Ion Conduction Mechanisms and Thermal Properties of Hydrated and Anhydrous Phosphoric Acids Studied with 1H, 2H, and 31P NMR

• Published in: The journal of physical chemistry. B Vol. 110; no. 49; pp. 24999 - 25006
• Main Authors: Aihara, Yuichi, Sonai, Atsuo, Hattori, Mineyuki, Hayamizu, Kikuko
• Format: Journal Article
• Language: English
• Published: United States American Chemical Society 14.12.2006
• ISSN: 1520-6106; 1520-5207
• DOI: 10.1021/jp064452v

To understand the behaviors of phosphoric acids in fuel cells, the ion conduction mechanisms of phosphoric acids in condensed states without free water and in a monomer state with water were studied by measuring the ionic conductivity (σ) using AC impedance, thermal properties, and self-diffusion coefficients (D) and spin−lattice relaxation times (T 1) with multinuclear NMR. The self-diffusion coefficient of the protons (H+ or H3O+), H2O, and H located around the phosphate were always larger than the diffusion coefficients of the phosphates and the disparity increased with increasing phosphate concentration. The diffusion coefficients of the samples containing D2O paralleled those in the protonated samples. Since the 1H NMR T 1 values exhibited a minimum with temperature, it was possible to determine the correlation times and they were found to be of nanosecond order for a distance of nanometer order for a flip. The agreement of the ionic conductivities measured directly and those calculated from the diffusion coefficients indicates that the ion conduction obeys the Nernst−Einstein equation in the condensed phosphoric acids. The proton diffusion plays a dominant role in the ion conduction, especially in the condensed phosphoric acids.