Hydroxide-ion incorporation and conduction mechanisms in tin pyrophosphate – a first-principles study

Abstract

The incorporation and conduction mechanisms of hydroxide ions in tin pyrophosphate (SnP 2 O 7 ) have been investigated theoretically on the basis of first-principles calculations. Hydroxide ions are not simply incorporated into interstitial sites in the crystal, and the incorporation is accompanied by dissociation of a P 2 O 7 unit (pyrophosphate ion) into two PO 4 units. From the calculated formation energies of various native defects, it was found that the interstitial proton and hydroxide ion are the dominant defect species and their concentrations can be controlled by doping heterovalent cations. The long-range migration of the hydroxide ion was observed in the first-principles molecular dynamics simulations, but its frequency during the simulation was extremely low. In fact, the calculated potential barrier for the conduction pathway was extremely high (1.92 eV), and the estimated bulk conductivity in SnP 2 O 7 was much lower than the experimentally reported conductivities. These results indicate that the experimentally observed hydroxide-ion conductivity of SnP 2 O 7 cannot be simply explained by motion of hydroxide ions through the crystal lattice.

A First-Principles Study on Proton Conductivity of Acceptor-Doped Tin Pyrophosphate

“…In the present study, the crystal structure with the space group of P 2 1 / c (No. 14) was employed in light of the calculated total energies of the reported polymorphs as previously reported Figure shows the calculated crystal structure, in which there are one type of Sn site, two P sites (P1, P2), and seven O sites (O1–O7) from the crystallographic point of view.…”