scholarly journals Electrochemical Reduction of Oxygen on Anthraquinone/Carbon Nanotubes Nanohybrid Modified Glassy Carbon Electrode in Neutral Medium

2013 ◽  
Vol 2013 ◽  
pp. 1-9 ◽  
Author(s):  
Zheng Gong ◽  
Guoquan Zhang ◽  
Song Wang
Keyword(s):  
Carbon Nanotubes ◽  
Electron Microscope ◽  
Glassy Carbon ◽  
Multiwall Carbon Nanotubes ◽  
Rotating Disk ◽  
Reduction Reaction ◽  
Rotating Disk Electrode ◽  
Neutral Medium ◽  
Potential Range ◽  
Buffer Solution

The electrochemical behaviors of monohydroxy-anthraquinone/multiwall carbon nanotubes (MHAQ/MWCNTs) nanohybrid modified glassy carbon (MHAQ/MWCNTs/GC) electrodes in neutral medium were investigated; also reported was their application in the electrocatalysis of oxygen reduction reaction (ORR). The resulting MHAQ/MWCNTs nanohybrid was characterized by scanning electron microscope (SEM) and transmission electron microscope (TEM). It was found that the ORR at the MHAQ/MWCNTs/GC electrode occurs irreversibly at a potential about 214 mV less negative than at a bare GC electrode in pH 7.0 buffer solution. Cyclic voltammetric and rotating disk electrode (RDE) techniques indicated that the MHAQ/MWCNTs nanohybrid has high electrocatalytic activity for the two-electron reduction of oxygen in the studied potential range. The kinetic parameters of ORR at the MHAQ/MWCNTs nanohybrid modified GC electrode were also determined by RDE and EIS techniques.

scholarly journals N8− Polynitrogen Stabilized on Nitrogen-Doped Carbon Nanotubes as an Efficient Electrocatalyst for Oxygen Reduction Reaction

Catalysts ◽  
2020 ◽  
Vol 10 (8) ◽  
pp. 864 ◽  
Author(s):  
Zhenhua Yao ◽  
Ruiyang Fan ◽  
Wangyang Ji ◽  
Tingxuan Yan ◽  
Maocong Hu
Keyword(s):  
Carbon Nanotubes ◽  
Oxygen Reduction Reaction ◽  
Oxygen Reduction ◽  
Rotating Disk ◽  
Reduction Reaction ◽  
Rotating Disk Electrode ◽  
Nitrogen Doped ◽  
Metal Free ◽  
Temperature Programmed ◽  
Nitrogen Doped Carbon

In this work, non-traditional metal-free polynitrogen chain N8− deposited on a nitrogen-doped carbon nanotubes (PN-NCNT) catalyst was successfully synthesized by a facile cyclic voltammetry (CV) approach, which was further tested in an oxygen reduction reaction (ORR). The formation of PN on NCNT was confirmed by attenuated total reflectance–Fourier transform infrared spectroscopy (ATR-FTIR) and Raman spectroscopy. Partial positive charge of carbon within NCNT facilitated electron transfer and accordingly induced the formation of more PN species compared to CNT substrate as determined by temperature-programmed decomposition (TPD). Rotating disk electrode (RDE) measurements suggested that a higher current density was achieved over PN-NCNT than that on PN-CNT catalyst, which can be attributed to formation of the larger amount of N8− on NCNT. Kinetic study suggested a four-electron pathway mechanism over PN-NCNT. Moreover, it showed long stability and good methanol tolerance, which indicates its great potential application. This work provides insights on designing and synthesizing non-traditional metal-free catalysts for ORR in fuel cells.

