scholarly journals Catalytic Performances of Au–Pt Nanoparticles on Phosphorous Functionalized Carbon Nanofibers towards HMF Oxidation

2018 ◽  
Vol 4 (3) ◽  
pp. 48 ◽  
Author(s):  
Sebastiano Campisi ◽  
Sofia Capelli ◽  
Davide Motta ◽  
Felipe Trujillo ◽  
Thomas Davies ◽  
...  
Keyword(s):  
Carbon Nanofibers ◽  
Photoelectron Spectroscopy ◽  
Pt Nanoparticles ◽  
Carbon Surface ◽  
Protective Agent ◽  
Transmission Electron ◽  
Functionalized Materials ◽  
Furandicarboxylic Acid ◽  
Key Parameter ◽  
Catalytic Performances

Herein, we reported the utilization of pre-formed Au–Pt nanoparticles deposited on phosphorus functionalized carbons as effective catalysts for the oxidation of 5-hydroxymethylfurfural (HMF) to furandicarboxylic acid (FDCA). Au–Pt nanoparticles have been prepared by a two-step methodology using polyvinyl alcohol (PVA) as protective agent and a combination of NaBH4 and H2 as reducing agents. Three carbon nanofibers (CNFs) with different graphitization degrees have been functionalized through treatment with an H3PO4–HNO3 mixture at 150 °C, in order to incorporate P groups on carbon surface. Surface and structural properties of the synthesized functionalized materials have been investigated by transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and Raman spectroscopy. The structural and surface properties of carbon nanofibers determine the amount of P-functionalities, which is a key parameter affecting the catalytic performances of Au–Pt. Indeed, the highest activity and stability has been achieved for Au–Pt deposited on the sample, which showed the largest amount of P-groups on the surface.

scholarly journals Ruling Factors in Cinnamaldehyde Hydrogenation: Activity and Selectivity of Pt-Mo Catalysts

Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 362
Author(s):  
Marta Stucchi ◽  
Maela Manzoli ◽  
Filippo Bossola ◽  
Alberto Villa ◽  
Laura Prati
Keyword(s):  
Photoelectron Spectroscopy ◽  
Pt Nanoparticles ◽  
Carbon Support ◽  
Catalytic Performance ◽  
Acid Sites ◽  
Hydrogenation Catalysts ◽  
Cinnamaldehyde Hydrogenation ◽  
Transmission Electron ◽  
Heat Treated ◽  
Heating Treatment

To obtain selective hydrogenation catalysts with low noble metal content, two carbon-supported Mo-Pt bimetallic catalysts have been synthesized from two different molybdenum precursors, i.e., Na2MoO4 and (NH4)6Mo7O24. The results obtained by X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM) combined with the presence and strength of acid sites clarified the different catalytic behavior toward cinnamaldehyde hydrogenation. After impregnating the carbon support with Mo precursors, each sample was used either as is or treated at 400 °C in N2 flow, as support for Pt nanoparticles (NPs). The heating treatment before Pt deposition had a positive effect on the catalytic performance. Indeed, TEM analyses showed very homogeneously dispersed Pt NPs only when they were deposited on the heat-treated Mo/C supports, and XPS analyses revealed an increase in both the exposure and reduction of Pt, which was probably tuned by different MoO3/MoO2 ratios. Moreover, the different acid properties of the catalysts resulted in different selectivity.

Electroless Synthesis of 1.4 nm Pd and Pt Nanoparticles on Self-Assembled Rosette Nanotubes

2011 ◽  
Vol 1301 ◽  
Author(s):  
Rahul Chhabra ◽  
Hicham Fenniri
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Pt Nanoparticles ◽  
Hierarchical Organization ◽  
X Ray ◽  
Force Microscopy ◽  
Rosette Nanotubes ◽  
Atomic Force ◽  
Transmission Electron ◽  
Self Assembled

ABSTRACTElectroless synthesis and hierarchical organization of 1.4 nm Pd and Pt nanoparticles (NPs) on self-assembled Rosette Nanotubes (RNTs) is described. The nucleated NPs are nearly monodisperse and reveal supramolecular organizations guided by RNT templates. Interestingly, the narrow size distribution is attributable to unique templating behavior of RNTs. The resulting metal NP-RNT composites were characterized by Atomic Force Microscopy (AFM), Scanning Electron Microscopy (SEM) and Transmission Electron Microscopy (TEM). X-ray Photoelectron Spectroscopy (XPS) was also performed to confirm the nature and composition of RNT-templated NPs.

