Aspects of the thermodynamics of liquid alloys of noble metals and transition metals

1984 ◽  
Vol 61-62 ◽  
pp. 101-111 ◽  
Author(s):  
O.J. Kleppa
Nanomaterials ◽  
2019 ◽  
Vol 9 (9) ◽  
pp. 1235 ◽  
Author(s):  
Norihiko Fukuoka ◽  
Katsuaki Tanabe

The plasmonic enhancement of electromagnetic field energy density at the sharp tips of nanoparticles or nanoscale surface roughnesses of hydrogen-absorbing transition metals, Pd, Ti, and Ni, is quantitatively investigated. A large degree of energy focusing is observed for these transition metals in the microwave region, even surpassing the enhancement for noble metals according to the conditions. Pd, for instance, exhibits peak field enhancement factors of 6000 and 2 × 108 in air for morphological aspect ratios of 10 and 100, respectively. Metal surfaces possibly contain such degrees of nano- or micro-scale native random roughnesses, and, therefore, the field enhancement effect may have been unknowingly produced in existing electrical and optical systems. In addition, for future devices under development, particularly in hydrogen-related applications, it is desirable to design and optimize the systems, including the choice of materials, structures, and operating conditions, by accounting for the plasmonic local energy enhancement effect around the metal surfaces.


1975 ◽  
Vol 30 (4) ◽  
pp. 485-491 ◽  
Author(s):  
Y. Waseda ◽  
M. Ohtani

Abstract Recent X-ray diffraction data on molten noble and transition metals have been used to calculate effective interionic potentials by means of the Born-Green equation. The results on the noble metals are compared with the generalized pseudopotential calculations of Moriarty. In all cases the potentions were found to be insensitive to temperature and to have long-range oscillations. The results suggest that the effective valence number is close to unity in these molten metals, this giving reasonable values of the electrical resistivity when calculated in the framework of the usual Ziman theory.The self-diffusion coefficients, viscosities and surface tensions were calculated from the poten-tials and radial distribution functions using the kinetic theory of fluids. Adequate agreement with experimental data was obtained.


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