The catalytic and optical properties of metal nanoparticles can be combined to create
platforms for light-driven chemical energy storage and enhanced in-situ
reaction monitoring. However, the heavily damped plasmon resonances of many
catalytically active metals (e.g. Pt, Pd) prevent this dual functionality in pure
nanostructures. The addition of catalytic metals at the surface of efficient
plasmonic particles thus presents a unique opportunity if the resonances can be
conserved after coating. Here, nanometer resolution electron-based techniques
(electron energy loss, cathodoluminescence, and energy dispersive X-ray
spectroscopy) are used to show that Au particles incorporating a catalytically
active but heavily damped metal, Pd, sustain multiple size-dependent localized
surface plasmon resonances (LSPRs) that are narrow and strongly localized at the
Pd-rich tips. The resonances also couple with a dielectric substrate and other
nanoparticles, establishing that the full range of plasmonic behavior is observed in
these multifunctional nanostructures despite the presence of Pd.