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Jeong, Hu Young
UNIST Central Research Facilities (UCRF)
Research Interests
  • Soft material characterization such as graphene using a low kV Cs-corrected TEM
  • Insitu-TEM characterization of carbon-based materials using nanofactory STM holder for Li-ion battery application
  • Structural characterization of mesoporous materials using SEM & TEM
  • Interface analysis between various oxides and metals through Cs-corrected (S)TEM
  • Resistive switching mechanism of graphene oxide thin films for RRAM application

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Nature of Rh Oxide on Rh Nanoparticles and Its Effect on the Catalytic Activity of CO Oxidation

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Title
Nature of Rh Oxide on Rh Nanoparticles and Its Effect on the Catalytic Activity of CO Oxidation
Author
Kim, Sun MiQadir, KamranSeo, BoraJeong, Hu YoungJoo, Sang HoonTerasaki, OsamuPark, Jeong Young
Keywords
Catalytic activity; CO oxidation; Oxidation state; Rh nanoparticles; Surface oxide layer; UV-ozone (UV/O3) dosing
Issue Date
2013-11
Publisher
SPRINGER
Citation
CATALYSIS LETTERS, v.143, no.11, pp.1153 - 1161
Abstract
Surface oxide layers formed on transition metal catalysts are well known as one of the controlling factors in enhancing or suppressing the catalytic activity of metal catalysts. We investigated the growth of a surface oxide layer on two sizes of Rh metal nanoparticles (NPs) as a function of UV-ozone (UV/O3) dosing as well as how the oxide layer formed on the surface of the Rh NPs affects the catalytic activity for CO oxidation. Monodisperse Rh NPs were synthesized via one-pot polyol reduction using poly(vinylpyrrolidone) as a capping agent. Varying the concentration of the Rh precursors controlled the size of the NPs. The changes that occurred as a function of UV/O3 dosing were characterized using X-ray photoelectron spectroscopy, which showed that the oxidation state increased with increasing surface modification time. The catalytic activity and activation energy of the two-dimensional Rh NPs arrays were measured as the UV/O3 exposure time increased. Our reaction studies indicate that the turnover rate of CO oxidation on the Rh NPs is enhanced as the quantity of the surface oxide layer formed during UV/O3 surface treatment increases, indicating that the oxides grown on the surface of the Rh metal are catalytically active. These results suggest an intriguing way to tune catalytic activity via engineering of the nanoscale surface oxide.
URI
https://scholarworks.unist.ac.kr/handle/201301/3889
DOI
10.1007/s10562-013-1087-2
ISSN
1011-372X
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UCRF_Journal Papers
ECHE_Journal Papers
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