Effect of Reducing Agent on the Dispersion of Pt Nanoparticles on Electrospun Nb0.1Ti0.9O2 Nanofibers

2013 ◽  
Vol 1542 ◽  
Author(s):  
Esmaeil Navaei Alvar ◽  
Biao Zhou ◽  
S. Holger Eichhorn
Keyword(s):  
Electron Microscopy ◽  
Ethylene Glycol ◽  
Surface Area ◽  
Sodium Borohydride ◽  
Chemical Reduction ◽  
Pt Nanoparticles ◽  
Surfactant Solution ◽  
Pem Fuel Cells ◽  
Active Surface Area ◽  
X Ray

ABSTRACTDegradation of the catalyst and catalyst support is an essential limitation of polymer electrolyte membrane (PEM) fuel cells containing commercial platinum on carbon catalysts. Catalysts based on platinum nanoparticles coated onto nanostructured TiO2 materials are presently investigated as a more stable and equally cost effective alternative. Reported here is the synthesis of two different Pt/Nb0.1Ti0.9O2 catalysts that were prepared by chemical reduction of H2PtCl6 with either sodium borohydride in ethanolic surfactant solution or ethylene glycol. X-ray diffraction, scanning electron microscopy, energy-dispersive X-ray spectroscopy, and high-resolution transmission electron microscopy confirmed the deposition of Pt nanoparticles on the surface of the nanofibers and revealed average sizes of 5.4 nm and 7.6 nm for reduction with ethylene glycol and sodium borohydride, respectively. The formation of smaller sized Pt nanoparticles in ethylene glycol is reasoned with the passivation of the nanoparticle surface by glycolic anions. Cyclic voltammetry measurements confirmed a higher electrochemical specific surface area (ESCA) of about 5.45 m2/gPt for the catalyst with smaller nanoparticles while the other catalyst reached only 4.96m2/gPt. Both catalysts retain about 60% of their electrochemically active surface area after 1000 voltammetric cycles in the range of 0.03 to 1.4 V vs. RHE. This relatively high value of activity retention is explained with a strong interaction between Pt nanoparticles and Nb0.1Ti0.9O2 support.

Pt Nanoparticles Decorated on Fe2O3/N, P-Doped Mesoporous Carbon for Enhanced Oxygen Reduction Activity and Durability

2020 ◽  
Vol 18 (2) ◽  
Author(s):  
Sabarinathan Ravichandran ◽  
Narayanamoorthy Bhuvanendran ◽  
Kai Peng ◽  
Weiqi Zhang ◽  
Qian Xu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Oxygen Reduction ◽  
Photoelectron Spectroscopy ◽  
Active Sites ◽  
Chemical Reduction ◽  
Pt Nanoparticles ◽  
Active Surface ◽  
Alkaline Media ◽  
Active Surface Area ◽  
X Ray

Abstract The Pt–Fe2O3 nanoparticles embedded over N, P-doped carbon (Pt–Fe2O3/NPC) was successfully synthesized by chemical reduction method demonstrating an enhanced electrocatalytic efficacy in alkaline media toward oxygen reduction reaction (ORR). The surface morphology of Pt–Fe2O3/NPC has been characterized by electron microscopy scanning, X-ray diffraction, electron microscopy transmission, Raman spectra, and X-ray photoelectron spectroscopy. The ORR electrocatalytic activity of Pt–Fe2O3/NPC was found to be the superior mass activity of 0.120 mA µg−1, which are almost twice higher than those for Pt–Fe2O3/VC (0.068 mA µg−1) and Pt/C (0.061 mA µg−1) catalysts. The durability tests revealed that the Pt–Fe2O3/NPC exhibited enhanced stability observed from the order of electrochemical active surface area (ECA) loss determined as Pt–Fe2O3/NPC (45.67%) <Pt–Fe2O3/VC (62.5%) <(Pt/C (72.13%) after 5000 cycles. This present investigation unveiled a facile approach to develop the number of active sites with the combination between P–Fe2O3 and N, P-doped carbon for improved electrocatalytic performance toward ORR.

