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  • 1
    Online Resource
    Online Resource
    The Electrochemical Society ; 2011
    In:  ECS Transactions Vol. 41, No. 1 ( 2011-10-04), p. 539-548
    In: ECS Transactions, The Electrochemical Society, Vol. 41, No. 1 ( 2011-10-04), p. 539-548
    Abstract: A segmented cell system was employed to investigate the impact of localized gas diffusion layer (GDL) PTFE content variations on fuel cell performance. An artificial defect was created by exchanging the standard cathode GDL with 13 wt. % PTFE located at segment 4 with a similar GDL (8, 17, 26, or 35 wt. % PTFE loading). An increase in PTFE loading caused a local performance decrease at high current density. For the 8 wt. % PTFE case, the local performance variation was relatively small. Other segments and the whole cell performance were not significantly affected by the defect. Spatially distributed data analysis with polarization and electrochemical impedance spectroscopy (EIS) revealed that such performance decreases are attributed to an increase in mass transfer overpotential ascribe to a decrease in porosity, average pore size and gas permeability with an increase in GDL defect PTFE loading.
    Type of Medium: Online Resource
    ISSN: 1938-5862 , 1938-6737
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2011
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  • 2
    Online Resource
    Online Resource
    IOP Publishing ; 2023
    In:  Materials Research Express Vol. 10, No. 1 ( 2023-01-01), p. 015501-
    In: Materials Research Express, IOP Publishing, Vol. 10, No. 1 ( 2023-01-01), p. 015501-
    Abstract: A model for PEM fuel cell impedance taking into account the pore size distribution (PSD) in the cathode catalyst layer is developed. Experimental PSD is approximated by pores of three sizes (small, medium and large) and in each kind of pores, the oxygen diffusion coefficient is allowed to have a separate value. The model is fitted to experimental impedance spectra of a low–Pt PEM fuel cell. The oxygen diffusivities of small and medium pores exhibit rapid growth with the cell current density, while in large pores, this parameter remains nearly constant. We show that oxygen reduction occurs mainly in the small and medium pores, leaving the large pores for mass transport only. This effect explains the discrepancy between small effective oxygen diffusivity of PEMFC catalyst layer measured in situ in operating cells by limiting current method, and much larger value of this parameter determined from ex situ experiments using Loschmidt cell.
    Type of Medium: Online Resource
    ISSN: 2053-1591
    Language: Unknown
    Publisher: IOP Publishing
    Publication Date: 2023
    detail.hit.zdb_id: 2760382-9
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  • 3
    Online Resource
    Online Resource
    The Electrochemical Society ; 2016
    In:  ECS Meeting Abstracts Vol. MA2016-02, No. 38 ( 2016-09-01), p. 2716-2716
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2016-02, No. 38 ( 2016-09-01), p. 2716-2716
    Abstract: The successful commercial deployment of proton exchange membrane fuel cells (PEMFCs) depends on the achievement of stringent performance and durability requirements. Currently, air is the most convenient oxidant for fuel cell applications, and its quality is an important consideration for operation because airborne contaminants can negatively affect fuel cell performance, cause premature degradation and decrease durability (1). Aromatic compounds are hazardous pollutants produced or used in many industrial processes. Benzene and naphthalene are the main representatives of aromatic hydrocarbons and are widely used as precursors for chemical syntheses. More than half of the entire benzene production is processed to styrene to manufacture polymers and plastics. Benzene is originated in the air from emissions of chemical plants, burning coal and oil, gasoline stations and vehicle exhausts. Naphthalene is used in the production of phthalic anhydride and as a pest control agent. Determination of the impact of C 6 H 6 and C 10 H 8 on PEMFC performance is critical to establish environmental requirements for fuel cell usage, define specifications for air filtration systems and support understanding of fundamental aspects of PEMFC operation and maintenance. A segmented cell and data acquisition system were used (2) with a commercially available 100 cm 2 membrane/electrode assembly (MEA). Each electrode contained a Pt/C catalyst with a loading of 0.4 mg Pt  cm -2 . A segmented SGL 25BC gas diffusion layer (GDL, 10 segments of 7.6 cm 2 ) and a Teflon gasket were employed at the cathode whereas a single GDL piece was applied at the anode. The MEA was operated under galvanostatic control of the whole cell current. Other operating conditions were: 80°C, 48.3 kPa g back pressure, 100/50% relative humidity and 2/2 stoichiometry for the anode and cathode respectively. The dry contaminant