TY - JOUR
T1 - Evolution of morphological and optical properties of various Au x Pd 1−x bimetallic nanostructures by the systematic control of composition
AU - Pandey, Puran
AU - Kunwar, Sundar
AU - Sui, Mao
AU - Lee, Jihoon
N1 - Publisher Copyright:
© 2018 Elsevier B.V.
PY - 2018/8/30
Y1 - 2018/8/30
N2 - Bimetallic nanostructures (BMNSs) have gained significant attention because of their multi-functionality, site-specific response and electronic heterogeneity along with the additional opportunities to tune physical and optical properties. In this paper, the systematic evolution of Au x Pd 1−x BMNS is thoroughly investigated in terms of morphological and optical properties through the solid state dewetting on c-plane sapphire. The bilayer composition and deposition order change are coherently tested along with the conventional growth parameter control. By the systematic control of annealing temperature, annealing duration and deposition thickness, the formation of various BMNSs demonstrate sharp distinctions at different Au x Pd 1−x compositions (x = 0.25, 0.50 and 0.75). In specific, the high Au percentage in the Au x Pd 1−x bilayers shows an enhanced dewetting due to the higher diffusivity and lower surface energy of Au atoms as compared to the Pd. Furthermore, the deposition order also induces a significant alteration on the dewetting process. Upon annealing, the evolution of BMNSs relies on the combination of atomic diffusion, inter-diffusion, alloying, surface and interface energy minimization and Rayleigh-like instability. Furthermore, the analysis of reflectance spectra demonstrates the development of the quadrupolar and dipolar resonance peaks, absorption band and their shift, induced by the localized surface plasmon resonance (LSPR) of various Au x Pd 1−x BMNSs. Specifically, the quadrupolar resonance peak is consistent ∼380 nm whereas the dipolar resonance peak and absorption dip are readily blue-shifted and narrowed along with the evolution of isolated and uniform BMNSs.
AB - Bimetallic nanostructures (BMNSs) have gained significant attention because of their multi-functionality, site-specific response and electronic heterogeneity along with the additional opportunities to tune physical and optical properties. In this paper, the systematic evolution of Au x Pd 1−x BMNS is thoroughly investigated in terms of morphological and optical properties through the solid state dewetting on c-plane sapphire. The bilayer composition and deposition order change are coherently tested along with the conventional growth parameter control. By the systematic control of annealing temperature, annealing duration and deposition thickness, the formation of various BMNSs demonstrate sharp distinctions at different Au x Pd 1−x compositions (x = 0.25, 0.50 and 0.75). In specific, the high Au percentage in the Au x Pd 1−x bilayers shows an enhanced dewetting due to the higher diffusivity and lower surface energy of Au atoms as compared to the Pd. Furthermore, the deposition order also induces a significant alteration on the dewetting process. Upon annealing, the evolution of BMNSs relies on the combination of atomic diffusion, inter-diffusion, alloying, surface and interface energy minimization and Rayleigh-like instability. Furthermore, the analysis of reflectance spectra demonstrates the development of the quadrupolar and dipolar resonance peaks, absorption band and their shift, induced by the localized surface plasmon resonance (LSPR) of various Au x Pd 1−x BMNSs. Specifically, the quadrupolar resonance peak is consistent ∼380 nm whereas the dipolar resonance peak and absorption dip are readily blue-shifted and narrowed along with the evolution of isolated and uniform BMNSs.
KW - Au-Pd alloy
KW - Nanoparticles
KW - Nanostructures
KW - Plasmonics
KW - Solid state dewetting
UR - http://www.scopus.com/inward/record.url?scp=85046082465&partnerID=8YFLogxK
U2 - 10.1016/j.apsusc.2018.04.203
DO - 10.1016/j.apsusc.2018.04.203
M3 - Article
AN - SCOPUS:85046082465
SN - 0169-4332
VL - 450
SP - 336
EP - 347
JO - Applied Surface Science
JF - Applied Surface Science
ER -