“…The two 2p 3/2 BEs at 780.9-781.0 and 783.3-783.5 eV are further assigned to Co 2+ in CoO and Co 2+ in CoMoO x , respectively, due to their agreement with CoO (780.0-780.7 eV) [17,39,40,44,45] and CoMoO 4 (780.5-781.2) [37][38][39]46] references. The relatively large BE deviation of Co 2+ in CoMoO x from Co 2+ in CoMoO 4 might result from the polarization effect or the nonstoichiometry when Co 2+ ions are incorporated into highly oxidized MoO 3 matrix [39,46,47]. The BE intensity ratio of Co 2+ in CoMoO x to that in CoO increased from 1.3 to 2.6 after reduction, indicating that more CoMoO x was formed at the expense of CoO and MoO 3 .…”