Liquid metals offer unprecedented chemistry. Here it is shown that they can facilitate self-limiting oxidation processes on their surfaces, which enables the growth of metal oxides that are atomically thin. This claim is exemplified by creating atomically thin hydrated MnO 2 using a Galvanic replacement reaction between permanganate ions and a liquid gallium-indium alloy (EGaIn). The "liquid solution"-"liquid metal" process leads to the reduction of the permanganate ions, resulting in the formation of the oxide monolayer at the interface. It is presented that under mechanical agitation liquid metal droplets are established, and simultaneously, hydrated gallium oxides and manganese oxide sheets delaminate themselves from the interfacial boundaries. The produced nanosheets encapsulate a metallic core, which is found to consist of solid indium only, with the full migration of gallium out of the droplets. This process produces core/shell structures, where the shells are made of stacked atomically thin nanosheets. The obtained core/shell structures are found to be an efficient photocatalyst for the degradation of an organic dye under simulated solar irradiation. This study presents a new research direction toward the modification and functionalization of liquid metals through spontaneous interfacial redox reactions, which has implications for many applications beyond photocatalysis.

Colloidal liquid metal alloys of gallium, with melting points below room temperature, are potential candidates for creating electrically conductive and flexible composites. However, inclusion of liquid metal micro‐ and nanodroplets into soft polymeric matrices requires a harsh auxiliary mechanical pressing to rupture the droplets to establish continuous pathways for high electrical conductivity. However, such a destructive strategy reduces the integrity of the composites. Here, this problem is solved by incorporating small loading of nonfunctionalized graphene flakes into the composites. The flakes introduce cavities that are filled with liquid metal after only relatively mild press‐rolling (<0.1 MPa) to form electrically conductive continuous pathways within the polymeric matrix, while maintaining the integrity and flexibility of the composites. The composites are characterized to show that even very low graphene loadings (≈0.6 wt%) can achieve high electrical conductivity. The electrical conductance remains nearly constant, with changes less than 0.5%, even under a relatively high applied pressure of >30 kPa. The composites are used for forming flexible electrically‐conductive tracks in electronic circuits with a self‐healing property. The demonstrated application of co‐fillers, together with liquid metal droplets, can be used for establishing electrically‐conductive printable‐composite tracks for future large‐area flexible electronics.

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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.

Liquid metals can play an essential role in the generation of electrically conductive composites for electronic devices and environmental sensing and remediation applications. Here, a method for growing a polyaniline nanofibrous network at liquid metal nanoparticle interfaces is demonstrated for generating hybrid liquid metal–polymer nanocomposites. The investigation shows that an initial functionalization step of the liquid metal nanoparticles with a polymerization enhancer is essential for providing stable and specific nucleation points for the formation of the polyaniline nanofibrous network. The acidity and mechanical agitation conditions are carefully adjusted to control the fibrous polyaniline. The embedded gallium elements form an initial seeding layer around the liquid metal nanoparticles. The novel nanocomposites offer synergistic properties for environmental sensing and molecular separation applications. This study provides a road map for the direct synthesis of long organic molecular chains at the dynamic interfaces of liquid metals.

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Room‐temperature synthesis of 2D graphitic materials (2D‐GMs) remains an elusive aim, especially with electrochemical means. Here, it is shown that liquid metals render this possible as they offer catalytic activity and an ultrasmooth templating interface that promotes Frank–van der Merwe regime growth, while allowing facile exfoliation due to the absence of interfacial forces as a nonpolar liquid. The 2D‐GMs are formed at low onset potential and can be in situ doped depending on the choice of organic precursors and the electrochemical set‐up. The materials are tuned to exhibit porous or pinhole‐free morphologies and are engineered for their degree of oxidation and number of layers. The proposed liquid‐metal‐based room‐temperature electrochemical route can be expanded to many other 2D materials.