Suchergebnisse

Atomistic simulations have revealed an unconventional behavior of point defects at interfaces found in multilayer composites synthesized by physical vapor deposition but the observed mechanisms that involve point-defect annihilation are subject to time-scale limitations. So, a mathematical model that describes long-term evolution of point defects in such materials under irradiation is presented in this work. Firstly, the effect of interface point-defect trapping and recombination mechanisms on point-defect concentrations has been studied. In addition, the effect of interface self-interstitial atoms loading, which has been seen during collision cascades, and constitutional vacancies has been studied too. Two interface configurations have been considered between metals in a β-α-β three-layer system (α = Cu and β = Nb, or V), KSmin and KS1. These interfaces correspond to ground-state and defect-free KS structures respectively. The respond to irradiation of the systems investigated here, Cu/Nb and Cu/V, depends on both, interface characteristics and bulk properties. Nonetheless, the influence of the properties of one metal in the point-defect evolution of the other metal is only effective if there are constitutional vacancies at the interface, i.e., for KSmin. Especial attention has been paid to the behavior of the same metal (Cu) when it is surrounded by diverse metals (Nb, or V) with the aim of comparing quantitatively our model predictions with experimental results reported elsewhere. The lower concentration of vacancies in Cu layer of Cu/Nb system at steady state is due to the low mobility of vacancies in niobium. ; European Social Fund, Operational Programme of Castilla y León, and Junta de Castilla y León, through the Ministry of Education, as well as by the European Union Framework Programme 7, Multiscale Modelling and Materials by Design of Interface-Controlled Radiation Damage in Crystalline Materials (RADINTERFACES) under grant agreement no. 263273

AbstractSynthesis of silver nanoparticles (Ag NPs) using microalgae is gaining recognition for its environmentally friendly and cost-effective nature while maintaining high activity of NPs. In the present study, Ag NPs were synthesized using a methanolic extract of Chlorella vulgaris and subjected to calcination. The X-ray diffraction (XRD) analysis showed a crystalline nature of the products with Ag2O and Ag phases with an average crystalline size of 16.07 nm before calcination and an Ag phase with 24.61 nm crystalline size after calcination. Fourier transform infrared spectroscopy (FTIR) revealed the capping functional groups on Ag NPs, while scanning electron microscopy (SEM) displayed their irregular morphology and agglomeration after calcination. The organic coating was examined by energy-dispersive X-ray spectroscopy (EDX) and thermogravimetric (TGA) analyses, confirming the involvement of the metabolites. The UV–Vis analysis showed a difference in optical properties due to calcination. Synthesized Ag NPs were applied for the photodegradation of hazardous dye Brilliant Blue R in visible light. Different values of light intensity, catalyst dose, initial dye concentration, and pH were tested to identify the optimal set of operating conditions. The highest degradation efficiency of 90.6% with an apparent rate constant of 0.04402 min−1 was achieved after 90 min of irradiation in the highest tested catalyst dosage.