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   <subfield code="a">The physical and photo electrochemical characterization of the crednerite CuMnO2</subfield>
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   <subfield code="c">[Yassine Bessekhouad, Yamina Gabes, Aissa Bouguelia, Mohamed Trari]</subfield>
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   <subfield code="a">CuMnO2 is prepared via Cu+→Li+ exchange in molten copper (I) chloride. It crystallizes in a monoclinic structure (SG C2/m) where the MnO6 octahedra elongation is ascribed to the Yahn-Teller (Y-T) effect of Mn3+ ions. From chemical analysis, the oxide is more accurately formulated as CuMnO2.01. Above 250°C, it undergoes a reversible transition to spinel Cu x Mn3−x O4 and beyond 940°C it converts back to Cu1.1Mn0.9O2. Extrapolation of high-temperature magnetic data indicates T-intercept θ p of −450K and an effective moment of 5.22μB, consistent with strong antiferromagnetism in the basal plans and high spin (HS) configuration Mn3+. This value is slightly larger than that of the spin only moment, a behavior ascribed to Cu2+ originating from oxygen insertion. As prepared, CuMnO2 displays p-type conductivity with an activation energy of 0.16eV. Most holes generated upon band gap excitation are trapped on Cu+ ions and the conduction occurs by small polarons hopping between neighboring sites. The linear increase of thermopower for Cu1.05Mn0.95O2 with temperature indicates a hole mobility μ300K (3.5×10-6cm2V−1s−1) thermally activated. CuMnO2 is made p- and n-type and the difference in the carriers mobilities is attributed to different oxygen polyhedra. The title oxide, characterized photo electrochemically, exhibits a pH-insensitive flat band potential (+0.13VSCE). The valence band, located at 5.3eV below vacuum, is made up of Cu 3d orbital. As application, the powder showed a good performance for the H2-photo evolution.</subfield>
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