Facile Fabrication of ZnO-ZnFe2O4 Hollow Nanostructure by a One-Needle Syringe Electrospinning Method for a High-Selective H2S Gas Sensor

Herein, a facile fabrication process of ZnO-ZnFe2O4 hollow nanofibers through one-needle syringe electrospinning and the following calcination process is presented. The various compositions of the ZnO-ZnFe2O4 nanofibers are simply created by controlling the metal precursor ratios of Zn and Fe. Moreover, the different diffusion rates of the metal oxides and metal precursors generate a hollow nanostructure during calcination. The hollow structure of the ZnO-ZnFe2O4 enables an enlarged surface area and increased gas sensing sites. In addition, the interface of ZnO and ZnFe2O4 forms a p-n junction to improve gas response and to lower operation temperature. The optimized ZnO-ZnFe2O4 has shown good H2S gas sensing properties of 84.5 (S = Ra/Rg) at 10 ppm at 250 ∘C with excellent selectivity. This study shows the good potential of p-n junction ZnO-ZnFe2O4 on H2S detection and affords a promising sensor design for a high-performance gas sensor.

First of Its Kind Automotive Catalyst Prepared by Recycled PGMs-Catalytic Performance

The production of new automotive catalytic converters requires the increase of the quantity of Platinum Group Metals in order to deal with the strict emission standards that are imposed for vehicles. The use of PGMs coming from the recycling of spent autocatalysts could greatly reduce the cost of catalyst production for the automotive industry. This paper presents the synthesis of novel automotive Three-Way Catalysts (PLTWC, Pd/Rh = 55/5, 60 gPGMs/ft3) and diesel oxidation catalysts (PLDOC, Pt/Pd = 3/1, 110 gPGMs/ft3) from recovered PGMs, without further refinement steps. The catalysts were characterized and evaluated in terms of activity in comparison with benchmark catalysts produced using commercial metal precursors. The small-scale catalytic monoliths were successfully synthesized as evidenced by the characterization of the samples with XRF analysis, optical microscopy, and N2 physisorption. Hydrothermal ageing of the catalysts was performed and led to a significant decrease of the specific surface area of all catalysts (recycled and benchmarks) due to sintering of the support material and metal particles. The TWCs were studied for their activity in CO and unburned hydrocarbon oxidation reactions under a slightly lean environment of the gas mixture (λ > 1) as well as for their ability to reduce NOx under a slightly rich gas mixture (λ < 1). Recycled TWC fresh catalyst presented the best performance amongst the catalysts studied for the abatement of all pollutant gases, and they also showed the highest Oxygen Storage Capacity value. Moreover, comparing the aged samples, the catalyst produced from recycled PGMs presented higher activity than the one synthesized with the use of commercial PGM metal precursors. The results obtained for the DOC catalysts showed that the aged PLDOC catalyst outperformed both the fresh catalyst and the aged DOC catalyst prepared with the use of commercial metal precursors for the oxidation of CO, hydrocarbons, and NO. The latter reveals the effect of the presence of several impurities in the recovered PGMs solutions.

Formation of Pt-Based Alloy Nanoparticles Assisted by Molybdenum Hexacarbonyl

We report on an optimized, scalable solution-phase synthetic procedure for the fabrication of fine-tuned monodisperse nanostructures (Pt(NiCo), PtNi and PtCo). The influence of different solute metal precursors and surfactants on the morphological evolution of homogeneous alloy nanoparticles (NPs) has been investigated. Molybdenum hexacarbonyl (Mo(CO)6) was used as the reductant. We demonstrate that this solution-based strategy results in uniform-sized NPs, the morphology of which can be manipulated by appropriate selection of surfactants and solute metal precursors. Co-surfactants (oleylamine, OAm, and hexadecylamine, HDA) enabled the development of a variety of high-index faceted NP morphologies with varying degrees of curvatures while pure OAm selectively produced octahedral NP morphologies. This Mo(CO)6-based synthetic protocol offers new avenues for the fabrication of multi-structured alloy NPs as high-performance electrocatalysts.

