Synthesis of Highly Accessible and Reactive Sites in Gold Nanoparticles Using Bound Bis(Diphenylphosphine) Ligands

While bound organic ligands provide steric protection against aggregation for metallic nanoparticles in solution, they can block a large fraction of the surface atoms which are needed for binding in catalysis and sensing applications. In this work, highly accessible Au nanoparticles ligated with bis(diphenylphosphine) molecules are synthesized and characterized in solution. Characterization is performed using high angle annular dark field-scanning transmission electron microscopy (HAADF-STEM), ultraviolet-visible (UV-Vis) spectroscopy, and fluorescence chemisorption experiments. These synthesized nanoparticles are accessible to a 2-napthalenethiol (2-NT) probe molecule in solution. The highest 2-NT accessibility is observed when using 1,1-bis(diphenylphosphino)methane (dppm) ligand where 61 % of the total gold atoms are accessible. It is hypothesized that increasing the rigidity of the bis(diphenylphosphine) ligand increases the number of binding sites on the Au nanoparticles. These nanoparticles are catalytically active for resazurin reduction, and the resazurin reduction rate scales with the number of binding sites.

Automated summary

By using gold nanoparticles with bis(diphenylphosphine) ligands, the accessibility and catalytic activity can be enhanced, providing new possibilities for catalysis and sensing applications.