We demonstrate that supermolecular templating allows tuning the pore size of ordered mesoporous materials in the once elusive range from 30 nm to more than 60 nm through simple control of synthetic variables (salt/supermolecule concentration and hydrothermal temperature). Gold nanoparticles (AuNPs) within the extra-large pores exhibit dramatically increased lifetime compared to those located within relatively small mesopores due to the enhanced mass diffusion that suppresses coke deposition on AuNPs.

Recent years have witnessed considerable progress in the development of solar cells based on lead halide perovskite materials. However, their intrinsic instability remains a limitation. In this context, the interplay between the thermal degradation and the hydrophobicity of perovskite materials is investigated. To this end, the salt 1-(4-ethenylbenzyl)-3-(3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooctylimidazolium iodide (ETI), is employed as an additive in hybrid perovskites, endowing the photoactive materials with high thermal stability and hydrophobicity. The ETI additive inhibits methylammonium (MA) permeation in methylammonium lead triiodide (MAPbI 3 ) occurring due to intrinsic thermal degradation, by inhibiting out-diffusion of the MA + cation, preserving the pristine material and preventing decomposition. With this simple approach, high efficiency solar cells based on the unstable MAPbI 3 perovskite are markedly stabilized under maximum power point tracking, leading to greater than twice the preserved efficiency after 700 h of continuous light illumination and heating (60 °C). These results suggest a strategy to tackle the intrinsic thermal decomposition of MAI, an essential component in all state-of-the-art perovskite compositions.

Despite the excellent photovoltaic properties achieved by perovskite solar cells at the laboratory scale, hybrid perovskites decompose in the presence of air, especially at high temperatures and in humid environments. Consequently, high‐efficiency perovskites are usually prepared in dry/inert environments, which are expensive and less convenient for scale‐up purposes. Here, a new approach based on the inclusion of an in situ polymerizable ionic liquid, 1,3‐bis(4‐vinylbenzyl)imidazolium chloride ([bvbim]Cl), is presented, which allows perovskite films to be manufactured under humid environments, additionally leading to a material with improved quality and long‐term stability. The approach, which is transferrable to several perovskite formulations, allows efficiencies as high as 17% for MAPbI3 processed in air % relative humidity (RH) ≥30 (from an initial 15%), and 19.92% for FAMAPbI3 fabricated in %RH ≥50 (from an initial 17%), providing one of the best performances to date under similar conditions.

Single-atom catalysts are emerging as primary catalysts for many reactions due to their 100% utilization of active metal centers leading to high catalytic efficiencies.

Here, a soft robotic microgripper is presented that consists of a smart actuated microgel connected to a spatially photopatterned multifunctional base. When pressed onto a target object, the microgel component conforms to its shape, thus providing a simple and adaptive solution for versatile micromanipulation. Without the need for active visual or force feedback, objects of widely varying mechanical and surface properties are reliably gripped through a combination of geometrical interlocking mechanisms instantiated by reversible shape‐memory and thermal responsive swelling of the microgel. The gripper applies holding forces exceeding 400 µN, which is high enough to lift loads 1000 times heavier than the microgel. An untethered version of the gripper is developed by remotely controlling the position using magnetic actuation and the contractile state of the microgel using plasmonic absorption. Gentle yet stable robotic manipulation of biological samples under physiological conditions opens up possibilities for high‐throughput interrogation and minimally invasive interventions.