Catalytically active ceria-supported cobalt–manganese oxide nanocatalysts for oxidation of carbon monoxide. Issue 22 (24th May 2017)
- Record Type:
- Journal Article
- Title:
- Catalytically active ceria-supported cobalt–manganese oxide nanocatalysts for oxidation of carbon monoxide. Issue 22 (24th May 2017)
- Main Title:
- Catalytically active ceria-supported cobalt–manganese oxide nanocatalysts for oxidation of carbon monoxide
- Authors:
- Wang, Xu
Du, Lin-Ying
Du, Meng
Ma, Chao
Zeng, Jie
Jia, Chun-Jiang
Si, Rui - Abstract:
- Abstract : The crystallinity of the surface of the two-dimensional Co3 O4 phase governs the catalytic performance of ceria-supported cobalt–manganese oxide nanostructures. Abstract : A low-concentration cobalt (∼6 at%) and manganese (∼3 at%) bimetallic oxide catalyst supported on ceria nanorods (CoMnO x /CeO2 ), as well as its related single metal oxide counterparts (CoO x /CeO2 and MnO x /CeO2 ) was synthesized via a deposition–precipitation approach. The fresh samples after air-calcination at 400 °C were tested under the reaction conditions of CO oxidation, and showed the following order of reactivity: CoMnO x /CeO2 > CoO x /CeO2 > MnO x /CeO2 . X-ray diffraction (XRD) and transmission electron microscopy (TEM) data identified that the structure of the CeO2 support was maintained during deposition of metal (Co, Mn) ions while the corresponding vis-Raman spectra verified that more oxygen vacancies were created after deposition–precipitation than those in pure ceria nanorods. Aberration-corrected, high-angle, annular dark-field scanning transmission electron microscopy (HAADF-STEM) images with the help of electron energy loss spectroscopy (EELS) analyses determined two types of cobalt species, i.e. ultra-fine clusters (<2 nm) and smaller nanocrystals (up to 5 nm) in CoO x /CeO2 while only bigger nanostructures (∼10 nm) of cobalt–manganese oxides in CoMnO x /CeO2 . X-ray absorption fine structure (XAFS) measurements demonstrated the presence of a cubic Co3 O4 phase in all theAbstract : The crystallinity of the surface of the two-dimensional Co3 O4 phase governs the catalytic performance of ceria-supported cobalt–manganese oxide nanostructures. Abstract : A low-concentration cobalt (∼6 at%) and manganese (∼3 at%) bimetallic oxide catalyst supported on ceria nanorods (CoMnO x /CeO2 ), as well as its related single metal oxide counterparts (CoO x /CeO2 and MnO x /CeO2 ) was synthesized via a deposition–precipitation approach. The fresh samples after air-calcination at 400 °C were tested under the reaction conditions of CO oxidation, and showed the following order of reactivity: CoMnO x /CeO2 > CoO x /CeO2 > MnO x /CeO2 . X-ray diffraction (XRD) and transmission electron microscopy (TEM) data identified that the structure of the CeO2 support was maintained during deposition of metal (Co, Mn) ions while the corresponding vis-Raman spectra verified that more oxygen vacancies were created after deposition–precipitation than those in pure ceria nanorods. Aberration-corrected, high-angle, annular dark-field scanning transmission electron microscopy (HAADF-STEM) images with the help of electron energy loss spectroscopy (EELS) analyses determined two types of cobalt species, i.e. ultra-fine clusters (<2 nm) and smaller nanocrystals (up to 5 nm) in CoO x /CeO2 while only bigger nanostructures (∼10 nm) of cobalt–manganese oxides in CoMnO x /CeO2 . X-ray absorption fine structure (XAFS) measurements demonstrated the presence of a cubic Co3 O4 phase in all the cobalt-based catalysts. The fitting results of the extended X-ray absorption fine structure (EXAFS) indicated that the introduction of the secondary metal (Mn) oxide significantly enhanced the two-dimensional growth of cobalt oxide nanostructures on the surface of CeO2 . Therefore, the enhanced activity of CO oxidation reaction over the bimetallic cobalt–manganese oxide nanocatalyst can be attributed to the higher crystallinity of the Co3 O4 phase in this work. … (more)
- Is Part Of:
- Physical chemistry chemical physics. Volume 19:Issue 22(2017)
- Journal:
- Physical chemistry chemical physics
- Issue:
- Volume 19:Issue 22(2017)
- Issue Display:
- Volume 19, Issue 22 (2017)
- Year:
- 2017
- Volume:
- 19
- Issue:
- 22
- Issue Sort Value:
- 2017-0019-0022-0000
- Page Start:
- 14533
- Page End:
- 14542
- Publication Date:
- 2017-05-24
- Subjects:
- Chemistry, Physical and theoretical -- Periodicals
541.3 - Journal URLs:
- http://pubs.rsc.org/en/journals/journalissues/cp#!issueid=cp016040&type=current&issnprint=1463-9076 ↗
http://www.rsc.org/ ↗ - DOI:
- 10.1039/c7cp02004j ↗
- Languages:
- English
- ISSNs:
- 1463-9076
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 6475.306000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 171.xml