Relevant bibliographies by topics / Pt electrocatalyst

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers
  5. Reports

Academic literature on the topic 'Pt electrocatalyst'

Author: Grafiati
Published: 9 March 2023
Last updated: 31 July 2025

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Journal articles on the topic "Pt electrocatalyst"

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Kryukov, Yu I., V. I. Lukovtsev, Elena Mikhailovna Petrenko, and I. S. Khozyainova. "Electrochemical activity of the cathodes with platinum or platinum-palladium electrocatalysts for alkaline water electrolysis." Electrochemical Energetics 12, no. 1 (2012): 36–38. http://dx.doi.org/10.18500/1608-4039-2012-12-1-36-38.

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Electrochemical activity of cathodes with Pt or Pt-Pd-electrocatalysts was studied by voltammetry method under galvanostatic conditions. The dependence of the overvoltage of hydrogen evolution reaction on the logarithm of current density and on the test time of the cathode with Pt-Pd-electrocatalysts are defined. It is shown that the electrochemical activity of cathode with Pt-Pd-electrocatalyst is two times higher than with Pt-electrocatalyst at the hydrogen evolution reaction in 30% KOH solution at 90°C. As the temperature increases from 15 to 90° C the current density at 40 mV overvoltage a
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Cheng, Fengshun, Yuchen Guo, Xinhong Liang, et al. "Ionic Liquid Modification of High-Pt-Loading Pt/C Electrocatalysts for Proton Exchange Membrane Fuel Cell Application." Catalysts 14, no. 6 (2024): 344. http://dx.doi.org/10.3390/catal14060344.

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Ionic liquid modification for carbon-supported platinum (Pt/C) electrocatalysts to enhance their oxygen reduction reaction (ORR) activity has been well recognized. However, the research has only been reported on the low-Pt-loading Pt/C electrocatalysts, e.g., 20 wt%, while in practical applications, usually high-Pt-loading Pt/C electrocatalysts of 45–60 wt% are used. In this work, ionic liquid modification is systematically investigated for a Pt/C electrocatalyst with 60 wt% Pt loading for its ORR activity in the cathode in proton exchange membrane fuel cells (PEMFCs). Various adsorption amoun
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Miyamoto, Ryo, Taichi Ogawa, Ryosuke Nishiizumi, et al. "Pt-Ta-Co Electrocatalysts for Polymer Electrolyte Fuel Cells." ECS Meeting Abstracts MA2023-02, no. 40 (2023): 1958. http://dx.doi.org/10.1149/ma2023-02401958mtgabs.

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Introduction Electrocatalysts with both high catalytic activity and high potential cycling durability are required for polymer electrolyte fuel cells. It is of technological interest to develop electrocatalysts using mesoporous carbon as a support framework and Pt-Ta-Co as a catalyst. Fuel cells using this novel electrocatalyst have to be prepared to evaluate their electrochemical performance. Here in this study, we aim to examine polymer electrolyte fuel cells using these new electrocatalysts by evaluating the current-voltage characteristics and various overvoltages under different electrocat
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Miyamoto, Ryo, Kojiro Sanami, Takashi Suzuki, et al. "Electrochemical Characteristics of Polymer Electrolyte Fuel Cells Using Pt-Ta-Co Electrocatalysts." ECS Transactions 114, no. 5 (2024): 263–74. http://dx.doi.org/10.1149/11405.0263ecst.

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Polymer electrolyte fuel cells for heavy-duty applications need highly active and durable electrocatalysts. For this purpose, electrocatalysts based on Pt-Ta-Co materials are here developed. This study evaluates the cell performance, the various overvoltages, start-stop and load cycling durability, and electrocatalyst layer microstructure under different fabrication conditions. Guidelines for higher power, higher performance, and higher durability of polymer electrolyte fuel cells are proposed. Using Pt7Ta2Co1/KB electrocatalysts, the initial catalytic activity, start-stop cycle durability, an
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Miyamoto, Ryo, Kojiro Sanami, Takashi Suzuki, et al. "Electrochemical Characteristics of Polymer Electrolyte Fuel Cells Using Pt-Ta-Co Electrocatalysts." ECS Transactions 114, no. 5 (2024): 277–88. http://dx.doi.org/10.1149/11405.0277ecst.

