scholarly journals The Influence of the Electrodeposition Parameters on the Properties of Mn-Co-Based Nanofilms as Anode Materials for Alkaline Electrolysers

Materials ◽  
2020 ◽  
Vol 13 (11) ◽  
pp. 2662
Author(s):  
Karolina Cysewska ◽  
Maria Krystyna Rybarczyk ◽  
Grzegorz Cempura ◽  
Jakub Karczewski ◽  
Marcin Łapiński ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Nickel Foam ◽  
Catalytic Performance ◽  
X Ray ◽  
Synthesis Conditions ◽  
Β Phase ◽  
Metal Nitrates ◽  
Transmission Electron ◽  
Double Hydroxide

In this work, the influence of the synthesis conditions on the structure, morphology, and electrocatalytic performance for the oxygen evolution reaction (OER) of Mn-Co-based films is studied. For this purpose, Mn-Co nanofilm is electrochemically synthesised in a one-step process on nickel foam in the presence of metal nitrates without any additives. The possible mechanism of the synthesis is proposed. The morphology and structure of the catalysts are studied by various techniques including scanning electron microscopy, X-ray diffraction, X-ray photoelectron spectroscopy, and transmission electron microscopy. The analyses show that the as-deposited catalysts consist mainly of oxides/hydroxides and/or (oxy)hydroxides based on Mn2+, Co2+, and Co3+. The alkaline post-treatment of the film results in the formation of Mn-Co (oxy)hydroxides and crystalline Co(OH)2 with a β-phase hexagonal platelet-like shape structure, indicating a layered double hydroxide structure, desirable for the OER. Electrochemical studies show that the catalytic performance of Mn-Co was dependent on the concentration of Mn versus Co in the synthesis solution and on the deposition charge. The optimised Mn-Co/Ni foam is characterised by a specific surface area of 10.5 m2·g−1, a pore volume of 0.0042 cm3·g−1, and high electrochemical stability with an overpotential deviation around 330–340 mV at 10 mA·cm−2geo for 70 h.

scholarly journals Spinel-Type (FeCoCrMnZn)3O4 High-Entropy Oxide: Facile Preparation and Supercapacitor Performance

Materials ◽  
2020 ◽  
Vol 13 (24) ◽  
pp. 5798
Author(s):  
Bingliang Liang ◽  
Yunlong Ai ◽  
Yiliang Wang ◽  
Changhong Liu ◽  
Sheng Ouyang ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Nickel Foam ◽  
Spinel Type ◽  
X Ray ◽  
High Entropy ◽  
Transmission Electron ◽  
Coating Method ◽  
Potential Applications ◽  
Supercapacitor Performance

High-entropy oxides (HEOs) have attracted more and more attention because of their unique structures and potential applications. In this work, (FeCoCrMnZn)3O4 HEO powders were synthesized via a facile solid-state reaction route. The confirmation of phase composition, the observation of microstructure, and the analysis of crystal structure, distribution of elements, and valences of elements were conducted by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDS), and X-ray photoelectron spectroscopy (XPS), respectively. Furthermore, a (FeCoCrMnZn)3O4/nickel foam ((FeCoCrMnZn)3O4/NF) electrode was prepared via a coating method, followed by the investigation of its supercapacitor performance. The results show that, after calcining (FeCoCrMnZn)3O4 powders at 900 °C for 2 h, a single spinel structure (FCC, Fd-3m, a = 0.8399 nm) was obtained with uniform distribution of Fe, Co, Cr, Mn, and Zn elements, the typical characteristic of a high-entropy oxide. In addition, the mass specific capacitance of the (FeCoCrMnZn)3O4/NF composite electrode was 340.3 F·g−1 (with 1 M KOH as the electrolyte and 1 A·g−1 current density), which indicates that the (FeCoCrMnZn)3O4 HEO can be regarded as a prospective candidate for an electrode material in the field of supercapacitor applications.

scholarly journals Preparation of g-C3N4/MoS2 Composite Material and Its Visible Light Catalytic Performance

2021 ◽  
Author(s):  
Yu Fan ◽  
Yan-ning Yang ◽  
Chen Ding
Keyword(s):  
Electron Microscopy ◽  
Photocatalytic Activity ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
Photogenerated Electron ◽  
Catalytic Performance ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Calcination Method

