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    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
    Kurzfassung: 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
    Materialart: Online-Ressource
    ISSN: 2151-2043
    Sprache: Unbekannt
    Verlag: The Electrochemical Society
    Publikationsdatum: 2016
    ZDB Id: 2438749-6
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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