LAUSR.org creates dashboard-style pages of related content for over 1.5 million academic articles. Sign Up to like articles & get recommendations!

Self-Restraining Electroless Deposition for Shell@Core Particles and Influence of Lattice Parameter on the ORR Activity of Pt(Shell)@Pd(Core)/C Electrocatalyst

Photo from wikipedia

Ultrathin metal layer-coated particles have potential applications in various fields, especially in electrocatalysis, where catalytic activity can be increased by shell@core design. In this article, a synthetic method is introduced… Click to show full abstract

Ultrathin metal layer-coated particles have potential applications in various fields, especially in electrocatalysis, where catalytic activity can be increased by shell@core design. In this article, a synthetic method is introduced to synthesize shell@core nanoparticles, in which the selected reducing agent can be electrochemically oxidized preferentially on the core particle but not on the shell metal. Once the shell metal is deposited on the core metal, the oxidation of the reducing agent is inhibited, subsequently forming a shell@core particle with an ultrathin shell. By this method, carbon-supported shell(Pt)@core(Pd) nanoparticles with submonolayer Pt shell were synthesized using formic acid as reducing agent. Spectroscopic characterizations, X-ray photoelectron spectroscopy and energy-dispersive system, confirmed the Pt deposition. The shell@core structure of Pt@Pd was corroborated by scanning transmission electron microscopy analysis. This Pt(shell)@Pd(core) electrocatalyst was tested for electroch...

Keywords: core; metal; shell; deposition shell; core electrocatalyst; shell core

Journal Title: Journal of Physical Chemistry C
Year Published: 2018

Link to full text (if available)


Share on Social Media:                               Sign Up to like & get
recommendations!

Related content

More Information              News              Social Media              Video              Recommended



                Click one of the above tabs to view related content.