Enhanced hydrogen production via urea electrolysis over Ni-NiO electrodeposited on Ti mesh.

The sluggish kinetics of anodic oxygen evolution reaction (OER) is regarded as the main bottleneck for ineffective hydrogen production efficiency, limiting the industrial application of electrochemical water splitting. Substituting the OER by urea electrooxidation reaction (UOR) and simultaneously developing highly active and economical bifunctional electrocatalyst for UOR and hydrogen evolution reaction (HER) is a promising method to realize energy-saving hydrogen production and urea-rich wastewater abatement. Herein, self-supporting Ni-NiO film grown on Ti mesh (Ni-NiO/TM) was successfully prepared by a facile cathodic electrodeposition method with using nickel acetate as the only raw material. Electrodeposition process was optimized by modulating the electrodeposition time and potential. x-ray diffraction, scanning electron microscopy, transmission electron microscopy, x-ray photoelectron spectroscopy and Raman characterization revealed the optimized Ni-NiO/TM was comprised of crystalline Ni and amorphous NiO and its morphology exhibited nanosphere structure, assembled by nanosheets. Ni-NiO/TM sample prepared under the potential of -1.5 V and deposition time of 10 min illustrated the lowest UOR potential of 1.34 V at 50 mA cm-2and robust stability, superior to the recently reported literatures. Furthermore, the HER potential was only -0.235 V to drive the current density of 50 mA cm-2. The cell voltage of urea-assisted electrolysis for hydrogen production in Ni-NiO/TM||Ni-NiO/TM two-electrode system only required 1.56 V to deliver 50 mA cm-2, obviously lower than that (>1.72 V) for overall water splitting. This work demonstrated the potential of Ni-based material as bifunctional electrocatalyst for energy-saving H2production by urea-rich wastewater electrolysis.

Size-controlled growth of ZnSe nanocrystals for high-performance photocatalytic H2O2 production in pure water.

Semiconductor photocatalysis is deemed as a novel and promising process that can produce H2O2 from earth-abundant water and gaseous dioxygen using sunlight as the energy supply. The searching of novel catalysts for photocatalytic H2O2 production has received increasing attention in the last few years. Herein, size-controlled growth of ZnSe nanocrystals was realized via a solvothermal method by varying the amount of Se and KBH4. The performance of the as-obtained ZnSe nanocrystals towards photocatalytic H2O2 production depends on the mean size of the synthesized nanocrystals. Under O2-bubbling, the optimal ZnSe sample presented an excellent H2O2 production efficiency (8.596 mmol g-1 h-1), and the apparent quantum efficiency for H2O2 production reaches as high as 2.84% at λ = 420 nm. Under air-bubbling, the accumulation of H2O2 was as high as 1.758 mmol L-1 after 3 h irradiation at the ZnSe dosage of 0.4 g L-1. The photocatalytic H2O2 production performance is far superior to the most investigated semiconductors such as TiO2, g-C3N4, and ZnS.

Three-dimensional Nanoporous Cu-Doped Ni Coating as Bifunctional Electrocatalyst for Hydrazine Sensing and Hydrogen Evolution Reaction.

Developing a cost-effective and efficient bifunctional electrocatalyst with simple synthesis strategy for hydrazine sensing and H evolution reaction (HER) is of utmost importance. Herein, a three-dimensional porous Cu-doped metallic Ni coating on Ti mesh (Ni(Cu) coating/TM) was successfully electrodeposited by a facile electrochemical method. Electrochemical etching of the electrodeposited Ni(Cu) coating with metallic Ni and Cu mixed phase on a Ti mesh contributed to the formation of a three-dimensional porous Cu-doped metallic Ni coating. Owing to the large specific surface area and enhanced electroconductivity caused by the porous structure and Cu doping, respectively, the developed Ni(Cu) coating/TM exhibited superior hydrazine sensing performance and electrocatalytic activity toward hydrogen evolution reaction (HER). The Ni(Cu) coating/TM electrode presented a good sensitivity of 3909µA mM-1cm-2and two relatively broad linear ranges from 0.004 mM to 2.915 mM and from 2.915 mM to 5.691 mM as well as a low detection limit of 1.90µM. In addition, the Ni(Cu) coating/TM required a relatively low HER overpotential of 140 mV to reach -10 mA cm-2and exhibited robust durability in alkaline solution. The excellent hydrazine electrooxidation and HER performance guarantee its promising application in hydrazine detection and energy conversion.