scholarly journals Cyclic Voltammetry Characterization of Au, Pd, and AuPd Nanoparticles Supported on Different Carbon Nanofibers

Surfaces ◽  
2019 ◽  
Vol 2 (1) ◽  
pp. 205-215 ◽  
Author(s):  
Anna Testolin ◽  
Stefano Cattaneo ◽  
Wu Wang ◽  
Di Wang ◽  
Valentina Pifferi ◽  
...  
Keyword(s):  
Cyclic Voltammetry ◽  
Surface Chemistry ◽  
Carbon Nanofibers ◽  
Photoelectron Spectroscopy ◽  
Carbon Support ◽  
Carbon Surface ◽  
Carbon Supports ◽  
Heat Treated ◽  
Temperature Heat ◽  
Treated Carbon

Three types of carbon nanofibers (pyrolytically stripped carbon nanofibers (PS), low-temperature heat treated carbon nanofibers (LHT), and high-temperature heat treated carbon nanofibers (HHT)) with different graphitization degrees and surface chemistry have been used as support for Au, Pd, or bimetallic AuPd alloy nanoparticles (NPs). The carbon supports have been characterized using Raman, X-ray photoelectron spectroscopy (XPS), and cyclic voltammetry (CV). Moreover, the morphology of the metal nanoparticles was investigated using transmission electron microscopy (TEM) and CV. The different properties of the carbon-based supports (particularly the graphitization degree) yield different electrochemical behaviors, in terms of potential window widths and electrocatalytic effects. Comparing the electrochemical behavior of monometallic Au and Pd and bimetallic AuPd, it is possible to observe the interaction of the two metals when alloyed. Moreover, we demonstrate that carbon surface has a strong effect on the electrochemical stability of AuPd nanoparticles. By tuning the Au-Pd nanoparticles’ morphology and modulating the surface chemistry of the carbon support, it is possible to obtain materials characterized by novel electrochemical properties. This aspect makes them good candidates to be conveniently applied in different fields.

TEMPLATE STRATEGY FOR THE SYNTHESIS OF Cu2O–Pt HIERARCHICAL HETEROSTRUCTURES FOR THE DEGRADATION OF METHYLENE BLUE

NANO ◽  
2013 ◽  
Vol 08 (06) ◽  
pp. 1350062 ◽  
Author(s):  
SHIYONG BAO ◽  
HAN ZHU ◽  
PAN WANG ◽  
MEILING ZOU ◽  
MINGLIANG DU ◽  
...  
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Methylene Blue ◽  
Photoelectron Spectroscopy ◽  
Pt Nanoparticles ◽  
X Ray Diffraction ◽  
Electron Hole ◽  
X Ray ◽  
Transmission Electron ◽  
Green Route

A facile and green route was introduced to synthesize Pt nanoparticles (PtNPs) immobilized on Cu 2 O octahedrons to form Cu 2 O – Pt hierarchical heterostructure. Transmission electron microscopy (TEM), field emission scanning electron microscopy (FE-SEM), high resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS) and X-ray diffraction (XRD) were employed to study their morphology, chemical and crystallographic properties of the Cu 2 O – Pt hierarchical heterostructure. These novel Cu 2 O – Pt hierarchical heterostructures show fascinating degradations of methylene blue (MB), due to the suppressed electron/hole recombination phenomena and the efficient ability to capture the light.

Chemical Deposition Method for Synthesis of Pt-TiO2 Composite Nanotubes with Photoelectrochemical Activity

2012 ◽  
Vol 465 ◽  
pp. 276-282
Author(s):  
Zhong Hui Gao ◽  
Zhen Duo Cui ◽  
Xian Jin Yang
Keyword(s):  
Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Chemical Deposition ◽  
Pt Nanoparticles ◽  
High Density ◽  
Deposition Method ◽  
Photoelectrochemical Activity ◽  
X Ray ◽  
Transmission Electron ◽  
Chemical Deposition Method

Pt nanoparticles were successfully assembled in self-organized TiO2 nanotubes by a chemical deposition method. Scanning electron microscopy, transmission electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy were used for characterizing the surface morphology and phase composition. Photocurrent response activity was measured. Different morphology of Pt-TiO2 NTs exhibited different photocurrent generation efficiency. High density Pt nanoparticles depositing on TiO2 NTs decreased the photocurrent of Pt-TiO2 electrodes. It was because the high density Pt nanoparticles could become the recombination centers of photoelectrons and holes.