Investigation of ORR Performances on Graphene/Phthalocyanine Nanocomposite in Neutral Medium

2019 ◽  
Vol 25 (6) ◽  
pp. 1416-1421 ◽  
Author(s):  
Moumita Mukherjee ◽  
Madhupriya Samanta ◽  
Gour P. Das ◽  
Kalyan K. Chattopadhyay
Keyword(s):  
Metal Ion ◽  
Low Cost ◽  
Rotating Disk ◽  
Reduction Reaction ◽  
Rotating Disk Electrode ◽  
Zinc Phthalocyanine ◽  
Neutral Medium ◽  
Neutral Solution ◽  
Solution Ph ◽  
Onset Potential

AbstractThe drive to replace scarce and expensive Pt-based electrocatalysts for oxygen reduction reaction (ORR) has led to the development of a group of electrocatalysts composed of transition-metal ion centers coordinated with four nitrogen groups (M-N4). Among these, metal phthalocyanines (MPcs), due to low cost of preparation, highly conjugated structure as well as high thermal and chemical stability, have received a great interest. The catalytic activity of MPcs can be improved by employing conducting supports. Here, in this report, we have solvothermally synthesized graphene-supported zinc phthalocyanine nanostructures, and their ORR kinetics and mechanism have been investigated in neutral solution (pH = 7) by using the rotating disk electrode technique. The as-synthesized nanocomposite followed a 4e− reduction pathway. The onset potential (−0.04 V versus Ag/AgCl) found in this work can be comparable with other state-of-the-art material, demonstrating good performance in neutral solution. The fascinating performance leads the nanocomposite material toward future energy applications.

Electrochemical dioxygen reduction catalyzed by a (nitro)cobalt(perfluorophthalocyanine) complex and the possibility of a peroxynitro complex intermediate

2015 ◽  
Vol 19 (11) ◽  
pp. 1185-1196 ◽  
Author(s):  
John A. Goodwin ◽  
Johnson Agbo ◽  
Justin Zuczek ◽  
Auquilla Samuel ◽  
Tyler H. Aslund ◽  
...  
Keyword(s):  
Glassy Carbon Electrode ◽  
Glassy Carbon ◽  
Rotating Disk ◽  
Open Shell ◽  
Reduction Reaction ◽  
Rotating Disk Electrode ◽  
Carbon Electrode ◽  
Disk Electrode ◽  
Pyridine Ligand ◽  
Dioxygen Reduction

The (nitro)([Formula: see text],[Formula: see text]-dimethyl-4-aminopyridine) complex of perfluorinated cobalt(III) phthalocyanine Co(III)F16Pc(Me2Npy)(NO[Formula: see text] catalyzes the electrochemical oxygen reduction reaction (ORR) in pH 4.0, 7.0, and 10.0 buffer and 0.05 M sulfuric acid solution when deposited on a glassy carbon electrode. Cyclic voltammetry (CV), rotating disk electrode voltammetry (RDE), and rotating ring-disk electrode voltammetry (RRDE) have been used to determine the reduction product as hydrogen peroxide although in concentrations too small to observe by qualitative methods such as oxidation of NaI in solution. The dependence of the values of the peak potentials for the reduction on the pH of the solution and the -log[Me2Npy] are consistent with protonation up to pH 7.6 and pyridine ligand loss during the reduction. The addition of nitrite at 0.1 and 1 M to pH 7.0 solutions in contact with films of CoF16Pc on the glassy carbon electrode decreases the ORR current and shifts the peak potential of the ORR from -0.21 V vs. NHE to -0.19 V vs. NHE. The addition of nitrite at 0.1 and 1 M to films of Co(III)F16Pc(Me2Npy)(NO[Formula: see text] on glassy carbon, however, has no effect on either the current or the potential. While the electrochemical evidence for this proposal is not definitive, modeling has been used to examine the center of reduction in the alternative mechanisms by evaluation of the LUMOs of the hypothetical intermediates in both closed and open shell cases. The formation of five-coordinate Co(II)F16Pc(NO) is proposed to occur initially in the reduction mechanism. It is also possible that O2 reduction takes place at the NO ligand center by way of a nitrogen-bound peroxynitrite intermediate. The [Formula: see text] ligand appears to remain bound during the ORR. Direct coordination of O2 to the metal center requiring a six-coordinate species, Co(III)F16Pc(O[Formula: see text](NO[Formula: see text], Co(II)F16Pc(O[Formula: see text](NO) or [Co(II)F16Pc(O[Formula: see text](NO[Formula: see text]][Formula: see text] and has been considered in DFT modeling studies. The instability of the two-electron reduced, protonation species, [Co(I)F16Pc(NO2OH)][Formula: see text] in its loss of peroxynitrous acid suggests that the reduction of O2 may occur by two one-electron reduction steps rather than a two-electron step.

