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Full-Text Articles in Engineering
Sr2Fe1.5Mo0.5O6-Δ – Sm0.2Ce0.8O1.9 Composite Anodes For Intermediate-Temperature Solid Oxide Fuel Cells, Beibei He, Ling Zhao, Shuxiang Song, Tong Liu, Fanglin Chen, Changrong Xia
Sr2Fe1.5Mo0.5O6-Δ – Sm0.2Ce0.8O1.9 Composite Anodes For Intermediate-Temperature Solid Oxide Fuel Cells, Beibei He, Ling Zhao, Shuxiang Song, Tong Liu, Fanglin Chen, Changrong Xia
Faculty Publications
Sr2Fe1.5Mo0.5O6−δ (SFM) perovskite is carefully investigated as an anode material for solid oxide fuel cells with LaGaO3-based electrolytes. Its electronic conductivity under anodic atmosphere is measured with four-probe method while its ionic conductivity is determined with oxygen permeation measurement. Samaria doped ceria (SDC) is incorporated into SFM electrode to improve the anodic performance. A strong relation is observed between SDC addition and polarization losses, suggesting that the internal SFM-SDC contacts are active for H2 oxidation. The best electrode performance is achieved for the composite with 30 wt% SDC addition, resulting …
Aerosol-Assisted Synthesis Of Monodisperse Single-Crystalline Α-Cristobalite Nanospheres, Xingmao Jiang, Lihong Bao, Yung-Sung Cheng, Darren R. Dunphy, Xiaodong Li, C. Jeffrey Brinker
Aerosol-Assisted Synthesis Of Monodisperse Single-Crystalline Α-Cristobalite Nanospheres, Xingmao Jiang, Lihong Bao, Yung-Sung Cheng, Darren R. Dunphy, Xiaodong Li, C. Jeffrey Brinker
Faculty Publications
Monodisperse single-crystalline α-cristobalite nanospheres have been synthesized by hydrocarbon-pyrolysis-induced carbon deposition on amorphous silica aerosol nanoparticles, devitrification of the coated silica at high temperature, and subsequent carbon removal by oxidation. The nanosphere size can be well controlled by tuning the size of the colloidal silica precursor. Uniform, high-purity nanocrystalline α-cristobalite is important for catalysis, nanocomposites, advanced polishing, and understanding silica nanotoxicology.
Effect Of Titanium Dioxide Supports On The Activity Of Pt-Ru Toward Electrochemical Oxidation Of Methanol, Roderick E. Fuentes, Brenda L. García, John W. Weidner
Effect Of Titanium Dioxide Supports On The Activity Of Pt-Ru Toward Electrochemical Oxidation Of Methanol, Roderick E. Fuentes, Brenda L. García, John W. Weidner
Faculty Publications
TiO2and Nb-TiO2 were investigated as stable supports for Pt-Ru electrocatalysts towards methanol oxidation. X-ray photo-electron spectroscopy (XPS) data for all these TiO2-based supports show oxidation states of Ti4+, with no Ti3+, suggesting low electronic conductivity. However, the deposition of metal nanoparticles onto the supports at loadings of 60 wt% metal dramatically increased conductivity, making these electrodes (metal particles + support) suitable for electrochemistry even though the supports have low conductivity. For some of these TiO2-based supports, the activity of Pt-Ru towards methanol oxidation was excellent, even surpassing the activity …
Quantifying Individual Potential Contributions Of The Hybrid Sulfur Electrolyzer, John A. Staser, Maximilian B. Gorensek, John W. Weidner
Quantifying Individual Potential Contributions Of The Hybrid Sulfur Electrolyzer, John A. Staser, Maximilian B. Gorensek, John W. Weidner
Faculty Publications
The hybrid sulfur cycle has been investigated as a means to produce clean hydrogen efficiently on a large scale by first decomposing H2SO4 to SO2, O2, and H2O and then electrochemically oxidizing SO2 back to H2SO4 with the cogeneration of H2. Thus far, it has been determined that the total cell potential for the hybrid sulfur electrolyzer is controlled mainly by water transport in the cell. Water is required at the anode to participate in the oxidation of SO2 to H2SO4 …
Low-Temperature Synthesis Of A Ptru/Nb0.1ti0.9o2 Electrocatalyst For Methanol Oxidation, Brenda L. García, Roderick Fuentes, John W. Weidner
Low-Temperature Synthesis Of A Ptru/Nb0.1ti0.9o2 Electrocatalyst For Methanol Oxidation, Brenda L. García, Roderick Fuentes, John W. Weidner
Faculty Publications
Niobium was doped into anatase TiO2 support at 10 mol % (Nb0.1Ti0.9O2) using sol-gel chemistry. A PtRu/Nb0.1Ti0.9O2 catalyst was synthesized by LiBH4 reduction in tetrahydrofuran. The methanol electro-oxidation activity of the catalyst shows that this oxide support was electrically conductive. The current (A/gPt) was 6% higher on the PtRu/Nb0.1Ti0.9O2 catalyst compared to a commercial PtRu/C catalyst at 25°C. The electrochemically active surface area of the PtRu/C was 94% higher than PtRu/Nb0.1Ti0.9O2, thus the current per active site was 100% higher on PtRu/Nb0.1Ti0.9O2. A membrane electrode assembly with PtRu/Nb0.1Ti0.9O2 had 46% higher current (A/gPt) than an equivalent E-TEK membrane electrode assembly …
Development Of Method For Synthesis Of Pt–Co Cathode Catalysts For Pem Fuel Cells, Xuguang Li, Héctor R. Colón-Mercado, Gang Wu, Jong-Won Lee, Branko N. Popov
Development Of Method For Synthesis Of Pt–Co Cathode Catalysts For Pem Fuel Cells, Xuguang Li, Héctor R. Colón-Mercado, Gang Wu, Jong-Won Lee, Branko N. Popov
Faculty Publications
