The controlled aggregation of colloidal particles is not only a widespread natural phenomenon but also serves as a tool to design complex building blocks with tailored shape and functionalities. However, the quantitative characterization of such heteroaggregation processes remains challenging. Here, we demonstrate the use of analytical centrifugation to characterize the heteroaggregation of silica particles and soft microgels bearing similar surface charges. We investigate the attachment as well as the stability of the formed heteroaggregates as a function of particle to microgel surface ratio, microgel size and the influence of temperature. The attachment of microgels onto the colloidal particles induces a change in the sedimentation coefficient, which is used to quantitatively identify the number of attached microgels. We corroborate the shift in sedimentation coefficient by computer simulations of the frictional properties of heteroaggregates via a modified Brownian dynamic algorithm. The comparison between theoretical investigations and experiments suggest that the microgels deform and flatten upon attachment.The effect of humidity on the ionic transport in the amorphous phase of poly(ethylene oxide) thin films has been studied by local dielectric spectroscopy. We explored a controlled humidity range between 15% RH and 50% RH. AFM-based local dielectric imaging allowed the thin film topography and the corresponding dielectric contrast maps to be obtained simultaneously. No humidity effect on the film topography was observed whereas large variation of the dielectric signal could be detected. In addition, we observed a clear dielectric contrast in different locations on the thin film surface. At selected regions with high contrast in the dielectric maps, we performed nanoDielectric Spectroscopy (nDS) measurements covering the frequency range from 5 Hz to 100 kHz. By modeling these spectroscopy results, we quantified the conductivity of the amorphous phase of the semicrystalline poly(ethylene oxide) films. The crystalline fraction of the PEO thin films was extracted and found to be about 36%, independently of humidity. However, the average conductivity increased by a factor of 25 from 2 × 10-10 to 5 × 10-9 S cm-1, by changing environmental humidity in the explored % RH range.van der Waals (vdWs) heterostructures, combining different two-dimensional (2D) layered materials with diverse properties, have been demonstrated to be a very promising platform to explore a new physical phenomenon and realize various potential applications in atomically thin electronic and optoelectronic devices. Here, we report the controlled growth of vertically stacked β-In2Se3/MoS2 vdWs heterostructures (despite the existence of large lattice mismatching ∼29%) through a typical two-step chemical vapor deposition (CVD) method. The crystal structure of the achieved heterostructures is characterized by transmission electron microscopy, where evident Moiré patterns are observed, indicating well-aligned lattice orientation. Strong photoluminescence quenching is obeserved in the heterostructure, revealing effective interlayer charge transfer at the interface. Electrical devices are further constructed based on the achieved heterostructures, which have a high on/off ratio and a typical rectifying behavior. Upon laser irradiation, the devices show excellent photosensing properties. A high responsivity of 4.47 A W-1 and a detectivity of 1.07 × 109 Jones are obtained under 450 nm laser illumination with a bias voltage of 1 V, which are much better than those of heterostructures grown via CVD. Most significantly, the detection range can be extended to near-infrared due to the relatively small bandgap nature of β-In2Se3. With 830 nm laser illumination, the devices also show distinct photoresponses with fast response speed even when operating at room temperature.  https://www.selleckchem.com/products/6-benzylaminopurine.html  The high-quality β-In2Se3/MoS2 heterostructures broaden the family of the 2D layered heterostructure system and should have significant potential applications in high-performance broadband photodetectors.Magnesium hydride (MgH2) has been considered as a promising hydrogen storage material for buildings that are powered by hydrogen energy, but its practical application is hampered by poor kinetics and unstable thermodynamics. Herein, we describe a feasible method for preparing FeNi nanoparticles dispersed on reduced graphene oxide nanosheets (FeNi/rGO), and we confirmed that excellent catalytic effects increased the hydrogen storage performance of MgH2. 5 wt% FeNi/rGO-modified MgH2 began to release hydrogen at 230 °C and liberated 6.5 wt% H2 within 10 min at 300 °C. As for the hydrogenation process, the dehydrogenated sample absorbed 5.4 wt% H2 within 20 min at 125 °C under a hydrogen pressure of 32 bar. More importantly, a hydrogen capacity of 6.9 wt% was maintained after 50 cycles without compromising the kinetics during each cycle. A unique catalytic mechanism promoted synergetic effects between the in situ-formed Mg2Ni/Mg2NiH4, Fe, and rGO that efficiently promoted hydrogen dissociation and diffusion along the Mg/MgH2 interface, anchored the catalyst, and prevented MgH2 from aggregation and growth.We present the plasmon-enhanced nonlinear nanofocusing of a gold (Au) nanoprism array substrate (ANAS) driven via an ultrafast azimuthal vector beam (AVB). Theoretical calculations show that the electric-field intensity of the ANAS vertically excited via the femtosecond AVB is higher than that of LPB excitation. In this experiment, the second-order surface nonlinear optical response of the ANAS is adopted to examine the nonlinear plasmonic nanofocusing of the ANAS, and it was observed that the second harmonic (SH) intensity of the ANAS excited via the femtosecond AVB is ∼3.8 times higher than that of LPB excitation, revealing that the ANAS under AVB excitation has a better nonlinear plasmonic nanofocusing characteristic than that under LPB excitation. Furthermore, the GaSe nanosheets are transferred on the ANAS to examine the nonlinear plasmonic nanofocusing of the ANAS. The SH intensity of the GaSe nanosheets deposited on the ANAS via the femtosecond AVB excitation has been enhanced ∼4.7 times than that of LPB excitation, indicating that the ANAS via AVB excitation has better nonlinear plasmonic nanofocusing than that of LPB excitation.