Pt Nanoparticles Supported on Nitrogen-Doped Carbon-TiO2 Composite as a High-Performance Electrocatalyst for Methanol Oxidation

2020 ◽  
Vol 18 (1) ◽  
Author(s):  
Jun Zhang ◽  
Jiao Chen ◽  
Fan Zhou ◽  
Xuewen Zeng ◽  
An Xing ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Surface Area ◽  
Methanol Oxidation ◽  
Electrocatalytic Activity ◽  
Direct Methanol Fuel Cells ◽  
Pt Nanoparticles ◽  
Great Promise ◽  
X Ray ◽  
Nitrogen Doped ◽  
Nitrogen Doped Carbon

Abstract Monodispersed Pt nanoparticles supported on a TiO2 and nitrogen-doped carbon composite (TiO2/NDC) were successfully synthesized via an efficient in situ self-assembly strategy and microwave-assisted polyol process. The Pt/TiO2/NDC catalyst exhibited superior electrocatalytic activity toward the methanol oxidation reaction (MOR). The electrochemically active surface area of the Pt/TiO2/NDC catalyst was twofold higher than that of the Pt/C/NDC catalyst. In addition, the Pt/TiO2/NDC catalyst revealed a better electrocatalytic activity and CO-tolerance as well as a stability toward the MOR. The combined characterization from Fourier transform infrared spectrum, Brunauer-Emmett-Teller surface area, scanning electron microscopy, transmission electron microscopy, energy dispersive spectrometer, thermogravimetric analysis, inductively coupled plasma atomic emissions spectrometry, X-ray diffraction, and X-ray photoelectron spectroscopy analyses demonstrated that the superior catalytic performance and stability of the Pt/TiO2/NDC catalysts likely arose from the synergistic effect of their unique morphology and composition as well as the electronic effect between the TiO2/NDC and Pt. This electrocatalyst holds great promise for application in direct methanol fuel cells.

scholarly journals Reduced Graphene Oxide-Supported Pt-Based Catalysts for PEM Fuel Cells with Enhanced Activity and Stability

Catalysts ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 256
Author(s):  
Irina V. Pushkareva ◽  
Artem S. Pushkarev ◽  
Valery N. Kalinichenko ◽  
Ratibor G. Chumakov ◽  
Maksim A. Soloviev ◽  
...  
Keyword(s):  
Graphene Oxide ◽  
Reduced Graphene Oxide ◽  
Surface Area ◽  
Pem Fuel Cells ◽  
Polyol Process ◽  
Proton Exchange ◽  
Active Surface Area ◽  
Electrochemical Performances ◽  
Simultaneous Reduction ◽  
Reduced Graphene

Platinum (Pt)-based electrocatalysts supported by reduced graphene oxide (RGO) were synthesized using two different methods, namely: (i) a conventional two-step polyol process using RGO as the substrate, and (ii) a modified polyol process implicating the simultaneous reduction of a Pt nanoparticle precursor and graphene oxide (GO). The structure, morphology, and electrochemical performances of the obtained Pt/RGO catalysts were studied and compared with a reference Pt/carbon black Vulcan XC-72 (C) sample. It was shown that the Pt/RGO obtained by the optimized simultaneous reduction process had higher Pt utilization and electrochemically active surface area (EASA) values, and a better performance stability. The use of this catalyst at the cathode of a proton exchange membrane fuel cell (PEMFC) led to an increase in its maximum power density of up to 17%, and significantly enhanced its performance especially at high current densities. It is possible to conclude that the optimized synthesis procedure allows for a more uniform distribution of the Pt nanoparticles and ensures better binding of the particles to the surface of the support. The advantages of Pt/RGO synthesized in this way over conventional Pt/C are the high electrical conductivity and specific surface area provided by RGO, as well as a reduction in the percolation limit of the components of the electrocatalytic layer due to the high aspect ratio of RGO.

scholarly journals Surfactant-free synthesis of carbon-supported silver (Ag/C) nanobars as an efficient electrocatalyst for alcohol tolerance and oxidation of sodium borohydride in alkaline medium

2021 ◽  
Vol 3 (6) ◽  
Author(s):  
Santanu Dey ◽  
Pradipta Chakraborty ◽  
Dhiraj Kumar Rana ◽  
Subhamay Pramanik ◽  
Soumen Basu
Keyword(s):  
Cyclic Voltammetry ◽  
Ethylene Glycol ◽  
Alkaline Medium ◽  
Sodium Borohydride ◽  
Metallic Silver ◽  
Alcohol Tolerance ◽  
Current Ratio ◽  
X Ray ◽  
Scan Rate ◽  
Borohydride Oxidation

