scholarly journals Calcined Co(II)-Triethylenetetramine, Co(II)- Polyaniline-Thiourea as the Cathode Catalyst of Proton Exchanged Membrane Fuel Cell

Polymers ◽  
2020 ◽  
Vol 12 (12) ◽  
pp. 3070
Author(s):  
Wen-Yao Huang ◽  
Li-Cheng Jheng ◽  
Tar-Hwa Hsieh ◽  
Ko-Shan Ho ◽  
Yen-Zen Wang ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Linear Sweep Voltammetry ◽  
Conducting Medium ◽  
Membrane Electrode ◽  
X Ray Diffraction ◽  
Xps Spectra ◽  
X Ray ◽  
Co Catalysts ◽  
Electrode Assemblies ◽  
Diffraction Patterns

Triethylenetetramine (TETA) and thiourea complexed Cobalt(II) (Co(II)) ions are used as cathode catalysts for proton exchanged membrane fuel cells (PEMFCs) under the protection of polyaniline (PANI) which can become a conducting medium after calcination. Fourier-transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS) spectra clearly reveal the presence of typical carbon nitride and sulfide bonds of the calcined Nitrogen (N)- or Sulfur (S)-doped co-catalysts. Clear (002) and (100) planes of carbon-related X-ray diffraction patterns are found for co-catalysts after calcination, related to the formation of a conducting medium after the calcination of PANI. An increasing intensity ratio of the D to G band of the Raman spectra reveal the doping of N and S elements. More porous surfaces of co-catalysts are found in scanning electronic microscopy (SEM) micropictures when prepared in the presence of both TETA and thiourea (CoNxSyC). Linear sweep voltammetry (LSV) curves show the highest reducing current to be 4 mAcm−2 at 1600 rpm for CoNxSyC, indicating the necessity for both N- and S-doping. The membrane electrode assemblies (MEA) prepared with the cathode made of CoNxSyC produces the highest maximum power density, close to 180 mW cm−2.

Surface Characterization of Carbon-Bearing Magnetite (CBM) and Carbon-Bearing Ni(II)-Ferrite (CBNF)

1994 ◽  
Vol 344 ◽  
Author(s):  
T. Sano ◽  
K. Akanuma ◽  
M. Tsuji ◽  
Y. Tamaura
Keyword(s):  
Photoelectron Spectroscopy ◽  
Spinel Structure ◽  
Surface Characterization ◽  
Carbon Deposition ◽  
X Ray Diffraction ◽  
Xps Spectra ◽  
X Ray ◽  
Oxygen Ions ◽  
Diffraction Patterns

AbstractOxygen-deficient magnetite (ODM; Fe3O4-δ, δ>0) synthesized by reduction of magnetite with H2 at 300°C decomposed CO2 to carbon with an efficiency of nearly 100% at 300°C. In this reaction, two oxygen ions of the CO2 were incorporated into the spinel structure of ODM and carbon was deposited on the surface of ODM with zero valence to form visible particles. The particles of carbon separated from ODM were studied by Raman, energy-dispersive X-ray and wave-dispersive X-ray spectroscopies. The carbon which had been deposited on the ODM was found to be a mixture of graphite and amorphous carbon in at least two levels of crystallization. X-ray photoelectron spectroscopy and X-ray diffraction patterns of the carbon-bearing magnetite (CBM) showed no indication of carbide (Fe3C) or metallic iron (α-Fe) phase formation. In the C 1s XPS spectra of the CBM, no peaks were observed which could be assigned to CO2 or CO. X-ray diffractometry, chemical analysis and TG-MS measurement showed that the carbon-bearing Ni(II)-ferrite (CBNF) (Ni(II)/Fetotal = 0.15) synthesized by the carbon deposition reaction from CO2 with the H2-reduced Ni(II)-ferrite was represented by (Ni0.28Fe2.72O4.00)1-δ (Ni2+06.9Fe2+2.31O3.00)δCτ (δ= 0.27, τ= 0.17). The carbon of the CBNF gave the CIOlayer-like oxide containing some Ni2+ ions.

