Constructing core–shell
nanostructures is demonstrated to
be an effective strategy to improve catalytic activity of metal nanoparticles.
However, the impact of the atomic ordering of the metal core on the
performance of the shell remains unexplored. Here, ruthenium–platinum
(Ru–Pt) core–shell nanoparticles, with a crystalline
and amorphous Ru core of the same diameter and diverse Pt shell thicknesses,
are prepared and characterized by X-ray diffraction (XRD), X-ray photoelectron
spectroscopy (XPS), high-angle annular dark-field scanning transition
electron spectroscopy (HAADF-STEM), and CO tripping voltammetry. The
well-defined heterostructured Ru–Pt interface and anisotropic
growth of the Pt shell on the crystalline Ru core (Ru@Pt
x
) were observed, while the amorphous Ru core induces
a partial alloy at the Ru–Pt interface and isotropic growth
of the Pt shell. The core–shell structure also results in an
apparent down-shift of the d-band center of Pt, which dissipates much
faster on the amorphous Ru core than on crystalline ones, as demonstrated
by the XRD and CO desorption potential. The two sets of core–shell
nanoparticles show that a volcano-shape dependence of the catalytic
activity on the thickness of the Pt shell and the crystalline Ru core
markedly enhanced the catalytic performance and stability toward electro-oxidation
of formic acid and ethanol, which is ascribed to the lattice strain
of the Pt shell, down-shift of the d-band center, the weakened CO
adsorption, and thus alleviated poisoning.
The slow kinetics of oxygen evolution reaction (OER) has seriously hindered the development of electrical water splitting and rechargeable metal-air batteries. The ethanol oxidation reaction (EOR) to replace OER is...
Development
of low-cost and high-efficiency electrocatalysts for
hydrogen evolution reaction is a critical step toward sustainable
water splitting. Herein, in situ growth of heterostructured MoC/Mo2C nanoribbons and nanoflowers on copper foam (Mo
x
C/Cu), copper foil, and nickel foam (Mo
x
C/Ni) are prepared via a two-step method: hydrothermal
preparation of molybdenum precursors followed by pyrolysis at controlled
temperatures. The Mo
x
C/Cu hybrids are
found to exhibit an excellent catalytic activity, as compared to the
Mo
x
C/Ni and Cu foil counterparts, and
the sample prepared at 750 °C stands out as the best among the
series with a low overpotential of 169 mV to reach the current density
of 200 mA cm–2 in 1 M KOH, and 194 mV in 0.5 M H2SO4, and the corresponding Tafel slopes of 98 and
74 mV dec–1, respectively. The electrocatalytic
activity is also found to vary with the Mo2+/Mo3+ and N contents in the samples that impact the electrical conductivity
and electron-transfer kinetics of the hydrogen evolution reaction.
Results suggest that MoC/Mo2C heterostructured materials
supported on copper foam may be a viable candidate to catalyze hydrogen
evolution reaction in a wide range of pH.
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