AbstractWe have synthesized carbon-supported silver (Ag/C) nanobars by a simple surfactant-free hydrothermal method using glucose as the reducing reagent as well as the source of carbon in Ag/C nanobars. Physicochemical characterization of the materials was performed by X-ray Diffraction (XRD), field emission scanning electron microscopy, and energy-dispersive X-ray spectroscopy. The XRD pattern confirmed the presence of a pure metallic silver phase. No carbon phase was detected, which indicates that the carbon exists mainly in the amorphous form. The electrocatalytic activity of Ag/C in different electrolyte solutions such as 0.5 M NaOH, 0.5 M NaOH + 1 M ethanol (EtOH), 0.5 M NaOH + 1 M ethylene glycol (EG), and 0.5 M NaOH + 0.01 M NaBH4 (sodium borohydride) was studied by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and chronoamperometry (CA) study. Alcohol tolerance of the catalysts was also established in the presence of ethanol and ethylene glycol. The forward-to-backward current ratio from cyclic voltammetry (CV) study of Ag/C-20 (20 h) in 0.5 M NaOH + 1 M ethanol solution at 100 mV s−1 scan rate is 4.13 times higher compared to that of Ag/C-5 (5 h). Hence, Ag/C-20 is a better candidate for the tolerance of ethanol. In the presence of ethylene glycol (1 M) in 0.5 M NaOH solution, it is obtained that the forward-to-backward current ratio at the same scan rate for Ag/C-20 is lower than that in the presence of ethanol. The durability of the catalyst was studied by chronoamperometry measurement. We studied the electrochemical kinetics of Ag/C catalysts for borohydride oxidation in an alkaline medium. The basic electrochemical results for borohydride oxidation show that Ag/C has very well strength and activity for direct borohydride oxidation in an alkaline medium. The reaction of borohydride oxidation with the contemporaneous BH4−. hydrolysis was noticed at the oxidized silver surface. Among all the synthesized Ag/C catalysts, Ag/C-20 exhibited the best electrocatalytic performance for borohydride oxidation in an alkaline medium. The activation energy and the number of exchange electrons at Ag/C-20 electrode surface for borohydride electro-oxidation were estimated as 57.2 kJ mol−1 and 2.27, respectively.

scholarly journals Magnetically Recyclable Wool Keratin Modified Magnetite Powders for Efficient Removal of Cu2+ Ions from Aqueous Solutions

Nanomaterials ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 1068
Author(s):  
Xinyue Zhang ◽  
Yani Guo ◽  
Wenjun Li ◽  
Jinyuan Zhang ◽  
Hailiang Wu ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Aqueous Solutions ◽  
Adsorption Capacity ◽  
Surface Area ◽  
Ion Concentration ◽  
Bet Surface Area ◽  
Chemical Compositions ◽  
Ion Adsorption ◽  
X Ray ◽  
Wool Keratin

The treatment of wastewater containing heavy metals and the utilization of wool waste are very important for the sustainable development of textile mills. In this study, the wool keratin modified magnetite (Fe3O4) powders were fabricated by using wool waste via a co-precipitation technique for removal of Cu2+ ions from aqueous solutions. The morphology, chemical compositions, crystal structure, microstructure, magnetism properties, organic content, and specific surface area of as-fabricated powders were systematically characterized by various techniques including field emission scanning electron microscopy (FESEM), energy dispersive spectroscopy (EDS), X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), vibrating sample magnetometer (VSM), thermogravimetric (TG) analysis, and Brunauer–Emmett–Teller (BET) surface area analyzer. The effects of experimental parameters such as the volume of wool keratin hydrolysate, the dosage of powder, the initial Cu2+ ion concentration, and the pH value of solution on the adsorption capacity of Cu2+ ions by the powders were examined. The experimental results indicated that the Cu2+ ion adsorption performance of the wool keratin modified Fe3O4 powders exhibited much better than that of the chitosan modified ones with a maximum Cu2+ adsorption capacity of 27.4 mg/g under favorable conditions (0.05 g powders; 50 mL of 40 mg/L CuSO4; pH 5; temperature 293 K). The high adsorption capacity towards Cu2+ ions on the wool keratin modified Fe3O4 powders was primarily because of the strong surface complexation of –COOH and –NH2 functional groups of wool keratins with Cu2+ ions. The Cu2+ ion adsorption process on the wool keratin modified Fe3O4 powders followed the Temkin adsorption isotherm model and the intraparticle diffusion and pseudo-second-order adsorption kinetic models. After Cu2+ ion removal, the wool keratin modified Fe3O4 powders were easily separated using a magnet from aqueous solution and efficiently regenerated using 0.5 M ethylene diamine tetraacetic acid (EDTA)-H2SO4 eluting. The wool keratin modified Fe3O4 powders possessed good regenerative performance after five cycles. This study provided a feasible way to utilize waste wool textiles for preparing magnetic biomass-based adsorbents for the removal of heavy metal ions from aqueous solutions.

