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In this review, we describe the theory and mechanisms required for magnetic actuation, classify bio-hybrid actuators by their diverse organic components, and discuss their current limitations. Insights into the future of coupling cells and cell-derived components with magnetic materials to fabricate multi-functional actuators are also provided.Surfactants play a critical role in bottom-up nanotechnologies due to their peculiar nature of controlling the interfacial energy. Since their operational mechanism originates from the molecular-scale formation and disruption processes of molecular assemblies (i.e., micelles), conventional static-mode atomic force microscopy has made a significant contribution to unravel the detailed molecular pictures. Recently, we have successfully developed a local solvation measurement technique based on three-dimensional frequency-modulation atomic force microscopy, whose spatial resolution is not limited by jump-to-contact. Here, using this novel technique, we investigate molecular nanomechanics in the formation and disruption processes of micelles formed on a hydrophobic surface. Furthermore, an experiment employing a hetero-nanostructure reveals that the nanomechanics depends on the form of the molecular assembly. Namely, the hemifusion and disruption processes are peculiar to the micellar surface and cause a higher energy dissipation than the monolayer surface. The technique established in this study will be used as a generic technology for further development of bottom-up nanotechnologies.The total synthesis of (±)-vinoxine was achieved featuring the assembly of a multi-substituted tetrahydropyrido[1,2-a]indole skeleton through the Tf2O-mediated Bischler-Napieralski reaction. The characteristic diazabicyclo[3.3.1]nonane skeleton was stereoselectively constructed via radical cyclization based on the one stereochemistry of the C3 position. The established methodology provides new options for the synthesis of natural products and pharmaceuticals containing the multi-substituted pyrido[1,2-a]indole skeleton.Polarization-sensitive photodetectors are the core of optics applications and have been successfully demonstrated in photodetectors based on the newly-emerging metal-halide perovskites. However, achieving high polarization sensitivity is still extremely challenging. In addition, most of the previously reported photodetectors were concentrated on 1D lead-halide perovskites and 2D asymmetric intrinsic structure materials, but suffered from being external bias driven, lead-toxicity, poor stability and complex processes, severely limiting their practical applications. Here, we demonstrate a high-performance polarization-sensitive and stable polarization-sensitive UV photodetector based on a dendritic crystal lead-free metal-halide CsCu2I3/GaN heterostructure. By combining the anisotropic morphology and asymmetric intrinsic structure of CsCu2I3 dendrites with the isotropic material GaN film, a high specific surface area and built-in electric field are achieved, exhibiting an ultra-high polarization selectivity up to 28.7 and 102.8 under self-driving mode and -3 V bias, respectively. To our knowledge, such a high polarization selectivity has exceeded those of all of the reported perovskite-based devices, and is comparable to, or even superior to, those of the conventional 2D heterostructure materials. Interestingly, the unsealed device shows outstanding stability, and can be stored for over 2 months, and effectively maintained the performance even after repeated heating (373K)-cooling (300K) for different periods of time in ambient air, indicating a remarkable temperature tolerance and desired compatibility for applications under harsh conditions. Such excellent performance and simple method strongly show that the CsCu2I3/GaN heterojunction photodetector has great potential in practical applications with high polarization-sensitivity. This work provides a new insight into designing novel high-performance polarization-sensitive optoelectronic devices.High-entropy perovskite oxides (HEPOs) are attracting significant attention due to their unique structures, unprecedented properties and great application potential in many fields, while available synthetic methods have many shortcomings; so it is still a challenge to develop a simple, low-cost and environment-friendly synthetic strategy for HEPOs. Herein, a novel synthetic strategy is reported for HEPOs using an ionic liquid (IL)-hydroxide-mediated technique at a low temperature and normal atmospheric pressure. The synthesized HEPOs, including Ba(FeNbTiZrTa)O3, Ba(MnNbTiZrTa)O3, Ba(FeSnTiZrTa)O3 and Ba(FeVTiZrTa)O3, exhibit a cubic structure and a dispersed nanoparticle morphology (particle size of 20-60 nm). The formation process of HEPOs in an IL-KOH system can be described as follows first, B-site metal source compounds are dissolved in IL-KOH medium to form hydroxyl complexes; second, the complexes further dehydrate, condensate and react with Ba2+ ions to form the crystal nuclei of HEPOs under the synergistic effect of reaction temperature and basicity; third, the growth of HEPO nuclei is completed by the Ostwald ripening process. In these processes, KOH not only plays a role as a solvent, but also provides sufficient OH- concentration for the formation and condensation of B-site metal hydroxyl complexes, while the IL also makes significant contributions first, a lower reaction temperature and lower dosage of KOH are achieved by the use of the IL; second, the IL with good dissolving ability and low surface tensions can promote the nucleation rate of HEPOs and improve the Ostwald ripening process; third, the compact adsorption of the IL on the surface of products ensures a small particle size and high dispersion of