Abstract
Copper nanoparticles (CuNPs) are attractive as a low-cost alternative to their gold and silver analogues for numerous applications, although their potential has hardly been explored due to their higher susceptibility to oxidation in air. Here we show the unexpected findings of an investigation into the correlation between the air-stability of CuNPs and the structure of the thiolate capping ligand; of the eight different ligands screened, those with the shortest alkyl chain, –(CH2)2–, and a hydrophilic carboxylic acid end group are found to be the most effective at retarding oxidation in air. We also show that CuNPs are not etched by thiol solutions as previously reported, and address the important fundamental question of how the work function of small supported metal particles scales with particle size. Together these findings set the stage for greater utility of CuNPs for emerging electronic applications.
Highlights
Copper nanoparticles (CuNPs) are attractive as a low-cost alternative to their gold and silver analogues for numerous applications, their potential has hardly been explored due to their higher susceptibility to oxidation in air
We have shown that alkylamine ligands used in the synthesis of CuNPs can be readily exchanged with thiolate ligands without etching the Cu core, and that very short alkyl thiols with a carboxylic acid end group are exceptionally effective at retarding oxidation of CuNPs in air
We have addressed the important fundamental question of how the work function of small supported metal particles scales with size, a relation that has until now has been the subject of debate
Summary
Copper nanoparticles (CuNPs) are attractive as a low-cost alternative to their gold and silver analogues for numerous applications, their potential has hardly been explored due to their higher susceptibility to oxidation in air. We show that CuNPs are not etched by thiol solutions as previously reported, and address the important fundamental question of how the work function of small supported metal particles scales with particle size Together these findings set the stage for greater utility of CuNPs for emerging electronic applications. The way that the work function (φ) of supported metal NPs scales with size for sizes greater than that at which quantum size effects dominate; >2 nm, is a contentious issue[22,23,24,25,26,27,28] These gaps in the understanding of how to modify the surface of CuNPs to match the application, and how the properties of small metal NPs scale with size need to be addressed if CuNPs are to achieve their potential as a substitute for Au and Ag for emerging electronic applications
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