Tuning the transmittance of colloidal solution by changing the orientation of Ag nanoplates in ferrofluid.

Ag nanoplates and Fe(3)O(4) nanoparticle-based ferrofluids were utilized to fabricate a magnetic field controlled optic switch. The changing of light transmittance (LT) is caused by the rotation of Ag nanoplates, whose long axis always follows the orientation of external magnetic field to minimize the potential energy. The sensitivity of switching was optimized by choosing Ag nanoplates with appropriate size and concentration. The switching of transmission is proved to be fast and fully reversible. This phenomenon not only indicates an effective method to adjust the propagation of optical signals, but also reveals the possibility and great potential to develop magnetic controlled functional devices.

A Simple Electrochemical Route to Access Amorphous Co-Ni Hydroxide for Non-enzymatic Glucose Sensing.

Among the numerous transition metal hydroxide materials, cobalt- and nickel-based hydroxides have been extensively studied for their excellent electrochemical performances such as non-enzymatic electrochemical sensors. Binary cobalt-nickel hydroxide has received extensive attention for its exceptionally splendid electrochemical behaviors as a promising glucose sensor material. In this work, we report the synthesis of three-dimensional amorphous Co-Ni hydroxide nanostructures with homogeneous distribution of elements via a simple and chemically clean electrochemical deposition method. The amorphous Co-Ni hydroxide, as a non-enzymatic glucose sensor material, exhibits a superior biosensing performance toward glucose detection for its superior electron transfer capability, high specific surface area, and abundant intrinsic redox couples of Ni2+/Ni3+ and Co2+/Co3+/Co4+ ions. The as-synthesized amorphous Co-Ni hydroxide holds great potential in glucose monitoring and detection as non-enzymatic glucose sensors with high sensitivity 1911.5 µA mM-1 cm-2 at low concentration, wide linear range of 0.00025-1 mM and 1-5 mM, low detection limit of 0.127 µM, super long-term stability, and excellent selectivity in 0.5 M NaOH solution.

Control of the compositions and morphologies of uranium oxide nanocrystals in the solution phase: multi-monomer growth and self-catalysis.

The presence of mixed products and impurities, which always confuse researchers, are common during synthesizing nanomaterials. Even though many studies have been conducted with an objective to control the synthesis of nanomaterials, very few studies have investigated a mechanism to control the composition of nanomaterials. Various products include UO3·H2O, U3O8, UO2, and U4O9 were produced by simply adjusting the pH with ammonia. The morphology of UO2 and U3O8 are tunable. In this study, we suggest two mechanisms that can be used to control the nanomaterial composition. Various experiments have been conducted to understand the mechanism that controls the composition of nanomaterials. We indicate that a multi-monomer growth model can be used to control the uranium oxide composition. We have developed a new oxidation-reduction system using acetone, and this system is capable of controlling both the morphology and composition of uranium oxide micro/nanomaterials. Further, the presence of the self-catalysis mechanism can be used to regulate processes that control the monomer transformation. Thus, the results of this study can be applied to help in the construction of mixed-valence metal oxides.

A Novel TiZrHfMoNb High-Entropy Alloy for Solar Thermal Energy Storage.

An equiatomic TiZrHfMoNb high-entropy alloy (HEA) was developed as a solar thermal energy storage material due to its outstanding performance of hydrogen absorption. The TiZrHfMoNb alloy transforms from a body-centered cubic (BCC) structure to a face-centered cubic (FCC) structure during hydrogen absorption and can reversibly transform back to the BCC structure after hydrogen desorption. The theoretical calculations demonstrated that before hydrogenation, the BCC structure for the alloy has more stable energy than the FCC structure while the FCC structure is preferred after hydrogenation. The outstanding hydrogen absorption of the reversible single-phase transformation during the hydrogen absorption⁻desorption cycle improves the hydrogen recycling rate and the energy efficiency, which indicates that the TiZrHfMoNb alloy could be an excellent candidate for solar thermal energy storage.

Significant enhanced uranyl ions extraction efficiency with phosphoramidate-functionalized ionic liquids via synergistic effect of coordination and hydrogen bond.

The influence of the linking group between the phosphoryl and bridging moieties in phosphoryl-containing task-specific ionic liquids (TSILs) on the extraction of uranyl ions was experimentally and theoretically investigated. A novel phosphoramidate-based TSIL with an amine group as the linking moiety resulted in a higher uranyl ion extraction efficiency compared with that of other phosphoryl-based TSILs. A distribution ratio of 4999 ± 51 can be achieved for uranyl ions. The uranyl ions (76.7 ± 1.5%) were stripped from the loaded ionic liquid phase in a single stage using 0.05 M diethylenetriamine pentaacetic acid in a 1.0 M guanidine carbonate solution. The extraction stoichiometry of the uranyl ions was determined by a slope analysis of the extraction data. Furthermore, the fundamental nature of the interaction between the phosphoramidate-based TSIL and uranyl ions was theoretically studied for the first time. The theoretical calculations demonstrated that the synergistic effect of the complexation interaction and H-bond formation between the phosphoramidate-functional ionic liquid and uranyl nitrate led to the higher extraction efficiency. These results provide a basis for rational design, synthesis and potential applications of novel TSILs for uranyl extraction.

Physical justification for negative remanent magnetization in homogeneous nanoparticles.

The phenomenon of negative remanent magnetization (NRM) has been observed experimentally in a number of heterogeneous magnetic systems and has been considered anomalous. The existence of NRM in homogenous magnetic materials is still in debate, mainly due to the lack of compelling support from experimental data and a convincing theoretical explanation for its thermodynamic validation. Here we resolve the long-existing controversy by presenting experimental evidence and physical justification that NRM is real in a prototype homogeneous ferromagnetic nanoparticle, an europium sulfide nanoparticle. We provide novel insights into major and minor hysteresis behavior that illuminate the true nature of the observed inverted hysteresis and validate its thermodynamic permissibility and, for the first time, present counterintuitive magnetic aftereffect behavior that is consistent with the mechanism of magnetization reversal, possessing unique capability to identify NRM. The origin and conditions of NRM are explained quantitatively via a wasp-waist model, in combination of energy calculations.

The magnetic assembly of polymer colloids in a ferrofluid and its display applications.

Nonmagnetic polymer colloids have been assembled into colloidal photonic crystals in a ferrofluid by applying an external magnetic field based on the dipole-dipole interactions of "magnetic holes". The photonic crystal disassembles immediately when the magnetic field is removed. The mechanism of assembly can be explained by two simultaneous processes: phase separation and colloidal assembly. In this work, increasing the size of the building blocks still produces colorful photonic crystals due to their 2nd order diffraction. With a larger building block, the magnetic response between the polymer colloids is greatly enhanced so that an instant and reversible assembly/disassembly can be realized in a much weaker magnetic field and lower ferrofluid concentration. Based on these investigations, a magnetically controlled photonic display unit has been fabricated, which works in a weak magnetic field, has stable reflection signals and possesses fast and reversible on/off switching of reflections.