Stretchable and Soft Electronics using Liquid Metals

The use of liquid metals based on gallium for soft and stretchable electronics is discussed. This emerging class of electronics is motivated, in part, by the new opportunities that arise from devices that have mechanical properties similar to those encountered in the human experience, such as skin, tissue, textiles, and clothing. These types of electronics (e.g., wearable or implantable electronics, sensors for soft robotics, e‐skin) must operate during deformation. Liquid metals are compelling materials for these applications because, in principle, they are infinitely deformable while retaining metallic conductivity. Liquid metals have been used for stretchable wires and interconnects, reconfigurable antennas, soft sensors, self‐healing circuits, and conformal electrodes. In contrast to Hg, liquid metals based on gallium have low toxicity and essentially no vapor pressure and are therefore considered safe to handle. Whereas most liquids bead up to minimize surface energy, the presence of a surface oxide on these metals makes it possible to pattern them into useful shapes using a variety of techniques, including fluidic injection and 3D printing. In addition to forming excellent conductors, these metals can be used actively to form memory devices, sensors, and diodes that are completely built from soft materials. The properties of these materials, their applications within soft and stretchable electronics, and future opportunities and challenges are considered.     

Genome engineering allows selective conversions of terephthalaldehyde to multiple valorized products in bacterial cells

Deconstruction of polyethylene terephthalate (PET) plastic waste generates opportunities for valorization to alternative products. We recently designed an enzymatic cascade that could produce terephthalaldehyde (TPAL) from terephthalic acid. Here, we showed that the addition of TPAL to growing cultures of Escherichia coli wild-type strain MG1655 and an engineered strain for reduced aromatic aldehyde reduction (RARE) strain resulted in substantial reduction. We then investigated if we could mitigate this reduction using multiplex automatable genome engineering (MAGE) to create an E. coli strain with 10 additional knockouts in RARE. Encouragingly, we found this newly engineered strain enabled a 2.5-fold higher retention of TPAL over RARE after 24 h. We applied this new strain for the production of para-xylylenediamine (pXYL) and observed a 6.8-fold increase in pXYL titer compared with RARE. Overall, our study demonstrates the potential of TPAL as a versatile intermediate in microbial biosynthesis of chemicals that derived from waste PET.     

Segregated and Non-Settling Liquid Metal Elastomer via Jamming of Elastomeric Particles

Liquid metal elastomer (LME)—that is, liquid metal particles dispersed in elastomer—is a soft material that has useful electric, dielectric, and thermal properties. Two issues with LME are sought to be addressed: 1) the dense liquid metal (LM) particles can settle before curing of the elastomer, and 2) the LM particles are separated by a thin layer of insulating elastomer and therefore require some “mechanical sintering” to break this layer to create conductive paths. These issues are addressed using an LME containing elastic particles (LMEP). Elastic polydimethylsiloxane particles (PPs) and LM particles jam to prevent particle settling. Meanwhile, the PPs reduce the loading necessary to create conductive paths, thus decreasing the density and cost relative to LME. Surprisingly, the particles percolate into conductive paths prior to curing the LMEP but not in LME. The dielectric constant, electrical conductivity, and thermal conductivity of LMEPs are investigated by changing the volume fraction of LM particles, polydimethylsiloxane pre-polymer and PPs, and propose an LMEP with the optimal ratio. In addition, LMEP-based sensors and circuits are demonstrated for wearable electronics.