was injected into the humidified cathode air stream. The poisoning proceeded until the cell voltage reached a steady value. Subsequently, the contaminant injection was stopped to evaluate the cell self-recovery. Fig. 1 a) shows the voltage response and normalized current density for each segment at 1.0 A cm -2 under benzene contamination. For the first 18 hours, the cell was operated with pure air resulting in a cell voltage of 0.670 V. The injection of 2 ppm C 6 H 6 decreased the voltage to a steady state of 0.560 V and caused a redistribution of local current densities. Operation with pure air fully recovered the initial cell performance. Effects of naphthalene are shown in Fig. 1 b). The introduction of 2.3 ppm C 10 H 8 to air stream led to a significant voltage drop within 10 h and a different current redistribution pattern. Voltage oscillations from 0.100 to 0.170 V were observed as soon as the cell reached 0.12 V. Recovery took 2 h and was accompanied by further redistribution of localized currents. Benzene and naphthalene have similar electrochemical properties (3, 4). Cathodic desorption of the adsorbed species on Pt occurs at hydrogen adsorption potentials ( 〈  0.1 V) and is accompanied by partial hydrogenation, while electrooxidation takes place at 1.35 V with formation of CO 2 as the main product. The strong adsorption of C 6 H 6 and C 10 H 8 occurs at 0.1-0.6 V without electrochemical reactions, and results in an in-plane adsorbate configuration due to the interaction between the aromatic ring and the Pt surface (5). Contaminant adsorption results in a decrease of the electrochemical area, suppression of O 2 adsorption and shift the oxygen reduction from a 4-electron to a 2-electron mechanism, which negatively impact PEMFC performance. The data demonstrated that C 10 H 8 has a severer effect on PEMFC than C 6 H 6 which is most likely due to a higher adsorption energy and abilty to form multilayer adsorption (6, 7). A detailed discussion of the results and a poisoning mechanism will be presented. ACKNOWLEDGMENTS We gratefully acknowledge ONR (N00014-13-1-0463), DOE EERE (DE-EE0000467) and Hawaiian Electric Company. REFERENCES O.A. Baturina, Y. Garsany, B.D. Gould, K.E. Swider-Lyons, in: H. Wang, H. Li, X.-Z. Yuan (Eds.), PEM fuel cell failure mode analysis, CRC Press, 2011, p. 199. T.V. Reshetenko, G. Bender, K. Bethune, R. Rocheleau, Electrochim. Acta , 56 , 8700 (2011). F. Montilla, F. Huerta, E. Morallon, J.L. Vazquez, Electrochim. Acta , 45 , 4271 (2000). T. Löffler, E. Drbalkova, P. Janderka, P. Königshoven, H. Baltruschat, J. Electroanal. Chem. , 550-551 , 81 (2003). M.P. Soriaga, A.T. Hubbard, J. Am. Chem. Soc. , 104 , 2735 (1982). C. Morin, D. Simon, P. Sautet, J. Phys. Chem. B , 108 , 12084 (2004). J.M. Gottfried, E.K. Vestergaard, P. Bera, C.T. Campbell, J. Phys. Chem. B , 110 , 17539 (2006). Figure 1
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2016
    detail.hit.zdb_id: 2438749-6
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  • 4
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2020-02, No. 36 ( 2020-11-23), p. 2280-2280
    Abstract: The unprecedented situation with global COVID-19 pandemic exposed a significant vulnerability of world economics related to rearrangement and in some cases disappearance of supply chains. The Platinum Group Metals (PGMs) are listed critical minerals in practically all developed countries including USA, EU, UK and others. To ensure uninterrupted development of clean energy technologies, such as fuel cells and electrolysis, which are heavily depend on PGMs a significant breakthrough should be made to switch to completely PGM-free materials. Pajarito Powder in a close collaboration with world leader in MEA manufacturing IRD Fuel Cells, Hawaii Natural Energy Institute, University of Hawaii, and a number of US DOE National Labs (ANL, ORNL, LANL, NREL and other) developed under US DOE ElectroCat project Fe-N-C PGM-free catalysts for the Oxygen Reduction Reaction which are ready for commercial evaluation in some fuel cells applications [1-7]. The main focus of the project was not only to synthesize ORR catalysts with the highest activity and durability, but also in the way which can be easily scaled up to the hundreds of metric tons of catalysts. Pajarito Powder used the VariPore™ method for manufacturing several sets of PGM-free catalysts (with more than 30 synthesized at the time of abstract submission) with variation of surface area, level of graphitization, particle and pore size distribution, bulk and surface chemical composition as well as hydrophobic properties. These materials were synthesized by a bottom-up approach using nitrogen-rich organic compounds, transition metal salts, and particle/pore formers (either one or series of them). Pajarito’s method include aggressive catalyst cleaning where unreacted metal nanoparticles, remaining particle/pore formers, and admixtures from acids are removed. The resulting materials are active towards ORR