Surface patterning of liquid metals (LMs) is a key processing step for LM‐based functional systems. Current patterning methods are substrate specific and largely suffer from undesired imperfections—restricting their widespread applications. Inspired by the universal catechol adhesion chemistry observed in nature, LM inks stabilized by the assembly of a naturally abundant polyphenol, tannic acid, has been developed. The intrinsic adhesive properties of tannic acid containing multiple catechol/gallol groups, allow the inks to be applied to a variety of substrates ranging from flexible to rigid, metallic to plastics and flat to curved, even using a ballpoint pen. This method can be further extended from hand‐written texts to complex conductive patterns using an automated setup. In addition, capacitive touch and hazardous heavy metal ion sensors have been patterned, leveraging from the synergistic combination of polyphenols and LMs. Overall, this strategy provides a unique platform to manipulate LMs from hand‐written pattern to complex designs onto the substrate of choice, that has remained challenging to achieve otherwise.

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Liquid metals (LMs) are electronic liquid with enigmatic interfacial chemistry and physics. These features make them promising materials for driving chemical reactions on their surfaces for designing nanoarchitectonic systems. Herein, we showed the interfacial interaction between eutectic gallium−indium (EGaIn) liquid metal and graphene oxide (GO) for the reduction of both substrate-based and free-standing GO. NanoIR surface mapping indicated the successful removal of carbonyl groups. Based on the gained knowledge, a composite consisting of assembled reduced GO sheets on LM microdroplets (LM−rGO) was developed. The LM enforced Ga 3+ coordination within the rGO assembly found to modify the electrochemical interface for selective dopamine sensing by separating the peaks of interfering biologicals. Subsequently, paper-based electrodes were developed and modified with the LM−rGO that presented the compatibility of the assembly with low-cost commercial technologies. The observed interfacial interaction, imparted by LM's interfaces, and electrochemical performance observed for LM−rGO will lead to effective functional materials and electrode modifiers.

Gut microbiota dynamically participate in diverse physiological activities with direct impact on the host’s health. A range of factors associated with the highly complex intestinal flora ecosystem poses challenges in regulating the homeostasis of microbiota. The consumption of live probiotic bacteria, in principle, can address these challenges and confer health benefits. In this context, one of the major problems is ensuring the survival of probiotic cells when faced with physical and chemical assaults during their intake and subsequent gastrointestinal passage to the gut. Advances in the field have focused on improving conventional encapsulation techniques in the microscale to achieve high cell viability, gastric and temperature resistance, and longer shelf lives. However, these microencapsulation approaches are known to have limitations with possible difficulties in clinical translation. In this Perspective, we present a brief overview of the current progress of different probiotic encapsulation methods and highlight the contemporary and emerging single-cell encapsulation strategies using nanocoatings for individual probiotic cells. Finally, we discuss the relative advantages of various nanoencapsulation approaches and the future trend toward developing coated probiotics with advanced features and health benefits.

Low melting point eutectic systems, such as the eutectic gallium–indium (EGaIn) alloy, offer great potential in the domain of nanometallurgy; however, many of their interfacial behaviors remain to be explored. Here, a compositional change of EGaIn nanoalloys triggered by polydopamine (PDA) coating is demonstrated. Incorporating PDA on the surface of EGaIn nanoalloys renders core–shell nanostructures that accompany Ga–In phase separation within the nanoalloys. The PDA shell keeps depleting the Ga3+ from the EGaIn nanoalloys when the synthesis proceeds, leading to a Ga3+-coordinated PDA coating and a smaller nanoalloy. During this process, the eutectic nanoalloys turn into non-eutectic systems that ultimately result in the solidification of In when Ga is fully depleted. The reaction of Ga3+-coordinated PDA-coated nanoalloys with nitrogen dioxide gas is presented as an example for demonstrating the functionality of such hybrid composites. The concept of phase-separating systems, with polymeric reservoirs, may lead to tailored materials and can be explored on a variety of post-transition metals.

Liquid metal dispersion stabilized by natural phenolics for conductive paper composites has been demonstrated.

Liquid metal (LM) catalysts have been demonstrated to accelerate chemical reactions, providing an intriguing route to fine chemical synthesis with immense technological implications. Herein, we explore gallium-based LMs as catalysts to promote the oxidative self-polymerization of natural polyphenols, an emerging class of natural building blocks for surface functionalization with diverse biochemical properties. The oxidative polymerization of polyphenols, triggered by eutectic alloy of gallium and indium, results in nanocoatings with remarkably high reaction kinetics. The oxidative polymerization occurs in a wide pH range including an acidic environmenta condition previously unexplored for the deposition of phenolic coatings. The LM triggers the generation of highly active radical species from the oxidant causing the rapid oxidation of the polyphenols and their subsequent deposition on a range of different substrates. We further show that the LM-based catalytic system addresses several other limitations of existing coating methods including a narrow pH range, substrate specificity (precursor–dependent), and low coating uniformity. Finally, we demonstrate that the phenolic nanocoatings obtained from the acidic pH environment have excellent antioxidant and antibacterial properties without requiring any post-functionalization step. This process for creating phenolic nanocoatings may find applications in a wide range of industries, food science, and biomedicine.

The use of cell‐mediated chemistry is an emerging strategy that exploits the metabolic processes of living cells to develop biomimetic materials with advanced functionalities and enhanced biocompatibility. Here, a concept of a cell‐mediated catalytic process for forming protective nano‐shells on individual probiotic cells is demonstrated. This process is leveraged by the cell environment to induce oxidative polymerization of phenolic compounds, and simultaneously these phenolic polymers assemble to form nano‐coatings around individual cell surfaces. The detailed analysis reveals that the oxidation process is triggered by an essential nutrient (manganese) of the probiotic cells, which significantly increases the oxidation rate of phenolic compounds. The phenolic coatings, encapsulating each cell in nanometre scale, demonstrate excellent biocompatibility and biodegradability. Additionally, the in situ encapsulated probiotic cells display an improved gastric tolerance of up to ≈1.4 times higher than the native cells and enhanced adhesion as high as ≈1.6 times onto a model of intestinal epithelial cells. Finally, the coated probiotic cells exhibit a high antioxidant activity as an advanced feature. Overall, this method provides a unique approach to improve the probiotic delivery using the cell machinery to engineer encapsulating nanocoatings with protective benefits and new functionalities.