scholarly journals Comparative Study of Ag Nanostructures: Molecular Simulations, Electrochemical Behavior, and Antibacterial Effect

2016 ◽  
Vol 2016 ◽  
pp. 1-9 ◽  
Author(s):  
Álvaro de Jesús Ruíz-Baltazar ◽  
Simón Yobanny Reyes-López ◽  
D. Larrañaga ◽  
R. Pérez
Keyword(s):  
Cyclic Voltammetry ◽  
Ethylene Glycol ◽  
Comparative Study ◽  
Sodium Borohydride ◽  
Electrochemical Behavior ◽  
Antibacterial Effect ◽  
Chemical Reduction ◽  
Molecular Simulations ◽  
The Other ◽  
E Coli

Nanoparticles of Ag with different sizes and structures were obtained and studied. Two methods for reductions of Ag ions were employed, chemical reduction by sodium borohydride and ethylene glycol. Cuboctahedral and icosahedral structures were obtained. Molecular simulations were carried out in order to evaluate the reactivity of both structures. On the other hand, the electrochemical activity and antibacterial effect (E. coli) of the cuboctahedral and icosahedral structures were measured experimentally. The results obtained by molecular simulation, cyclic voltammetry, and antibacterial effect were compared and discussed in this work.

scholarly journals SINTESIS NANOKOMPOSIT Nata de coco/TiO2/Ag DAN EFEKTIVITASNYA SEBAGAI ANTIBAKTERI TERHADAP BAKTERI Escherichia coli dan Staphylococcus aureus

2021 ◽  
Vol 14 (1) ◽  
Author(s):  
Heriyanto Tinentang ◽  
Henry F Aritonang ◽  
Harry S. J. Koleangan
Keyword(s):  
Electron Microscopy ◽  
Escherichia Coli ◽  
Scanning Electron Microscopy ◽  
Staphylococcus Aureus ◽  
Chemical Reduction ◽  
Bacterial Activity ◽  
Energy Dispersive ◽  
X Ray ◽  
Escherichia Coli Bacteria ◽  
Scanning Electron

Telah dilakukan penelitian tentang kemampuan aktivitas anti bakteri untuk bakteri Staphylococcus aureus (gram positif) dan Escherichia coli (gram negatif) dengan menggunakan nanokomposit nata de coco/TiO2, nata de coco/Ag, dan nata de coco/TiO2/Ag dengan variasi konsentrasi Ag 0,5 M; 0,6 M; 0,7 M; 0,8 M dan 0,9 M  menggunakan metode reduksi kimia. Nanopartikel tersebut dikarakterisasi menggunakan X-Ray Diffractometry (XRD), scanning electron microscopy-energy dispersive X-ray spectroscopy  (SEM-EDS) dan anti bakteri. Untuk uji aktivitas antibakteri menggunakan metode kertas cakram dan dilakukan sebanyak dua kali ulangan untuk tiap-tiap sampel dan bakteri yang diuji. Hasil penelitian menunjukan, aktivitas anti bakteri nanokomposit yang paling baik dalam menghambat pertumbuhan bakteri adalah nanokomposit Nata de coco/TiO2/Ag mampu menghambat pertumbuhan bakteri Escherichiacoli dan Staphylococcusaureus, namun nanokomposit tersebut lebih efektif menghambat pertumbuhan bakteri Escherichiacoli.ABSRACT Research on the ability of anti-bacterial activity for Staphylococcus aureus (gram positive) and Escherichia coli (gram negative) bacteria using nata de coco / nanocomposites TiO2, nata de coco / Ag, and nata de coco / TiO2 / Ag with variations of Ag 0,5 M; 0.6 M; 0.7 M; 0.8 M and 0.9 M using the chemical reduction method. Nanoparticles were characterized using X-Ray Diffractometry (XRD), scanning electron microscopy-energy dispersive X-ray spctroscopy  (SEM-EDS) and anti-bacterial actvity. Test the antibacterial activity using the paper disc method and repeated two times for each sample and bacteria tested. The results showed that the good anti-bacterial activity of nanocomposites in inhibiting bacterial growth was nanocomposite nata de coco /TiO2/Ag  able to inhibit the growth of Escherichia coli and S. aureus, but the nanocomposite is more effective in inhibiting the growth of Escherichia  coli bacteria.

