Ultralow charge-transfer resistance with ultralow Pt loading for hydrogen evolution and oxidation using Ru@Pt core-shell nanocatalysts
نویسندگان
چکیده
We evaluated the activities of well-defined Ru@Pt core-shell nanocatalysts for hydrogen evolution and oxidation reactions (HER-HOR) using hanging strips of gas diffusion electrode (GDE) in solution cells. With gas transport limitation alleviated by micro-porous channels in the GDEs, the charge transfer resistances (CTRs) at the hydrogen reversible potential were conveniently determined from linear fit of ohmic-loss-corrected polarization curves. In 1 M HClO4 at 23 °C, a CTR as low as 0.04 Ω cm(-2) was obtained with only 20 μg cm(-2) Pt and 11 μg cm(-2) Ru using the carbon-supported Ru@Pt with 1:1 Ru:Pt atomic ratio. Derived from temperature-dependent CTRs, the activation barrier of the Ru@Pt catalyst for the HER-HOR in acids is 0.2 eV or 19 kJ mol(-1). Using the Ru@Pt catalyst with total metal loadings <50 μg cm(-2) for the HER in proton-exchange-membrane water electrolyzers, we recorded uncompromised activity and durability compared to the baseline established with 3 mg cm(-2) Pt black.
منابع مشابه
Ni@Pt core-shell nanoparticles as an improved electrocatalyst for ethanol electrooxidation in alkaline media
Core-shell nanostructures are emerging as more important materials than alloy nanostructures and have much more interesting potential applications in various fields. In this work, we demonstrated the fast and facile synthesis of core-shell nanoparticles consisting of Pt thin layer as the shell and Ni nanoparticles as the cores. The described method herein is suitable for large-scale and low-cos...
متن کاملEthanol electrooxidation on the Co@Pt core-shell nanoparticles modified carbon-ceramic electrode in acidic and alkaline media
In this study, the electrocatalytic activity of the Co@Pt core-shell nanoparticles toward the ethanol oxidation reaction has been investigated by cyclic voltammetry and chronoamperometry in acidic and alkaline media in details. The physicochemical data obtained in alkaline solution are compared to those in acidic solution. The obtained results demonstrate that while in the both media Co@Pt core...
متن کاملTailoring Au-core Pd-shell Pt-cluster nanoparticles for enhanced electrocatalytic activity†
We have rationally synthesized and optimized catalytic nanoparticles consisting of a gold core, covered by a palladium shell, onto which platinum clusters are deposited (Au@Pd@Pt NPs). The amount of Pt and Pd used is extremely small, yet they show unusually high activity for electrooxidation of formic acid. The optimized structure has only 2 atomic layers of Pd and a half-monolayer equivalent o...
متن کاملAg/Pt Core-Shell Nanoparticles on Graphene Nanocomposite for Effective Anodic Fuels Electro-oxidation
The nanocomposite consists of the Ag as a core and Pt as shell on the surface of graphene nanosheets (Ag/Pt-G) was synthesized with a simple method and used as a novel electrochemical platform for an efficient catalyst for oxidation of the ethanol, methanol and formic acid. The morphology and electrochemical properties of Ag/Pt-G nanocomposite were investigated by TEM, X-ray diffraction, and vo...
متن کاملRu-Pt core-shell nanoparticles for preferential oxidation of carbon monoxide in hydrogen.
Most of the world's hydrogen supply is currently obtained by reforming hydrocarbons. 'Reformate' hydrogen contains significant quantities of CO that poison current hydrogen fuel-cell devices. Catalysts are needed to remove CO from hydrogen through selective oxidation. Here, we report first-principles-guided synthesis of a nanoparticle catalyst comprising a Ru core covered with an approximately ...
متن کامل