sites and predominantly consists of atomically dispersed Fe-N x moieties [1-4]. Pajarito’s unique capability to prepare these materials reproducibly at a 50+ grams per batch level allowed IRD Fuel Cells to produce industrial quality MEAs with reproducible performance (~300 MEAs with 25cm 2 active area are made at the time of abstract submission). This oral presentation will report results of physical-chemical characterization of PGM-free catalysts, their comprehensive analysis at HNEI, modeling done by Dr. Andrei Kulikovsky, and structure-to-properties correlations obtained by our Team in collaboration with ElectroCat consortium. The critical challenges and path to overcome them will be discussed [1-3]. Acknowledgments: We would like to acknowledge the financial support from US DOE EERE under the grant DE-EE0008419 “Active and Durable PGM-free Cathodic Electrocatalysts for Fuel Cell Application” (PI: Alexey Serov). References: [1] T. Reshetenko, G. Randolf, M. Odgaard, B. Zulevi, A. Serov, A. Kulikovsky "The Effect of Proton Conductivity of Fe–N–C–Based Cathode on PEM Fuel cell Performance" Journal of The Electrochemical Society 167 (2020) 084501. [2] A. Baricci, A. Bisello, A. Serov, M. Odgaard, P. Atanassov, A. Casalegno "Analysis of the effect of catalyst layer thickness on the performance and durability of platinum group metal-free catalysts for polymer electrolyte membrane fuel cells" Sustainable Energy Fuels 3 (12) (2019) 3375-3386. [3] C.L. Vecchio, A. Serov, H. Romero, A. Lubers, B. Zulevi, A.S. Aricò, V. Baglio "Commercial platinum group metal-free cathodic electrocatalysts for highly performed direct methanol fuel cell applications" J. of Power Sources 437 (2019) 226948. [4] S. Stariha, K. Artyushkova, M. J. Workman, A. Serov, S. McKinney, B. Halevi, P. Atanassov "PGM-free Fe-N-C catalysts for oxygen reduction reaction: Catalyst layer design" J. Power Sources 326 (2016) 43–49. [5] S. Rojas-Carbonell, K. Artyushkova, A. Serov, C. Santoro, I. Matanovic, P. Atanassov "Effect of pH on the activity of platinum group metal- free catalysts in oxygen reduction reaction" ACS Catalysis 8 (2018) 3041-3053. [6] M.J. Workman, A. Serov, L. Tsui, P. Atanassov, K. Artyushkova "Fe-N-C Catalyst Graphitic Layer Structure and Fuel Cell Performance" ACS Energy Lett. 2 (2017) 1489–1493. [7] M. J. Workman, M. Dzara, C. Ngo, S. Pylypenko, A. Serov, S. McKinney, J. Gordon, P. Atanassov, K. Artyushkova "Platinum group metal-free electrocatalysts: Effects of synthesis on structure and performance in proton-exchange membrane fuel cell cathodes" J. Power Sources 348 (2017) 30-39.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2020
    detail.hit.zdb_id: 2438749-6
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  • 5
    Online Resource
    Online Resource
    The Electrochemical Society ; 2008
    In:  ECS Meeting Abstracts Vol. MA2008-02, No. 11 ( 2008-08-29), p. 943-943
    In: ECS Meeting Abstracts, The Electrochemical Society, Vol. MA2008-02, No. 11 ( 2008-08-29), p. 943-943
    Abstract: Abstract not Available.
    Type of Medium: Online Resource
    ISSN: 2151-2043
    Language: Unknown
    Publisher: The Electrochemical Society
    Publication Date: 2008
    detail.hit.zdb_id: 2438749-6
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  • 6
    In: Electrochimica Acta, Elsevier BV, Vol. 80 ( 2012-10), p. 368-376
    Type of Medium: Online Resource
    ISSN: 0013-4686
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2012
    detail.hit.zdb_id: 1483548-4
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  • 7
    In: Electrochimica Acta, Elsevier BV, Vol. 76 ( 2012-8), p. 16-25
    Type of Medium: Online Resource
    ISSN: 0013-4686
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2012
    detail.hit.zdb_id: 1483548-4
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  • 8
    In: Applied Catalysis B: Environmental, Elsevier BV, Vol. 312 ( 2022-09), p. 121424-
    Type of Medium: Online Resource
    ISSN: 0926-3373
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2022
    detail.hit.zdb_id: 2017331-3
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  • 9
    Online Resource
    Online Resource
    Elsevier BV ; 2013
    In:  Journal of Power Sources Vol. 241 ( 2013-11), p. 597-607
    In: Journal of Power Sources, Elsevier BV, Vol. 241 ( 2013-11), p. 597-607
    Type of Medium: Online Resource
    ISSN: 0378-7753
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2013
    detail.hit.zdb_id: 1491915-1
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  • 10
    Online Resource
    Online Resource
    Elsevier BV ; 2006
    In:  Journal of Power Sources Vol. 160, No. 2 ( 2006-10), p. 925-932
    In: Journal of Power Sources, Elsevier BV, Vol. 160, No. 2 ( 2006-10), p. 925-932
    Type of Medium: Online Resource
    ISSN: 0378-7753
    Language: English
    Publisher: Elsevier BV
    Publication Date: 2006
    detail.hit.zdb_id: 1491915-1
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