Stephan Handschuh-Wang

Liquid metal sponges for mechanically durable, all-soft, electrical conductors

Liquid metal sponges were developed by loading liquid metals (GaInSn) into elastomer sponges. The elasticity of 3D-interconnected networks and the fluidic nature of liquid metals led to the formation of all-soft structures for electrical conductors with high electrical conductivity and mechanical flexibility.

Liquid metal droplets with high elasticity, mobility and mechanical robustness

Non-stick, ultra-elastic liquid metal droplets were fabricated by coating polytetrafluoroethylene (PTFE) particles onto the surface of NaOH-treated liquid metal droplets. The liquid metal droplets consisted of a liquid metal core, a thin anti-oxidation layer to maintain the high surface tension of the liquid metal and a particle-interpenetrated shell to enhance the mobility of the droplet.

Recent progress in fabrication and application of polydimethylsiloxane sponges

Owing to their structural advantages in comparison with bulk polydimethylsiloxane (PDMS), porous 3D substrates, which are also known as PDMS sponges, possess immense potential in energy generation, transport and storage, absorption, separation, photocatalysis, wearable electronics and life science applications. Extensive effort has therefore been devoted to the design and synthesis of porous PDMS sponges. The key to excellent performance in high-value applications is a deep knowledge of the beneficial aspects of their porosity, structure and morphology for a specific application. Several new routes for the fabrication of PDMS sponges, as well as novel applications, have been developed recently. Therefore, this review focuses on advances in the field of the fabrication and application of PDMS sponges since 2011. After a concise introduction, which includes remarks on the benefits of PDMS in comparison with other materials, strategies for the synthesis/fabrication of PDMS sponges are presented and their advantages and drawbacks are concisely discussed. A summary of the potential fabrication procedures will be beneficial for those entering the field, as it gives a quick overview of the feasible applications of a PDMS sponge fabricated via a specific method. Afterwards, different high-value applications of PDMS sponges are described in conjunction with specific and detailed examples of all the abovementioned applications. In this regard, suggestions are also made regarding which fabrication method is most beneficial for the application being discussed. Finally, recent advances in the fabrication and application of PDMS sponges are summarized, as well as issues, such as surface functionalization and pore size limitations, which are impeding reasonable future applications. We envision that this review will be helpful to those entering the field, as well as experienced researchers who need rapid access to recent literature, and will give new stimuli for the development of novel porous materials.

Hydrophilic Sponges for Leaf-Inspired Continuous Pumping of Liquids

A bio‐inspired, leaf‐like pumping strategy by mimicking the transpiration process through leaves is developed for autonomous and continuous liquid transport enabled by durable hydrophilic sponges. Without any external power sources, flows are continuously generated ascribed to the combination of capillary wicking and evaporation of water. To validate this method, durable hydrophilic polydimethylsiloxane sponges modified with polyvinyl alcohol via a “dip‐coat‐dry” method have been fabricated, which maintains hydrophilicity more than 2 months. The as‐made sponges are further applied to achieve stable laminar flow patterns, chemical gradients, and “stop‐flow” manipulation of the flow in microfluidic devices. More importantly, the ease‐of‐operation and excellent pumping capacity have also been verified with over 24 hs pumping and quasi‐stable high flow rates up to 15 µL min−1. The present strategy can be easily integrated to other miniaturized systems requiring pressure‐driven flow and should have potential applications, such as cell culture, micromixing, and continuous flow reaction.

Enhancing the colloidal stability of detonation synthesized diamond particles in aqueous solutions by adsorbing organic mono-, bi- and tridentate molecules

Colloidal stability of nanoparticles with particle sizes smaller than 100nm is a critical issue for various research areas, including material science, electronics and biomedicine. We propose a facile, fast and cost-efficient method to increase the colloidal stability by simply adding organic molecules as ligands, which adsorb to the nanoparticle surface subsequently. Citric acid, oxalic acid, glutamic acid and propylamine were found to stabilize the nanodiamond (ND) particles with a mean diameter of approx. 30-100nm. The charge of the particles could be controlled by the pH of the dispersions and by stabilizing with carboxylic acids or amino acids mentioned above. ND particles stabilized with citric acid and oxalic acid at a pH higher than 2.5 were negatively charged, while ND dispersions stabilized with glutamic acid were charged positively below a pH of 3.2. Furthermore, the stability of the dispersion was found to be dependent on the concentration of the stabilizing agent and the pH of the dispersion. Finally, we proposed the stabilizing mechanism of ND particles with propylamine. Glutamic acid and propylamine stabilized ND dispersions can be utilized for high seeding densities on negatively charged surfaces due to the amino-groups, which can be helpful for adsorption processes in electronics and material science. Due to the high biocompatibility, non-cytotoxicity and chemical inertness of ND particles, carboxylic acids and amino acids stabilized ND particles are envisaged to be useful in the biomedical field, i.e. bio-labels, drug delivery vehicles, and effective enterosorbent.

Rational Fabrication of Anti‐Freezing, Non‐Drying Tough Organohydrogels by One‐Pot Solvent Displacement

Tough hydrogels, polymeric network structures with excellent mechanical properties (such as high stretchability and toughness), are emerging soft materials. Despite their remarkably mechanical features, tough hydrogels exhibit two flaws (freezing around the icing temperatures of water and drying under arid conditions). Inspired by cryoprotectants (CPAs) used in the inhibition of the icing of water in biological samples, a versatile and straightforward method is reported to fabricate extreme anti-freezing, non-drying CPA-based organohydrogels with long-term stability by partially displacing water molecules within the pre-fabricated hydrogels. CPA-based Ca-alginate/polyacrylamide (PAAm) tough hydrogels were successfully fabricated with glycerol, glycol, and sorbitol. The CPA-based organohydrogels remain unfrozen and mechanically flexible even up to -70 °C and are stable under ambient conditions or even vacuum.

