Abstract
The atom oxidation states were determined using the binding energies of the core S2p-, Cu2p-, Cr2p-, and Ln3d-levels in CuCr0.99Ln0.01S2 (Ln = Dy-Lu) solid solutions. The charge distribution on the matrix elements (Cu, Cr, and S) remained unaffected after cationic substitution. The sulfur atoms were found to be in the S2- oxidation state, the copper-Cu+, and the chromium-Cr3+. The cationic substitution of the initial CuCrS2-matrix occurred via the isovalent mechanism. The obtained results were compared with the electrophysical properties for CuCr0.99Ln0.01S2. The measured carrier concentration was from 1017 to 1018 cm-3. The largest Seebeck coefficient value of 157 µV/K was measured for CuCr0.99Yb0.01S2 at 500 K. The cationic substitution with lanthanides allowed one to enhance the Seebeck coefficient of the initial CuCrS2-matrix.
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