Probing the Catalyst-Ionomer Interface in Catalyst Layers with Sulfo-Phenylated Polyphenylene Ionomers Using CO-Displacement and Stripping Techniques

Robert James Anton, Shikai Sun, Karen Swider-Lyons, Cortney Mittelsteadt, Michael Adamski, Benjamin Britton, Yu Morimoto, Iryna Zenyuk
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Abstract

An investigation of ionomer-catalyst interfaces for electrodes containing sulfo-phenylated polyphenylene (sPPP) ionomers is conducted with CO displacement and stripping experiments. We find that at fully humidified conditions, catalyst layers containing sPPP ionomers show a CO displacement peak that is almost entirely suppressed. This suppression corresponds to adsorption of sulfonic acid group adsorption on only 2% of the available Pt surface. We also observe that at 100% RH, the double-layer capacitance of the catalyst layer is higher when poisoned by CO. This is inverse of the behavior observed with PFSA electrodes, indicating that there might be different ionomer-catalyst interactions present with an sPPP ionomer. We hypothesize that differences between sPPP and perfluorinated sulfonic acid (PFSA) ionomer backbones may account for this difference due to the presence of phenyl rings, which could adsorb to Pt surfaces preferentially at high humidification.
用co置换和汽提技术探测亚苯基聚苯离聚物在催化剂层中的催化剂-离聚物界面
采用CO置换和汽提实验研究了含硫苯基化聚苯(sPPP)离聚体电极的离聚体-催化剂界面。我们发现在完全加湿的条件下,含有sPPP离聚体的催化剂层显示出几乎完全抑制的CO置换峰。这种抑制对应于仅在2%的铂表面吸附磺酸基团。我们还观察到,在100% RH下,当CO中毒时,催化剂层的双层电容更高。这与PFSA电极观察到的行为相反,表明sPPP离聚体可能存在不同的离聚体-催化剂相互作用。我们假设sPPP和全氟磺酸(PFSA)离子单体骨架之间的差异可能是由于苯环的存在造成的,苯环在高湿度下可以优先吸附到Pt表面。
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