Defect-free, high resolution patterning of liquid metals using reversibly sealed, reusable polydimethylsiloxane microchannels for flexible electronic applications

This paper describes a simple and reliable approach for high-resolution patterning of liquid metals onto elastomeric substrates and their applications in flexible and wearable electronics. In this method, the liquid metal eutectic gallium indium (EGaIn) alloy was first dispensed into an air plasma-treated polydimethylsiloxane (PDMS) substrate through a reversibly sealed PDMS microchannel. The liquid metal-filled substrate was then placed on a cold plate, where the liquid metal was solidified. Finally, defect-free patterns were obtained by directly peeling off the PDMS microchannel on a hot plate while the liquid metal started to melt. The as-made liquid metal patterns exhibited excellent electrical and mechanical performance. As a proof of concept, the as-made flexible patterns of liquid metals were applied as flexible electrical conductors, capacitive sensors, and touch keyboards.

Softening and Shape Morphing of Stiff Tough Hydrogels by Localized Unlocking of the Trivalent Ionically Cross-Linked Centers

The mechanical properties (e.g., stiffness, stretchability) of prefabricated hydrogels are of pivotal importance for diverse applications in tissue engineering, soft robotics, and medicine. This study reports a feasible method to fabricate ultrasoft and highly stretchable structures from stiff and tough hydrogels of low stretchability and the application of these switchable hydrogels in programmable shape-morphing systems. Stiff and tough hydrogel structures are first fabricated by the mechanical strengthening of Ca2+ -alginate/polyacrylamide tough hydrogels by addition of Fe3+ ions, which introduces Fe3+ ionically cross-linked centers into the Ca2+ divalent cross-linked hydrogel, forming an additional and much less flexible trivalent ionically cross-linked network. The resulting stiff and tough hydrogels are exposed to an L-ascorbic acid (vitamin C, VC) solution to rapidly reduce Fe3+ to Fe2+ . As a result, flexible divalent ionically cross-linked networks are formed, leading to swift softening of the stiff and tough hydrogels. Moreover, localized stiffness variation of the tough hydrogels can be realized by precise patterning of the VC solution. To validate this concept, sequential steps of VC patterning are carried out for local tuning of the stiffness of the hydrogels. With this strategy, localized softening, unfolding, and sequential folding of the tough hydrogels into complex 3D structures is demonstrated.

Enhanced nucleation of diamond on three dimensional tools via stabilized colloidal nanodiamond in electrostatic self-assembly seeding process

Nanocrystalline diamond particles are promising candidates for copious applications in materials science, biology and electronics. In this work, diamond nucleation density was unprecedentedly enhanced via a non-invasive electrostatic self-assembly seeding approach. By addition of glutamic acid to the nanodiamond seeding solution, the positively charged amino-group of glutamic acid, which is adsorbed on nanodiamond particles, enhances the adsorption on negative charged cemented carbide substrate. The highest nucleation density (1.0×1010cm-2) was achieved by utilizing glutamic acid at pH 4 as well as DI water at pH 2.2. This density was 20-1000 times higher than most earlier published results on WC-Co substrate. The concentration of the organic molecule, pH, concentration of ND particles and ultrasonication seeding time were found to be important for the seeding process. The colloidal stability was tweaked by pH of the dispersion and concentration of glutamic acid. The optimized parameters for nanodiamond adsorption on WC-Co substrate were found to be pH 4 at a concentration of 7×10-5M of glutamic acid at a nanodiamond concentration of 0.005wt%, while the seeding was conducted for 30min. The short ultrasonication time inhibits aggregation and void formation due to peeling off of nanodiamond patches at prolonged seeding times. Moreover, diamond thin films were deposited uniformly and densely on end mills made of cemented carbide. This work indicates that electrostatic induced adsorption of diamond nanoparticles is crucial for the development of ultra-high nucleation densities for the growth of high performance nanocrystalline diamond films, especially for micro sized tools with sharp cutting edges. It may serve as an approach for pinhole-free ultra-thin films deposition on micro-electromechanical system, and encapsulation coating in harsh environment.

Bioinspired, Mechano-Regulated Interfaces for Rationally Designed, Dynamically Controlled Collection of Oil Spills from Water

This study describes the fabrication of bioinspired mechano‐regulated interfaces (MRI) for the separation and collection of oil spills from water. The MRI consists of 3D‐interconnected, microporous structures of sponges made of ultrasoft elastomers (Ecoflex). To validate the MRI strategy, ecoflex sponges are first fabricated with a low‐cost sugar‐leaching method. This study then systematically investigates the absorption capacity (up to 1280% for chloroform) of the sponges to different oils and organic solvents. More importantly, the oil flux through the as‐made sponges is controlled by mechanical deformation, which increases up to ≈33‐fold by tensile strain applied to the sponge from 0 to 400%. On the basis of MRI, this study further demonstrates the application of ecoflex sponges in oil skimmers for selective collecting oil from water with high efficiency and durable recyclability. The as‐developed MRI strategy has opened a new path to allow rational design and dynamical control toward developing high performance devices for oil permeation and selective collection of oil spills from water.