scholarly journals Green synthesis of single phase hausmannite Mn3O4 nanoparticles via Aspalathus linearis natural extract

2021 ◽  
Vol 3 (5) ◽  
Author(s):  
A. Diallo ◽  
N. Tandjigora ◽  
S. Ndiaye ◽  
Tariq Jan ◽  
I. Ahmad ◽  
...  

Abstract Nowadays, green synthesis of nanoparticles using plant precursors has been extensively studied. However, less attention has been given to Mn3O4. This contribution validates the synthesis of single-phase Hausmannite Mn3O4 nanoparticles by a green approach without using any standard acid/base compounds, surfactants, and organic/inorganic dissolving agents. The chemical chelation of the Mn precursor was performed via bioactive compounds of the Aspalathus Linearis’ extract, an African indigenous plant. Annealing at 400 °C for ~ 1 h was required to crystallize the small amorphous nanoparticles with an initial bimodal size distribution peaking at $$\left\langle {\phi_{1} } \right\rangle$$ ϕ 1  ~ 4.21 nm and $$\left\langle {\phi_{2} } \right\rangle$$ ϕ 2  ~ 8.51 nm respectively. Such annealing lead to increase in the diameter of the nanoparticles from 17 to 28 nm.The morphological, structural, vibrational, surface, and photoluminescence properties of the single-phase Hausmannite nanoparticles were comprehensively investigated by High Resolution Transmission Electron Microscopy(HRTEM),Energy Dispersive X-ray Spectroscopy (EDS), X-ray Diffraction (XRD), Raman and X-rays Photoelectron Spectroscopy (XPS), spectroscopy as well as room temperature photoluminescence. Structural and morphological investigations revealed the formation of quasi-spherical nanoparticles having a single phase Hausmannite Mn3O4 crystal structure. XPS results also validated the XRD results about the formation of Hausmannite Mn3O4 nanoparticles. Raman investigations allowed a crystal-clear distinction between the Mn3O4 nature of the nanoparticles from the potential γ -Mn2O3 phase as both phases belong to the same space group and both assume tetragonally-distorted cubic lattices of nearly similar dimensions. The optical studies of the single phase Hausmannite crystalline nanoparticles exhibited a broad photoluminescence in the spectral range of 300–700 nm, which is ideal for emission devices. Graphic abstract

2020 ◽  
Vol 2020 ◽  
pp. 1-12
Author(s):  
Xuan Nui Pham ◽  
Hoa Thi Nguyen ◽  
Ngan Thi Pham

In recent years, the green synthesis of nanoparticles via biological processes has attracted considerable attention. Herein, we introduce a facile and green approach for the synthesis of poriferous silver nanoparticles (Ag-NPs) decorated hydroxylapatite (HAp@Ag) nanoparticles with excellent antibacterial properties. All the nanocomposites were fully characterized in the solid state via various techniques such as X-ray powder diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), and energy-dispersive X-ray spectrometer (EDX), in which the synthesized Ag-NPs (24 nm in diameter) and their homogeneous incorporation on HAp have been studied by ultraviolet-visible (UV-vis) technique, transmission electron microscopy (TEM), and dynamic light scattering (DLS) analysis. The obtained results indicate that the structure and morphology of HAp have no significant changes after the incorporation of Ag-NPs on its surface. Moreover, an impressive antibacterial activity of HAp@Ag nanocomposite against Gram-positive bacterium Staphylococcus aureus and Gram-negative bacteria Escherichia coli and Pseudomonas aeruginosa has been recorded by using the agar well diffusion method. As a result, the HAp@Ag nanocomposite promises to be a great biomedical material with high antibacterial properties.


Nano Research ◽  
2021 ◽  
Author(s):  
Alevtina Smekhova ◽  
Alexei Kuzmin ◽  
Konrad Siemensmeyer ◽  
Chen Luo ◽  
Kai Chen ◽  
...  