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Polymer electrolyte fuel cells for heavy-duty applications need highly active and durable electrocatalysts. For this purpose, electrocatalysts based on Pt-Ta-Co materials are here developed. This study evaluates the cell performance, the various overvoltages, start-stop and load cycling durability, and electrocatalyst layer microstructure under different fabrication conditions. Guidelines for higher power, higher performance, and higher durability of polymer electrolyte fuel cells are proposed. Using Pt7Ta2Co1/KB electrocatalysts, the initial catalytic activity, start-stop cycle durability, an
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Miyamoto, Ryo, Taichi Ogawa, Ryosuke Nishiizumi, et al. "Pt-Ta-Co Electrocatalysts for Polymer Electrolyte Fuel Cells." ECS Transactions 112, no. 4 (2023): 353–60. http://dx.doi.org/10.1149/11204.0353ecst.

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Polymer electrolyte fuel cells for heavy-duty applications require highly active and durable electrocatalysts. Our research group has developed electrocatalysts with Pt-Ta-Co-based alloy. This study evaluates the cell performance with the Pt-Ta-Co-based alloy catalysts by varying the fabrication conditions of the electrocatalyst layers, such as the ionomer and solid ratio of the electrocatalyst paste. In addition, the effect of the carbon catalyst support on the cell performance is evaluated using mesoporous carbon and typical Ketjen black carbon supports. The cells using these new catalysts e
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Sharma, Shuchi, and Ranga Rao Gangavarapu. "(Digital Presentation) Synthesis and Promoting Activity of Gd2O3 for Methanol Electro-Oxidation on Pt/C." ECS Meeting Abstracts MA2022-02, no. 50 (2022): 2426. http://dx.doi.org/10.1149/ma2022-02502426mtgabs.

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One of the challenges in electrocatalysis is to design either an efficient non-noble electrocatalyst or improve the electrocatalytic activity of Pt/C by incorporating promoters such as metal oxides, carbides and nitrides. Rare earth metal oxides such as CeO2 have been explored to promote methanol electro-oxidation on Pt/C electrocatalyst. It has been noted that the synthesis method has profound effect on the physiochemical and in turn electrochemical properties of metal oxide promoted Pt/C electrocatalysts. This concept is tested on Gd2O3 promoted Pt/C. Gd2O3 is prepared by precipitation (GdO-
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Pan, Hong Cheng, Jiang Tao Liu, Jin Ming Liang, et al. "Preparation of Pt Colloids via a Wet-Chemical Method for Methanol Sensor." Advanced Materials Research 295-297 (July 2011): 527–30. http://dx.doi.org/10.4028/www.scientific.net/amr.295-297.527.

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Pt colloids were synthesized by a wet-chemical method. The Pt colloids were modified on the glassy carbon electrode (GCE). The electrochemical behavior and electrocatalyst for methanol of the colloidal Pt-modified electrode in H2SO4medium were investigated. The results show that the as-prepared Pt colloids are good electrocatalysts for methanol oxidation and the oxidation current increases with methanol concentration in the range of 0.002 to 0.5 M. The colloidal Pt-modified electrode is simple, easy-to-use and reusable, showing promising applications in the electrocatalyst and determination of
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Lim, Seongje, and Jong Hyeok Park. "MOF-Derived High Entropy Alloy Electrocatalyst with Low Amount of Noble Metal for Alkaline HER." ECS Meeting Abstracts MA2024-02, no. 56 (2024): 3782. https://doi.org/10.1149/ma2024-02563782mtgabs.

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Although numerous researches for electrochemical hydrogen generation reactions have been conducted, they have the limitation of requiring the use of large amounts of several noble metal elements such as Pt, Ru, and Ir for hydrogen evolution electrocatalysts. In addition, there are increasing researches of high-entropy alloy electrocatalysts, which has many advantages for electrocatalysis like high stability, tunability of element composition and ratio, various active sites, etc., while their synthesis methods usually require harsh consition. In this research, we introduce CoNiCuMnRu/C high ent
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Sanami, Kojiro, Kakeru Kubo, Ryo Miyamoto, et al. "A Tantalum-Rich Pt-Ta-Co Electrocatalyst for Polymer Electrolyte Fuel Cells." ECS Transactions 114, no. 5 (2024): 85–92. http://dx.doi.org/10.1149/11405.0085ecst.

