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The present study was reported with synthesize of copper oxide nanoparticles by ethno botanical species. Bio convivial and compatible approaches were made to utilize the renewable source of leaves extract of Achyranthes aspera Linn as efficient capping and stabilizing agent as well. Also, natural A. aspera was functioned as reductant in the formation of CuO NPs. The phytosynthesized CuO nanoparticles were extensively characterized by X-ray diffraction analysis, Fourier transform infrared spectroscopy, Scanning electron microscopy, Energy dispersive X-ray diffraction, High resolution tunnelling electron microscopy and also comprehensively examined their biological applications like antibacterial and antifungal susceptibility against E. lenta, E. aerogenes and C. albicans strains. An XRD result of prepared CuO nanoparticles reveals the monoclinic crystalline structure and average crystallite size of 11–16 nm. The morphology variations for different concentrations of precursor material were noticed by SEM image. Furthermore, the crystalline planes found in SAED pattern of synthesized CuO NPs were coincide to the analysed XRD spectra. In the present study, a novel green approach was used to synthesize of CuO NPs for the antibacterial activity of poorly characterized and emerging pathogens of E. lenta and E. aerogenes. Further, the physicochemical, morphological and biological properties of CuO NPs are discussed. [ABSTRACT FROM AUTHOR]

BiSb nanoparticles were synthesized by solvothermal method. The synthesized material having a trigonal structure with space group R3m was confirmed through X-ray diffraction pattern. The Williamson-Hall method was employed to analyze the lattice stress and micro-strain produced in the BiSb nanoparticles. On the prepared material surface morphology studies were carried out using HR-SEM with EDXA. UV-visible absorption spectrum shows a wide absorption peak at 287 nm and the estimated band gap value is at Eg = 1.6 eV (from Tauc plot). The values of remanent polarization Pr = 0.156 μC/cm2, saturation polarization Ps = 0.253 μC/cm2, and coercive electric field Ec = 13.5 kV/cm obtained from the loop were close to the value. The BiSb nanoparticles exhibit semi-metallic-reported characteristics. This material is useful for thermoelectric power generation applications. [ABSTRACT FROM AUTHOR]

Development of new superparamagnetic materials with narrow size distribution is crucial for biomedical and environmental applications. Hence, we report the synthesis of narrow size distributed single grain MnFe2O4 nanoparticles of average particle size 9 nm by solvothermal reflux method. Synthesized compound crystallized in face centered cubic spinel structure and is confirmed by X-ray diffraction profiles. Transmission electron micrograph shows narrow size distributed particles with an average particle size of 9 nm and is equal to crystallite diameter estimated from Scherrer equation. The spinel crystal structure is further confirmed by electron diffraction profiles, Fourier transformed infrared spectrum, and Raman spectrum at room temperature. Magnetic properties of the sample show superparamagnetic nature at room temperature with moderate saturated magnetization of 56.4 emug−1. Magnetic heating properties of nanoparticles dispersion show the attainment of hyperthermia temperature (43 °C) in a short span of time of 1.6 min for 2 mg/mL and 2.6 min for 1 mg/mL concentrations. Estimated specific heat generation rate or specific power absorption rate, from temporal temperature plots, is 145.78 Wg−1 and is useful for magnetic hyperthermia application in cancer therapy. Photocatalysis properties of sample show 96% of rhodamine B dye degradation in little less than 6 h under UV light irradiation and are useful for photocatalytic applications in wastewater treatment in industries. [ABSTRACT FROM AUTHOR]