scholarly journals Optical, XPS and XRD Studies of Semiconducting Copper Sulfide Layers on a Polyamide Film

2009 ◽  
Vol 2009 ◽  
pp. 1-8 ◽  
Author(s):  
Valentina Krylova ◽  
Mindaugas Andrulevičius
Keyword(s):  
Photoelectron Spectroscopy ◽  
Copper Sulfide ◽  
Diffusion Method ◽  
X Ray Diffraction ◽  
Xps Spectra ◽  
X Ray ◽  
Xrd Studies ◽  
Polyamide Film ◽  
Indirect Band Gap ◽  
Xrd Method

Copper sulfide layers were formed on polyamide PA 6 surface using the sorption-diffusion method. Polymer samples were immersed for 4 and 5 h in 0.15 mol⋅  solutions and acidified with HCl (0.1 mol⋅) at . After washing and drying, the samples were treated with Cu(I) salt solution. The samples were studied by UV/VIS, X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) methods. All methods confirmed that on the surface of the polyamide film a layer of copper sulfide was formed. The copper sulfide layers are indirect band-gap semiconductors. The values of are 1.25 and 1.3 eV for 4 h and 5 h sulfured PA 6 respectively. Copper XPS spectra analyses showed Cu(I) bonds only in deeper layers of the formed film, while in sulfur XPS S 2p spectra dominating sulfide bonds were found after cleaning the surface with ions. It has been established by the XRD method that, beside , the layer contains as well. For PA 6 initially sulfured 4 h, grain size forchalcocite, , was  nm and fordjurleite, , it was 54.17 nm. The sheet resistance of the obtained layer varies from 6300 to 102 .

Study Behavior of XPS Spectra of Ni, Mn, Y and O in Y2NiMnO6 Ceramics

2015 ◽  
Vol 804 ◽  
pp. 97-103 ◽  
Author(s):  
Panakamon Deeyai ◽  
Thanapong Sareein ◽  
Bundit Putasaeng ◽  
Naphat Chathirat
Keyword(s):  
Photoelectron Spectroscopy ◽  
Ceramic Materials ◽  
Effect Of Temperature ◽  
Decomposition Technique ◽  
X Ray Diffraction ◽  
Xps Spectra ◽  
X Ray ◽  
Study Behavior ◽  
Sintering Time ◽  
Effects Of Temperature

Bulk Y2NiMnO6 samples were prepared by thermal decomposition technique at 800 °C for 6 hours. The effects of temperature on the structure of ceramics were investigated for different sintering temperatures in the range of 1000-1300 °C, while kept constant the sintering time of 12 hours. Structural characterization had been investigated via X-ray diffraction (XRD) on samples of different sintering temperatures. Results from the experiment had revealed that high temperature affected oxide in ceramic materials. Further analysis with X-ray photoelectron spectroscopy (XPS) technique had revealed an outstanding point of ceramics by investigating the Ni 2p, 2p3/2, Mn 2p1/2, 2p3/2, and Y 3d3/2, 3d5/2 at the surface of Y2NiMnO6 ceramics. The changes in relative intensity of XPS peaks and the shifts in their binding energy (eV) were observed in the results, while the effect of temperature on oxide in ceramics may be investigated with dielectric property in the future.

