CO oxidation of bare and TiO₂-coated NiO–Ni(OH)₂ nanoparticles

CO oxidation reactivity of bare and TiO₂-coated nanoparticles consisting of both NiO and Ni(OH)₂ surfaces was studied. For the deposition of TiO₂, atomic layer deposition was used, and formation of three-dimensional domains of TiO₂ on NiO–Ni(OH)₂ could be identified. Based on the data of X-ray Photo...

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Published inCurrent applied physics Vol. 12; no. 2; pp. 429 - 433
Main Authors Nam, Jong Won, Kim, Kwang-Dae, Kim, Dong Wun, Seo, Hyun Ook, Kim, Young Dok, Lim, Dong Chan
Format Journal Article
LanguageEnglish
Published Elsevier B.V 01.03.2012
한국물리학회
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ISSN1567-1739
1878-1675
DOI10.1016/j.cap.2011.07.044

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Summary:CO oxidation reactivity of bare and TiO₂-coated nanoparticles consisting of both NiO and Ni(OH)₂ surfaces was studied. For the deposition of TiO₂, atomic layer deposition was used, and formation of three-dimensional domains of TiO₂ on NiO–Ni(OH)₂ could be identified. Based on the data of X-ray Photoelectron Spectroscopy, we suggest that upon TiO₂ deposition only Ni(OH)₂ was remained on the surface, whereas NiO surface disappeared. Both CO adsorption and CO oxidation took place on NiO–Ni(OH)₂ surfaces under our experimental conditions. CO adsorption was almost completely suppressed after TiO₂ deposition, whereas CO oxidation activity was maintained to large extent. It is proposed that bare NiO cannot be active for CO oxidation, and can only uptake CO under our experimental condition, whereas hydroxylated surface of NiO can be active for CO oxidation.
Bibliography:http://dx.doi.org/10.1016/j.cap.2011.07.044
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G704-001115.2012.12.2.021
ISSN:1567-1739
1878-1675
DOI:10.1016/j.cap.2011.07.044