Space cooling and heating currently result in huge amounts of energy consumption and various environmental problems. Herein, a switching strategy is described for efficient energy‐saving cooling and heating based on the dynamic cavitation of silicone coatings that can be reversibly and continuously tuned from a highly porous state to a transparent solid. In the porous state, the coatings can achieve efficient solar reflection (93%) and long‐wave infrared emission (94%) to induce a subambient temperature drop of about 5 °C in hot weather (≈35 °C). In the transparent solid state, the coatings allow active sunlight permeation (95%) to induce solar heating to raise the ambient temperature from 10 to 28 °C in cold weather. The coatings are made from commercially available, cheap materials via a facile, environmentally friendly method, and are durable, reversible, and patternable. They can be applied immediately to various existed objects including rigid substrates.

Earthworms are able to pass through sticky soil without inducing stains through a self-forming thick lubricating layer on their rough skins. To mimic this earthworm-like lubricating capability, an attempt to create a textured structure on the surface of liquid-releasable polymer coatings by a "breath figure" process is described herein. The resulting coatings exhibit fast and site-specific release behavior under external triggers such as solid-based friction. The released oil is then stabilized by the surface texture to form thick lubricating layers, reducing friction and enhancing wear resistance. Moreover, the coatings also exhibit excellent antifouling property in a sticky soil environment. Because the lubricating layer can be regenerated after consumption, the potential of this self-replenished lubricating mechanism in preparing friction-reduction, antiwear, and antifouling coatings used in solid-based environments is therefore envisioned.

Two click-based porous organic polymers (CPP-1 and CPP-2) are readily synthesized through a click reaction. Using CPP-1 and CPP-2 as supports, palladium nanoparticles (NPs) with uniform and dual distributions were prepared through H 2 and NaBH 4 reduction routes, respectively. Ultrafine palladium NPs are effectively immobilized in the interior cavities of polymers. The coordination of 1,2,3-triazolyl to palladium and the confinement effect of polymers on palladium NPs are verified by solid-state 13 C NMR and IR spectra, XPS analyses, EDX mapping, and computational calculation. The steric and electronic properties of polymers have a considerable influence on the interaction between polymers and palladium NPs, as well as the catalytic performances of NPs. The ultrafine palladium NPs with uniform distribution exhibit superior stability and recyclability over palladium NPs with dual distributions and palladium on charcoal in the hydrogenation of nitroarenes, and no obvious agglomeration and loss of catalytic activity were observed after recycling several times. The excellent performances mainly result from synergetic effects between palladium NPs and polymers.