Abstract The g-C3N4 nanosheet was prepared by calcination method, the MoS2 nanosheet was prepared by hydrothermal method. The g-C3N4/MoS2 composites were prepared by ultrasonic composite in anhydrous ethanol. X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), ultraviolet-visible spectroscopy (UV-Vis), and photoluminescence (PL) techniques were used to characterize the materials. The photocatalytic degradation of Rhodamine B (Rh B) by g-C3N4/MoS2 composites with different mass ratios was investigated under visible light. The results show that a small amount of MoS2 combined with g-C3N4 can significantly improve photocatalytic activity. The g-C3N4/MoS2 composite with a mass ratio of 1:8 has the highest photocatalytic activity, and the degradation rate of Rh B increases from 50% to 99.6%. The main reason is that MoS2 and g-C3N4 have a matching band structure. The separation rate of photogenerated electron-hole pairs is enhanced. So the g-C3N4/MoS2 composite can improve the photocatalytic activity. The photocatalytic mechanism was proposed through the active matter capture experiment.

scholarly journals The Preparation of Pd/Foam-Ni Electrode and Its Electrocatalytic Hydrodechlorination for Monochlorophenol Isomers

Catalysts ◽  
2018 ◽  
Vol 8 (9) ◽  
pp. 378 ◽  
Author(s):  
Junjing Li ◽  
Huan Wang ◽  
Liang Wang ◽  
Chang Ma ◽  
Cong Luan ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Catalytic Performance ◽  
Order Kinetic ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Order Kinetic Model ◽  
Good Catalytic Activity ◽  
Promising Application

Noble metal palladium modified foamed nickel electrode (Pd/foam-Ni) was prepared by electrodeposition method. The fabricated electrode showed better catalytic performance than the Pd/foam-Ni prepared by conventional electroless deposition. The catalysts were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). Electrocatalytic activity of the Pd/Ni was studied for the hydrodechlorination of monochlorophenol isomers. The Pd/Ni exhibited good catalytic activity for 3-chlorophenol (3-CP). Complete decomposition of chlorophenol isomers could be achieved within 2 h, and the hydrodechlorination process conformed to the pseudo-first-order kinetic model. It showed a supreme stability after recycling for 5 times. The Pd/Ni exhibited a promising application prospect with high effectiveness and low Pd loading.

scholarly journals Green Synthesis and Characterization of Carbon Nanotubes/Polyaniline Nanocomposites

2015 ◽  
Vol 2015 ◽  
pp. 1-9 ◽  
Author(s):  
Van Hoa Nguyen ◽  
Jae-Jin Shim
Keyword(s):  
Electron Microscopy ◽  
Carbon Nanotubes ◽  
Photoelectron Spectroscopy ◽  
Interfacial Polymerization ◽  
Nickel Foam ◽  
Green Solvents ◽  
X Ray ◽  
Transmission Electron ◽  
Two Phases

Carbon nanotubes/polyaniline (CNT/PANI) nanocomposites were synthesized by the interfacial polymerization of aniline in the presence of CNTs using two green solvents, water and an ionic liquid (1-butyl-3-methylimidazolium tetrafluoroborate, [bmim][BF4]), as the two phases. The formation and incorporation of PANI on the surface of the CNTs were confirmed by scanning electron microscopy, transmission electron microscopy, X-ray diffraction, Fourier transform infrared spectroscopy ultraviolet-visible spectroscopy, and X-ray photoelectron spectroscopy. The analyses showed that the surface of the CNTs was coated with different morphologies of thin PANI layers depending on whether a HCl or HNO3solution was used. The thermal stability of the composites was much better than that of the bare CNTs and pure PANI. The as-prepared composites were also used to modify the nickel foam electrodes for characterization of the electrochemical properties.

scholarly journals Selective Catalytic Reduction of NOx with NH3 over Mn2O3 supported with different morphology of CeO2 Catalysts

2021 ◽  
Author(s):  
Shyam Rao ◽  
VIVEK PATEL ◽  
Sweta Sharma
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Catalytic Reduction ◽  
Catalytic Performance ◽  
X Ray Diffraction ◽  
Wet Impregnation ◽  
X Ray ◽  
Nh3 Scr ◽  
Transmission Electron ◽  
Reduction Of Nox