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In polymer electrolyte fuel cells (PEFCs), Pt catalyst particle growth due to load fluctuation potential cycling, and oxidative corrosion of the carbon support due to start-stop potential cycling are important issues for cathode electrocatalysts affecting their durability. Here, we incorporate tantalum into the electrocatalyst to improve both the catalytic activity and durability. This is achieved via self-assembly of a nanocomposite electrocatalyst via dealloying to form Pt-Co alloy and TaOx support nanoparticles. Half-cell electrochemical measurements confirm that the catalytic activity and
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Dissertations / Theses on the topic "Pt electrocatalyst"

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geng, xi. "synthesis and characterization of nanostructured carbon supported Pt-based electrocatalysts." Digital WPI, 2012. https://digitalcommons.wpi.edu/etd-theses/83.

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Fuel cell, as an alternative green power source for automobiles and portable electronics, has attracted worldwide attention due to its desirable properties such as high energy density and low greenhouse gas emission. Despite great progress in the past decades, several challenges still remain as obstacles for the large-scale commercialization. Among them, the high cost of Pt-based electrode material is considered as a major barrier, while the life span or stability of electrode catalysts is another concern since the electrocatalysts can be easily poisoned during the fuel cell operation. In orde
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Ying, Qiling. "Preparation and characterization of highly active nano pt/c electrocatalyst for proton exchange membrane fuel cell." Thesis, University of the Western Cape, 2006. http://etd.uwc.ac.za/index.php?module=etd&action=viewtitle&id=gen8Srv25Nme4_3791_1188474883.

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<p>Catalysts play an essential role in nearly every chemical production process. Platinum supported on high surface area carbon substrates (Pt/C) is one of the promising candidates as an electrocatalyst in low temperature polymer electrolyte fuel cells. Developing the activity of the Pt/C catalyst with narrow Pt particle size distribution and good dispersion has been a main concern in current research.</p> <p><br /> In this study, the main objective was the development and characterization of inexpensive and effective nanophase Pt/C electrocatalysts. A set of modified Pt/C electrocatalysts wit
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Huang, Shiow-Jing. "Study of copper underpotential deposition on Au and Pt disk electrode and electrocatalyst." Case Western Reserve University School of Graduate Studies / OhioLINK, 2012. http://rave.ohiolink.edu/etdc/view?acc_num=case1323447585.

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STASSI, ALESSANDRO. "Preparation and characterization of electrocatalysts for high temperature polymer electrolyte fuel cells." Doctoral thesis, Università degli Studi di Roma "Tor Vergata", 2010. http://hdl.handle.net/2108/1338.

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E’ noto che per una effettiva immissione nel settore automotive delle celle a combustibile ad elettrolita polimerico (PEFCs) alimentate a idrogeno, una delle principali barriere da superare è legata durata dei materiali adoperati. Il fenomeno di sintering del platino e la corrosione che quest’ultimo assieme al supporto, subiscono operando alle alte temperature richieste dal settore automotive (120 ÷ 130 °C), si traduce in una riduzione del tempo di vita del catalizzatore nel suo complesso. Gli effetti del sintering e della corrosione del catalizzatore si traducono in una perdita di area super
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Perazzolo, Valentina. "NITROGEN, SULPHUR AND PLATINUM FUNCTIONAL MESOPOROUS CARBONS: SYNTHESIS, CHARACTERIZATION AND PERFORMANCE TOWARD OXYGEN REDUCTION REACTION." Doctoral thesis, Università degli studi di Padova, 2017. http://hdl.handle.net/11577/3424872.

