부산대학교 도서관

We report on quasielastic neutron scattering (QENS) andab initiomolecular dynamics (AIMD) simulations of the mechanism of proton diffusionin the partially and fully hydrated barium indate oxide proton conductorsBa(2)In(2)O(5)(H2O)( x ) (x = 0.30 and 0.92). Structurally,these materials are featured by an intergrowth of cubic and "pseudo-cubic"layers of InO6 octahedra, wherein two distinct proton sites,H(1) and H(2), are present. We show that the main localized dynamicsof these protons can be described as rotational diffusion of O-H(1)species and H(2) proton transfers between neighboring oxygen atoms.The mean residence times of both processes are in the order of picosecondsin the two studied materials. For the fully hydrated material, Ba2In2O5(H2O)(0.92), we also reveal the presence of a third proton site, H(3), whichbecomes occupied upon increasing the temperature and serves as a saddlestate for the interexchange between H(1) and H(2) protons. Crucially,the occupation of the H(3) site enables long-range diffusion of protons,which is highly anisotropic in nature and occurs through a two-dimensionalpathway. For the partially hydrated material, Ba2In2O5(H2O)(0.30), the occupationof the H(3) site and subsequent long-range diffusion are not observed,which is rationalized by hindered dynamics of H(2) protons in thevicinity of oxygen vacancies. A comparison to state-of-the-art proton-conductingoxides, such as barium zirconate-based materials, suggests that thegenerally lower proton conductivity in Ba2In2O5(H2O)( x ) is dueto a large occupation of the H(1) and H(2) sites, which, in turn,means that there are few sites available for proton diffusion. Thisinsight suggests that the chemical substitution of indium by cationswith higher oxidation states offers a novel route toward higher protonconductivity because it reduces the proton site occupancy while preservingan oxygen-vacancy-free structure.