Polymer composites with electrically conductive fillers have been developed as mechanically flexible, easily processable electromagnetic interference (EMI) shielding materials. Although there are a few elastomeric composites with nanostructured silvers and carbon nanotubes showing moderate stretchability, their EMI shielding effectiveness (SE) deteriorates consistently with stretching. Here, a highly stretchable polymer composite embedded with a three‐dimensional (3D) liquid‐metal (LM) network exhibiting substantial increases of EMI SE when stretched is reported, which matches the EMI SE of metallic plates over an exceptionally broad frequency range of 2.65–40 GHz. The electrical conductivities achieved in the 3D LM composite are among the state‐of‐the‐art in stretchable conductors under large mechanical deformations. With skin‐like elastic compliance and toughness, the material provides a route to meet the demands for emerging soft and human‐friendly electronics.

High‐temperature dielectric materials for capacitive energy storage are in urgent demand for modern power electronic and electrical systems. However, the drastically degraded energy storage capabilities owing to the inevitable conduction loss severely limit the utility of dielectric polymers at elevated temperatures. Herein, a new approach based on the in situ preparation of oxides onto polyimide (PI) films to high‐temperature laminated polymer dielectrics is described. As confirmed by computational simulations, the charge injection at the electrode/dielectric interface and electrical conduction in dielectric films are substantially depressed via engineering the in situ prepared oxide layer in the laminated composites. Consequently, ultrahigh dielectric energy densities and high efficiencies are simultaneously achieved at elevated temperatures. Especially, an excellent energy density of 1.59 J cm−3 at a charge–discharge efficiency of above 90% has been achieved at 200 °C, outperforming the current dielectric polymers and composites. Together with its excellent discharging capability and cyclic reliability, the laminate‐structured film is demonstrated to be a promising class of polymer dielectrics for high‐power energy storage capacitors operating at elevated temperatures. The facile preparation method reported herein is readily adaptable to a variety of polymer thin films for energy applications under extreme environments.

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