Abstract

Metallic nanostructures can find various applications such as in optoelectronic devices, nanostructure synthesis and catalytic applications and their applicability vary depending on their size, density and configuration dependent properties. In this paper, the dimensional and configurational evolution of self-assembled palladium (Pd) nanostructures is systematically studied on c-plane sapphire with the control of annealing temperature (AT) and annealing duration with the initial Pd layers of various thicknesses. Depending on the AT, two distinct growth regimes are observed based on the concurrent effect of surface diffusion, surface energy minimization and Pd sublimation: i.e. (i) agglomeration of Pd nano-clusters from voids (500<AT≤650°C) and (ii) round nanoparticle (NP) fabrication (650°C<AT≤900°C). At 950°C, due to the sublimation of Pd atoms, substantial decrease in the NP dimension is witnessed and results in the ring patterns around the NPs. Additional investigation is performed at 950°C to reveal the annealing duration effect on the NP evolution. Due to the dual effect of the Oswald ripening and atom sublimation, initially the dimension of NPs is grown and then gradually decays along with the duration, resulting in an inverted ‘V’ pattern evolution in diameter and height. Moreover, the evolution of optical properties such as absorption band and average reflectance are studied with the corresponding reflectance spectra as a function of wavelength over UV, visible and NIR region. The Raman spectra analysis depicts the variation of lattice vibration peak intensity and position based on the surface morphology of the Pd nanostructures.

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