Abstract
The hyperfine structure of divalent and trivalent iron in CoO has been obtained from the Mössbauer effect of Fe57 produced by the electron-capture decay of Co57. The two valence states are obtained respectively by x ray and Auger effect de-excitation of the K-shell hole resulting from electron capture in divalent Co57. Higher valence states which could be produced by multiple Auger de-excitation are not observed, indicating that their lifetimes are short. The magnetic field at a divalent iron nucleus at low temperature is 2.0×105 oe while that at a trivalent one is 5.6×105 oe. The quadrupole coupling in this almost cubic environment is less than 1.0 Mc/sec.