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It is proposed that primary nucleation of amorphous microspherulites of hydrated silica in natural proto-precious-opal can be followed by a long range superlattice ordering process by means of electrostatic self-assembly. Necessary conditions in the thermodynamics are a high surface charge density on microspherulite surfaces, a long Debye length and an appropriate number density of nucleation centres. A further chemical requirement is a high alkaline environmental pH from 9 to 10. It is also proposed that the characteristic concentric spherical shell-like structure of spherulites, centred on primary nuclei, are due to sequential deposition of intrinsic salts which precipitate out when the corresponding solubility limits in the liquid are successively exceeded. It can be that the better-known sedimentation of microspherulites under gravity only plays part in the final stabilization period of overall growth.
Efficient coupling between solid state quantum emitters and plasmonic waveguides is important for the realization of integrated circuits for quantum information, communication and sensing. However, realization of plasmonic circuits is still scarce, p
The complete symmetry characterization of eigenstates in bare opal systems is obtained by means of group theory. This symmetry assignment has allowed us to identify several bands that cannot couple with an incident external plane wave. Our prediction
Codeposition of two molecular species [CuPc (donor) and PFP (acceptor)] on noble metal (111) surfaces leads to the self-assembly of an ordered mixed layer with maximized donor-acceptor contact area. The main driving force behind this arrangement is a
We report the fabrication of self-assembled, strain-free GaAs/Al$_{0.27}$Ga$_{0.73}$As quantum dot pairs which are laterally aligned in the growth plane, utilizing the droplet epitaxy technique and the anisotropic surface potentials of the GaAs (100)
Glycine on Cu(001) is used as an example to illustrate the critical role of molecular polarity and finite temperature effect in self-assembly of biomolecules at a metal surface. A unified picture for glycine self-assembly on Cu(001) is derived based