Transparent nanostructured BaTiO3 film electrodes were synthesized on conductive substrates from BaTiO3 nanocrystals forming at low temperature. Electrochemical and spectroelectrochemical methods were employed to inve...Transparent nanostructured BaTiO3 film electrodes were synthesized on conductive substrates from BaTiO3 nanocrystals forming at low temperature. Electrochemical and spectroelectrochemical methods were employed to investigate its properties of band energetics and the trap state at different pH values. The flat band edges greatly depended on the pH value of electrolyte, and the flat band edges were -0.70, -0.92 and -1.20 V vs saturated Ag/AgCl at the pH value of 3.0, 6.8 and 13.0, respectively. The results showed that trap state densities also highly depended on pH. The total trap state densities were 3.73 × 1015, 4.02 × 1015 and 6.48 × 1016 cm-2 at pH value of 3.0, 6.8 and 13.0 respectively with maximum located at -0.36 V, -0.50 V and -0.80 V. The results obtained from CVs were in good agreement with that obtained from the measurements of time resolved currents. The size of the peak potentials in the cyclic voltammograms experiments was increased dramatically with the pH value increasing, indicating that traps were surface-related.展开更多
文摘Transparent nanostructured BaTiO3 film electrodes were synthesized on conductive substrates from BaTiO3 nanocrystals forming at low temperature. Electrochemical and spectroelectrochemical methods were employed to investigate its properties of band energetics and the trap state at different pH values. The flat band edges greatly depended on the pH value of electrolyte, and the flat band edges were -0.70, -0.92 and -1.20 V vs saturated Ag/AgCl at the pH value of 3.0, 6.8 and 13.0, respectively. The results showed that trap state densities also highly depended on pH. The total trap state densities were 3.73 × 1015, 4.02 × 1015 and 6.48 × 1016 cm-2 at pH value of 3.0, 6.8 and 13.0 respectively with maximum located at -0.36 V, -0.50 V and -0.80 V. The results obtained from CVs were in good agreement with that obtained from the measurements of time resolved currents. The size of the peak potentials in the cyclic voltammograms experiments was increased dramatically with the pH value increasing, indicating that traps were surface-related.