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Proton Exchange Membrane (PEM) Fuel Cells are a promising technology for the clean energy production, especially in the automotive field. Actually, the main commercial catalysts employed in this system are based on Pt Nanoparticles supported on high surface area Carbon. The main issues associated to PEM Fuel Cells deal with the sluggish kinetic of oxygen reduction (ORR) at Platinum based electrode, with the low stability of both the carbon support and the metal phase, that tend respectively to oxidize and dissolve or diffuse and with the high cost due to rare and expensive Pt. In fact, nowaday
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Schmidt, Thomas Justus, Methap Oezaslan, W. Liu, et al. "Homogeneity and elemental distribution in self-assembled bimetallic Pd–Pt aerogels prepared by a spontaneous one-step gelation process." Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2017. http://nbn-resolving.de/urn:nbn:de:bsz:14-qucosa-222784.

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Multi-metallic aerogels have recently emerged as a novel and promising class of unsupported electrocatalyst materials due to their high catalytic activity and improved durability for various electrochemical reactions. Aerogels can be prepared by a spontaneous one-step gelation process, where the chemical co-reduction of metal precursors and the prompt formation of nanochain-containing hydrogels, as a preliminary stage for the preparation of aerogels, take place. However, detailed knowledge about the homogeneity and chemical distribution of these three-dimensional Pd–Pt aerogels at the nano-sca
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Schmidt, Thomas Justus, Methap Oezaslan, W. Liu, et al. "Homogeneity and elemental distribution in self-assembled bimetallic Pd–Pt aerogels prepared by a spontaneous one-step gelation process." Royal Society of Chemistry, 2016. https://tud.qucosa.de/id/qucosa%3A30258.

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Multi-metallic aerogels have recently emerged as a novel and promising class of unsupported electrocatalyst materials due to their high catalytic activity and improved durability for various electrochemical reactions. Aerogels can be prepared by a spontaneous one-step gelation process, where the chemical co-reduction of metal precursors and the prompt formation of nanochain-containing hydrogels, as a preliminary stage for the preparation of aerogels, take place. However, detailed knowledge about the homogeneity and chemical distribution of these three-dimensional Pd–Pt aerogels at the nano-sca
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CARDOSO, ELISANGELA S. "Síntese e caracterização de eletrocatalisadores Pt/C, PtAu/C e PtAuBi/C pelo método da redução via feixe de elétrons para oxidação direta de metanol e etanol." reponame:Repositório Institucional do IPEN, 2012. http://repositorio.ipen.br:8080/xmlui/handle/123456789/10132.

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Made available in DSpace on 2014-10-09T12:35:07Z (GMT). No. of bitstreams: 0<br>Made available in DSpace on 2014-10-09T14:00:26Z (GMT). No. of bitstreams: 0<br>Dissertação (Mestrado)<br>IPEN/D<br>Instituto de Pesquisas Energeticas e Nucleares - IPEN-CNEN/SP
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Gu, Zhihui. "Dissolution of oxygen reduction electrocatalysts in acidic environment." [College Station, Tex. : Texas A&M University, 2007. http://hdl.handle.net/1969.1/ETD-TAMU-2458.

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Curnick, Oliver J. "Ionomer-stabilised Pt and Pt-Ti bimetallic electrocatalysts for the proton exchange membrane fuel cell." Thesis, University of Birmingham, 2012. http://etheses.bham.ac.uk//id/eprint/3732/.

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This work aims to address the need for more durable electrocatalysts with lower precious metal content for proton exchange membrane fuel cells (PEMFCs), through the development of novel electrocatalyst materials and preparation routes. In this work, 'Nafion-Pt/C' electrocatalysts have been derived from ionomer-stabilised Pt nanoparticles synthesised via a novel, wet-chemical route that offers unprecedented control over the formation of the Pt-ionomer interface, with a view towards maximising the utilisation of the electrocatalyst. Nafion-Pt/C electrocatalysts have been characterised using ex-s
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Book chapters on the topic "Pt electrocatalyst"

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Astravukh, Yana, Angelina Pavlets, Aleksey Nikulin, Ilya Pankov, Danil Alekseenko, and Anastasia Alekseenko. "Hybrid Electrocatalyst Based on Pt/C with Varying Mass Fraction of Platinum for PEMFC." In Springer Proceedings in Materials. Springer Nature Switzerland, 2025. https://doi.org/10.1007/978-3-031-87677-6_1.