AbstractModern design of superior multi-functional alloys composed of several principal components requires in-depth studies of their local structure for developing desired macroscopic properties. Herein, peculiarities of atomic arrangements on the local scale and electronic states of constituent elements in the single-phase face-centered cubic (fcc)- and body-centered cubic (bcc)-structured high-entropy Alx-CrFeCoNi alloys (x = 0.3 and 3, respectively) are explored by element-specific X-ray absorption spectroscopy in hard and soft X-ray energy ranges. Simulations based on the reverse Monte Carlo approach allow to perform a simultaneous fit of extended X-ray absorption fine structure spectra recorded at K absorption edges of each 3d constituent and to reconstruct the local environment within the first coordination shells of absorbers with high precision. The revealed unimodal and bimodal distributions of all five elements are in agreement with structure-dependent magnetic properties of studied alloys probed by magnetometry. A degree of surface atoms oxidation uncovered by soft X-rays suggests different kinetics of oxide formation for each type of constituents and has to be taken into account. X-ray magnetic circular dichroism technique employed at L2.3 absorption edges of transition metals demonstrates reduced magnetic moments of 3d metal constituents in the sub-surface region of in situ cleaned fcc-structured Al0.3-CrFeCoNi compared to their bulk values. Extended to nanostructured versions of multicomponent alloys, such studies would bring new insights related to effects of high entropy mixing on low dimensions.


2020 ◽  
Vol 62 (7) ◽  
pp. 1123
Author(s):  
Е.В. Богданов ◽  
Е.И. Погорельцев ◽  
А.В. Карташев ◽  
М.В. Горев ◽  
М.С. Молокеев ◽  
...  

Abstract The (NH_4)_3VOF_5 crystals have been synthesized and their homogeneity and single-phase structure has been established by the X-ray diffraction, energy dispersive spectroscopy, and X-ray photoelectron spectroscopy studies. The investigations of the temperature dependences of specific heat, entropy, strain, and pressure susceptibility show the occurrence of three phase transitions caused by the structural transformations in the (NH_4)_3VOF_5 crystals. The T – p phase diagram shows the temperature limits of stability of the crystalline phases implemented in (NH_4)_3VOF_5. The optical and dielectric studies disclose the ferroelastic nature of the phase transitions. An analysis of the experimental data together with the data on the isostructural (NH_4)_3VO_2F_4 crystal makes it possible to distinguish the physical properties of oxyfluorides containing vanadium of different valences (IV and V).


Coatings ◽  
2020 ◽  
Vol 10 (7) ◽  
pp. 659 ◽  
Author(s):  
Marcela Elisabeta Barbinta-Patrascu ◽  
Camelia Ungureanu ◽  
Nicoleta Badea ◽  
Mihaela Bacalum ◽  
Andrada Lazea-Stoyanova ◽  
...  

The objective of the present study is the valorization of natural resources and the recycling of vegetal wastes by converting them into novel plasmonic bio-active hybrids. Thus, a “green” approach was used to design pectin-coated bio-nanosilver. Silver nanoparticles were generated from two common garden herbs (Mentha piperita and Amaranthus retroflexus), and pectin was extracted from lemon peels. The samples were characterized by the following methods: Ultraviolet–visible (UV-Vis) absorption spectroscopy, Fourier Transform Infrared (FT-IR), X-ray Diffraction (XRD), X-ray Photoelectron Spectroscopy (XPS), dynamic light scattering (DLS), Atomic Force Microscopy (AFM), Scanning Electron Microscopy (SEM)–Energy-dispersive X-ray Spectroscopy (EDX), and zeta potential measurements. Microscopic investigations revealed the spherical shape and the nano-scale size of the prepared biohybrids. Their bioperformances were checked in terms of antioxidant and antibacterial activity. The developed plasmonic materials exhibited a strong ability to scavenge short-life (96.1% ÷ 98.7%) and long-life (39.1% ÷ 91%) free radicals. Microbiological analyses demonstrated an impressive antibacterial effectiveness of pectin-based hybrids against Escherichia coli. The results are promising, and the obtained biomaterials could be used in many bio-applications, especially as antioxidant and antimicrobial biocoatings.


