- Chuang, Cheng-Hao;
- Chen, Chieh-Ming;
- Shao, Yu-Cheng;
- Yeh, Ping-Hung;
- Chang, Chih-Ming;
- Pong, Way-Faung;
- Kapilashrami, Mukes;
- Glans, Per-Anders;
- Gul, Sheraz;
- Wang, Gongming;
- Li, Yat;
- Zhang, Jin;
- Miyawaki, Jun;
- Niwa, Hideharu;
- Harada, Yoshihisa;
- Chen, Jin-Ming;
- Guo, Jinghua
The identification of lattice multiphases in TiO2 nanocrystals is studied by high resolution transmission electron microscope and electron diffraction patterns. Based on the spectroscopic analysis using soft x-ray absorption and resonant inelastic soft x-ray scattering, it is believed that the oxygen vacancies at the interface exhibit structural distortion of the TiO68−cluster around the defect site as for the multiphase lattice. We elucidate that the extra 3d electrons nearby induce the inelastic scattering features with the excitation energy dependence owing to different energy relaxation processes, a characteristic of the electron-phonon coupling or the nature of the electron-hole pair at the intermediate state. The manifold dd excitations driven by the strong interaction between Ti-3d and O-2p electrons are noticeably rich, coexisting on both Ti and O sites. This sophisticated experiment can advance the perspective of nanocomposite TiO2 for various interactions of surface Ti3+ in applications of future devices.