Abstract
Multi-metallic alloy nanoparticles (NPs) can enable the advanced applications in the energy, biology, electronics, optics and catalysis due to their multi-functionality, wide tunable range and electronic heterogeneity. In this work, various mono-, bi- and tri-metallic nanostructures composed of Ag, Au and Pt are demonstrated on transparent c-plane sapphire (0001) substrates and the corresponding morphological and optical characteristics are thoroughly investigated. The resulting Pt and AuPt NPs in this study demonstrate much enhanced LSPR responses as compared to the pure Pt NPs from the previous studies, which was contributed by the synergistic effect of Au and Pt and improved surface morphology. These results are sharply distinct in terms of surface morphology and elemental variability from those obtained by the dewetting of monometallic Ag, Au and Pt films under the similar growth conditions, which is due to the distinct dewetting kinetics of the bi-layer and tri-layer films. These NPs exhibit strongly enhanced localized surface plasmon resonance (LSPR) bands in the UV-VIS wavelengths such as dipolar, quadrupolar, multipolar and higher order resonance modes depending upon the size and elemental composition of NPs. The LSPR bands are much stronger with the high Ag content and gradually attenuated with the Ag sublimation. Furthermore, the VIS region LSPR bands are readily blue shifted along with the reduction of NP size. The Ag/Pt bi-layers and Ag/Au/Pt tri-layers are systematically dewetted and transformed into various AgPt and AgAuPt nanostructures such as networked, elongated and semispherical configurations by means of enhanced surface diffusion, intermixing and energy minimization along with the temperature control. The sublimation of Ag atoms plays a significant role in the structural and elemental composition of NPs such that more isolated and semispherical Pt and AuPt NPs are evolved from the AgPt and AgAuPt NPs respectively.
On the localized surface plasmon resonance modes in nanoporous gold films
