifunctional systems, such as Co@SiO2 and Fe@SiO2.

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Metadata

Authors
Park, J. C., Bang, J. U., Lee, J., Ko, C. H., & Song, H.
Venue
J. Mater. Chem.
Published
2010
Volume
20
Issue
7
Pages
1239-1246
ISSN
  • 0959-9428 (ISSN-L)
  • 1364-5501
OpenAlex
W2034495469
Cited by
218
References
4
FWCI
5.76
Type
journal article
Language
en
Open access
closed

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CoChat. (2026). Citation check: Ni@SiO2yolk-shell nanoreactor catalysts: High temperature stability and recyclability. https://app.cochat.ai/papers/10.1039/b918446e
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Park, J. C., Bang, J. U., Lee, J., Ko, C. H., & Song, H. (2010). Ni@SiO2yolk-shell nanoreactor catalysts: High temperature stability and recyclability. J. Mater. Chem. https://doi.org/10.1039/b918446e

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