A procedure was developed to synthesize a platinum–cobalt (Pt–Co) alloy electrocatalyst for oxygen reduction using Co/C composite as a support. The Pt–Co/C catalysts were synthesized through: (i) chemical oxidation of carbon black, (ii) Co deposition on the oxidized carbon using a chelation method, (iii) chemical treatment in an acidic medium to remove excess of Co on the carbon surface, (iv) Pt deposition onto the Co/C support, and (v) postheat treatment to form the Pt–Co alloy catalyst. The synthesized Pt–Co/C catalyst showed improved activity and long-term stability in polymer electrolyte membrane …
Electrochemical Filtering Of Co From Fuel-Cell Reformate, Balasubramanian Lakshmanan, Wayne Huang, John W. Weidner
Electrochemical Filtering Of Co From Fuel-Cell Reformate, Balasubramanian Lakshmanan, Wayne Huang, John W. Weidner
Faculty Publications
A proton exchange membrane fuel cell was used as a flow reactor for continuous preferential oxidation of CO over H2 from 1.0% CO in H2 under pulse-potential control. By varying the pulse profile ~e.g., on-time, off-time, pulse potential! the CO and H2 oxidation currents were varied independently. The improvement in faradaic selectivity between CO and H2 oxidation results from the promotion of CO adsorption during the off ~i.e., open-circuit! portion of the pulse. Therefore, during the on portion CO oxidation was preferred while the surface was covered with CO.
Development Of A Novel Co Tolerant Proton Exchange Membrane Fuel Cell Anode, Andrew T. Haug, Ralph E. White, John W. Weidner, Wayne Huang
Development Of A Novel Co Tolerant Proton Exchange Membrane Fuel Cell Anode, Andrew T. Haug, Ralph E. White, John W. Weidner, Wayne Huang
Faculty Publications
Typically Pt is alloyed with metals such as Ru, Sn, or Mo to provide a more CO-tolerant, high-performance proton exchange membrane fuel cell (PEMFC) anode. In this work, a layer of carbon-supported Ru is placed between the Pt catalyst and the anode flow field to form a filter. When oxygen is added to the fuel stream, it was predicted that the slow H2 kinetics of Ru in this filter would become an advantage compared to Pt and Pt:Ru alloy anodes, allowing a greater percentage of O2 to oxidize adsorbed CO to CO2. With an anode feed …
Studies On Capacity Fade Of Spinel-Based Li-Ion Batteries, Ramadass Premanand, Anand Durairajan, Bala Haran, Ralph E. White, Branko N. Popov
Studies On Capacity Fade Of Spinel-Based Li-Ion Batteries, Ramadass Premanand, Anand Durairajan, Bala Haran, Ralph E. White, Branko N. Popov
Faculty Publications
The performance of Cell-Batt® Li-ion cells using nonstoichiometric spinel as the positive electrode material has been studied at different charging rates. The capacity of the cell was optimized based on varying the charging current and the end potential. Subsequent to this, the capacity fade of these batteries was studied at different charge currents. During cycling, cells were opened at intermittent cycles and extensive material and electrochemical characterization was done on the active material at both electrodes. For all charge currents, the resistance of both the electrodes does not vary significantly with cycling. This result is in contrast with cells …
Synthesis And Characterization Of Hydrous Ruthenium Oxide-Carbon Supercapacitors, Manikandan Ramani, Bala S. Haran, Ralph E. White, Branko N. Popov
Synthesis And Characterization Of Hydrous Ruthenium Oxide-Carbon Supercapacitors, Manikandan Ramani, Bala S. Haran, Ralph E. White, Branko N. Popov
Faculty Publications
It is shown that composite Ru oxide-carbon based supercapacitors possess superior energy and power densities as compared to bare carbon. An electroless deposition process was used to synthesize the ruthenium oxide-carbon composites. Ru is dispersed on the carbon matrix as small particles. The effect of electrochemical oxidation and temperature treatment on the material performance has been studied extensively. Increasing the oxidation temperature reduces the proton transport rate and also increases the degree of crystallinity of the deposits. This adversely affects the performance of the composite. Loading a small amount of Ru oxide (9 wt %) on carbon increases the capacitance …
Anodic Oxidation Of Ethylenediaminetetraacetic Acid On Platinum Electrode In Alkaline Medium, S. N. R. Pakalapati, Branko N. Popov, Ralph E. White
Anodic Oxidation Of Ethylenediaminetetraacetic Acid On Platinum Electrode In Alkaline Medium, S. N. R. Pakalapati, Branko N. Popov, Ralph E. White
Faculty Publications
The anodic oxidation of ethylenediaminetetraacetic acid (EDTA) was studied in alkaline medium on a smooth platinum electrode. Bulk electrolysis indicated that stable organic intermediates (formaldehyde and glyoxal) are formed during the oxidation of EDTA and that complete oxidation to CO2 can be achieved. The proposed pathway suggests that the acetate groups in EDTA are initially oxidized, generating formaldehyde and ethylenediamine. The rest potential of EDTA (0.066 to 0.164 V vs. Hg/HgO) was observed to be higher than for other organic species. In alkaline medium, very little EDTA oxidation was found to occur on bare platinum. Limiting-current behavior due to …
Linear Algebra Used To Determine Independent Half‐Cell Equations, D. H. Coleman, Ralph E. White
Linear Algebra Used To Determine Independent Half‐Cell Equations, D. H. Coleman, Ralph E. White
Faculty Publications
No abstract provided.
