High‐Power Actuation from Molecular Photoswitches in Enantiomerically Paired Soft Springs

Motion in plants often relies on dynamic helical systems as seen in coiling tendrils, spasmoneme springs, and the opening of chiral seedpods. Developing nanotechnology that would allow molecular‐level phenomena to drive such movements in artificial systems remains a scientific challenge. Herein, we describe a soft device that uses nanoscale information to mimic seedpod opening. The system exploits a fundamental mechanism of stimuli‐responsive deformation in plants, namely that inflexible elements with specific orientations are integrated into a stimuli‐responsive matrix. The device is operated by isomerization of a light‐responsive molecular switch that drives the twisting of strips of liquid‐crystal elastomers. The strips twist in opposite directions and work against each other until the pod pops open from stress. This mechanism allows the photoisomerization of molecular switches to stimulate rapid shape changes at the macroscale and thus to maximize actuation power.     

An Ultrastable and Easily Regenerated Hydrogen‐Bonded Organic Molecular Framework with Permanent Porosity

A robust hydrogen‐bonded organic framework HOF‐TCBP (H₄TCBP=3,3′,5,5′‐tetrakis‐(4‐carboxyphenyl)‐1,1′‐biphenyl) has been successfully constructed and structurally characterized. It possesses a permanent 3D porous structure with a 5‐fold interpenetrated dia topological network. This activated HOF‐TCBP has a high BET surface area of 2066 m² g⁻¹ and is capable of highly selective adsorption and separation of light hydrocarbons under ambient conditions. It shows excellent thermal stability, as demonstrated by PXRD experiments and N₂ adsorption tests. Practical use of HOF‐TCBP is facilitated by the ease of its preparation and renewal through rotary evaporation.     

Mechanochemical Friedel–Crafts Alkylation—A Sustainable Pathway Towards Porous Organic Polymers

This study elucidates an innovative mechanochemical approach applying Friedel–Crafts alkylation to synthesize porous covalent triazine frameworks (CTFs). Herein, we pursue a counterintuitive approach by utilizing a rather destructive method to synthesize well‐defined materials with intrinsic porosity. Investigating a model system including carbazole as monomer and cyanuric chloride as triazine node, ball milling is shown to successfully yield porous polymers almost quantitatively. We verified the successful structure formation by an in‐depth investigation applying XPS, solid‐state NMR and FT‐IR spectroscopy. An in situ study of pressure and temperature developments inside the milling chamber in combination with two‐dimensional liquid‐state NMR spectroscopy reveals insights into the polymerization mechanism. The versatility of this mechanochemical approach is showcased by application of other monomers with different size and geometry.     

Black Tungsten Nitride as a Metallic Photocatalyst for Overall Water Splitting Operable at up to 765 nm

Semiconductor photocatalysts are hardly employed for overall water splitting beyond 700 nm, which is due to both thermodynamic aspects and activation barriers. Metallic materials as photocatalysts are known to overcome this limitation through interband transitions for creating electron–hole pairs; however, the application of metallic photocatalysts for overall water splitting has never been fulfilled. Black tungsten nitride is now employed as a metallic photocatalyst for overall water splitting at wavelengths of up to 765 nm. Experimental and theoretical results together confirm that metallic properties play a substantial role in exhibiting photocatalytic activity under red‐light irradiation for tungsten nitride. This work represents the first red‐light responsive photocatalyst for overall water splitting, and may open a promising venue in searching of metallic materials as efficient photocatalysts for solar energy utilization.     

Mass Production and Pore Size Control of Holey Carbon Microcages

Architectural control of porous solids, such as porous carbon cages, has received considerable attention for versatile applications because of their ability to interact with liquids and gases not only at the surface, but throughout the bulk. Herein we report a scalable, facile spray‐pyrolysis route to synthesize holey carbon microcages with mosquito‐net‐like shells. Using the surfaces of water droplets as the growth templates, styrene–butadiene rubber macromolecules are controllably cross‐linked, and size‐controllable holes on the carbon shells are generated. The as‐formed carbon microcages encapsulating Si nanoparticles exhibit enhanced lithium‐storage performances for lithium‐ion batteries. The scalable, inexpensive synthesis of porous carbon microcages with controlled porosity and the demonstration of outstanding electrochemical properties are expected to extend their uses in energy storage, molecular sieves, catalysis, adsorbents, water/air filters, and biomedical engineering.