Fe-loaded zeolites as catalysts in the formation of humic substance-like darkcoloured polymers in polycondensation reactions of humic precursors

Clay Minerals ◽  
2012 ◽  
Vol 47 (3) ◽  
pp. 355-364 ◽  
Author(s):  
S. Fukuchi ◽  
M. Fukushima ◽  
R. Nishimoto ◽  
G. Qi ◽  
T. Sato
Keyword(s):  
Cation Exchange ◽  
Photoelectron Spectroscopy ◽  
Ionic Species ◽  
Exchange Capacity ◽  
X Ray Diffraction ◽  
Xps Spectra ◽  
X Ray ◽  
Catalytic Activities ◽  
Ion Exchange Reaction ◽  
Xrd Patterns

AbstractTo enhance the catalytic activities of zeolites for the polycondensation reactions of humic precursors, Fe was loaded into a zeolite via an ion-exchange reaction and the resulting product was subjected to calcination at 773 K. Two types iron-loaded zeolites were prepared using one equivalent (Fe-Z-1) and 10-equivalents (Fe-Z-10) of Fe2+ to the cation-exchange capacity of a natural zeolite from Niki town (Hokkaido, Japan). X-ray diffraction (XRD) patterns and X-ray photoelectron spectroscopy (XPS) spectra showed that the Fe(II) that was originally loaded into the cation-exchange sites in the zeolite became oxidized to a Fe(III) ionic species during the preparation. The catalytic activities of each zeolite were evaluated, based on the degree of darkening for reaction mixtures containing catechol, glycine and glucose as model humic precursors. The catalytic activities of Fe-Z-1 and Fe-Z-10 were higher than that for an untreated zeolite, and increased with the amount of Fe in the zeolite.

scholarly journals Ag/AgCl/MIL-101(Fe) Catalyzed Degradation of Methylene Blue under Visible Light Irradation

Materials ◽  
2019 ◽  
Vol 12 (9) ◽  
pp. 1453 ◽  
Author(s):  
Yun Liu ◽  
Yuanhong Xie ◽  
Mingjin Dai ◽  
Qingjiao Gong ◽  
Zhi Dang
Keyword(s):  
Methylene Blue ◽  
Catalytic Activity ◽  
Visible Light ◽  
Photoelectron Spectroscopy ◽  
X Ray Diffraction ◽  
Box Behnken Design ◽  
X Ray ◽  
Plasmonic Material ◽  
Fenton Catalyst ◽  
Diffraction Patterns

A novel photo-Fenton catalyst named Ag/AgCl/MIL-101(Fe) was synthesized by the method of precipitation and photo reduction and characterized by X-ray diffraction patterns (XRD), Brunauer-Emmett-Teller (BET) measurements, Fourier transform infrared spectra (FTIR), scanning electron microscopy with energy dispersive X-ray spectroscopy (SEM-EDX), X-ray photoelectron spectroscopy (XPS) and UV-vis diffuse reflectance spectra. Moreover, the catalytic activity of the synthesized catalyst was tested using methylene blue (MB) as the target pollutant. The obtained results illustrated that the plasmonic material Ag/AgCl was successfully loaded on MIL-101(Fe) and the obtained catalyst exhibited an excellent catalytic activity under visible light at the neutral pH. According to the analyses of Plackett-Burman and Box-Behnken design, the optimum conditions for MB degradation were obtained. Under these conditions, the MB decolorization and mineralization efficiencies could reach to 99.75% and 65.43%, respectively. The recycling experiments also showed that the as-prepared catalyst displayed good reusability. In addition, the possible reaction mechanisms for the heterogeneous photo-Fenton system catalyzed by Ag/AgCl/MIL-101(Fe) were derived. The synthesized catalyst provides a promising approach to degrade organic pollutants in waste water.

scholarly journals Zn/F-doped tin oxide nanoparticles synthesized by laser pyrolysis: structural and optical properties

2019 ◽  
Vol 10 ◽  
pp. 9-21 ◽  
Author(s):  
Florian Dumitrache ◽  
Iuliana P Morjan ◽  
Elena Dutu ◽  
Ion Morjan ◽  
Claudiu Teodor Fleaca ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Laser Energy ◽  
Xrd Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Laser Pyrolysis ◽  
One Step ◽  
Diffraction Patterns ◽  
Tin Oxide Nanoparticles ◽  
Co Doped

