A significant challenge in conventional heat-shrinkable polymers is to produce controllable microstructures. Here we report that the polymer material fabricated by three-dimensional (3D) printing technique has a heat-shrinkable property, whose initial microstructure can undergo a spontaneous pattern transformation under heating. The underlying mechanism is revealed by evaluating internal strain of the printed polymer from its fabricating process. It is shown that a uniform internal strain is stored in the polymer during the printing process and can be released when heated above its glass transition temperature. Furthermore, the internal strain can be used to trigger the pattern transformation of the heat-shrinkable polymer in a controllable way. Our work provides insightful ideas to understand a novel mechanism on the heat-shrinkable effect of printed material, but also to present a simple approach to fabricate heat-shrinkable polymer with a controllable thermo-structural response.

The development of solution-processed photovoltaic (PV) devices for indoor applications has recently attracted widespread attention owing to their outstanding potential in harvesting energy efficiently for low-power-consumption electronic devices, such as...

Shell buckling is central in many biological structures and advanced functional materials, even if, traditionally, this elastic instability has been regarded as a catastrophic phenomenon to be avoided for engineering structures. Either way, predicting critical buckling conditions remains a long-standing challenge. The subcritical nature of shell buckling imparts extreme sensitivity to material and geometric imperfections. Consequently, measured critical loads are inevitably lower than classic theoretical predictions. Here, we present a robust mechanism to dynamically tune the buckling strength of shells, exploiting the coupling between mechanics and magnetism. Our experiments on pressurized spherical shells made of a hard-magnetic elastomer demonstrate the tunability of their buckling pressure via magnetic actuation. We develop a theoretical model for thin magnetic elastic shells, which rationalizes the underlying mechanism, in excellent agreement with experiments. A dimensionless magneto-elastic buckling number is recognized as the key governing parameter, combining the geometric, mechanical, and magnetic properties of the system.

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Flexible pressure sensors offer a wide application range in health monitoring and human-machine interaction. However, their implementation in functional textiles and wearable electronics is limited because existing devices are usually small, 0D elements, and pressure localization is only achieved through arrays of numerous sensors. Fiber-based solutions are easier to integrate and electrically address, yet still suffer from limited performance and functionality. An asymmetric cross-sectional design of compressible multimaterial fibers is demonstrated for the detection, quantification, and localization of kPa-scale pressures over m 2 -size surfaces. The scalable thermal drawing technique is employed to coprocess polymer composite electrodes within a soft thermoplastic elastomer support into long fibers with customizable architectures. Thanks to advanced mechanical analysis, the fiber microstructure can be tailored to respond in a predictable and reversible fashion to different pressure ranges and locations. The functionalization of large, flexible surfaces with the 1D sensors is demonstrated by measuring pressures on a gymnastic mat for the monitoring of body position, posture, and motion.