Key points are not available for this paper at this time.
A family of photocatalysts for water splitting into hydrogen was prepared by distributing TiO(6) units in an MTi-layered double hydroxide matrix (M = Ni, Zn, Mg) that displays largely enhanced photocatalytic activity with an H(2)-production rate of 31.4 μmol h(-1) as well as excellent recyclable performance. High-angle annular dark-field scanning transmission electron microscopy (HAADF-STEM) mapping and XPS measurement reveal that a high dispersion of TiO(6) octahedra in the layered doubled hydroxide (LDH) matrix was obtained by the formation of an M(2+)-O-Ti network, rather different from the aggregation state of TiO(6) in the inorganic layered material K(2)Ti(4)O(9). Both transient absorption and photoluminescence spectra demonstrate that the electron-hole recombination process was significantly depressed in the Ti-containing LDH materials relative to bulk Ti oxide, which is attributed to the abundant surface defects that serve as trapping sites for photogenerated electrons verified by positron annihilation and extended X-ray absorption fine structure (EXAFS) techniques. In addition, a theoretical study on the basis of DFT calculations demonstrates that the electronic structure of the TiO(6) units was modified by the adjacent MO(6) octahedron by means of covalent interactions, with a much decreased bandgap of 2.1 eV, which accounts for its superior water-splitting behavior. Therefore, the dispersion strategy for TiO(6) units within a 2D inorganic matrix can be extended to fabricate other oxide or hydroxide catalysts with greatly enhanced performance in photocatalysis and energy conversion.
Zhao et al. (Mon,) studied this question.