Related Experiment Video
Updated: Dec 25, 2025

Epitaxial Growth of Perovskite Strontium Titanate on Germanium via Atomic Layer Deposition
Published on: July 26, 2016
Influence of Surface Potential on the Capacitive Performance of the TiO2 Thin-Film Electrode with Different
Wei Tan1, Tian Gao1, Yang Wang1,2
1School of Chemical Engineering and Technology, Tianjin University, No. 135 Yaguan Road, Tianjin 300350, People's Republic of China.
Abstract:
Electrochemical capacitor and capacitive deionization store energy through the interface layer formed between electrodes and electrolytes. The crystalline form and surface potential of the oxide electrode can be changed in order to improve the capacitance. By characterizing the surface property and crystalline form of the TiO2 thin-film electrode at different sintering temperatures, it is showed that each electrode has its own surface potential which is affected by the crystalline structure. At elevated sintering temperature, TiO2 transfers from anatase to rutile with an increased surface potential. The electrochemical tests show that the electrode capacitance increases from 19.50 to 41.82 mF/cm2. Therefore, rutile TiO2 has a higher surface potential and better capacitive performance when used on a positive electrode compared with anatase TiO2. In general, the relation between the surface potential, the crystalline forms, and the capacitive performance is achieved in this work. We hope it can promote the investigation of oxide materials in the application for electrochemical capacitors and capacitive deionization.
Related Concept Videos
MOS Capacitor
The metal gate is typically made from highly conductive materials such as aluminum or polysilicon. Beneath the metal gate lies a thin layer of...
Dielectric Polarization in a Capacitor
Crystal Field Theory - Tetrahedral and Square Planar Complexes
Crystal field theory (CFT) is applicable to molecules in geometries other than octahedral. In octahedral complexes, the lobes of the dx2−y2 and dz2 orbitals point directly at the ligands. For tetrahedral complexes, the d orbitals remain in place, but with only four ligands located between the axes. None of the orbitals points directly at the tetrahedral ligands. However, the dx2−y2 and dz2 orbitals (along the Cartesian axes) overlap with the ligands less than the dxy,...
Crystal Field Theory - Octahedral Complexes
To explain the observed behavior of transition metal complexes (such as colors), a model involving electrostatic interactions between the electrons from the ligands and the electrons in the unhybridized d orbitals of the central metal atom has been developed. This electrostatic model is crystal field theory (CFT). It helps to understand, interpret, and predict the colors, magnetic behavior, and some structures of coordination compounds of transition metals.
CFT focuses on...