scholarly journals Synthesis and electrocatalytic activity towards oxygen reduction reaction of gold-nanostars

2018 ◽  
Vol 18 (44) ◽  
pp. 36-40
Author(s):  
Oyunbileg G ◽  
Batnyagt G ◽  
Enkhsaruul B ◽  
T Takeguchi
Keyword(s):  
Electron Microscope ◽  
Oxygen Reduction Reaction ◽  
Oxygen Reduction ◽  
Electrocatalytic Activity ◽  
Electrical Energy ◽  
Rotating Disk ◽  
Reduction Reaction ◽  
Rotating Disk Electrode ◽  
Alkaline Electrolyte ◽  
Study Results

The oxygen reduction reaction (ORR) is a characteristic reaction which determines the performance of fuel cells which convert a chemical energy into an electrical energy. Aims of this study are to synthesize Au-based nanostars (AuNSs) and determine their preliminary electro-catalytic activities towards ORR by a rotating-disk electrode method in alkaline electrolyte. The images obtained from a scanning electron microscope (SEM) and a transmission electron microscope (TEM) analyses confirm the formation of the star-shaped nanoparticles. Among the investigated nanostar catalysts, an AuNS5 with smaller size and a few branches showed the higher electrocatalytic activity towards ORR than other catalysts with a bigger size. In addition, the electron numbers transferred for all the catalysts are approximately two. The present study results infer that the size of the Au-based nanostars may influence greatly on their catalytic activity. The present study results show that the further improvement is needed for Au-based nanostar catalysts towards the ORR reaction.

scholarly journals Preparation of Bimetallic Pd-Co Nanoparticles on Graphene Support for Use as Methanol Tolerant Oxygen Reduction Electrocatalysts

2012 ◽  
Vol 2 (6) ◽  
pp. 295-301 ◽  
Author(s):  
R. N. Singh ◽  
C. S. Sharma
Keyword(s):  
Oxygen Reduction ◽  
Multiwall Carbon Nanotubes ◽  
Rotating Disk ◽  
Lattice Parameter ◽  
Reduction Reaction ◽  
Rotating Disk Electrode ◽  
Partial Substitution ◽  
Methanol Tolerant ◽  
Orr Activity ◽  
Co Nanoparticles

Graphene-supported (40-x) wt% Pd x wt% Co (0≤x≤13.33) alloys/composites have been prepared by a microwave-assisted polyol reduction method and been investigated for their structural and electrocatalytic properties for the oxygen reduction reaction (ORR) in 0.5 M H2SO4 at 298 K. The study demonstrated that the bimetallic Pd-Co composite nanoparticles are, in fact, alloy nanoparticles with fcc crystalline structure. Partial substitution of Pd by Co (from 3.64 to 13.33 wt%) in 40 wt% Pd/graphene decreases the lattice parameter as well as the crystallite size and increases the apparent catalytic activity, the latter, however, being the greatest with 8 wt% Co. The ORR activity of the active 32 wt% Pd 8wt% Co is found to be considerably low when it was deposited on the support multiwall carbon nanotubes under similar conditions. The rotating disk electrode study indicated that the ORR on 32 wt% Pd 8 wt% Co/GNS in 0.5 M H2SO4 follows approximately the four-electron pathway.

