One-step electrodeposition of ligand-free PdPt alloy nanoparticles from water droplets: Controlling size, coverage, and elemental stoichiometry
Author(s) -
Andrew D. Pendergast,
Matthew W. Glasscott,
Christophe Renault,
Jeffrey E. Dick
Publication year - 2018
Publication title -
electrochemistry communications
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.223
H-Index - 192
eISSN - 1873-1902
pISSN - 1388-2481
DOI - 10.1016/j.elecom.2018.11.005
Subject(s) - highly oriented pyrolytic graphite , stoichiometry , nanoparticle , phase (matter) , chemical engineering , scanning electron microscope , materials science , alloy , metal , particle size , graphite , inorganic chemistry , analytical chemistry (journal) , chemistry , nanotechnology , metallurgy , organic chemistry , engineering , composite material
We present a robust and facile method to produce metal nanoparticle (NP) alloys in a one-step synthesis using direct electrodeposition onto highly oriented pyrolytic graphite (HOPG). Precursor salts, H2PtCl6 and Pd(NO3)2, were dissolved in a 1 mM sodium dodecylsulfate (SDS) water droplet with 1× phosphate buffered saline solution and suspended in a dichloroethane (DCE) continuous phase. Tetrabutylammonium perchlorate was added to the DCE continuous phase to maintain charge balance during electrodeposition. NP fabrication via electrodeposition was driven by droplet collisions onto HOPG, which was biased at a potential where the metal precursor salts would reduce to their respective zero-valent atoms. Scanning Electron Microscopy (SEM) and Energy Dispersive X-ray Spectroscopy (EDX) were used to study the size, coverage, and morphology of the NPs as well as the atomic stoichiometry. EDX mapping indicated homogeneous distribution of Pd and Pt at the single NP level. Homogeneously alloyed PdPt NPs were realized from this study with demonstrated control over metal composition, surface coverage, and NP size.
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