4.6 Article

DRIFTS-MS Investigation of Low-Temperature CO Oxidation on Cu-Doped Manganese Oxide Prepared Using Nitrate Aerosol Decomposition

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MOLECULES
卷 28, 期 8, 页码 -

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MDPI
DOI: 10.3390/molecules28083511

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doping; Cu-Mn2O4; CO oxidation; oxygen vacancy; water resistance; DRIFTS-MS

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Cu-doped manganese oxide (Cu-Mn2O4) prepared using aerosol decomposition showed excellent CO oxidation performance. The 0.5Cu-Mn2O4 catalyst with a hollow sphere morphology and high Mn3+, Cu+, and Oads ratios exhibited the best CO oxidation activity, with low T-50 and T-90 values. DRIFTS-MS analysis revealed that terminal-type oxygen (M=O) and bridge-type oxygen (M-O-M) on 0.5Cu-Mn2O4 were reactive at low temperatures and water had limited inhibitory effects on CO oxidation.
Cu-doped manganese oxide (Cu-Mn2O4) prepared using aerosol decomposition was used as a CO oxidation catalyst. Cu was successfully doped into Mn2O4 due to their nitrate precursors having closed thermal decomposition properties, which ensured the atomic ratio of Cu/(Cu + Mn) in Cu-Mn2O4 close to that in their nitrate precursors. The 0.5Cu-Mn2O4 catalyst of 0.48 Cu/(Cu + Mn) atomic ratio had the best CO oxidation performance, with T-50 and T-90 as low as 48 and 69 degrees C, respectively. The 0.5Cu-Mn2O4 catalyst also had (1) a hollow sphere morphology, where the sphere wall was composed of a large number of nanospheres (about 10 nm), (2) the largest specific surface area and defects on the interfacing of the nanospheres, and (3) the highest Mn3+, Cu+, and Oads ratios, which facilitated oxygen vacancy formation, CO adsorption, and CO oxidation, respectively, yielding a synergetic effect on CO oxidation. DRIFTS-MS analysis results showed that terminal-type oxygen (M=O) and bridge-type oxygen (M-O-M) on 0.5Cu-Mn2O4 were reactive at a low temperature, resulting in-good low-temperature CO oxidation performance. Water could adsorb on 0.5Cu-Mn2O4 and inhibited M=O and M-O-M reaction with CO. Water could not inhibit O-2 decomposition to M=O and M-O-M. The 0.5Cu-Mn2O4 catalyst had excellent water resistance at 150 degrees C, at which the influence of water (up to 5%) on CO oxidation could be completely eliminated.

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