2016
DOI: 10.1016/j.catcom.2015.10.024
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Low-temperature efficient degradation of ethyl acetate catalyzed by lattice-doped CeO2–CoOx nanocomposites

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Cited by 57 publications
(19 citation statements)
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“…It might be due to the high dispersion of Co nanoparticles beyond the detection limit or the existence of amorphous metal species . Moreover, the ionic radius of Co 2+ (0.820 Å) and Co 3+ (0.650 Å) were smaller than that of Ce 4+ (1.110 Å) . Therefore, the Co ions might be incorporated into the CeO 2 lattice to form the Ce−Co‐O x solid solution, which might also be confirmed by the slight shift (0.15 °) of the characteristic peak of CeO 2 (111) at 28.6° in Figure b.…”
Section: Resultsmentioning
confidence: 90%
“…It might be due to the high dispersion of Co nanoparticles beyond the detection limit or the existence of amorphous metal species . Moreover, the ionic radius of Co 2+ (0.820 Å) and Co 3+ (0.650 Å) were smaller than that of Ce 4+ (1.110 Å) . Therefore, the Co ions might be incorporated into the CeO 2 lattice to form the Ce−Co‐O x solid solution, which might also be confirmed by the slight shift (0.15 °) of the characteristic peak of CeO 2 (111) at 28.6° in Figure b.…”
Section: Resultsmentioning
confidence: 90%
“…This was associated with the enriched lattice oxygen. 760 Catalytic oxidation of EA over noble metal (Pt, Ru and Au) supported catalysts were also reported in several works. 516,709,[761][762][763][764] In general, supported Ru catalysts show higher acitivity in this reaction compared with Pt-and Au-based catalysts.…”
Section: Ethyl Acetatementioning
confidence: 77%
“…Considering the smaller radii of Mn 3+ (0.65 Å) and Mn 4+ (0.53 Å) than that of Ce 4+ (1.11 Å), this led to the formation of Ce‐Mn‐O solid solution. [ 43–45 ] The presence of the solid solution was considered to promote the emergence of structural defects (such as oxygen vacancies), which could increase the oxygen storage/release capacity of catalysts, resulting in better catalytic oxidation activity. The effect of different hydrothermal conditions on the structure of Ce‐Mn‐O x catalysts therefore might lead to different element valence states and redox properties, which was discussed in detail below.…”
Section: Resultsmentioning
confidence: 99%