The influence of the electrode geometry on the microstructure and corrosion behaviour of Co-Mo nano-crystalline coatings elaborated by electrodeposition is studied. The corrosion behaviour was determined in the Ringer’s solution at 25°C. Electrodeposition mechanisms are also discussed as a function of the electrode geometry. The electrode geometry was found to affect the growth rate and, under certain conditions, the microstructure (existence of channels and pores). It does not have influence on the corrosion behaviour.
The effect of cationic, anionic and nonionic surface active additives, organic compounds and polymers on the electrodeposition of Zn-Mo coatings on steel substrate and detailed characterization in chosen optimal conditions was studied. The influence of polyethylene glycol (PEG) various concentration, sodium dodecyl sulphate (SDS), triton X-100, d-sorbitol, cetyl trimethyl ammonium bromide (CTAB), thiourea and disodium ethylenediaminetetraacetate (EDTA) on the electrodeposition process was examined. The composition of deposits was defined by wavelength dispersive X-ray fluorescence spectrometry (WDXRF). Results has shown that the current efficiency of the electrodeposition of Zn-Mo coatings is 71.4%, 70.7%, 66.7% for 1.5 g/dm3 PEG 20000, 0.1 g/dm3 Triton X-100 and 0.75 M D-sorbitol respectively. The surface topography and roughness of selected coatings on steel was investigated by atomic force microscopy (AFM). The attendance of D-sorbitol of 0.75 M in the solution cause clear reduction of grain size and the value of roughness parameter (Ra) in relation to SDS, PEG, Triton X-100 and the sample prepared without the additives. The morphology of electrodeposited layers was studied by scanning electron microscopy (SEM). The addition of selected additives to the electrolytic bath results in the formation of smoother, brighter and more compact Zn-Mo coatings in comparison to layers obtained from similar electrolytes but without the addition of surfactants. The optimal concentration of the most effective additives such as PEG 20000, Triton X-100 and D-sorbitol is 1.5 g/dm3, 0.1 g/dm3, 0.75 M respectively.
The influence on the corrosion behaviour of Co-Mo nano-crystalline coatings of dissolved oxygen is studied in the Ringer’s solution and artificial saliva at 25°C. This was done by means of potentiodynamic tests and surface observations. It was shown that dissolved oxygen has no influence on passivity, oxidation of the coating and selective dissolution of cobalt. By contrast, dissolved oxygen affects corrosion. General corrosion was observed in the Ringer’s solution whereas pitting corrosion was found in artificial saliva.
In this study, a molybdenum alloy with dispersed high-entropy particles was fabricated using the powder metallurgy method. The high-entropy powder, composed of Nb, Ta, V, W, and Zr elements with a same atomic fraction, was prepared via high-energy ball milling. Using this powder, an ideal core-shell powder, composed of high-entropy powder as core and Mo powder as shell, was synthesized via the milling and reduction processes. These processes enabled the realization of an ideal microstructure with the high-entropy phase uniformly dispersed in the Mo matrix. The sintered body was successfully fabricated via uniaxial compaction followed by pressureless sintering. The sintered body was analyzed by X-ray diffraction and scanning electron microscope, and the high-entropy phase is uniformly dispersed in the Mo matrix.
The subject of the study was the production and characterization of three ceramic-metal graded composites, which differed in addition of the metallic phase. The following composites systems were investigated: Al2O3-Mo, Al2O3-Cu, Al2O3-W. Composites were produced by centrifugal slip casting method. This technique combines the classic casting of the slurry into porous molds with the action of centrifugal force. As a result, sleeve-shaped shapes with a metallic phase gradient were obtained. X-ray phase analysis have not revealed new phases in the produced composites. The type of metallic phase and its distribution in the ceramic matrix influenced the hardness of the produced composites.
We demonstrated a tunable Q-switched ytterbium-doped fiber laser (YDFL) using MoWS2/rGO nanocomposite as passive saturable absorber. Further, the Mo1−xWxS2/rGO nanosheets, with x proportion of 0.2, are synthesized using hydrothermal exfoliation technique. The proposed nanocomposite-PVA based thin film is fabricated by mixing the MoWS2/rGO nanosheets with polyvinyl alcohol (PVA). The fabricated thin film is sandwiched between two fiber ferrules to realize the proposed saturable absorber (SA). Further, the proposed MoWS2/rGO-PVA based thin film SA exhibits a fast relaxation time and a high damage threshold which are suitable to realize a Q-switched pulsed laser with a tunable wavelength range of 10 nm that extends from 1028 nm to 1038 nm. For the highest pump power of 267.4 mW, the generated Q-switched pulses exhibit a narrow pulse width of 1.22 μs, the pulse repetition rate of 90.4 kHz, the highest pulse energy of 2.13 nJ and its corresponding average power of 0.193 mW. To the best of author’s knowledge, this is the first realization of a tunable Q-switching fiber laser in a 1 μm wavelength using MoWS2/rGO nanocomposite saturable absorber.