We demonstrate a general non-Derjaguin-Landau-Verwey-Overbeek method to stabilize colloids in liquids. By this method, colloidal particles that initially form unstable suspension and sediment from the liquid are stabilized by the addition of salt to the suspending liquid. Yet, the salt is not expected to adsorb or directly interact with the surface of the colloids. For the method to work, the liquid should be a mixture, and the salt needs to be antagonistic such that each ion is preferentially solvated by a different component of the mixture. The stabilization may depend on the salt content, mixture composition, or distance from the mixture's coexistence line.

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Improved understanding of complex interactions between nanoparticles will facilitate the control over the ensuing self-assembled structures. In this work, we consider the dynamic changes occurring upon dilution in the self-assembly of a system of ferromagnetic cobalt nanoparticles that combine magnetic, electric, and steric interactions. The systems examined here vary in the strength of the magnetic dipole interactions and the amount of point charges per particle. Scattering techniques are employed for the characterization of the self-assembly aggregates, and zeta-potential measurements are employed for the estimation of surface charges. Our experiments show that for particles with relatively small initial number of surface electric dipoles, an increase in particle concentration results in an increase in diffusion coefficients; whereas for particles with relatively high number of surface dipoles, no effect is observed upon concentration changes. We attribute these changes to a shift in the adsorption/desorption equilibrium of the tri-n-octylphosphine oxide (TOPO) molecules on the particle surface. We put forward an explanation, based on the combination of two theoretical models. One predicts that the growing concentration of electric dipoles, stemming from the addition of tri-n-octylphosphine oxide (TOPO) as co-surfactant during particle synthesis, on the surface of the particles results in the overall repulsive interaction. Secondly, using density functional theory, we explain that the observed behaviour of the diffusion coefficient can be treated as a result of the concentration dependent nanoparticle self-assembly: additional repulsion leads to the reduction in self-assembled aggregate size despite the shorter average interparticle distances, and as such provides the growth of the diffusion coefficient.

Laser micromachining is the chosen method for vertical interconnect access point (VIA) formation in flex PCB layers. Even so, this method suffers from several inherent physical issues as a result of the intense localized heating causing strong Marangoni convection and the buildup of recast along the VIA upper crater walls while also scattered particle debris and oxidation of copper across the surface. The mitigation of the height and radius of this recast layer is critical for the following build-up process and device functionality and reliability. This is currently a major technology inhibitor to the adoption of flex PCBs for high-power electronics. In this study, we present experimental results showing the use of engineered sacrificial layers that coat the surface of the flex PCB substrate during the laser micromachining process. Optimization of this engineered sacrificial layer resulted in a major improvement in recast quality and debris control as well as reducing the oxide formation while increasing the laser drilling efficiency, attributable to increased surface pressure on the substrate. In this paper, we describe the methods and materials used in the development of sacrificial layers and show the positive impact it achieves on improving and modifying the plasma characteristics throughout the overall laser drilling process.

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