Synthesis of stable ligand-free gold–palladium nanoparticles using a simple excess anion method

Meenakshisundaram Sankar, Qian He, Moataz Morad, James Pritchard, Simon J Freakley, Jennifer K Edwards, Stuart H Taylor, David J Morgan, Albert F Carley, David W Knight

Research output: Contribution to journalArticle

87 Citations (Scopus)

Abstract

We report a convenient excess anion modification and post-reduction step to the impregnation method which permits the reproducible preparation of supported bimetallic AuPd nanoparticles having a tight particle size distribution comparable to that found for sol-immobilization materials but without the complication of ligands adsorbed on the particle surface. The advantageous features of the modified impregnation materials compared to those made by conventional impregnation include a smaller average particle size, an optimized random alloy composition, and improved compositional uniformity from particle-to-particle resulting in higher activity and stability compared to the catalysts prepared using both conventional impregnation and sol immobilization methods. Detailed STEM combined with EDX analyses of individual particles have revealed that an increase in anion concentration increases the gold content of individual particles in the resultant catalyst, thus providing a method to control/tune the composition of the nanoalloy particles. The improved activity and stability characteristics of these new catalysts are demonstrated using (i) the direct synthesis of hydrogen peroxide and (ii) the solvent-free aerobic oxidation of benzyl alcohol as case studies.
Original languageEnglish
Pages (from-to)6600-6613
Number of pages14
JournalACS Nano
Volume6
Issue number8
DOIs
Publication statusPublished - 7 Jul 2012

Cite this

Sankar, M., He, Q., Morad, M., Pritchard, J., Freakley, S. J., Edwards, J. K., Taylor, S. H., Morgan, D. J., Carley, A. F., & Knight, D. W. (2012). Synthesis of stable ligand-free gold–palladium nanoparticles using a simple excess anion method. ACS Nano, 6(8), 6600-6613. https://doi.org/10.1021/nn302299e