Fabricating polyoxometalates-stabilized single-atom site catalysts in confined space with enhanced activity for alkynes diboration

Effecting the synergistic function of single metal atom sites and their supports is of great importance to achieve high-performance catalysts. Herein, we successfully fabricate polyoxometalates (POMs)-stabilized atomically dispersed platinum sites by employing three-dimensional metal-organic frameworks (MOFs) as the finite spatial skeleton to govern the accessible quantity, spatial dispersion, and mobility of metal precursors around each POM unit. The isolated single platinum atoms (Pt1) are steadily anchored in the square-planar sites on the surface of monodispersed Keggin-type phosphomolybdic acid (PMo) in the cavities of various MOFs, including MIL-101, HKUST-1, and ZIF-67. In contrast, either the absence of POMs or MOFs yielded only platinum nanoparticles. Pt1-PMo@MIL-101 are seven times more active than the corresponding nanoparticles in the diboration of phenylacetylene, which can be attributed to the synergistic effect of the preconcentration of organic reaction substrates by porous MOFs skeleton and the decreased desorption energy of products on isolated Pt atom sites.

Secondary granulation-assisted CVD growth of WS2, TiS2 and NbS2 crystals

Chemical vapor deposition (CVD) is a cost-effective and scalable approach to prepare high-quality two-dimensional (2D) transition metal dichalcogenides (TMDCs), which is crucial for practical applications. Nevertheless, how to sublimate metal precursors with high melting point efficiently is still challenging. Herein, we demonstrate a novel secondary granulation-assisted route to adjust the supply of WO3 at moderate temperature (730 [Formula: see text]C), guarantee the appropriate tungsten/chalcogen ratio, and then achieve the controllable growth of monolayer WS2 crystals. Transmission electron microscopy, Raman and other characterizations indicate their high crystallinity. Notably, the domain size, nucleation density and morphology can be regulated by the size of the granulated WO3 particles. Moreover, the related mechanism is explained in detail, which applies equally to the steerable growth of TiS2 and NbS2, confirming the versatility of this method for growing 2D TMDCs. Therefore, this work offers a facile route for the microthermal CVD growth of 2D TMDCs crystals and drives the development of applications.

Tantalum-Doped TiO2 Prepared by Atomic Layer Deposition and Its Application in Perovskite Solar Cells

Tantalum (Ta)-doped titanium oxide (TiO2) thin films are grown by plasma enhanced atomic layer deposition (PEALD), and used as both an electron transport layer and hole blocking compact layer of perovskite solar cells. The metal precursors of tantalum ethoxide and titanium isopropoxide are simultaneously injected into the deposition chamber. The Ta content is controlled by the temperature of the metal precursors. The experimental results show that the Ta incorporation introduces oxygen vacancies defects, accompanied by the reduced crystallinity and optical band gap. The PEALD Ta-doped films show a resistivity three orders of magnitude lower than undoped TiO2, even at a low Ta content (0.8–0.95 at.%). The ultraviolet photoelectron spectroscopy spectra reveal that Ta incorporation leads to a down shift of valance band and conduction positions, and this is helpful for the applications involving band alignment engineering. Finally, the perovskite solar cell with Ta-doped TiO2 electron transport layer demonstrates significantly improved fill factor and conversion efficiency as compared to that with the undoped TiO2 layer.

Effect of Organic Linkers on Metal-Organic Frameworks Electrode Fabrication for Battery Supercapacitor Hybrid Application

Metal organic framework (MOFs) of ternary metal precursors with different organic linkers are synthesized and fabricated on Ni-foam as the electrodes via hydrothermal reaction aiming to enhance the electrical conductivity and the specific capacitance, Cs. We report the preparation of ternary metal with different organic linkers named CoCuNi-bi using terephthalic acid (H2bdc), CoCuNi-tri using trimellitic acid and CoCuNi-tetra using pyromellitic acid with increasing of active sites on Ni-foam substrate respectively. The CoCuNi-tetra demonstrates the highest Cs of 740 F g-1 at 2 mV/s & 791 F g-1 (87.9 mAh g­­­-1) at 1 Ag-1 respectively followed by CoCuNi-tri (674 F g-1 at 1 A g-1; 74.9 mAh g-1) and CoCuNi-bi (591 F g-1 at 1 A g-1; 65.7 mAh g-1). CoCuNi-tetra shows the best electrochemical performance hence it could be the encouraging electrode for supercapacitor materials.