Identify the Active Phase of Fe–CN Composites for Oxidation Removal of Rhodamine B with H2O2

2019 ◽  
Vol 233 (7) ◽  
pp. 1035-1045
Author(s):  
Tingting Diao ◽  
Wenyao Wang ◽  
Xuelian Xu ◽  
Ping Xiao ◽  
Duihai Tang ◽  
...  
Keyword(s):  
Rhodamine B ◽  
Photoelectron Spectroscopy ◽  
Guanidine Hydrochloride ◽  
Active Phase ◽  
Atomic Emission ◽  
Gravimetric Analysis ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Catalytic Performances

AbstractFe-containing carbon nitrides (Fe–CN) prepared with various CN precursors, including dicyandiamide, melamine, guanidine hydrochloride and urea, were characterized by X-ray diffraction, thermal gravimetric analysis, N2physisorption, transmission electron microscopy, X-ray photoelectron spectroscopy and atomic emission spectrometer measurements, and used as catalysts to catalyze the rhodamine B oxidation with H2O2as oxidant. Characteristic results showed that Fe–CN exhibits different compositions, properties and catalytic performances if different CN precursors are used. The Fe–CN prepared from dicyandiamide contains mainly CN phase and certain amounts of surface Fe2O3phase, exhibits the best activity; while that prepared from urea contains mainly Fe2O3phase and few amounts of CN phase, exhibits the worst activity. Contrasting experiments conducted under light irradiation, with a supported Fe/CN_D catalyst, and that using a washed catalyst, suggested that the surface Fe2O3is the active site of the reaction.

Carbon Film Deposition On Silicon Using Low Energy Ion Beams

1991 ◽  
Vol 223 ◽  
Author(s):  
Qin Fuguang ◽  
Yao Zhenyu ◽  
Ren Zhizhang ◽  
S.-T. Lee ◽  
I. Bello ◽  
...  
Keyword(s):  
Photoelectron Spectroscopy ◽  
Ion Beam ◽  
Carbon Film ◽  
Carbon Films ◽  
Film Deposition ◽  
Ion Energy ◽  
Transmission Electron ◽  
Higher Temperature ◽  
Post Implantation ◽  
Beam Deposition

ABSTRACTDirect ion beam deposition of carbon films on silicon in the ion energy range of 15–500eV and temperature range of 25–800°C has been studied using mass selected C+ ions under ultrahigh vacuum. The films were characterized with X-ray photoelectron spectroscopy, Raman spectroscopy, and transmission electron microscopy and diffraction analysis. Films deposited at room temperature consist mainly of amorphous carbon. Deposition at a higher temperature, or post-implantation annealing leads to formation of microcrystalline graphite. A deposition temperature above 800°C favors the formation of microcrystalline graphite with a preferred orientation in the (0001) direction. No evidence of diamond formation was observed in these films.

Investigation of Polyoxometalate-(Poly)pyrrole Heterogeneous Nanostructures as Cathodes for Rechargeable Magnesium-Ion Batteries

2018 ◽  
Author(s):  
Hakeem K. Henry ◽  
Sang Bok Lee
Keyword(s):  
Electron Microscopy ◽  
Transmission Electron Microscopy ◽  
Photoelectron Spectroscopy ◽  
Active Material ◽  
Conductive Polymer ◽  
Current Collector ◽  
Constant Current ◽  
Anodized Aluminum ◽  
Transmission Electron ◽  
Pyrrole Monomer

