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Creatures, such as Venus flytrap and hummingbirds, capable of rapid predation through snap‐through transition, provide paradigms for the design of soft actuators and robots with fast actions. However, these artificial "snappers" usually need contact stimulations to trigger the flipping. Reported here is a constrained anisotropic poly(N‐isopropylacrylamide) hydrogel showing fast snapping upon light stimulation. This hydrogel is prepared by flow‐induced orientation of nanosheets (NSs) within a rectangular tube. The precursor containing gold nanoparticles is immediately exposed to UV light for photopolymerization to fix the ordered structure of NSs. Two ends of the slender gel are clamped to form a buckle with bistability nature, which snaps to the other side upon laser irradiation. Systematic experiments are conducted to investigate the influences of power intensity and irradiation angle of the laser, as well as thickness and buckle height of the gel, on the snapping behaviors. The fast snapping is further used to kick a plastic bead and control the switch state. Furthermore, synergetic or oscillated snapping of the gel with two buckles of opposite directions is realized by inclined irradiation of a laser or horizontal irradiation with two lasers, respectively. Such light‐steered snapping of hydrogels should merit designing soft robots, energy harvests, etc. [ABSTRACT FROM AUTHOR]

Upcycling waste plastics (e.g., polyethylene (PE)) into value‐added carbon products is regarded as a promising approach to address the increasingly serious waste plastic pollution and simultaneously achieve carbon neutrality. However, developing new carbonization technology routes to promote the oxidation of PE at low temperature and construct the stable cross‐linking network remains challenging. Here, a facile carbon‐grown‐on‐carbon strategy is proposed using carbon black (CB) to convert waste PE into core/shell carbon nanoparticles (CN) in high yields at low temperature. The yield of CN remarkably increases when the heating temperature decreases or the dosage of CB increases. The obtained CN displays turbostratic structure and closely aggregated granular morphology with a size of ≈80 nm. It is found that, prior to the oxidation and carbonization of PE, CB forms a 3D network architecture in the PE matrix. More importantly, CB not only catalyzes the partial oxidation of PE to form PE macromolecular radicals and introduce oxygen‐containing groups at low temperature in the early stage, but also favors for the construction of a stable cross‐linking network in the latter stage. This work offers a facile sustainable strategy for chemical upcycling of PE into value‐added carbon products without post‐treatments or usage of metallic catalysts. [ABSTRACT FROM AUTHOR]