Anodes of SnO were charged reversibly with Li to capacities greater than 600 mAh/g. The anode materials were characterized by Sn-119 Mossbauer spectrometry at 11 and 300 K, and by X-ray diffractometry at 300 K. Trends in the valence of Sn were as expect ed when the Sn oxides are reduced in the presence of Li. At low Li capacities the SnO is reduced to small particles of beta-Sn, and with increasing Li capacity an alloy of Li22Sn5 is formed. Although the Li22Sn5 develops over a range of Li concentrations in the anode material, the Li22Sn5 that forms at low Li insertions is not typical of bulk Li22Sn5 in either its structural or electrochemical properties. The recoil-free fraction of the Sn oxide (and perhaps the metallic Sn) in the anode materials showed an anomalously large temperature dependence. This is indicative of nanoparticles or a severely defective structure. We monitored the changes in the Li-SnO and Li-Sn materials during atmospheric exposure over times up to 2 months. This oxidation process of Sn was very much the reverse of the Sn reduction during the Li insertion, although it occurred over a much longer time scale. We also report the temperature dependencies of recoil-free fractions for standard samples of beta-Sn, SnO2, and the alloy Li22Sn5.