scholarly journals Oxygen Reduction Reaction Electrocatalysis in Alkaline Electrolyte on Glassy-Carbon-Supported Nanostructured Pr6O11 Thin-Films

Catalysts ◽  
2018 ◽  
Vol 8 (10) ◽  
pp. 461 ◽  
Author(s):  
Rakesh Sharma ◽  
Verónica Müller ◽  
Marian Chatenet ◽  
Elisabeth Djurado

In this work, hierarchical nanostructured Pr6O11 thin-films of brain-like morphology were successfully prepared by electrostatic spray deposition (ESD) on glassy-carbon substrates. These surfaces were used as working electrodes in the rotating disk electrode (RDE) setup and characterized in alkaline electrolyte (0.1 M NaOH at 25 ± 2 °C) for the hydrogen evolution reaction (HER), the oxygen evolution reaction (OER), and the oxygen reduction reaction (ORR) for their potential application in alkaline electrolyzers or in alkaline fuel cells. The electrochemical performances of these electrodes were investigated as a function of their crystallized state (amorphous versus crystalline). Although none of the materials display spectacular HER and OER activity, the results show interesting performances of the crystallized sample towards the ORR with regards to this class of non-Pt group metal (non-PGM) electrocatalysts, the activity being, however, still far from a benchmark Pt/C electrocatalyst.

2018 ◽  
Vol 18 (44) ◽  
pp. 36-40
Author(s):  
Oyunbileg G ◽  
Batnyagt G ◽  
Enkhsaruul B ◽  
T Takeguchi

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.


Author(s):  
N. F. Daudt ◽  
A. Poozhikunnath ◽  
H. Yu ◽  
L. Bonville ◽  
R. Maric

Abstract Proton exchange membrane fuel cells (PEMFC) play a key role for sustainable energy; however, catalyst degradation remains one of the main challenges for competing with traditional energy technologies. The Pt/C commercially available electrocatalysts are susceptible to Pt dissolution and carbon support corrosion. In this context, we design a Pt–NbOx catalyst supported on TiN nanoparticles as an alternative electrocatalyst for the oxygen reduction reaction (ORR). The use of Pt–NbOx reduces materials’ costs by lowering the required platinum loading and improving catalyst performance. The TiN support is selected to improve support stability. The electrocatalyst is successfully synthesized by a one-step flame spray process called reactive spray deposition technology. Electrocatalyst with two different very low Pt loadings (0.032 mg cm−2 and 0.077 mg cm−2) are investigated and their performance as cathode is evaluated by the rotating disk electrode method. The new electrocatalyst based on Pt–NbOx supported on TiN has ORR performance that is comparable to the state-of-the-art Pt/C electrocatalyst. A half-wave potential of 910 mV was observed in the polarization curves, as well as a mass activity of 0.120 A∙mgPt−1 and a specific activity of 283 μA∙cmPt−2 at 0.9 V. These results demonstrate that Pt–NbOx on TiN electrocatalyst has the potential for replacing Pt/C cathode in PEMFC.


Author(s):  
Busra Ergul-Yilmaz ◽  
Zhiwei Yang ◽  
Assem O. Basurrah ◽  
Mike L. Perry ◽  
Kimberly S Reeves ◽  
...  

Abstract Self-supported nanocolumnar Pt:Ni thin films (TFs) with varying Pt:Ni atomic ratios and Pt mass loadings were produced on a microporous layer (MPL)-like surface composed of carbon particles by high pressure sputtering and examined as oxygen reduction reaction (ORR) electrocatalysts for polymer electrolyte membrane fuel cells. Cauliflower-like microstructures were observed from scanning electron microscopy imaging. Various Pt:Ni atomic ratios were obtained by simply changing the relative deposition power between Pt and Ni source and investigated by X-ray diffraction and quartz crystal microbalance analysis. Electrochemical characterization of the Pt:Ni-TF/MPL-like-layer/glassy-carbon samples was conducted through benchtop cyclic voltammetry and rotating disk electrode measurements. The electrochemically active surface area (ECSA) was found to be between 22-42 m2/g for different Pt:Ni atomic ratios. Lower Pt mass loadings exhibited a higher ECSA and the catalytic activity of all Pt:Ni ratios increased with the increase in Pt mass loading. The ORR activity of the Pt:Ni-TFs increased in the order of 3:1 < 1:1 < 1:3 with exhibiting a specific activity of 1781 µA/cm2 and mass activity of 0.66 A/mg for the Ni-rich film with 1:3 ratio. The catalytic performance of Pt:Ni-TFs were higher than traditional high surface area carbon supported Pt nanoparticles, elemental Pt nanorods, and Pt-Ni nanorods.


Molecules ◽  
2021 ◽  
Vol 26 (13) ◽  
pp. 3858
Author(s):  
Monica Dan ◽  
Adriana Vulcu ◽  
Sebastian A. Porav ◽  
Cristian Leostean ◽  
Gheorghe Borodi ◽  
...  

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.


Author(s):  
A. Mary Remona ◽  
K. L. N. Phani

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.


2008 ◽  
Vol 258 (1) ◽  
pp. 235-242 ◽  
Author(s):  
L ZHU ◽  
D SUSAC ◽  
M TEO ◽  
K WONG ◽  
P WONG ◽  
...  

2017 ◽  
Vol 19 (45) ◽  
pp. 30464-30472 ◽  
Author(s):  
Tao Yang ◽  
Jian Liu ◽  
Yang Yu ◽  
Yueh-Lin Lee ◽  
Harry Finklea ◽  
...  

In the present study, the oxygen reduction reaction mechanism is investigated using numerical methods on a dense thin (La1−xSrx)yMnO3±δ film deposited on a YSZ substrate.


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