Joint Experimental and Computational O-17 and H-1 Solid State NMR Study of Ba2In2O4(OH)(2) Structure and Dynamics

摘要

A structural characterization of the hydrated form of the brownmillerite-type phase Ba2In2O5, Ba2In2O4(OH)(2), is reported using experimental multinuclear NMR spectroscopy and density functional theory (DFT) energy and GIPAW NMR calculations. When the oxygen ions from H2O fill the inherent O vacancies of the brownmillerite structure, one of the water protons remains in the same layer (O-3) while the second proton is located in the neighboring layer (O-2) in sites with partial occupancies, as previously demonstrated by Jayaraman et al. ( Solid State Ionics 2004, 170, 25-32) using X-ray and neutron studies. Calculations of possible proton arrangements within the partially occupied layer of Ba2In2O4(OH)(2) yield a set of low energy structures; GIPAW NMR calculations on these configurations yield H-1 and O-17 chemical shifts and peak intensity ratios, which are then used to help assign the experimental MAS NMR spectra. Three distinct H-1 resonances in a 2:1:1 ratio are obtained experimentally, the most intense resonance being assigned to the proton in the O-3 layer. The two weaker signals are due to O2 layer protons, one set hydrogen bonding to the O-3 layer and the other hydrogen bonding alternately toward the O3 and O1 layers. H-1 magnetization exchange experiments reveal that all three resonances originate from protons in the same crystallographic phase, the protons exchanging with each other above approximately 150 degrees C. Three distinct types of oxygen atoms are evident from the DFT GIPAW calculations bare oxygens (O), oxygens directly bonded to a proton (H-donor O), and oxygen ions that are hydrogen bonded to a proton (H-acceptor O). The O-17 calculated shifts and quadrupolar parameters are used to assign the experimental spectra, the assignments being confirmed by H-1-O-17 double resonance experiments.