Zn/F co-doped SnO2 nanoparticles with a mean diameter of less than 15 nm and a narrow size distribution were synthesized by a one-step laser pyrolysis technique using a reactive mixture containing tetramethyltin (SnMe4) and diethylzinc (ZnEt2) vapors, diluted Ar, O2 and SF6. Their structural, morphological, optical and electrical properties are reported in this work. The X-ray diffraction (XRD) analysis shows that the nanoparticles possess a tetragonal SnO2 crystalline structure. The main diffraction patterns of stannous fluoride (SnF2) were also identified and a reduction in intensity with increasing Zn percentage was evidenced. For the elemental composition estimation, energy dispersion X-ray spectroscopy (EDX) and X-ray photoelectron spectroscopy (XPS) measurements were performed. In general, both analyses showed that the Zn percentage increases with increasing ZnEt2 flow, accompanied at the same time by a decrease in the amount of F in the nanopowders when the same SF6 flow was employed. The Raman spectra of the nanoparticles show the influence of both Zn and F content and crystallite size. The fluorine presence is due to the catalytic partial decomposition of the SF6 laser energy transfer agent. In direct correlation with the increase in the Zn doping level, the bandgap of co-doped nanoparticles shifts to lower energy (from 3.55 to 2.88 eV for the highest Zn dopant concentration).

scholarly journals A multi-method characterization of natural terrestrial birnessites

2020 ◽  
Vol 105 (6) ◽  
pp. 833-847
Author(s):  
Florence T. Ling ◽  
Jeffrey E. Post ◽  
Peter J. Heaney ◽  
Cara M. Santelli ◽  
Eugene S. Ilton ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Large Set ◽  
X Ray Diffraction ◽  
Full Spectrum ◽  
X Ray ◽  
High Concentrations ◽  
Diffraction Patterns ◽  
X Ray Absorption ◽  
Crystal Structure And Chemistry

Abstract With a focus on a large set of natural birnessites collected from terrestrial, freshwater systems, we applied and compared the capabilities of X-ray diffraction (XRD), extended X-ray absorption fine structure (EXAFS), Fourier-transform infrared spectroscopy (FTIR), and X-ray photoelectron spectroscopy (XPS) to characterize crystal structure and chemistry. Using XRD, we successfully identified 3 of the 11 natural birnessite samples as hexagonal ranciéite-like phases, but the remaining samples yielded less interpretable “3-line” diffraction patterns with broad, asymmetrical peaks at d-spacings of ~7.2, ~2.4, and ~1.4 Å. EXAFS analysis suggested that many of these samples had characteristics of both triclinic and hexagonal birnessite. However, application of EXAFS to the ranciéite-like phases yielded unreasonably high concentrations of triclinic birnessite as an intergrowth, calling into question the use of synthetic hexagonal H-birnessite as an appropriate standard in the linear combination fitting of EXAFS data for natural birnessites. FTIR spectroscopy of the “3-line” birnessite samples successfully distinguished triclinic and hexagonal constituents, and analyses of peak positions suggested that natural birnessites occur as a full spectrum of triclinic and hexagonal intergrowths. XPS analysis of these samples revealed that higher Mn3+ concentrations relative to Mn2+ and Mn4+ are correlated to increased proportions of triclinic birnessite.

CO2 Adsorption Performance of N-Doped Ordered Microporous Carbons Templated from Zeolite HY

2011 ◽  
Vol 284-286 ◽  
pp. 2102-2105 ◽  
Author(s):  
Jin Zhou ◽  
Wen Li ◽  
Shu Ping Zhuo
Keyword(s):  
Photoelectron Spectroscopy ◽  
Carbon Deposition ◽  
X Ray Diffraction ◽  
Step Method ◽  
X Ray ◽  
Microporous Carbons ◽  
Adsorption Performance ◽  
Basic Nitrogen ◽  
Diffraction Patterns ◽  
Very High

Several microporous carbons were prepared by a two-step method using zeolite HY as a template, and were used as CO2 adsorbents. X-ray diffraction patterns present that the structure regularity of the zeolite has been well-replicated by the templated carbons. X-ray photoelectron spectroscopy confirms that the prepared carbons possess abundant nitrogen-containing groups due to the carbon deposition of acetonitrile. The prepared carbons show high CO2 adsorption capacity due to its very high microporous surface area and abundant basic nitrogen-containing groups.