Iron reduction and diopside-based glass ceramic preparation based on mineral carbonation of steel slag.

In this article, a new process for treating steel slag and CO2 simultaneously and preparing calcium carbonate, metallic iron, and glass ceramics without wastewater or gas production is proposed. The reduction of iron and preparation of diopside glass ceramics are studied in this paper, and the results show that the carbon thermal reduction product of the original slag does not reach its melting point, and the slag and iron are well separated in the samples containing the leached steel slag and added silica. Part of the parent glass is converted into a glass ceramic after heat treatment, and the crystalline phases of samples are melilite, diopside, and partial melilite, and diopside and anorthite, respectively. The crystallization activation energy of the best sample in this article is E = 660.664 kJ/mol. The Avrami indices calculated at different heating rates are all less than 3, which indicates that the crystallization mode of the glass involves surface crystallization. This finding is consistent with the results for the prepared glass ceramics.

Visible-Light-Driven Photocatalytic Activity of Magnetic BiOBr/SrFe12O19 Nanosheets.

Magnetic BiOBr/SrFe12O19 nanosheets were successfully synthesized using the hydrothermal method. The as-prepared samples were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), and UV-visible diffused reflectance spectra (UV-DRS), and the magnetic properties were tested using a vibration sample magnetometer (VSM). The as-produced composite with an irregular flaky-shaped aggregate possesses a good anti-demagnetization ability (Hc = 861.04 G) and a high photocatalytic efficiency. Under visible light (λ > 420 nm) and UV light-emitting diode (LED) irradiation, the photodegradation rates of Rhodamine B (RhB) using BiOBr/SrFe12O19 (5 wt %) (BOB/SFO-5) after 30 min of reaction were 97% and 98%, respectively, which were higher than that using BiOBr (87%). The degradation rate of RhB using the recovered BiOBr/5 wt % SrFe12O19 (marked as BOB/SFO-5) was still more than 85% in the fifth cycle, indicating the high stability of the composite catalyst. Meanwhile, after five cycles, the magnetic properties were still as stable as before. The radical-capture experiments proved that superoxide radicals and holes were main active species in the photocatalytic degradation of RhB.

Design and synthesis of hierarchical NiO/Ni3V2O8 nanoplatelet arrays with enhanced lithium storage properties.

Hierarchical NiO/Ni3V2O8 nanoplatelet arrays (NPAs) grown on Ti foil were prepared as free-standing anodes for Li-ion batteries (LIBs) via a simple one-step hydrothermal approach followed by thermal treatment to enhance Li storage performance. Compared to the bare NiO, the fabricated NiO/Ni3V2O8 NPAs exhibited significantly enhanced electrochemical performances with superior discharge capacity (1169.3 mA h g-1 at 200 mA g-1), excellent cycling stability (570.1 mA h g-1 after 600 cycles at current density of 1000 mA g-1) and remarkable rate capability (427.5 mA h g-1 even at rate of 8000 mA g-1). The excellent electrochemical performances of the NiO/Ni3V2O8 NPAs were mainly attributed to their unique composition and hierarchical structural features, which not only could offer fast Li+ diffusion, high surface area and good electrolyte penetration, but also could withstand the volume change. The ex situ XRD analysis revealed that the charge/discharge mechanism of the NiO/Ni3V2O8 NPAs included conversion and intercalation reaction. Such NiO/Ni3V2O8 NPAs manifest great potential as anode materials for LIBs with the advantages of a facile, low-cost approach and outstanding electrochemical performances.

Mineralogical characterisation and magnetic separation of vanadium-bearing converter slag.

The recycling of metallic iron is commonly the first step to fully use the converter slag, which is the biggest waste discharge in the steelmaking process. This study presents a proposed improved process of separating metallic iron from vanadium-bearing converter slag more efficiently. The mineralogical and morphological characteristics of the converter slag were first investigated, and the results showed that most of the iron was incorporated in the spinel and olivine. Grinding, sieving and magnetic separation were combined to recover metallic iron from the converter slag, and yielded approximately 41.5% of iron in which the iron content was as high as 85%, and the non-magnetic concentrate contains 8.56% vanadium with a yield of 95.3% and 8.63% titanium with a yield of 85.3%. The magnetic part can be used as the raw materials in the steel making process, whereas the non-magnetic part can be used as the raw materials for the further extraction of vanadium.