Comparison of Corrosion Performance of Extruded and Forged WE43 Mg Alloy.

Adjusting the microstructure through the deformation process is one of the ways to improve the properties of Mg alloys. Most studies have focused on the influence of the microstructure after deformation treatment on the mechanical properties of Mg alloys. In this paper, extruded and forged Mg-Gd-Y-Nd-Zr alloys were selected to investigate the corrosion performance of two deformed magnesium alloys immersed in 0.6 M NaCl solution using a hydrogen evolution test, a weight loss test, an immersion experiment, and an electrochemical test. The results showed that WE43 alloys undergoing different deformation treatments presented different microstructures, which led to different corrosion behaviors and corrosion resistance. The extruded WE43 alloy showed uniform corrosion, while the forged WE43 alloy suffered severe local galvanic corrosion. Meanwhile, the corrosion rate of the forged WE43 alloy was about four times faster than that of the extruded WE43 alloy.

Microgalvanic Corrosion of Mg-Ca and Mg-Al-Ca Alloys in NaCl and Na2SO4 Solutions.

As a kind of potential biomedical material, Mg-Ca alloy has attracted much attention. However, the role of Ca-containing intermetallics in microgalvanic corrosion is still controversial. In 0.6 mol/L NaCl and Na2SO4 solutions, the microgalvanic corrosion behavior of the second phase and Mg matrix of Mg-Ca and Mg-Al-Ca alloys was examined. It was confirmed that the Mg2Ca phase acts as a microanode in microgalvanic corrosion in both NaCl and Na2SO4 solutions, with the Mg matrix acting as the cathode and the Al2Ca phase acting as the microcathode to accelerate corrosion of the adjacent Mg matrix. It was also found that Cl- and SO42- have different sensibilities to microgalvanic corrosion.

Fe-Ion-Catalyzed Synthesis of CdSe/Cu Core/Shell Nanowires.

CdSe/Cu core/shell nanowires (NWs) are successfully synthesized by a wet chemical method for the first time. By utilizing the solution-liquid-solid (SLS) mechanism, CdSe NWs are fabricated by Bi seeds, which act as catalysts. In the subsequent radial overcoating of the Cu shell on the CdSe NWs, Fe ions have been proven to be an indispensable and efficient catalyzer. The thickness of the Cu shell could be well controlled in the range of 3 to 6 nm by varying the growth temperature (from 300 to 360 °C). Our synthetic strategy pioneers a new possibility for the controlled synthesis of semiconductor-metal heterostructure NWs (especially for II-VI semiconductors), such as CdS/Cu, ZnS/Au, and ZnO/Ag, which had broad application prospects in photoconductors, thin-film transistors, and light-emitting diodes. Theoretically, electrons flow from a higher Fermi-level material to the bottom Fermi-level at the metal-semiconductor heterojunction interface, which aligns the Fermi level and establishes the Schottky barrier. It leads to excess negative charges in metals and excess positive charges in semiconductors. Therefore, those effective electron traps reduce the probability of photogenerated electron-hole pair recombination efficiently, which has been widely applied in solar cells, sensors, photocatalysis, and energy storage. The breakthrough and innovation of this synthesis method have opened up a new synthetic route with a mild reaction environment, low energy consumption, and convenience.

Recycling of Spent Pot Lining First Cut from Aluminum Smelters by Utilizing the Two-Step Decomposition Characteristics of Dolomite.

Spent Pot Lining First Cut (shortened to SPL-1cut) is a solid waste discharged from a primary aluminum electrolytic production process. SPL-1cut is classified as hazardous waste in China because it contains large amounts of soluble sodium fluoride and a tiny amount of cyanide. Most of SPL-1cut is carbon-about 65%-and its calorific value is 22.587 MJ∙kg-1. There is a high level of sodium fluoride in SPL-1cut-about 15%-and sodium fluoride is randomly distributed in the carbon granule. The recycling of SPL-1cut using dolomite as a reactant, based on the characteristics of the two-step decomposition of dolomite at a high temperature, is discussed. The recycling of SPL-1cut was performed under the following heating conditions: the heating temperature was 850 °C, the holding time was 120 min, and 40% of the dolomite was added to the SPL-1cut. It was found that the cyanides are completely oxidized and decomposed, and dolomite is decomposed into MgO and active CaCO3. At the same time, NaF reacts with active CaCO3 and converts into CaF2. The results provide references for using SPL-1cut as an alternative fuel in the dolomite calcination process of the Pidgeon Process.

CuInTe2 Nanocrystals: Shape and Size Control, Formation Mechanism and Application, and Use as Photovoltaics.

We report on the synthesis of CuInTe2 nanoparticles and their function in photovoltaic equipment, such as solar cells. Under certain synthesis conditions, the CuInTe2 nanocrystals form shape with nanocrystals, nanorods or nanocubes. It was found that CuTe nanocrystals could be converted to CuInTe2 by addition of an In reactant. CuInTe2 nanorods were synthesized using this method.

Sulfur-free synthesis of size tunable rickardite (Cu3-x Te2) spheroids and planar squares.

We report a novel synthesis of monodisperse samples of copper telluride with crystallinity and stoichiometry corresponding to forms of rickardite, Cu3-x Te2 (x < 1). This synthesis makes use of a ligand balanced reaction to allow control over shape and size by varying the relative and absolute concentration of oleylamine to stearic acid. The rickardite samples presented here display size dependent plasmon peaks in the near infrared and direct energy band gaps between 1.7 and 2.3 eV. As such they may find utility in photovoltaic, thermoelectric or as novel optical materials for study of surface plasmons.

Cation exchange synthesis of CuIn x Ga1-x Se2 nanowires and their implementation in photovoltaic devices.

CuIn x Ga1-x Se2 (CIGS) nanowires were synthesized for the first time through an in situ cation exchange reaction by using CuInSe2 (CIS) nanowires as a template material and Ga-OLA complexes as the Ga source. These CIGS nanowires maintain nearly the same morphology as CIS nanowires, and the Ga/In ratio can be controlled through adjusting the concentration of Ga-OLA complexes. The characteristics of adjustable band gap and highly effective light-absorbances have been achieved for these CIGS nanowires. The light-absorbing layer in photovoltaic devices (PVs) can be assembled by employing CIGS nanowires as a solar-energy material for enhancing the photovoltaic response. The highest power conversion efficiency of solar thin film semiconductors is more than 20%, achieved by the Cu(In x Ga1-x )Se2 (CIGS) thin-film solar cells. Therefore, these CIGS nanowires have a great potential to be utilized as light absorber materials for high efficiency single nanowire solar cells and to generate bulk heterojunction devices.