2020
DOI: 10.1016/j.jechem.2020.03.063
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Enhancement of oxygen reduction activity and stability via introducing acid-resistant refractory Mo and regulating the near-surface Pt content

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Cited by 32 publications
(21 citation statements)
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“…The difference of lattice shrinkage is caused by the alloy formed by Pt and Ni. It will affect the overlapping degree of Pt electron states, causing a downshift of the d-band center that weakens the adsorption strength of the oxygenated intermediate on the surface of the catalyst, which is beneficial for re-exposure of active sites. …”
Section: Resultsmentioning
confidence: 99%
“…The difference of lattice shrinkage is caused by the alloy formed by Pt and Ni. It will affect the overlapping degree of Pt electron states, causing a downshift of the d-band center that weakens the adsorption strength of the oxygenated intermediate on the surface of the catalyst, which is beneficial for re-exposure of active sites. …”
Section: Resultsmentioning
confidence: 99%
“…In practice, there is a need to increase the stability of PtNi nanomaterials [ 88 ]. This necessity can be achieved by introducing a third element to form a ternary alloy or by modification through surface doping [ 89 , 90 , 91 , 92 , 93 , 94 , 95 ]. The enhanced durability and activity of PtNiCu nanoparticles, relative to octahedral PtNi [ 91 ], seems to reflect the surface elemental distribution of metal components.…”
Section: Alloyed Pt Nanostructuresmentioning
confidence: 99%
“…Relative to PtNi/C and the conventional Pt/C, the superior ORR-performance of Ga−PtNi/C, both during half-cell and single-cell tests, has been attributed to changes in the binding energies of the ORR intermediates, the reduced oxyphilic surface, and the Pt-lattice compression induced by Ga doping. The beneficial role of the doping of PtNi/C with Mo (mostly in the form of oxides) has also been reported [ 90 , 93 , 96 ]. The fact that molybdenum surface dopant preferentially occupies the vertex and edge sites of Mo-PtNi/C results in stabilization of the desired octahedral morphology of PtNi (enriched with exposed (111) facets in acid environment) as well as the increase in concentration of the sub-surface Ni and the stabilized under-coordinated Pt sites, thus preventing their migration and dissolution.…”
Section: Alloyed Pt Nanostructuresmentioning
confidence: 99%
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“…are regarded as the most effective catalysts to boost the sluggish kinetics of these reactions [20][21][22][23]. Unfortunately, their high cost, limited reserves, and low stabilities have hindered practical applications [24][25][26][27]. To resolve these issues, lots of researches have been dedicated to minimizing the usage and improving the stability of Pt/Pd-based catalysts [28][29][30].…”
Section: Introductionmentioning
confidence: 99%