(Digital Presentation) Rotating Ring-Disk Electrodes Studies on Oxygen Reduction Reaction at Hydrophobic Ionic Liquids Layer Modified Pt/C Catalyst

Abstract

Polymer electrolyte fuel cells (PEFCs) are expected as one of the clean, highly effective energy conversion systems, and have been actively studied. Pt nanoparticles on carbon supports (Pt/C) are commonly used as a cathode catalyst for PEFCs, because of the high activity on oxygen reduction reaction (ORR). However, its durability in long term driving and high mass activity for ORR have not sufficiently fulfilled at the present. More improvements of Pt/C catalyst for ORR activity and the durability are required for the spread of PEFCs To improve the activity and durability of Pt/C, ionic liquids (ILs) modified catalysts, called Pt/C-Solid catalysis with an IL layer (SCILL) catalysts, have recently attracted much attention [1]. ILs are liquid salts around room temperature, which have high ionic conductivity and electrochemical stability. We focused on hydrophobic ionic liquids with quaternary phosphonium cations [2]. Quaternary phosphonium cations ionic liquids have higher ionic conductivity and hydrophobicity than quaternary ammonium ionic liquids with the same structure and the same counter ions. Because of interference in the oxygen reduction reaction on platinum by water, increasing the hydrophobicity of the surface is expected to improve the activity on Pt/C catalysis. Hence, by using the quaternary phosphonium cations ILs for Pt/C-SCILL catalysts, it promises to improve the ORR activities for the catalyst. On the other hand, proton conduction and oxygen permeation rate are also important factors for ORR activity enhancement. In this study, we report the ORR activity for Pt/C-SCILL catalysts with ILs composed of highly hydrophobic cations and hydrophobic anions. Quaternary phosphonium based ILs (PXXXY+TFSA-[alkyl chain X= 4 Y= 1, 12, 16]) were used for Pt/C-SCILL modified electrodes. Commercially available 20 wt% or 30 wt% Pt/C (Cabot, Vulcan XC-72R🄬) catalyst was used for bare Pt/C modified electrodes. The ultrasonicated Pt/C catalyst suspension was dropped on the mirror polished glassy carbon disk electrodes. Pt/C-SCILL modified electrodes were prepared by recasting the ILs-2-propanol solution on the bare Pt/C modified electrodes or adding ILs to the catalyst suspension. Moreover, the mixture of the ILs and bis(trifluoromethanesulfonyl)imide (HTFSA) were also examined. The thickness of the ILs layer was calculated relative to the BET surface area of the carbon support. A platinum wire and a reversible hydrogen electrode (RHE) were used as the counter and reference electrodes, respectively. CV and LSV were carried out in 0.1 M HClO4 solution under Ar (CV) or O2 (LSV) atmosphere, respectively. The Pt/C-SCILL catalyst was prepared by recasting (thin layers, ~0.4 nm) or mixing (thick layers, 1nm~) methods. In the case of the thin layer (~0.4 nm) of ILs, the ORR activity increased as the size of the cations increased. However, for the thicker (1 nm ~) ILs layers, the ORR activity was lower than for the bare Pt/C catalysts. It seems that the aprotic ILs interfered with the proton supply, making the four-electron reduction reaction of oxygen less likely to occur. Therefore, we attempted to supply protons to the thick ILs layer by mixing an ionic liquid with a proton source. HTFSA was dissolved in P444(12)TFSA, which showed relatively good ORR activity in thin film studies. The Pt/C-SCILL catalyst was prepared by adding the mixture with a catalyst dispersion. This proton mixing Pt/C-SCILL catalyst showed a significant improvement in ORR activity compared to bare Pt/C catalyst. References [1] S. Silvia et al., Adv. Energy Sustainability Res., 2, 2000062 (2021). [2] K. Tsunashima and M. Sugiya, Electrochem. Commun., 9, 2353 (2007).