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Adzic, Radoslav, and Nebojsa Marinkovic. "Catalytic Properties of Pt Monolayer Electrocatalysts." In Platinum Monolayer Electrocatalysts. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-49566-4_8.

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Zhang, Junliang, and Shuiyun Shen. "Pt-MS Electrocatalysts for ORR." In Energy and Environment Research in China. Springer Berlin Heidelberg, 2020. http://dx.doi.org/10.1007/978-3-662-56070-9_3.

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Adzic, Radoslav, and Nebojsa Marinkovic. "Performance Stability and Scale-Up Syntheses of Pt Monolayer Electrocatalysts." In Platinum Monolayer Electrocatalysts. Springer International Publishing, 2020. http://dx.doi.org/10.1007/978-3-030-49566-4_9.

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Yao, Jun, Yufeng Yao, and Hossein Mirzaii. "Proton Modified Pt Zeolite Fuel Cell Electrocatalysts." In Renewable Energy in the Service of Mankind Vol I. Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-17777-9_16.

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Theerthagiri, Jayaraman, and Jagannathan Madhavan. "Pt Electrocatalysts for I-Mediated Dye-Sensitized Solar Cells." In Counter Electrodes for Dye-sensitized and Perovskite Solar Cells. Wiley-VCH Verlag GmbH & Co. KGaA, 2018. http://dx.doi.org/10.1002/9783527813636.ch2.

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Saravanan, Chandra, N. M. Markovic, M. Head-Gordon, and P. N. Ross. "Multi-Scale Modeling of CO Oxidation on Pt-Based Electrocatalysts." In Topics in Applied Physics. Springer New York, 2009. http://dx.doi.org/10.1007/978-0-387-78691-9_20.

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Chen, Rongrong, Junsong Guo, and Andrew Hsu. "Non-Pt Cathode Electrocatalysts for Anion-Exchange-Membrane Fuel Cells." In Lecture Notes in Energy. Springer London, 2013. http://dx.doi.org/10.1007/978-1-4471-4911-8_15.

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Dao, Van-Duong, Liudmila L. Larina, and Ho-Suk Choi. "Pt-Loaded Composite Electrocatalysts for I-Mediated Dye-Sensitized Solar Cells." In Counter Electrodes for Dye-sensitized and Perovskite Solar Cells. Wiley-VCH Verlag GmbH & Co. KGaA, 2018. http://dx.doi.org/10.1002/9783527813636.ch9.

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Zhang, Ruizhong, and Wei Chen. "Synthesis and Electrocatalysis of Pt-Pd Bimetallic Nanocrystals for Fuel Cells." In Nanostructure Science and Technology. Springer International Publishing, 2016. http://dx.doi.org/10.1007/978-3-319-29930-3_4.

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Conference papers on the topic "Pt electrocatalyst"

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Andresen, Peter L., Young J. Kim, Thomas P. Diaz, and Sam Hettiarachchi. "Online Catalytic Mitigation of SCC at Parts per Trillion Level." In CORROSION 2008. NACE International, 2008. https://doi.org/10.5006/c2008-08601.

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Abstract In oxidizing environments, electrocatalysis is highly effective in mitigating SCC, provided there is a stoichiometric excess of reductants over oxidants. This paper summarizes the mechanisms and criteria for effective SCC mitigation, with emphasis on the critical location for the catalyst in a crack and recent experimental support for these concepts. Optimization of electrocatalysis using an on-line process is described, and the experimental evidence for mitigation at ≤ 0.1 ppb Pt is presented.
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Andresen, Peter L., and Young J. Kim. "SCC Mitigation by Electrocatalysis." In CORROSION 2012. NACE International, 2012. https://doi.org/10.5006/c2012-01189.

