Electrochemical detection of hydrogen peroxide using micro and nanoporous CeO2 catalysts.

In this research work, focus has been made on a glassy carbon electrode (GCE) modified commercial micro and synthesized nano-CeO2 for the detection of hydrogen peroxide (H2O2). Firstly, CeO2 nanoleaves were prepared by solvothermal route. Both commercially available micro CeO2 and synthesized nano-CeO2 structures were analyzed by different characterization techniques. The Raman spectra of synthesized nano CeO2 has more oxygen vacancies than micro CeO2. SEM images revealed that the synthesized CeO2 acquired leaf-like morphology. The catalyst nano CeO2 offered mesoporosity from nitrogen adsorption-desorption isotherms with massive sites of activation for increasing efficiency. Experiments on determining H2O2 using micro CeO2 or nano-CeO2/GCE was conducted using cyclic voltammetry (CV) and amperometry. Enhanced H2O2 reduction peak current with lower potential was observed in nano-CeO2/GCE. The influence of scan rate and H2O2 concentration on the performance of nano-CeO2/GCE were also studied. The obtained results have indicated that nano-CeO2/GCE showed improved electrochemical sensing behavior towards the reduction of H2O2 than micro-CeO2/GCE and bare GCE. A linear relationship was obtained over 0.001 µM-0.125 µM concentration of H2O2, with good sensitivity 141.96 µA µM-1 and low detection limit of 0.4 nM. Hence, the present nano-CeO2 system will have a great potential with solvothermal synthesis approach in the development of electrochemical sensors.

A Self-Assembly of Single Layer of Co Nanorods to Reveal the Magnetostatic Interaction Mechanism.

In this work, we report a self-assembly method to fabricate a single layer of Co nanorods to study their magnetostatic interaction behavior. The Co nanorods with cambered and flat tips were synthesized by using a solvothermal route and an alcohol-thermal method, respectively. Both of them represent hard magnetic features. Co nanorods with cambered tips have an average diameter of 10 nm and length of 100 nm with coercivity of 6.4 kOe, and flat-tip nanorods with a 30 nm diameter and 100 nm length exhibit a coercivity of 4.9 kOe. They are further assembled on the surface of water in assistance of surfactants. The results demonstrate that the assembly type is dependent on the magnetic induction lines direction. For Co nanorods with flat tips, most of magnetic induction lines are parallel to the length direction, leading to an assembly that is tip to tip. For Co nanorods with cambered tips, they are prone to holding together side by side for their random magnetic induction lines. Under an applied field, the Co nanorods with flat tips can be further aligned into a single layer of Co nanorods. Our work gives a possible mechanism for the magnetic interaction of Co nanorods and provides a method to study their magnetic behavior.

The Effects of Various Parameters of the Microwave-Assisted Solvothermal Synthesis on the Specific Surface Area and Catalytic Performance of MgF2 Nanoparticles.

High-specific-surface-area MgF2 was prepared by microwave-assisted solvothermal synthesis. The influences of the solvent and the magnesium precursors, and the calcination atmospheres, on the nanoparticle sizes and specific surface areas, estimated by X-Ray Powder Diffraction, N2 sorption and TEM analyses, were investigated. Nanocrystallized (~7 nm) magnesium partially hydroxylated fluorides (MgF2-x(OH)x) with significant specific surface areas between 290 and 330 m2∙g-1 were obtained. After activation under gaseous HF, MgF2-x(OH)x catalysts underwent a large decrease of both their surface area and their hydroxide, rates as shown by their 19F and 1H solid-state NMR spectra. Expect for MgF2 prepared from the acetate precursor, an activity of 30-32 mmol/h∙g was obtained which was about 40% higher compared with that of MgF2 prepared using Trifluoroacetate method (21.6 mmol/h∙g).

Improving Photocatalytic Degradation Activity of Organic Pollutant by Sn4+ Doping of Anatase TiO2 Hierarchical Nanospheres with Dominant {001} Facets.

Herein, high-energy {001} facets and Sn4+ doping have been demonstrated to be effective strategies to improve the surface characteristics, photon absorption, and charge transport of TiO2 hierarchical nanospheres, thereby improving their photocatalytic performance. The TiO2 hierarchical nanospheres under different reaction times were prepared by solvothermal method. The TiO2 hierarchical nanospheres (24 h) expose the largest area of {001} facets, which is conducive to increase the density of surface active sites to degrade the adsorbed methylene blue (MB), enhance light scattering ability to absorb more incident photons, and finally, improve photocatalytic activity. Furthermore, the SnxTi1-xO2 (STO) hierarchical nanospheres are fabricated by Sn4+ doping, in which the Sn4+ doping energy level and surface hydroxyl group are beneficial to broaden the light absorption range, promote the generation of charge carriers, and retard the recombination of electron-hole pairs, thereby increasing the probability of charge carriers participating in photocatalytic reactions. Compared with TiO2 hierarchical nanospheres (24 h), the STO hierarchical nanospheres with 5% nSn/nTi molar ratio exhibit a 1.84-fold improvement in photodegradation of MB arising from the enhanced light absorption ability, increased number of photogenerated electron-hole pairs, and prolonged charge carrier lifetime. In addition, the detailed mechanisms are also discussed in the present paper.

MIL-125-NH2@TiO2 Core-Shell Particles Produced by a Post-Solvothermal Route for High-Performance Photocatalytic H2 Production.

Metal-organic frameworks (MOFs) have proven to be an interesting class of sacrificial precursors of functional inorganic materials for catalysis, energy storage, and conversion applications. However, the controlled synthesis of MOF-derived materials with desirable compositions, structures, and properties still remains a big challenge. Herein, we propose a post-solvothermal route for the outer-to-inner loss of organic linkers from MOF, which is simple, rapid, and controllable and can be operated at temperature much lower than that of the commonly adopted pyrolysis method. By such a strategy, the MIL-125-NH2 particles coated by TiO2 nanosheets were produced, and the thickness of TiO2 shell can be easily tuned. The MIL-125-NH2@TiO2 core-shell particles combine the advantages of highly active TiO2 nanosheets, MIL-125-NH2 photosensitizer, plenty of linker defects and oxygen vacancies, and mesoporous structure, which allows them to be utilized as photocatalysts for the visible-light-driven hydrogen production reaction. It is remarkable that the hydrogen evolution rate by MIL-125-NH2@TiO2 can be enhanced 70 times compared with the pristine MIL-125-NH2. Such a route can be easily applied to the synthesis of different kinds of MOF-derived functional materials.

Tunable solar-heat shielding property of transparent films based on mesoporous Sb-doped SnO2 microspheres.

In this paper, mesoporous antimony doped tin oxide (ATO) microspheres are synthesized via a solvothermal method from a methanol system with the surfactant followed by a thermal treatment process. Morphology studies reveal that the spherical products obtained by polyvinylpyrrolidone (PVP) templating result in a higher uniformity in size. Such obtained ATO microspheres with a secondary particle size ranging between 200 and 800 nm consist of packed tiny nanocrystals and have high specific surface area (∼98 m(2) g(-1)). The effect of Sb doping on the structural and electrical properties of SnO2 microspheres is studied. Because of the substitution of Sn(4+) with Sb(5+) accompanied by forming a shallow donor level close to the conduction band of SnO2, a lower resistivity of powder pellet can be achieved, which corresponds to the spectrally selective property of films. The application of ATO microspheres provides an example of transparent coatings; depending on Sb concentration in SnO2 and solid content of coatings, transparent films with tunable solar-heat shielding property are obtained.