2014 ◽  
Vol 32 (4) ◽  
pp. 702-708 ◽  
Author(s):  
M. Behera ◽  
G. Giri

AbstractHerein, we report a facile green synthesis of Cu2O nanoparticles (NPs) using copper sulfate as precursor salt and hydrazine hydrate as reducing agent in presence of bio-surfactant (i.e. leaves extract of arka — a perennial shrub) at 60 to 70 °C in an aqueous medium. A broad band centered at 460 nm in absorption spectrum reveals the formation of surfactant stabilized Cu2O NPs. X-ray diffraction pattern of the surfactant stabilized NPs suggests the formation of only Cu2O phase in assistance of a bio-surfactant with the crystallite size of ∼8 nm. A negative zeta potential of −12 mV at 8.0 pH in surfactant stabilized Cu2O NPs hints non-bonding electron transfer from O-atom of saponin to the surface of NP. Red-shift in the vibrational band (Cu-O stretching) of Cu2O from 637 cm−1 to 640 cm−1 in presence of bio-surfactant suggests an interfacial interaction between NPs and O-atoms of -OH groups of saponin present in the plant (i.e. Calotropis gigantean) extract. From X-ray photoelectron spectroscopy spectra, a decrease in binding energy of both 2p3/2 and 2p1/2 bands in Cu2O with saponin molecules as compared to bulk Cu atom reveals a charge transfer interaction between NP and saponin surfactant molecules. Transmission electron microscopy images show crystalline nature of Cu2O NPs with an fcc lattice.


1997 ◽  
Vol 04 (05) ◽  
pp. 919-922 ◽  
Author(s):  
A. FANELSA ◽  
R. SCHELLENBERG ◽  
F. U. HILLEBRECHT ◽  
E. KISKER

Magnetic dichroism has been observed in the angular distribution of p-core level photoemission spectra excited from crystalline ferromagnets by unpolarized X-rays. The angular dependence of the angular and energy-resolved photoemission intensity was recorded as a function of the emission direction with respect to the crystal, revealing a strong variation of the magnetic dichroism with emission angle due to photoelectron diffraction. This variation is particularly strong around the forward scattering peaks, including sign reversals close to these directions. The results demonstrate that any standard X-ray photoelectron spectroscopy apparatus possesses the potential for combined analysis of surface magnetic structure and geometric structure in a chemically specific way.


2009 ◽  
Vol 24 (8) ◽  
pp. 2483-2498 ◽  
Author(s):  
Axel Flink ◽  
Manfred Beckers ◽  
Jacob Sjölén ◽  
Tommy Larsson ◽  
Slawomir Braun ◽  
...  

(Ti1–xSix)Ny (0 ≤ x ≤ 0.20; 0.99 ≤ y(x) ≤ 1.13) thin films deposited by arc evaporation have been investigated by analytical transmission electron microscopy, x-ray diffraction, x-ray photoelectron spectroscopy, and nanoindentation. Films with x ≤ 0.09 are single-phase cubic (Ti,Si)N solid solutions with a dense columnar microstructure. Films with x > 0.09 have a featherlike microstructure consisting of cubic TiN:Si nanocrystallite bundles separated by metastable SiNz with coherent-to-semicoherent interfaces and a dislocation density of as much as 1014 cm−2 is present. The films exhibit retained composition and hardness between 31 and 42 GPa in annealing experiments to 1000 °C due to segregation of SiNz to the grain boundaries. During annealing at 1100–1200 °C, this tissue phase thickens and transforms to amorphous SiNz. At the same time, Si and N diffuse out of the films via the grain boundaries and TiN recrystallize.


2010 ◽  
Vol 1250 ◽  
Author(s):  
Xinghua Wang ◽  
Sarjoosing Goolaup ◽  
Peng Ren ◽  
Wen Siang Lew

AbstractThin films of magnetite (Fe3O4) are grown on a single-crystal Si/SiO2 (100) substrate with native oxide using DC reactive sputtering technique at room tempreture (RT) and 300C. The x-ray diffraction(XRD) result shows the thermal energy during deposition enhances the crystallization of the Fe3O4 and x-ray photoelectron spectroscopy confirms the film deposited at 300C is single-phase Fe3O4 while the film deposited at RT is mostly ν-Fe2O3. The electrical measurements show that the resistivity of the Fe3O4 film increases exponentially with decreasing temperature, and exhibit a sharp metal-insulator transition at around 100 K, indicating the Verwey transition feature. The saturation magnetization Ms of Fe3O4 film measured by vibrating sample measurement (VSM) at RT was found to be 445 emu/cm3.


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