Three different morphologies of CeO2 supports (NP, NC, and NR) were prepared by hydrothermal method and further Mn2O3 is impregnated on CeO2 supports using wet-impregnation methods, and their activity for NO reduction using NH3-SCR technique is analysed. The prepared catalysts and supports are further characterized through scanning electron microscopy (SEM), Energy-dispersive X-ray spectroscopy (EDX), X-ray diffraction (XRD), X-ray Photoelectron Spectroscopy (XPS), and transmission electron microscopy (TEM), and Brunauer–Emmett–Teller (BET). The catalytic performance of Mn2O3/CeO2-NP has shown the highest conversion (76.06 %) compared to the other two catalysts in the temperature range of 50 - 450°C.

scholarly journals Synthesis of Ce1−xPdxO2−δ Solid Solution in Molten Nitrate

Catalysts ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 640
Author(s):  
Hideaki Sasaki ◽  
Keisuke Sakamoto ◽  
Masami Mori ◽  
Tatsuaki Sakamoto
Keyword(s):  
Electron Microscopy ◽  
Solid Solution ◽  
Solid Solutions ◽  
Photoelectron Spectroscopy ◽  
Synthesis Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Co Precipitation ◽  
Ionic States

CeO2-based solid solutions in which Pd partially substitutes for Ce attract considerable attention, owing to their high catalytic performances. In this study, the solid solution (Ce1−xPdxO2−δ) with a high Pd content (x ~ 0.2) was synthesized through co-precipitation under oxidative conditions using molten nitrate, and its structure and thermal decomposition were examined. The characteristics of the solid solution, such as the change in a lattice constant, inhibition of sintering, and ionic states, were examined using X-ray diffraction (XRD), scanning electron microscopy–energy-dispersive X-ray spectroscopy (SEM−EDS), transmission electron microscopy (TEM)−EDS, and X-ray photoelectron spectroscopy (XPS). The synthesis method proposed in this study appears suitable for the easy preparation of CeO2 solid solutions with a high Pd content.

Characterization of columns grown during KrF laser micromachining of Al2O3–TiC ceramics

2003 ◽  
Vol 18 (5) ◽  
pp. 1123-1130 ◽  
Author(s):  
V. Oliveira ◽  
R. Vilar
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Laser Pulses ◽  
Formation Mechanisms ◽  
X Ray ◽  
Reducing Conditions ◽  
Transmission Electron ◽  
Column Formation ◽  
Krf Laser

This paper aims to contribute to the understanding of column formation mechanisms in Al2O3–TiC ceramics micromachined using excimer lasers. Chemical and structural characterization of columns grown in Al2O3–TiC composite processed with 200 KrF laser pulses at 10 J/cm2 was carried out by scanning electron microscopy, transmission electron microscopy, x-ray photoelectron spectroscopy, and x-ray diffraction analysis. Fully developed columns consist of a core of unprocessed material surrounded by an outer layer of Al2TiO5, formed in oxidizing conditions, and an inner layer, formed in reducing conditions, composed of TiC and Al3Ti or an AlTi solid solution. Possible mechanisms of column formation are discussed.

scholarly journals Green Synthesis of Feather-Shaped MoS2/CdS Photocatalyst for Effective Hydrogen Production

2013 ◽  
Vol 2013 ◽  
pp. 1-5 ◽  
Author(s):  
Yang Liu ◽  
Hongtao Yu ◽  
Xie Quan ◽  
Shuo Chen
Keyword(s):  
Electron Microscopy ◽  
Hydrogen Production ◽  
Photoelectron Spectroscopy ◽  
Diffuse Reflectance ◽  
Sulfur Source ◽  
X Ray ◽  
Transmission Electron ◽  
Microscopy Images ◽  
Effective Hydrogen ◽  
Better Than