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Abstract SCC growth rates are strongly influenced by water chemistry parameters, especially when crack chemistry can be concentrated from differential aeration or thermal gradients or boiling. Mitigation of the effects of the high corrosion potential associated with oxidants is most efficiently achieved by electrocatalysis, which requires that there be a stoichiometric excess of reductants over oxidants. Mechanisms and criteria for effective SCC mitigation are summarized, with particular focus on the critical location for the catalyst in a crack and experimental support for these concepts. Opt
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Andresen, Peter L. "Mitigation of Stress Corrosion Cracking by Underwater Thermal Spray Coating of Noble Metals." In CORROSION 1995. NACE International, 1995. https://doi.org/10.5006/c1995-95412.

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Abstract Numerous approaches have been developed for mitigating stress corrosion cracking in existing BWRs. Among these, reduction of the corrosion potential provides the most efficient, consistent, and dramatic decrease in the crack growth rate of unirradiated and irradiated materials of all types. Historically, reduction in corrosion potential has been accomplished by adding H2 to the feed water to decrease the dissolved O2 and H2O2 concentrations. However, H2 concentrations greatly in excess of the stoichiometric amount are required, and factors such as the cost of H2, increased N16 in the
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Strasser, Peter. "Combinatorial Development of Ternary Electrocatalysts for Methanol Oxidation." In ASME 2007 2nd Energy Nanotechnology International Conference. ASMEDC, 2007. http://dx.doi.org/10.1115/enic2007-45060.

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We report a combinatorial and high throughput catalyst optimization of ternary Pt-Co-Ru alloy electrocatalysts for the oxidation of methanol in Direct Methanol Fuel Cell anodes. A densely sampled ternary Pt alloy catalyst library was prepared and electrochemically tested in parallel for catalytic activity. A composition-activity map was obtained from which suitable catalyst candidates with improved activity were identified. Then, high throughput methods for evaluating corrosion stability of the alloy catalysts were developed based on structural and compositional criteria. Finally, combining st
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Diloyan, Georgiy, and Parsaoran Hutapea. "Platinum Dissolution in Proton Exchange Membrane Fuel Cell Under Mechanical Vibrations." In ASME 2011 9th International Conference on Fuel Cell Science, Engineering and Technology collocated with ASME 2011 5th International Conference on Energy Sustainability. ASMEDC, 2011. http://dx.doi.org/10.1115/fuelcell2011-54944.

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One of the factors that affect the performance of proton exchange membrane fuel cells (PEMFC) is the loss of electrochemically active surface area of the Platinum (Pt) based electrocatalyst due to platinum dissolution and sintering. The intent of the current research is to understand the effect of mechanical vibrations on the Pt particles dissolution and overall PEMFC performance. This study is of great importance for the automotive application of fuel cells, since they operate under a vibrating environment. Carbon supported platinum plays an important role as an electrocatalyst in PEMFC. Pt p
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Passalacqua, E., P. L. Antonucci, M. Vivaldi, A. Patti, N. Giordano, and K. Kinoshita. "Electrooxidation Behaviour of Pt/Carbon Electrocatalyst for Phosphoric Acid Fuel Cells (PAFC)." In 27th Intersociety Energy Conversion Engineering Conference (1992). SAE International, 1992. http://dx.doi.org/10.4271/929294.

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Maleki, Nasim, and Erfan Maleki. "Modeling of Cathode Pt /C Electrocatalyst Degradation and Performance of a PEMFC using Artificial Neural Network." In the The International Conference. ACM Press, 2015. http://dx.doi.org/10.1145/2832987.2833000.

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Gribov, Evgeniy N., Ivan M. Krivobokov, and Aleksey G. Okunev. "Effect of MEAs Preparation Procedure on Their Performance in Room Temperature DMFC." In ASME 2010 8th International Conference on Fuel Cell Science, Engineering and Technology. ASMEDC, 2010. http://dx.doi.org/10.1115/fuelcell2010-33160.

