We confirm that the unusual purple color of the intermetallic compound AuAl2 is of a plasmonic origin by launching surface plasmons (SPs) in thin AuAl2 films. We measure the SP dispersion relation and also use the films to measure the index of refraction of sucrose solutions using standard SP resonance sensing. We find that the SP energy in planar AuAl2 is approximately 2.1 eV, about 0.4 eV lower than in gold, and the material is highly resistant to oxidation. This is close to what is expected from previously reported measurements of the dielectric function of AuAl2. On this basis we predict that AuAl2 nanoparticles will a have very strong, spectrally nearly uniform light absorbance about an order of magnitude greater than standard carbon black. Such particles may therefore find applications as obscurants or as an alternative to more complex light absorbing gold structures in areas such as photothermal therapy or solar steam generation, or in plasmonic catalysis.

HypothesisPlasmon nanorulers are exquisitely sensitive distance sensors that are based on the electromagnetic interaction between metal nanoparticles and surfaces. We hypothesize that nanorulers can act as quantitative probes of processes such as particle aggregation and adsorption, and deploy them to investigate particle adsorption onto stimulus-responsive polymer films. While such systems have previously been qualitatively investigated with plasmon nanorulers, our quantitative analysis should provide deeper insights. ExperimentGold nanospheres are adsorbed from solution onto pH-responsive, amine-rich polyelectrolyte multilayer (PEM) films that are either directly deposited on a gold substrate or onto an intermediate selfassembled monolayer (SAM) of charged thiols. Fitting the optical scattering spectrum to a full-wave calculation, we quantify the sphere-substrate gap distance with good accuracy. FindingsWe find that the gold spheres partially embed into the PEMs rather than ride on top of them, and that although the amount of actuation of the spheres afforded by tuning the pH is well controlled, it is significantly smaller than the corresponding thickness changes in unstrained films. Further, the presence of a SAM below the PEM increases the amount of polymer in the PEM, except for the thickest and most highly charged films, where the SAM instead appears to displace from the area below the nanospheres.