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To quantify how the viscosities of silicone oil (SO) and liquid metal (LM) relate to emulsion-formation (LM-in-SO versus SO-in-LM), a process was developed to produce LM pastes with adjustable viscosity... 

Abstract Gallium-based liquid metals (LM) have surface tension an order of magnitude higher than water and break up into micro-droplets when mixed with other liquids. In contrast, silicone oil readily mixes into LM foams to create oil-in-LM emulsions with oil inclusions. Previously, the LM was foamed through rapid mixing in air for an extended duration (over 2 hours). This process first results in the internalization of oxide flakes that form at the air-liquid interface. Once a critical fraction of these randomly shaped solid flakes is reached, air bubbles internalize into the LM to create foams that can internalize secondary liquids. Here, we introduce an alternative oil-in-LM emulsion fabrication method that relies on the prior addition of SiO2 micro-particles into the LM before mixing it with the silicone oil. This particle-assisted emulsion formation process provides a higher control over the composition of the LM-particle mixture before oil addition, which we employ to systematically study the impact of particle characteristics and content on the emulsions' composition and properties. We demonstrate that the solid particle size (0.8 µm to 5 µm) and volume fraction (1% to 10%) have a negligible impact on the internalization of the oil inclusions. The inclusions are mostly spherical with diameters of 20 to 100 µm diameter and are internalized by forming new, rather than filling old, geometrical features. We also study the impact of the particle characteristics on the two key properties related to the functional application of the LM emulsions in the thermal management of microelectronics. In particular, we measure the impact of particles and silicone oil on the emulsion's thermal conductivity and its ability to prevent deleterious gallium-induced corrosion and embrittlement of contacting metal substrates. 

Gallium-based liquid metals (LMs) are suitable for many potential applications due to their unique combination of metallic and liquid properties. However, due to their high surface tension and low viscosity, LMs are challenging to apply to substrates in useful shapes, such as dots, wires, and films. These issues are mitigated by mixing the LMs in air with other materials, such as mixing with solid particles to form LM solid pastes or mixing with gases to form LM foams. Underlying these deceivingly simple mixing processes are complex and highly intertwined microscale mechanisms. Air microbubbles are inevitably incorporated while making LM pastes, making them partly foams. On the other hand, for foaming of the LM to occur, a critical volume content of solid particles must be internalized first. Consequently, both LM pastes and foams are multiphase composites containing solid and fluid microcomponents. Here, we systematically study the impact of the mixing procedure, solid particle size, and volume fraction (SiO2) on the air content of the multiphase LM composites. We demonstrate that decreasing the particle size and increasing their volume fraction substantially decrease the composite density (i.e., increases air entrapment). The foaming process can also be enhanced with the use of high-speed mechanical mixing, although leading to the formation of a more disordered internal structure. In contrast, manual mixing with larger microparticles can promote the formation of more paste-like composites with minimal air content. We explain the microscopic mechanisms underlying these trends by correlating macroscopic measurements with cross-sectional electron microscopy of the internal structure. 

Gallium based liquid metals (LM) have prospective biomedical, stretchable electronics, soft robotics, and energy storage applications, and are being widely adopted as thermal interface materials. The danger of gallium corroding most metals used in microelectronics requires the cumbersome addition of “barrier” layers or LM break-up into droplets within an inert matrix such as silicone oil. Such LM-in-oil emulsions are stabilized by native oxide on the droplets but have decreased thermal performance. Here we show that mixing of the silicone oil into an LM-air foam yields emulsions with inverted phases. We investigate the stability of these oil-in-LM emulsions through a range of processing times and oil viscosities, and characterize the impact of these parameters on the materials’ structure and thermal property relationships. We demonstrate that the emulsion with 40 vol% of 10 cSt silicone oil provides a unique thermal management material with a 10 W m −1 K −1 thermal conductivity and an exterior lubricant thin film that completely prevents corrosion of contacting aluminum. 

Abstract Sorption thermal energy storage (TES) seems to be an auspicious solution to overcome the issues of intermittent energy sources and utilization of low-grade heat. Ultrasound-assisted adsorption/desorption of water vapor on activated alumina is proposed as a means of low-grade heat utilization through TES. The effects of ultrasonic power on the storing stage (desorption of water vapor) were analyzed to optimize the desorption and overall efficiencies. To determine and justify the effectiveness of incorporating ultrasound from an energy-savings point of view, an approach of constant total (heat plus ultrasound) input power of 25 W was adopted. To measure the extent of the effectiveness of using ultrasound, ultrasonic-power-to-total power ratios of 0.2 and 0.4 were investigated and the results compared with those of no-ultrasound (heat only) at the same total power. The regeneration temperature and desorption rate were measured simultaneously to investigate the effects of ultrasonication on regeneration temperature and utilization of low-grade heat. The experimental results showed that using ultrasound facilitates the regeneration of activated alumina at both power ratios without increasing the total input power. With regard to regeneration temperature, incorporating ultrasound decreases the regeneration temperature hence justifying the utilization of low-grade heat for thermal energy purposes. In terms of overall energy recovery of the adsorption thermal storage process, a new metric is proposed to justify incorporating ultrasound and any other auxiliary energy along with low-grade heat.