Hollow structured CoSn(OH)6-supported Pt for effective room-temperature oxidation of gaseous formaldehyde

2016 ◽  
Vol 09 (06) ◽  
pp. 1642009 ◽  
Author(s):  
Jing Zhou ◽  
Yong Zhao ◽  
Lifan Qin ◽  
Chen Zeng ◽  
Wei Xiao
Keyword(s):  
Electron Microscopy ◽  
Catalytic Activity ◽  
Room Temperature ◽  
Synergetic Effect ◽  
Hollow Structure ◽  
Pt Nanoparticles ◽  
Hydroxyl Groups ◽  
High Catalytic Activity ◽  
Temperature Oxidation ◽  
X Ray

Uniform CoSn(OH)6 hollow nanoboxes and the derivative with Pt loading (Pt/CoSn(OH)6) were herein synthesized and characterized by means of X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). SEM and TEM analyses showed that CoSn(OH)6 possessed mesoporous hollow structure and Pt nanoparticles with size of 2–8[Formula: see text]nm were uniformly dispersed on the surface of CoSn(OH)6 nanoboxes. The performances of the catalysts for the formaldehyde (HCHO) removal at room temperature were evaluated. These Pt/CoSn(OH)6 catalysts exhibited a remarkable catalytic activity as well as stability for room-temperature oxidative decomposition of gaseous HCHO, while the corresponding CoSn(OH)6 only showed adsorption. The synergetic effect between the highly dispersed Pt nanoparticles and the CoSn(OH)6 nanoboxes with mesoporous hollow structure, a large surface area and abundant surface hydroxyl groups is considered to be the main reason for the observed high catalytic activity of Pt/CoSn(OH)6.

Facile deposition of Pt nanoparticles on Sb-doped SnO2 support with outstanding active surface area for the oxygen reduction reaction

2018 ◽  
Vol 8 (10) ◽  
pp. 2672-2685 ◽  
Author(s):  
Rhiyaad Mohamed ◽  
Tobias Binninger ◽  
Patricia J. Kooyman ◽  
Armin Hoell ◽  
Emiliana Fabbri ◽  
...  
Keyword(s):  
Oxygen Reduction Reaction ◽  
Oxygen Reduction ◽  
Surface Area ◽  
Pt Nanoparticles ◽  
Active Surface ◽  
Reduction Reaction ◽  
Active Surface Area

Synthesis of Sb–SnO2 supported Pt nanoparticles with an outstanding ECSA for the oxygen reduction reaction.

Copper-based MOF, Cu3(SDBA)2(HSDBA), as catalyst for efficient reduction of 4-nitrophenol in the presence of sodium borohydride

2022 ◽  
Author(s):  
Manel Mansour ◽  
Hamza Kahri ◽  
Mouhieddinne Guergueb ◽  
Houcine Barhoumi ◽  
Enrique Gutierrez-Puebla ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Scanning Electron Microscopy ◽  
Physicochemical Properties ◽  
Sodium Borohydride ◽  
Solvothermal Method ◽  
X Ray Diffraction ◽  
X Ray ◽  
Prepared Sample ◽  
Efficient Reduction ◽  
Scanning Electron

Herein, we report the synthesis of the copper-based MOF, Cu3(SDBA)2(HSDBA), using solvothermal method. The physicochemical properties of the as-prepared sample were examined by X-ray diffraction, scanning electron microscopy, energy-dispersive X-ray...

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