4.6 Article

Lanthanum-based double perovskite nanoscale motifs as support media for the methanol oxidation reaction

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CATALYSIS SCIENCE & TECHNOLOGY
卷 12, 期 2, 页码 613-629

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ROYAL SOC CHEMISTRY
DOI: 10.1039/d1cy01668g

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  1. U.S. National Science Foundation [CHE-1807640]
  2. U.S. Department of Energy [DE-SC0012704]

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Perovskite oxides show high activity as support media for the methanol oxidation reaction, with Ni-containing perovskites being more favorable for MOR. The activity of MOR is enhanced as the size of perovskite increases, and one-dimensional morphology of nanorods exhibits greater activity compared to nanocubes of similar diameter.
We have not only analyzed the performance of perovskite oxides as support media for the methanol oxidation reaction (MOR) but also examined the impact and significance of various reaction parameters on their synthesis. Specifically, we have generated (a) La2NiMnO6, LaMnO3, and LaNiO3 nanocubes with average sizes of similar to 200 nm, in addition to a series of La2NiMnO6 (b) nanocubes possessing average sizes of similar to 70 and 400 nm and (c) anisotropic nanorods characterized by average diameters of 40-50 nm. All of these samples, when used as supports for Pt nanoparticles, exhibited activities which were at least twice that measured for Pt/C. We have investigated and correlated the effect of varying perovskite (i) composition, (ii) size, and (iii) morphology upon the measured MOR activity. (i) The Ni-containing perovskites yielded generally higher performance metrics than LaMnO3 alone, suggesting that the presence of Ni is favorable for MOR, a finding supported by a shift in the Pt d-band in XPS. (ii) MOR activity is enhanced as the perovskite size increases in magnitude, suggesting that a growth in the perovskite particle size enables favorable, synergistic metal-support interactions. (iii) A comparison of the nanorods and nanocubes of a similar diameter implied that the one-dimensional morphology achieved a greater activity, a finding which can be attributed not only to the anisotropic structure but also to a desirable surface structure. Overall, these data yield key insights into the tuning of metal-support interactions via rational control over the composition, size, and morphology of the underlying catalyst support.

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