We demonstrate how to control the reorientation or the spinning of complex samples, for instance for 3D visual inspection or for volumetric reconstruction. Whether continuous rotation or transient reorientation takes place depends on the strength of the acoustic radiation torque, arising from pressure gradients, compared to the acoustic viscous torque, arising from the shear forces at the viscous boundary layer around the particle. Based on numerical simulations and experimental insights, we develop a strategy to achieve a desired alignment or continuous rotation around a chosen axis, by tuning the relative strengths of the transducers and thus adjusting the relative contributions of viscous and radiation torques. The approach is widely applicable, as we discuss in several generic examples, with limitations dictated by size and shape asymmetry of the samples.Correction for 'Perspective on multi-scale simulation of thermal transport in solids and interfaces' by Ming Hu et al., Phys. Chem. Chem. Phys., 2021, 23, 1785-1801, DOI 10.1039/D0CP03372C.An innovative tactic to prepare porous organic polymer membranes was developed via interfacial azo-coupling polymerization.  https://www.selleckchem.com/products/ON-01910.html  The membranes possess plentiful anchoring sites for loading Pd nanoparticles, and served as a membrane reactor, which exhibits high-performance catalytic reduction with a flux of 27.3 t m-2 day-1 and good long-term stability due to almost zero Pd leaching.The process of combining heterogeneous catalysts and direct current (DC) electric fields can achieve high catalytic activities, even under mild conditions ( less then 500 K) with relatively low electrical energy consumption. Hydrogen production by steam reforming of methane, aromatics and alcohol, dehydrogenation of methylcyclohexane, dry reforming of methane, and ammonia synthesis are known to proceed at low temperatures in an electric field. In situ/operando analyses are conducted using IR, Raman, X-ray absorption fine structure, electrochemical impedance spectroscopy, and isotopic kinetic analyses to elucidate the reaction mechanism for these reactions at low temperatures. The results show that surface proton hopping by a DC electric field, called surface protonics, is important for these reactions at low temperatures because of the higher surface adsorbate concentrations at lower temperatures.We examined the modified electronic structure and single-carrier transport of individual hybrid core-shell metal-semiconductor Au-ZnS quantum dots (QDs) using a scanning tunnelling microscope. Nearly monodisperse ultra-small QDs are achieved by a facile wet chemical route. The exact energy structures are evaluated by scanning tunnelling spectroscopy (STS) measurements at 300 mK for the individual nanoobjects starting from the main building block Au nanocrystals (NCs) to the final Au-ZnS QDs. The study divulges the evolution of the energy structure and the charge transport from the single metallic building block core to the core-shell metal-semiconductor QDs. Furthermore, we successfully determined the contributions related to the quantum-confinement-induced excitonic band structure of the ZnS nano-shell and the charging energy of the system by applying a semi-empirical approach considering a double barrier tunnel junction (DBTJ) arrangement. We detect strong conductance peaks in Au-ZnS QDs due to the overlapping of the energy structure of the Au nano-core and the discrete energy states of the semiconductor ZnS nano-shell. Our findings will help in understanding the electronic properties of metal-semiconductor QDs. The outcomes therefore have the potential to fabricate tailored metal-semiconductor QDs for single-electron devices.First-principles calculations have been performed to investigate the interaction between solute impurity O and H/He/vacancy irradiation defects in Ti3AlC2. The formation energy and occupation of O atoms within different defects as well as the trapping progress of O/H clusters are discussed. It is found that the O atom preferentially occupies the hexahedral interstitial site (Ihex-1) in bulk Ti3AlC2, whereas it prefers to occupy the neighbouring tetrahedral interstitial site (Itetr-2) within pre-exisiting Al monovacancy (VAl), Al divacancy (2VAl-Al) and the 2VAl-C divacancy composed of Al and C vacancies. The appearance of C vacancy could greatly reduce the oxygen formation energy and make an O atom more inclined to occupy the center of C vacancy. Vacancy could capture more O atoms than H/He atoms, where VAl and 2VAl-Al could hold up to fifteen and eighteen O atoms, respectively. Meanwhile, the O could also promote the formation of Al vacancy. On the other hand, O atoms tend to occupy the interstitial sites near the Al atomic layer and have attraction to Al atoms, which is likely to enable the O atoms to combine with the Al atoms to form a Al2O3 protective layer, thus effectively inhibiting further oxidation inside the Ti3AlC2. In addition, the H-O exhibits repulsion interaction, but strong attraction occurs in the He-O interaction. Therefore, the O atom has an inhibitory effect on the formation of the H cluster, while it could bind more He atoms to form a large number of He bubbles. Besides, the O impurity greatly reduces the trapping ability of vacancy to H atoms, and O and He have a synergistic interaction for inhibiting the aggregation of H clusters. The present results are expected to provide a new insight into the behaviour of Ti3AlC2 under irradiation and oxidation conditions so that structural materials could be better designed.Hydrogen adsorption on different benzenes, both organic and inorganic, decorated with Li cations (Li+) was systematically studied by using quantum chemistry techniques. Our calculations demonstrate that Li+-decoration enhances the hydrogen storage ability of the complexes. MP2 calculations reveal that one to five hydrogen molecules per Li+ have high adsorption energies (Ead), up to -4.77 kcal mol-1, which is crucial for effective adsorption/desorption performance. The assessed hydrogen capacity of studied complexes is in the range of 10.0-10.6 wt%. SAPT2 calculations confirmed that induction and electrostatic interactions play the major role for H2 adsorption of the investigated systems, whereas London dispersion contributes to Ead moderately only in the cases of large number of hydrogen molecules adsorbed. Independent gradient model (IGM) analysis showed that there exists non-covalent bonding between Li+ and H2. The obtained van't Hoff desorption temperatures substantially exceed the temperature of liquid nitrogen.