A novel experimental method for in situ strain measurement during selective laser melting

Selective laser Melting (SLM), a powder bed-based additive manufacturing technology, has been developed and applied in multiple industrial fields in the last decade. However, the distortion and swelling in the SLM process resulting from thermal stress cannot be predicted subject to measurement. In this work, an in situ distortion measurement system applied to the SLM process is presented. The distortion behaviour of component under laser scanning can be precisely recorded in real-time by this system. The detailed evolution and driving force of specimen distortion in the SLM process are discussed based on the experimental results. The distortion in single laser scanning presents a strong instantaneous upward motion of the central section during laser heating and a relatively slow downward recovery motion of the central section during cooling. The distortion behaviour of the sample with and without a layer of metal powder are compared, and laser scanning on the bare sample surface leads to a significantly higher residual distortion. The influence of SLM parameter variables (such as scanning speed, laser power, scanning width, layer thickness and scanning times) on SLM distortion is also analysed. At last, the stress distribution of laser melting is verified by the high-resolution EBSD analysis

A highly active hydrogen evolution electrocatalyst based on a cobalt–nickel sulfide composite electrode

A novel Co9S8–NixSy/Ni foam composite material was synthesized through the thermal decomposition of a cobalt–thiourea molecular precursor onto a 3D metallic support. The obtained electrode exhibited good activity toward the hydrogen evolution reaction in an alkaline medium, requiring a small overpotential of 163 mV at a current density of 10 mA cm?2, which is one of the lowest ever reported among transition metal sulfide materials

The effect of crystallinity on photocatalytic performance of Co3O4 water-splitting cocatalysts

Cocatalysts, when loaded onto a water splitting photocatalyst, accelerate the gas evolution reaction and improve the efficiency of the photocatalyst. In this paper, we report that the efficiency of the photocatalyst is enhanced using an amorphous cobalt oxide cocatalyst. The WO3 film, when loaded with amorphous or nanocrystalline Co3O4, shows an improvement of up to 40% in photocurrent generation and 34% in hydrogen gas evolution. The effect of cocatalyst crystallinity on performance was systematically studied, and we found that the photocurrent deteriorates with the conversion of the cocatalyst to a highly crystalline phase at an annealing temperature of 500 degrees C. The mechanism of this effect was studied in detail using electrochemical impedance spectroscopy, and the enhancement effect produced by the amorphous cocatalyst is attributed to the large density of unsaturated catalytically active sites in the amorphous material

Effect of La-Doping on optical bandgap and photoelectrochemical performance of hematite nanostructures

© the Partner Organisations 2014.La-doped hematite nanotubes are fabricated by electrospinning of a sol-gel solution consisting of La(iii) acetylacetonate hydrate/polyvinylpyrrolidone(PVP)/ferric acetylacetonate, and subsequent sintering at 500 °C for 5 h in air. Further grinding of these nanotubes affords La-doped hematite nanoparticles. FESEM EDX indicates that the La content is 3.66 mol% in La-doped hematite. HRTEM and XRD reveal that La3+ cations are doped into the hematite crystal lattice. UV-Vis diffuse reflectance shows increased light absorption for La-doped hematite, with the bandgap reduced from 2.58 eV to 2.46 eV. EIS and four-probe characterization demonstrate that La-doping reduces charge transfer resistance and increases the electrical conductivity, thus leading to improved charge transportation. Photoelectrochemical (PEC) water splitting studies show that under 100 mW cm-2 simulated solar irradiation, La-doped hematite nanoparticles demonstrate a net photocurrent density up to 0.112 and 0.270 mA cm-2 at 1.23 and 1.60 V vs. RHE, which are 187% and 63% higher than pristine hematite nanoparticles, respectively. The effect of La-doping on improving electrical conductivity, light absorption, and PEC performance is mainly attributed to the intensification of crystal orientation along the (110) plane and the lattice expansion caused by the La3+ cations, which have much larger radii and are more electron-rich than Fe3+.Link_to_subscribed_fulltex

Aqueous synthesis, doping, and processing of n-type Ag₂Se for high thermoelectric performance at near-room-temperature

Herein, we have successfully synthesized binary Ag2Se, composite Ag0:Ag2Se, and ternary Cu+:Ag2Se through an ambient aqueous-solution-based approach in a one-pot reaction at room temperature and atmospheric pressure without involving high-temperature heating, multiple-processes treatment, and organic solvents/surfactants. Effective controllability over phases and compositions/components are demonstrated with feasibility for large-scale production through an exquisite alteration in reaction parameters especially pH for enhancing and understanding thermoelectric properties. Thermoelectric ZT reaches 0.8-1.1 at near-room-temperature for n-type Ag2Se and Cu+ doping further improves to 0.9-1.2 over a temperature range of 300-393 K, which is the largest compared to that reported by wet chemistry methods. This improvement is related to the enhanced electrical conductivity and the suppressed thermal conductivity due to the incorporation of Cu+ into the lattice of Ag2Se at very low concentrations (x%Cu+:Ag2Se, x = 1.0, 1.5, and 2.0).Agency for Science, Technology and Research (A*STAR)The authors acknowledge financial support from the A*STAR SERC PHAROS program under grant number 1527200023

Amorphous ruthenium nanoparticles for enhanced electrochemical water splitting

© 2015 IOP Publishing Ltd.This paper demonstrates an optimized fabrication of amorphous Ru nanoparticles through annealing at various temperatures ranging from 150 to 700 °C, which are used as water oxidation catalyst for effective electrochemical water splitting under a low overpotential of less than 300 mV. The amorphous Ru nanoparticles with short-range ordered structure exhibit an optimal and stable electrocatalytic activity after annealing at 250 °C. Interestingly, a small quantity of such Ru nanoparticles in a thin film on fluorine-doped tin oxide glass is also effectively driven by a conventional crystalline silicon solar cell that has excellent capability for harvesting visible light. Remarkably, it achieves an overall solar-to-hydrogen efficiency of 11.3% in acidic electrolyte.Link_to_subscribed_fulltex

Cu(I)/Cu(II) Creutz-Taube Mixed-Valence 2D Coordination Polymers

Graphene-like two-dimensional (2D) coordination polymers (GCPs) have been of central research interest in recent decades with significant impact in many fields. According to classical coordination chemistry, Cu(II) can adopt the dsp2 hybridization to form square planar coordination geometry, but not Cu(I); this is why so far, there has been no 2D layered structures synthesized from Cu(I) precursors. Herein we report a pair of isostructural GCPs synthesized by the coordination of benzenehexathiol (BHT) ligands with Cu(I) and Cu(II) ions, respectively. Various spectroscopic characterizations indicate that Cu(I) and Cu(II) coexist with a near 1:1 ratio in both GCPs but remain indistinguishable with a fractional oxidation state of +1.5 on average, making these two GCPs a unique pair of Creutz-Taube mixed-valence 2D structures. Based on DFT calculations, we further uncovered an intramolecular pseudo-redox mechanism whereby the radicals on BHT ligands can oxidize Cu(I) or reduce Cu(II) ions upon coordination, thus producing isostructures yet with distinct electron configurations. For the first time, we demonstrate that using Cu(I) or Cu(II), one can achieve atomically isostructural 2D structures, indicating that a neutral periodic structure can host a different number of total electrons as ground states, which may open a new chapter for 2D materials