The Self-Discharge Of The Niooh/Ni(Oh)2 Electrode Constant Potential Study, Z. Mao, Ralph E. White
The Self-Discharge Of The Niooh/Ni(Oh)2 Electrode Constant Potential Study, Z. Mao, Ralph E. White
Faculty Publications
Hydrogen oxidation currents at a NiOOH/Ni(OH)2 electrode were measured directly at constant potentials for various hydrogen pressures and states of charge. It was found that the hydrogen oxidation current is linearly proportional to the hydrogen pressure at all electrode potentials and that the logarithm of the anodic current is a linear function of electrode potential. It was also found that hydrogen oxidation on the nickel substrate material was strongly inhibited by the presence of nickel hydroxide on the substrate surface. By comparing the currents for hydrogen oxidation and oxygen evolution on the NiOOH/Ni(OH)2 electrode and on a nickel …
The Effect Of The Tribromide Complex Reaction On The Oxidation/Reduction Current Of The Br2/Br– Electrode, P K. Adanuvor, Ralph E. White, S. E. Lorimer
The Effect Of The Tribromide Complex Reaction On The Oxidation/Reduction Current Of The Br2/Br– Electrode, P K. Adanuvor, Ralph E. White, S. E. Lorimer
Faculty Publications
The Br2/Br– electrode reaction with tribromide complex formation reaction in the solution, a chemical-electrochemical (C-E) type reaction, has been investigated in order to determine the effect of the chemical reaction on the electrode kinetics. It is shown that the chemical reaction has little effect on the electrode kinetics at very slow homogeneous reaction rates, but has a more drastic effect on the electrode kinetics at faster homogeneous reaction rates. Also, the kinetics at the electrode are affected by changes in the concentrations of the active species (Br2, Br–, and Br3–) …
An Analysis Of A Back Fed Porous Electorde For The Br2/Br- Redox Reaction, John W. Van Zee, Ralph E. White
An Analysis Of A Back Fed Porous Electorde For The Br2/Br- Redox Reaction, John W. Van Zee, Ralph E. White
Faculty Publications
No abstract provided.
An Analysis Of A Back Fed Porous Electrode For The Br2/Br Reaction, John Van Zee, Ralph E. White
An Analysis Of A Back Fed Porous Electrode For The Br2/Br Reaction, John Van Zee, Ralph E. White
Faculty Publications
An experimental analysis of the Br2/Br– redox reaction in a porous back fed ruthenium-coated titanium electrode is described. A mathematical model of the steady-state process is presented. Nonlinear regression of the model against the experimental data gives physically meaningful parameter estimates; these parameters and the model provide a design equation for the porous electrode current as a function of specific surface area, bulk Br2 concentration, average total overpotential, and the Reynolds number. The design equation shows that the back fed electrode could reduce the loss of Br2 across the separator and the ohmic loss in …
Electrochemical Reduction Of Molybdenum(Vi) Compounds In Molten Lithium Chloride-Potassium Chloride Eutectic, Branko N. Popov, H. A. Laitinen
Electrochemical Reduction Of Molybdenum(Vi) Compounds In Molten Lithium Chloride-Potassium Chloride Eutectic, Branko N. Popov, H. A. Laitinen
Faculty Publications
Molybdenum (VI) oxide reacts with molten LiCl-KCl eutectic at 450° to form MoO2CI2, which probably is present as an anion MoO2Cl4=, and pyromolybdate, Mo2O7=. Both of these species are electrochemically reduced to MoO2, which can be reoxidized to MoO2Cl2 by current reversal. A second reduction step, observed whether MoO3 or Mo2O72− is added to the melt, can be attributed to the reduction of MoO4−−, formed as a secondary reaction product in the first …