A novel method to bind soybean protein onto the surface of poly(ethylene terephthalate) fabric

2016 ◽  
Vol 87 (4) ◽  
pp. 460-473
Author(s):  
Jianfeng Zhou ◽  
Dandan Zheng ◽  
Fengxiu Zhang ◽  
Guangxian Zhang
Keyword(s):  
Photoelectron Spectroscopy ◽  
Ethylene Terephthalate ◽  
Soybean Protein ◽  
X Ray Diffraction ◽  
X Ray ◽  
Pet Fabric ◽  
Poly Ethylene Terephthalate ◽  
Pet Fibers ◽  
Diffraction Patterns ◽  
Poly Ethylene

In this study, –NH2 groups were introduced to a poly(ethylene terephthalate) (PET) fabric to make the fabric hydrophilic and, then, soybean protein was bonded on the surface of the modified PET fabric to obtain a soybean protein/PET composite fabric. The –NH2 groups allowed the soybean protein to be firmly bonded on the surface of the modified PET fabric. Scanning electron microscopy images showed that the surface of each modified PET fiber had a small number of grooves and that there was a thin film on each soybean protein/PET fiber. Attenuated total reflectance Fourier transform infrared spectra demonstrated that the nitrated and reduced PET fibers were introduced –NH2 groups and that there were –CO–NH– groups on the surface of soybean protein/PET fibers. X-ray photoelectron spectroscopy analyses showed that there was a nitrogen element on the modified PET fibers. The X-ray diffraction patterns suggested that the crystal structures of the modified fibers did not change significantly during the modification processes. The thermogravimetry results showed that the thermal stability of soybean protein/PET fiber kept well. The wearability tests indicated that the breaking strength and elasticity of the original fabric were well retained by the modified fabrics. The soybean protein/PET fabric had good levels of hydrophilicity and softness when the binding rate was below 3.0%.

Reactive Gas Condensation Synthesis of Aluminum Nitride Nanoparticles

2006 ◽  
Vol 6 (1) ◽  
pp. 146-150 ◽  
Author(s):  
Colin C. Baker ◽  
Abdullah Ceylan ◽  
S. Ismat Shah
Keyword(s):  
Thermal Conductivity ◽  
Aluminum Nitride ◽  
Photoelectron Spectroscopy ◽  
Temporal Stability ◽  
Gas Mixture ◽  
X Ray Diffraction ◽  
X Ray ◽  
Gas Condensation ◽  
Diffraction Patterns ◽  
Reactive Gas

Aluminum Nitride (AlN) nanoparticles were synthesized using a Reactive Gas Condensation (RGC) technique in which a mixture of ammonia (NH3) and nitrogen (N2) gases were used for the nitridation of aluminum. NH3 served as the reactive gas, while N2 served as both a carrier gas and the inert source for particle condensation. X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) analyses revealed that at reactive gas compositions greater than 10% NH3 in N2, samples were composed entirely of hexagonal AlN nanoparticles. Electron diffraction patterns showed single crystal hexagonal AlN structure. The particle size was controlled by varying the pressure of the gas mixture. AlN nanoparticles were dispersed in a liquid matrix to enhance thermal conductivity. Results showed that a minimal addition of AlN increased the thermal conductivity of hydrocarbon pump oil by approximately 27%. The thermal conductivity became constant after reaching a maximum above 0.01 wt% AlN. Temporal stability of AlN was studied by XRD. Samples exposed to air for extended periods of time and analyzed by XRD show no degradation of crystalline AlN nanoparticles.

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