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Direction specific adhesion induced by subsurface liquid filled microchannels
While directional effects in adhesion and locomotion have in general been generated by creating symmetry breaking topographic features on the surface of a soft bodied object, here we present a novel method for imparting this effect to thin adhesive layers by embedding liquid filled microchannels arranged in pairs with specific intra and inter pair distances. The adhesive exhibits uniform adhesion in classical peel tests when both the channels are filled with either air or a wetting liquid. But the asymmetric effect shows up when only one of the channels in the pair is filled with the liquid. The liquid alters the surface tension of the inner wall of the channel, which results in bulging deformation of the thin skin of the adhesive over the channel. The bulging however remains asymmetric, the extent of asymmetry depending on the intra-pair spacing between the channels. Besides the bulging effect, filling in one channel of a pair with liquid also leads to an asymmetric variation in its modulus. As a result, when an adherent is peeled off the adhesive from two opposite directions, significantly different adhesion strengths result. A similar directional effect also results when channels of two different diameters are used in the pair, thus opening up the possibility of generating several different adhesion strengths simply by altering the geometric features of the embedded microstructure and its filling status. We show also that for both channels in a pair filled with liquid, the adhesion strength increases significantly, by over 60 times of what is achieved for a smooth, featureless, adhesive layer.
Carbon onion / sulfur hybrid cathodes via inverse vulcanization for lithium sulfur batteries
A sulfur–1,3-diisopropenylbenzene copolymer was synthesized by ring-opening radical polymerization and hybridized with carbon onions at different loading levels. The carbon onion mixing was assisted by shear in a two-roll mill to capitalize on the softened state of the copolymer. The sulfur copolymer and the hybrids were thoroughly characterized in structure and chemical composition, and finally tested by electrochemical benchmarking. An enhancement of specific capacity was observed over 140 cycles at higher content of carbon onions in the hybrid electrodes. The copolymer hybrids demonstrate a maximum initial specific capacity of 1150 mA h gsulfur−1 (850 mA h gelectrode−1) and a low decay of capacity to reach 790 mA h gsulfur−1 (585 mA h gelectrode−1) after 140 charge/discharge cycles. All carbon onion/sulfur copolymer hybrid electrodes yielded high chemical stability, stable electrochemical performance superior to conventional melt-infiltrated reference samples having similar sulfur and carbon onion content. The amount of carbon onions embedded in the sulfur copolymer has a strong influence on the specific capacity, as they effectively stabilize the sulfur copolymer and sterically hinder the recombination of sulfur species to the S8 configuration.
On the behaviour of nanoparticles in oil-in-water emulsions with different surfactants
The distribution of narrowly dispersed gold nanoparticles in hexane-in-water emulsions was studied for different surfactants. Good surfactants such as SDS and Triton X-100 block the oil-water interfaces and confine particles in the droplet. Other surfactants (Tween 85 and Span 20) form synergistic mixtures with the nanoparticles at the interfaces that lower the surface tension more than any component. Supraparticles with fully defined particle distribution form in the droplets only for surfactants that block the interface. Other surfactants promote the formation of fcc agglomerates. Nanoparticles in emulsions behave markedly different from microparticles-their structure formation is governed by free energy minimization, while microparticles are dominated by kinetics.
Carbon onion–sulfur hybrid cathodes for lithium–sulfur batteries
In this study, we explore carbon onions (diameter below 10 nm), for the first time, as a substrate material for lithium sulfur cathodes. We introduce several scalable synthesis routes to fabricate carbon onion–sulfur hybrids by adopting in situ and melt diffusion strategies with sulfur fractions up to 68 mass%. The conducting skeleton of agglomerated carbon onions proved to be responsible for keeping active sulfur always in close vicinity to the conducting matrix. Therefore, the hybrids are found to be efficient cathodes for Li–S batteries, yielding 97–98% Coulombic efficiency over 150 cycles with a slow fading of the specific capacity (ca. 660 mA h g−1 after 150 cycles) in long term cycle test and rate capability experiments.