skip to main content
US FlagAn official website of the United States government
dot gov icon
Official websites use .gov
A .gov website belongs to an official government organization in the United States.
https lock icon
Secure .gov websites use HTTPS
A lock ( lock ) or https:// means you've safely connected to the .gov website. Share sensitive information only on official, secure websites.


Title: Lanthanum-based double perovskite nanoscale motifs as support media for the methanol oxidation reaction
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) La 2 NiMnO 6 , LaMnO 3 , and LaNiO 3 nanocubes with average sizes of ∼200 nm, in addition to a series of La 2 NiMnO 6 (b) nanocubes possessing average sizes of ∼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 LaMnO 3 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.  more » « less
Award ID(s):
1807640
PAR ID:
10315345
Author(s) / Creator(s):
; ; ; ;
Date Published:
Journal Name:
Catalysis Science & Technology
Volume:
12
Issue:
2
ISSN:
2044-4753
Format(s):
Medium: X
Sponsoring Org:
National Science Foundation
More Like this
  1. null (Ed.)
    We synthesized and subsequently rationalized the formation of a series of 3D hierarchical metal oxide spherical motifs. Specifically, we varied the chemical composition within a family of ATiO3 (wherein “A” = Ca, Sr, and Ba) perovskites, using a two-step, surfactant-free synthesis procedure to generate structures with average diameters of ~3 microns. In terms of demonstrating the practicality of these perovskite materials, we have explored their use as supports for the methanol oxidation reaction (MOR) as a function of their size, morphology, and chemical composition. The MOR activity of our target systems was found to increase with decreasing ionic radius of the “A” site cation, in order of Pt/CaTiO3 (CTO) > Pt/SrTiO3 (STO) > Pt/BaTiO3 (BTO). With respect to morphology, we observed an MOR enhancement of our 3D spherical motifs, as compared with either ultra-small or cubic control samples. Moreover, the Pt/CTO sample yielded not only improved mass and specific activity values but also a greater stability and durability, as compared with both commercial TiO2 nanoparticle standards and precursor TiO2 templates. 
    more » « less
  2. Abstract We have successfully synthesized ultrathin nanowires of pure Pt, Pt99Ni1, Pt9Ni1, and Pt7Ni3using a modified room‐temperature soft‐template method. Analysis of both methanol oxidation reaction (MOR) and ethanol oxidation reaction (EOR) results found that the Pt7Ni3samples yielded the best performance with specific activities of 0.36 and 0.34 mA/cm2respectively. Additionally, formic acid oxidation reaction (FAOR) tests noted that both Pt and PtNi nanowires oxidize small organic molecules (SOMs) via an indirect pathway. CO oxidation data suggests little measurable performance without any pre‐reduction treatment; however, after annealing in H2, we detected significantly improved CO2formation for both Pt9Ni1and Pt7Ni3motifs. These observations highlight the importance of pre‐treating these nanowires under a reducing atmosphere to enhance their performance for CO oxidation. To explain these findings, we collected extended x‐ray adsorption fine structure (EXAFS) spectroscopy data, consistent with the presence of partial alloying with a tendency for Pt and Ni to segregate, thereby implying the formation of a Pt‐rich shell coupled with a Ni‐rich core. We also observed that the degree of alloying within the nanowires increased after annealing in a reducing atmosphere, a finding deduced through analysis of the coordination numbers and calculations of Cowley's short range order parameters. 
    more » « less
  3. Abstract Fabrication of 3dmetal‐based core@shell nanocatalysts with engineered Pt‐surfaces provides an effective approach for improving the catalytic performance. The challenges in such preparation include shape control of the 3dmetallic cores and thickness control of the Pt‐based shells. Herein, we report a colloidal seed‐mediated method to prepare octahedral CuNi@Pt‐Cu core@shell nanocrystals using CuNi octahedral cores as the template. By precisely controlling the synthesis conditions including the deposition rate and diffusion rate of the shell‐formation through tuning the capping ligand, reaction temperature, and heating rate, uniform Pt‐based shells can be achieved with a thickness of <1 nm. The resultant carbon‐supported CuNi@Pt‐Cu core@shell nano‐octahedra showed superior activity in electrochemical methanol oxidation reaction (MOR) compared with the commercial Pt/C catalysts and carbon‐supported CuNi@Pt‐Cu nano‐polyhedron counterparts. 
    more » « less
  4. We report a versatile method based on seed-mediated growth for the facile synthesis of trimetallic Pd@PtxAu1−x core-shell nanocubes. By simply varying the feeding ratio between the Pt(II) and Au(III) precursors, the atomic ratio of Pt to Au in the shell and thereby the ensemble state of Pt atoms on the surface can be tuned to control the binding configuration of O2 molecules. Specifically, discrete Pt atoms on the surface promote the adsorption of O2 molecules in the Pauling configuration to enhance the catalytic selectivity of the nanoparticles toward H2O2 via the two-electron oxygen reduction reaction, with the Pd@Pt0.025Au0.975 nanocubes showing selectivity as high as 91% at 0.45 VRHE. This work offers a viable means to augment the electrocatalytic performance of alloy nanocrystals by controlling their surface compositions. 
    more » « less
  5. null (Ed.)
    Chemical Looping Reaction is a key strategy to achieve both emission reduction and carbon utilization while producing various value-added chemicals, through redox reactions. Here we study the effect of nanoshape ceria supported Ru catalysts for plasma assisted Chemical Looping Reforming reduction step coupled with water splitting oxidation step reactions in the temperature range 150 ⁰C to 400 ⁰C at 1 atm pressure. The oxygen carrier/catalyst combination materials used are Ru/CeO2 nanorods (NR), Ru/CeO2 nanocubes (NC), Ru/SiO2 nanospheres (NS), and Ni-based perovskite mixed with CeO2. NRs and NCs showed the best catalytic performance followed by Ni-based perovskite and NS. Differences in the selectivity and reactivity for the NRs and NCs were noticed. The NCs showed slightly higher selectivity towards H2 formation during reduction step and lesser carbon deposition. From the analysis of data and literature, it is proposed that the spillover of species such as H adatoms and CHx radicals after activation at Ru sites into the CeO2 supports and lattice O mobility may be slightly faster in the case of NCs. During the oxidation step, the NR and NC materials showed increased H2 production by a factor of more than 4 when compared to Ni based perovskite material. 
    more » « less