scholarly journals Eco-Friendly Nitrogen-Doped Graphene Preparation and Design for the Oxygen Reduction Reaction

Molecules ◽  
2021 ◽  
Vol 26 (13) ◽  
pp. 3858
Author(s):  
Monica Dan ◽  
Adriana Vulcu ◽  
Sebastian A. Porav ◽  
Cristian Leostean ◽  
Gheorghe Borodi ◽  
...  
Keyword(s):  
Oxygen Reduction Reaction ◽  
Oxygen Reduction ◽  
Rotating Disk ◽  
Reduction Reaction ◽  
Machine Learning Algorithms ◽  
Rotating Disk Electrode ◽  
X Ray ◽  
Synthesis Conditions ◽  
Characterization Techniques ◽  
Doped Graphene

Four N-doped graphene materials with a nitrogen content ranging from 8.34 to 13.1 wt.% are prepared by the ball milling method. This method represents an eco-friendly mechanochemical process that can be easily adapted for industrial-scale productivity and allows both the exfoliation of graphite and the synthesis of large quantities of functionalized graphene. These materials are characterized by transmission and scanning electron microscopy, thermogravimetry measurements, X-ray powder diffraction, X-ray photoelectron and Raman spectroscopy, and then, are tested towards the oxygen reduction reaction by cyclic voltammetry and rotating disk electrode methods. Their responses towards ORR are analysed in correlation with their properties and use for the best ORR catalyst identification. However, even though the mechanochemical procedure and the characterization techniques are clean and green methods (i.e., water is the only solvent used for these syntheses and investigations), they are time consuming and, generally, a low number of materials can be prepared, characterized and tested. In order to eliminate some of these limitations, the use of regression learner and reverse engineering methods are proposed for facilitating the optimization of the synthesis conditions and the materials’ design. Thus, the machine learning algorithms are applied to data containing the synthesis parameters, the results obtained from different characterization techniques and the materials response towards ORR to quickly provide predictions that allow the best synthesis conditions or the best electrocatalysts’ identification.

Methanol-Tolerant Oxygen Reduction Reaction at Pt–Pd/C Alloy Nanocatalysts

2010 ◽  
Vol 8 (1) ◽  
Author(s):  
A. Mary Remona ◽  
K. L. N. Phani
Keyword(s):  
Oxygen Reduction Reaction ◽  
Oxygen Reduction ◽  
Rotating Disk ◽  
Reduction Reaction ◽  
Rotating Disk Electrode ◽  
Methanol Tolerance ◽  
Pd Catalysts ◽  
Onset Potential ◽  
Direct Methanol ◽  
Methanol Tolerant

Carbon-supported platinum and Pt–Pd alloy electrocatalysts with different Pt/Pd atomic ratios were synthesized by a microemulsion method at room temperature (metal loading is 10 wt %). The Pt–Pd/C bimetallic catalysts showed a single-phase fcc structure and the mean particle size of Pt–Pd/C catalysts was found to be lower than that of Pt/C. The methanol-tolerant studies of the catalysts were carried out by activity evaluation of oxygen reduction reaction (ORR) on Pt–Pd catalysts using a rotating disk electrode (RDE). The studies indicated that the order of methanol tolerance was found to be PtPd3/C>PtPd/C>Pt3Pd/C. The oxygen reduction activities of all Pt–Pd/C were considerably larger than that of Pt/C with respect to onset and overpotential values. The Pd-loaded catalysts shift the onset potential of ORR by 125 mVMSE, 53 mVMSE, and 41 mVMSE to less cathodic potentials for Pt3Pd/C, PtPd/C, and PtPd3/C, respectively, with reference to Pt/C and the Pt3Pd/C catalyst showed greater shift in the onset value than the other PtPd catalysts reported in literature. Moreover, the Pt–Pd/C catalysts exhibited much higher methanol tolerance during ORR than the Pt/C, assessing that these catalysts may function as a methanol-tolerant cathode catalysts in a direct methanol fuel cell.

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