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In this work the effect of the MEA preparation techniques on the performance of DMFC was evaluated using three different methods of electrocatalyst deposition: i) catalyst coated membrane; ii) catalyst coated carbon paper; and iii) decal deposition. Optimization of the nafion content (5–15 wt. %) at anode and cathode sides of the MEA and the pressure (150–500 atm) were also performed. Activities of both supported and unsupported Pt and PtRu catalysts (Johnson Matthew) were compared in room temperature DMFC (RT-DMFC) using polarization curves. All MEAs prepared were also characterized by electr
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De Oliveira Vigier, Karine, Christophe Coutanceau, and Steve Baranton. "Electro-oxidation of glycerol and diglycerol in the presence of Pt or Pd-based electrocatalyst follows by the reductive amination of the products obtained." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/olba8004.

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The selective electro-oxidation of bio-based organic molecules such as glycerol, polyglycerols, saccharides and furanic compounds has received particular attention in recent years, due to the high value-added compounds that result and their numerous industrial applications. Electrochemical methods are therefore well suited for the controlled oxidation of small organic molecules in aqueous media. Glycerol valorization through partial oxidation is a good way of obtaining many different molecules with high added value such as glyceric acid, tartronic acid, dihydroxyacetone, glyceraldehyde etc.,
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Ogawa, Kuniyasu, Yasuo Yokouchi, Tomoyuki Haishi, and Kohei Ito. "Measurement of Current-Density in PEFC With NMR Sensors." In ASME/JSME 2011 8th Thermal Engineering Joint Conference. ASMEDC, 2011. http://dx.doi.org/10.1115/ajtec2011-44370.

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In order to improve the power generation performance of polymer electrolyte fuel cells (PEFC), it is necessary to maintain high current density over the whole area of the membrane electrode assembly (MEA) that includes the additional Pt-carbon particles loaded on the Polymer Electrolyte Membrane (PEM) as an electrocatalyst layer. However, the current density generated at the MEA is distributed unevenly due to a lack of hydrogen, flooding, and so on. Therefore, achieving a higher current density in a PEFC requires monitoring the local current density. The local current density in a PEFC can be
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Reports on the topic "Pt electrocatalyst"

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Stechel, Ellen Beth, Elise E. Switzer, Cy H. Fujimoto, Plamen Borissov Atanassov, Christopher James Cornelius, and Michael R. Hibbs. Nanostructured electrocatalyst for fuel cells : silica templated synthesis of Pt/C composites. Office of Scientific and Technical Information (OSTI), 2007. http://dx.doi.org/10.2172/952106.

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Adzic, Radoslav, and Michael Furey. Investigation of New Pt Monolayer Electrocatalysts for O2 Reduction. Office of Scientific and Technical Information (OSTI), 2011. http://dx.doi.org/10.2172/1079918.

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Beard, B. C., and P. N. Jr Ross. Structure and activity of Pt-Co alloys as oxygen reduction electrocatalysts. Office of Scientific and Technical Information (OSTI), 1986. http://dx.doi.org/10.2172/5733309.

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Mukerjee, Sanjeev, Plamen Atanassov, Scott Barton, Nilesh Dale, and Bar Halevi. Development of Novel Non-Pt Group Metal Electrocatalysts for PEM Fuel Cell Applications. Office of Scientific and Technical Information (OSTI), 2016. http://dx.doi.org/10.2172/1332697.

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Adzic, Radoslav, and Michael Furey. Develop Novel Pt Monolayer Electrocatalysts to Facilitate Oxygen Reduction Reaction (ORR) for PEM Fuel Cells. Office of Scientific and Technical Information (OSTI), 2013. http://dx.doi.org/10.2172/1095905.

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Wang, Guofeng. SISGR: Theoretically relating the surface composition of Pt alloys to their performance as the electrocatalysts of low-temperature fuel cells. Office of Scientific and Technical Information (OSTI), 2010. http://dx.doi.org/10.2172/1105984.

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Yahnke, Mark S. The application of solid-state NMR spectroscopy to electrochemical systems: CO adsorption on Pt electrocatalysts at the aqueous-electrode interface. Office of Scientific and Technical Information (OSTI), 1996. http://dx.doi.org/10.2172/451231.

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Mustain, William. Understanding the Effects of Surface Chemistry and Microstructure on the Activity and Stability of Pt Electrocatalysts on Non-Carbon Supports. Office of Scientific and Technical Information (OSTI), 2015. http://dx.doi.org/10.2172/1169894.

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