The PMo<sub>12</sub>-PPy heterogeneous cathode was synthesized electrochemically. In doing so, the PMo<sub>12</sub> redox-active material was impregnated throughout the conductive polymer matrix of the poly(pyrrole) nanowires. All chemicals and reagents used were purchased from Sigma-Aldrich. Anodized aluminum oxide (AAO) purchased from Whatman served as the porous hard template for nanowire deposition. A thin layer of gold of approximately 200nm was sputtered onto the disordered side of the AAO membrane to serve as the current collector. Copper tape was connected to the sputtered gold for contact and the device was sealed in parafilm with heat with an exposed area of 0.32 cm<sup>2</sup> to serve as the electroactive area for deposition. All electrochemical synthesis and experiments were conducted using a Bio-Logic MPG2 potentiostat. The deposition was carried out using a 3-electrode beaker cell setup with a solution of acetonitrile containing 5mM and 14mM of the phosphomolybdic acid and pyrrole monomer, respectively. The synthesis was achieved using chronoamperometry to apply a constant voltage of 0.8V vs. Ag/AgCl (BASi) to oxidatively polymerize the pyrrole monomer to poly(pyrrole). To prevent the POM from chemically polymerizing the pyrrole, an injection method was used in which the pyrrole monomer was added to the POM solution only after the deposition voltage had already been applied. The deposition was well controlled by limiting the amount of charge transferred to 300mC. Following deposition, the AAO template was removed by soaking in 3M sodium hydroxide (NaOH) for 20 minutes and rinsed several times with water. After synthesis, all cathodes underwent electrochemical testing to determine their performance using cyclic voltammetry and constant current charge-discharge cycling in 0.1 M Mg(ClO<sub>4</sub>)<sub>2</sub>/PC electrolyte. The cathodes were further characterized using scanning electron microscopy (SEM), transmission electron microscopy (TEM), scanning transmission electron microscopy (STEM), and x-ray photoelectron spectroscopy (XPS).

scholarly journals α-Cellulose Fibers of Paper-Waste Origin Surface-Modified with Fe3O4 and Thiolated-Chitosan for Efficacious Immobilization of Laccase

Polymers ◽  
2021 ◽  
Vol 13 (4) ◽  
pp. 581
Author(s):  
Gajanan S. Ghodake ◽  
Surendra K. Shinde ◽  
Ganesh D. Saratale ◽  
Rijuta G. Saratale ◽  
Min Kim ◽  
...  
Keyword(s):  
Enzyme Immobilization ◽  
Photoelectron Spectroscopy ◽  
Cellulose Fibers ◽  
Relative Activity ◽  
Significant Activity ◽  
X Ray Diffraction ◽  
X Ray ◽  
Transmission Electron ◽  
Laccase Immobilization ◽  
Surface Modified

The utilization of waste-paper-biomass for extraction of important α-cellulose biopolymer, and modification of extracted α-cellulose for application in enzyme immobilization can be extremely vital for green circular bio-economy. Thus, in this study, α-cellulose fibers were super-magnetized (Fe3O4), grafted with chitosan (CTNs), and thiol (-SH) modified for laccase immobilization. The developed material was characterized by high-resolution transmission electron microscopy (HR-TEM), HR-TEM energy dispersive X-ray spectroscopy (HR-TEM-EDS), X-ray diffraction (XRD), vibrating sample magnetometer (VSM), X-ray photoelectron spectroscopy (XPS), and Fourier transform infrared spectroscopy (FT-IR) analyses. Laccase immobilized on α-Cellulose-Fe3O4-CTNs (α-Cellulose-Fe3O4-CTNs-Laccase) gave significant activity recovery (99.16%) and laccase loading potential (169.36 mg/g). The α-Cellulose-Fe3O4-CTNs-Laccase displayed excellent stabilities for temperature, pH, and storage time. The α-Cellulose-Fe3O4-CTNs-Laccase applied in repeated cycles shown remarkable consistency of activity retention for 10 cycles. After the 10th cycle, α-Cellulose-Fe3O4-CTNs possessed 80.65% relative activity. Furthermore, α-Cellulose-Fe3O4-CTNs-Laccase shown excellent degradation of pharmaceutical contaminant sulfamethoxazole (SMX). The SMX degradation by α-Cellulose-Fe3O4-CTNs-Laccase was found optimum at incubation time (20 h), pH (3), temperatures (30 °C), and shaking conditions (200 rpm). Finally, α-Cellulose-Fe3O4-CTNs-Laccase gave repeated degradation of SMX. Thus, this study presents a novel, waste-derived, highly capable, and super-magnetic nanocomposite for enzyme immobilization applications.

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