HEPO nanoparticles to a certain extent. In brief, the technique provides an innovative, low-cost, simple and nontoxic strategy for the synthesis of HEPOs, which can be extended to other high-entropy materials.The development of highly active and selective heterogeneous-based catalysts with tailorable properties is not only a fundamental challenge, but is also crucial in the context of energy savings and sustainable chemistry. Here, we show that ruthenium nanoparticles (RuNPs) stabilised with simple polymerised ionic liquids (PILs) based on N-vinyl imidazolium led to highly active and robust nano-catalysts in hydrogenation reactions, both in water and organic media. Of particular interest, their activity and selectivity could simply be manipulated through counter-anion exchange reactions. Hence, as a proof of concept, the activity of RuNPs could be reversibly turned on and off in the hydrogenation of toluene, while in the case of styrene, the hydrogenation could be selectively switched from ethylbenzene to ethylcyclohexane upon anion metathesis. According to X-ray photoelectron spectroscopy (XPS) and dynamic light scattering (DLS) analyses, these effects could originate not only from the relative hydrophobicity and solvation of the PIL corona but also from the nature and strength of the PIL-Ru interactions.Anti-(ds)-DNA antibodies are the serological hallmark of Systemic Lupus Erythematosus (SLE). They assemble in the bloodstream with (ds)-DNA, forming immunocomplexes, which spread all over the body causing, among the other symptoms, lupic glomerulonephritis. Pathological manifestations of the disease may be reduced by destabilizing or inhibiting the formation of the immunocomplexes. In this respect, glycodendrimers showed peculiar interacting abilities towards this kind of biomolecule. Various generations of open-shell maltose-decorated poly(amidoamine) (PAMAM) and poly(propyleneimine) (PPI) dendrimers and two oligopeptides with different polyethylene glycol units were synthesized and characterized, and then tested for their anti-SLE activity. The activity of glycodendrimers and oligopeptides was evaluated in human plasma from patients with SLE, compared to healthy plasma, by means of an enzyme-linked immunosorbent assay (ELISA), and electron paramagnetic resonance (EPR) characterization using spin-label and spin-probe techniques. Different strategies for the immunocomplex formation were tested. The results show that both kinds of glycodendrimers and oligopeptides inhibited the formation of immunocomplexes. Also, a partial breakdown of preformed immunocomplexes was observed. Both ELISA and EPR analyses indicated a better activity of glycodendrimers compared to oligopeptides, the 3rd generation PPI dendrimer being the most promising against SLE. This study highlights the possibility to develop a new class of dendritic therapeutics for the treatment of Lupus in pre-clinical studies.A self-powered wearable brain-machine-interface system with pulse detection and brain stimulation for ceasing action has been realized. The system is composed of (1) a power supply unit that employs a piezoelectric generator and converts the mechanical energy of human daily activities into electricity; (2) a neck pulse biosensor that allows continuous measurements of carotid pulse by using a piezoelectric polyvinylidene fluoride film; (3) a data analysis module that enables a coordinated brain-machine-interface system to output brain stimulation signals; and (4) brain stimulating electrodes linked to the brain that implement behavioral intervention. Demonstration of the system with stimulating electrodes implanted in the periaqueductal gray (PAG) in running mice reveals the great effect of forced ceasing action. The mice stop their running within several seconds when the stimulation signals are sent into the PAG brain region (inducing fear). This self-powered scheme for neural stimulation realizes specific behavioral intervention without any external power supply, thus providing a new concept for future behavior intervention.Organic cations are believed to have little influence on the charge carrier lifetime in hybrid organic-inorganic perovskites. Experiments defy this expectation. ML323 solubility dmso We consider formamidinium lead iodide (FAPbI3) doping with and without Br as two prototypical systems, and perform ab initio time-domain nonadiabatic (NA) molecular dynamics simulations to investigate nonradiative electron-hole recombination. The simulations demonstrate that correlated organic-inorganic motion stabilizes the lattice and inhibits nonradiative charge recombination in FAPbI3 upon Br doping. Br doping suppresses the rotation of FA and the vibrations of both organic and inorganic components, and leads to hole localization and the extent of localization is enhanced upon thermal impact, notably reducing the NA coupling by decreasing the overlap between the electron and hole wave functions. Doping also slightly increases the bandgap for further decreasing NA coupling and enhances the open-circuit voltage of perovskite solar cells. The small NA coupling and large bandgap beat the slow coherence loss, delaying electron-hole recombination and extending the charge carrier lifetime to 1.5 ns in Br-doped FAPbI3, which is on the order of 1.1 ns in pristine FAPbI3. The obtained time scales are in good agreement with experiments. Multiple phonon modes, including those of both the inorganic and organic components, couple to the electronic subsystem and accommodate the excess electronic energy lost during nonradiative charge recombination. The study reveals the unexpected atomistic mechanisms for the reduction of electron-hole recombination upon Br doping, rationalizes the experiments, and advances our understanding of the excited-state dynamics of perovskite solar cells.