Journal
ISOTOPES IN ENVIRONMENTAL AND HEALTH STUDIES
Volume 57, Issue 6, Pages 641-663Publisher
TAYLOR & FRANCIS LTD
DOI: 10.1080/10256016.2021.1985488
Keywords
Equilibrium isotope effects; Fuel cells; oxygen-16; oxygen-18; Reduced partition function ratios; Density functional theory; Platinum catalyst
Funding
- JSPS [15K06670]
- Grants-in-Aid for Scientific Research [15K06670] Funding Source: KAKEN
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By utilizing density functional theory calculations, this study investigated the oxygen isotope fractionation observed on Pt catalyst surfaces in polymer electrolyte membrane fuel cells (PEMFCs). The experimental observation of O-16 enrichment in water molecules at the cathode can be satisfactorily explained by considering oxygen isotope exchange equilibria between adsorbed oxygen species on Pt(111) surfaces.
A density functional theory (DFT) computation on oxygen species adsorbed on platinum (Pt) catalyst surfaces has been carried out to elucidate oxygen isotope fractionation observed at the cathode of a polymer electrolyte membrane fuel cell (PEMFC). The Pt(111) catalyst surface was modelled by a Pt-19 cluster, and O, OH, OHH, OO, OOH, OHOH and HOHOH were assumed to be the oxygen species adsorbed on the Pt(111) surface. The oxygen isotope reduced partition function ratios (RPFRs) of the adsorbed species were calculated using the vibrational frequencies obtained by normal mode analyses performed on the optimized structures. Various oxygen isotope exchange equilibria among the adsorbed oxygen species and oxygen and water molecules in the gas phase were examined using their RPFRs. Experimental observation that the lighter O-16 is enriched in water molecules exhausted from the cathode is explainable in a satisfactory manner by assuming oxygen isotope exchange equilibria of O-2 molecule with O, OH, OO and OOH adsorbed on the Pt(111) surface that appear in the first half of the conversion reaction from O-2 to H2O and those of H2O molecule with the adsorbed oxygen species, OHH, OHOH and HOHOH, formed in the latter half of the conversion reaction.
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