MoS2/CdS photocatalyst was fabricated by a hydrothermal method for H2production under visible light. This method used low toxic thiourea as a sulfur source and was carried out at 200°C. Thus, it was better than the traditional methods, which are based on an annealing process at relatively high temperature (above 400°C) using toxic H2S as reducing agent. Scanning electron microscopy and transmission electron microscopy images showed that the morphologies of MoS2/CdS samples were feather shaped and MoS2layer was on the surface of CdS. The X-ray photoelectron spectroscopy testified that the sample was composed of stoichiometric MoS2and CdS. The UV-vis diffuse reflectance spectra displayed that the loading of MoS2can enhance the optical absorption of MoS2/CdS. The photocatalytic activity of MoS2/CdS was evaluated by producing hydrogen. The hydrogen production rate on MoS2/CdS reached 192 μmol·h−1. This performance was stable during three repeated photocatalytic processes.

scholarly journals Enhanced Photocatalytic Activity of Cu2O Cabbage/RGO Nanocomposites under Visible Light Irradiation

Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1712
Author(s):  
Appusamy Muthukrishnaraj ◽  
Salma Ahmed Al-Zahrani ◽  
Ahmed Al Otaibi ◽  
Semmedu Selvaraj Kalaivani ◽  
Ayyar Manikandan ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Thermo Gravimetric Analysis ◽  
Visible Region ◽  
Catalytic Performance ◽  
Precipitation Method ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Dye Pollutants ◽  
Transmission Electron

Towards the utilization of Cu2O nanomaterial for the degradation of industrial dye pollutants such as methylene blue and methyl orange, the graphene-incorporated Cu2O nanocomposites (GCC) were developed via a precipitation method. Using Hummers method, the grapheme oxide (GO) was initially synthesized. The varying weight percentages (1–4 wt %) of GO was incorporated along with the precipitation of Cu2O catalyst. Various characterization techniques such as Fourier-transform infra-red (FT-IR), X-ray diffraction (XRD), UV–visible diffused reflectance (UV-DRS), Raman spectroscopy, thermo gravimetric analysis (TGA), energy-dispersive X-ray analysis (EDX), and electro chemical impedance (EIS) were followed for characterization. The cabbage-like morphology of the developed Cu2O and its composites were ascertained from field-emission scanning electron microscopy (FESEM) and high-resolution transmission electron microscopy (HR-TEM). In addition, the growth mechanism was also proposed. The results infer that 2 wt % GO-incorporated Cu2O composites shows the highest value of degradation efficiency (97.9% and 96.1%) for MB and MO at 160 and 220 min, respectively. Further, its catalytic performance over visible region (red shift) was also enhanced to an appreciable extent, when compared with that of other samples.

scholarly journals Aluminum Nitride-Silicon Carbide Alloy Crystals Grown on SiC Substrates by Sublimation

2005 ◽  
Vol 10 ◽  
Author(s):  
Z. Gu ◽  
L. Du ◽  
J.H. Edgar ◽  
E.A. Payzant ◽  
L. Walker ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
X Ray Diffraction ◽  
Original Source ◽  
X Ray ◽  
Alloy Crystal ◽  
Transmission Electron ◽  
Crystal Substrate ◽  
Vapor Distribution ◽  
Uniform Composition

AlN-SiC alloy crystals, with a thickness greater than 500 µm, were grown on 4H- and 6H-SiC substrates from a mixture of AlN and SiC powders by the sublimation-recondensation method at 1860-1990 °C. On-axis SiC substrates produced a rough surface covered with hexagonal grains, while 6H- and 4H- off-axis SiC substrates with different miscut angles (8° or 3.68°) formed a relatively smooth surface with terraces and steps. The substrate misorientation ensured that the AlN-SiC alloy crystals grew two dimensionally as identified by scanning electron microscopy (SEM). X-ray diffraction (XRD) and transmission electron microscopy (TEM) confirmed that the AlN-SiC alloys had the wurtzite structure. Electron probe microanalysis (EPMA) and x-ray photoelectron spectroscopy (XPS) demonstrated that the resultant alloy crystals had non-stoichiometric ratios of Al:N and Si:C and a uniform composition throughout the alloy crystal from the interface to the surface. The composition ratio of Al:Si of the alloy crystals changed with the growth temperature, and differed from the original source composition, which was consistent with the results predicted by thermodynamic calculation of the solid-vapor distribution of each element. XPS detected the bonding between Si-C, Si-N, Si-O for the Si 2p spectra. The dislocation density decreased with the growth, which was lower than 106 cm−2 at the alloy surface, more than two orders of magnitude lower compared to regions close to the crystal/substrate interface, as determined by TEM.

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