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Using a multilayer deposition approach, we first electrophoretically deposit (EPD) silicon dioxide (SiO2) as an intermediate layer between the metallic substrate and SOCAL. The necessity of EPD SiO2 is to smooth ( less then 10 nm roughness) as well as to enable the proper surface chemistry for SOCAL bonding. To characterize antiscaling performance, we utilized calcium sulfate (CaSO4) scale tests, showing a 20× reduction in scale deposition rate than untreated metallic substrates. Descaling tests revealed that SOCAL dramatically decreases scale adhesion, resulting in rapid removal of scale buildup. Our work not only demonstrates a robust methodology for depositing antiscaling SOCAL coatings on metals but also develops design guidelines for the creation of antifouling coatings for alternate applications such as biofouling and high-temperature coking.As a promising microwave absorber filler, molybdenum disulfide (MoS2), because of the unique structure, high electrical conductivity, and polarization effect, is receiving more and more interest. Developing MoS2-based composites with specific structure and morphology is a hot top in the field of microwave absorbers, because of its strong multiple scattering and reflecting for microwaves as well as its unique interfacial characteristics. Now, with a facile solvothermal method, a novel core-shell CoFe2O4@1T/2H-MoS2 composite is synthesized, where the CoFe2O4 nanospheres are entirely embedded in a special three-dimensional (3D) nest-like 1T/2H phase MoS2. Notably, in comparison with superparamagnetic CoFe2O4 nanospheres, the coercivities of as-synthesized CoFe2O4@1T/2H-MoS2 composites greatly increase. PTC209 Here, 1T/2H-MoS2 exhibits ferromagnetism superimposed onto large diamagnetism. It is noted that, by adjusting the content of 1T/2H-phase MoS2, the microwave absorption performance of as-synthesized composites can be effectively tuned. The combination of 1T/2H-MoS2 with CoFe2O4 helps to adjust the permittivity and optimize the impedance matching of the composites. Impressively, a minimum reflection loss (RLmin) of -68.5 dB for the as-synthesized composites with a thickness of 1.81 mm is gained at 13.2 GHz; meanwhile, a broad effective bandwidth of 4.56 GHz ranged from 13.2 to 17.76 GHz is achieved at 1.6 mm. Further, the overall effective bandwidth (RL  less then -10 dB) is obtained up to 14.5 GHz from 3.5 to 18.0 GHz, covering more than 90% of the measured frequency range. The high microwave absorption performance is ascribed to the special structure design with the core of magnetic CoFe2O4 nanospheres and the shell of dielectric nest-like 1T/2H-MoS2 as well as their appropriate impedance matching. From the perspective of basic research and practical microwave application, this study provides another feasible and effective pathway to design novel MoS2-based magnetic/dielectric microwave absorbers.The development of novel efficient and robust electrocatalysts with sufficient active sites is one of the key parameters for hydrogen evolution reactions (HER) catalysis, which plays a key role in hydrogen production for clean energy harvesting. Recently, two-dimensional (2D) materials, especially those based upon transition metal dichalcogenides such as molybdenum disulfide (MoS2), have gained attention for the catalysis of hydrogen production because of their exceptional properties. Innovative strategies have been developed to engineer these material systems for improvements in their catalytic activity. Toward this aim, the facile growth of MoS2 clusters by sulfurization of molybdenum dioxide (MoO2) particles supported on reduced graphene oxide (rGO) foams using the chemical vapor deposition (CVD) method is reported. This approach created various morphologies of MoS2 with large edges and defect densities on the basal plane of rGO supported MoS2 structures, which are considered as active sites for HER catalysis. In addition, MoS2 nanostructures on the surface of the porous rGO network show robust physical interactions, such as van der Waals and π-π interactions between MoS2 and rGO. These features result in an improved process to yield a suitable HER catalyst. In order to gain a better understanding of the improvement of this MoS2-based HER catalyst, fully atomistic molecular dynamics (MD) simulations of different defect geometries were also performed.We report on the chemical and electronic structure of cesium tin bromide (CsSnBr3) and how it is impacted by the addition of 20 mol % tin fluoride (SnF2) to the precursor solution, using both surface-sensitive lab-based soft X-ray photoelectron spectroscopy (XPS) and near-surface bulk-sensitive synchrotron-based hard XPS (HAXPES). To determine the reproducibility and reliability of conclusions, several (nominally identically prepared) sample sets were investigated. The effects of deposition reproducibility, handling, and transport are found to cause significant changes in the measured properties of the films. Variations in the HAXPES-derived compositions between individual sample sets were observed, but in general, they confirm that the addition of 20 mol % SnF2 improves coverage of the titanium dioxide substrate by CsSnBr3 and decreases the oxidation of SnII to SnIV while also suppressing formation of secondary Br and Cs species. Furthermore, the (surface) composition is found to be Cs-deficient and Sn-rich compared to the nominal stoichiometry. The valence band (VB) shows a SnF2-induced redistribution of Sn 5s-derived density of states, reflecting the changing SnII/SnIV ratio. Notwithstanding some variability in the data, we conclude that SnF2 addition decreases the energy difference between the VB maximum of CsSnBr3 and the Fermi level, which we explain by defect chemistry considerations.In this study, a serotonin-stearic acid (ST-SA)-based bioconjugate was synthesized for the surface modification of manganese oxide-based nanocuboids (MNCs) for delivering of anticancer drug (i.e., doxorubicin hydrochloride (DOX)) to human liver cancer cells. MNCs were synthesized by chemical precipitation method, and their surface was modified with ST-SA bioconjugate for targeting of MNCs to cancer cells. The ST-SA@MNCs along with DOX showed good colloidal stability, high drug encapsulation (98.3%), and drug loading efficiencies (22.9%) as well as pH-responsive biodegradation. Coating with ST-SA conjugate provided a shield to MNCs which sustained their degradation in an acidic environment. The release of DOX was higher (81.4%) in acidic media than under the physiological conditions (20.5%) up to 192 h. The in vitro anti-proliferation assay showed that ST-SA@MNCs exhibit higher cell growth inhibition compared to that of pure DOX after 48 h of treatment. The cellular uptake and apoptosis studies revealed the enhanced uptake of ST-SA@MNCs in contrast to the MNCs due to overexpressed ST receptor on hepatocellular carcinoma cells and triggered the generation of reactive oxygen species in the cells.