Low-melting liquid metal is a hugely promising material for flexible conductive patterns due to its excellent conductivity and supercompliance, especially low-cost and environmental liquid processing technology. However, the ever-present fluidity characteristic greatly limits the stable shape and reliability of prepared liquid metal conductive electronics. Herein, a novel solidification strategy of liquid GaIn alloys by Ni doping and heat treatment is first reported, which can efficiently create a solid phase in the liquid metal and provide an effective solution for practical applications. Particularly, the liquid characteristic is preserved for conveniently fabricating different flexible electronic circuits, and then the solidification is carried out on prepared conductive patterns by heat treatment. The solidification mechanism is revealed by the interface chemical reaction between Ni and GaIn, creating the solid phase of intermetallic compound (Ga 4 Ni 3 and InNi 3 ) during heat treatment. Moreover, a biphasic GaInNi can be obtained by regulating the atomic ratio of gallium, indium, and nickel. As a result, the obtained GaInNi possesses extremely low sheet resistance (15 ± 4.5 to 135 ± 2.5 mΩ sq −1 ) and the variation of ΔR/R 0 exhibits low level (0-2) when strained up to 100%, which offers a promising strategy to prepare stretchable and reliable liquid metal electronics.

As a critical part of flexible electronics, flexible circuits inevitably work in a dynamic state, which causes electrical deterioration of brittle conductive materials (i.e., Cu, Ag, ITO). Recently, gallium-based liquid metal particles (LMPs) with electrical stability and self-repairing have been studied to replace brittle materials owing to their low modulus and excellent conductivity. However, LMP-coated Ga 2 O 3 needs to activate by external sintering, which makes it more complicated to fabricate and gives it a larger short-circuit risk. Coreshell structural particles (Ag@LMPs) that exhibit excellent initial conductivity (8.0 Ω sq −1 ) without extra sintering are successfully prepared by coating nanosilver on the surface of LMPs through in situ chemical reduction. The critical stress at which rigid Ag shells rupture can be controlled by adjusting the Ag shell thickness so that LM cores with low moduli can release, achieving real-time self-repairing (within 200 ms) under external destruction. Furthermore, a flexible circuit utilizing Ag@LMPs is fabricated by screen printing, and exhibits outstanding stability and durability (R/R 0 < 1.65 after 10 000 bending cycles in a radius of 0.5 mm) because of the functional core-shell structure. The self-repairable Ag@LMPs prepared in this study are a candidate filler for flexible circuit design through multiple processing methods.

Dual-network conductive hydrogels have drawn wide attention in epidemic electronics such as epidemic sensors and electrodes because of their inherent low Young's modulus, high skincompliance, and tunable mechanical strength. However, it is still full of challenges to gain a dual-network hydrogel with high stretchability, low hysteresis, and skin-adhesive performance simultaneously. Herein, to address this issue, a novel dual-network hydrogel (denoted as PAa hydrogel) with polyacrylamide as the first network and topologically entangled polydopamine as the secondary network was prepared through a facile gel-phase in situ self-polymerization and soaking treatment. Benefiting from the topological enhancement as well as the synergetic effects of hydrogen bonds and metal coordination bonds, low modulus (∼10 kPa), excellent stretchability (1090.8%), high compression (90%), negligible hysteresis (η = 0.019, energy loss coefficient), rapid recovery in seconds, and selfadhesion are obtained in the PAa hydrogels. To demonstrate their practical use, a states-independent and skin-adhesive epidemic sensor was successfully attached on human skin for motion detection. What is more, by using the hydrogel as an epidemic electrode, electromyogram signals were accurately detected and wirelessly transmitted to a smart phone. This work offers a new insight to understand the strengthening mechanism of dual network hydrogels and a design strategy for both epidemic sensors and electrodes.

Printed electronics on elastomer substrates have found wide applications in wearable devices and soft robotics. For everyday usage, additional requirements exist for the robustness of the printed flexible electrodes, such as the ability to resist scratching and damage. Therefore, highly robust electrodes with self‐healing, and good mechanical strength and stretchability are highly required and challenging. In this paper, a cross‐linking polyurea using polydimethylsiloxane as the soft segment and dynamic urea bonds is prepared and serves as a self‐healing elastomer substrate for coating and printing of silver nanowires (AgNWs). Due to the dynamic exchangeable urea bond at 60 °C, the elastomer exhibits dynamic exchange of the cross‐linking network while retaining the macroscopic shape. As a result, the AgNWs are partially embedded in the surface of the elastomer substrate when coated or printed at 60 °C, forming strong interfacial adhesion. As a result, the obtained stretchable electrode exhibits high mechanical strength and stretchability, the ability to resist scratching and sonication, and self‐healing. This strategy can be applied to a variety of different conducting electrode materials including AgNWs, silver particles, and liquid metal, which provides a new way to prepare robust and self‐healing printed electronics.

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