Efficient photocatalytic reductive dechlorination of 4-chlorophenol to phenol on {0 0 1}/{1 0 1} facets co-exposed TiO2 nanocrystals

4-chlorophenol could be efficiently photoreductively dechlorinated over anatase TiO 2 nanocrystals with co-exposed {0   0   1} and {1   0   1} facets, which were synthesized and further characterized by scanning electron microscope (SEM), transmission electron microscope (TEM), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). Although fluorine could adsorb on {0   0   1} facets to decrease their surface energy, enabling TiO 2 to expose high energy {0   0   1} facets, the surface bonded fluorine might depress the photoreductive dechlorination efficiency of 4-chlorophenol, attributed to the electron trapping role of surface ≡Ti F groups. Due to the formation of a surface heterojunction between {1   0   1} and {0   0   1} facets in a single TiO 2 nanocrystal, electrons and holes were spontaneously self-separated and selectively migrate to {1   0   1} and {0   0   1} facets, respectively. Electron trapping experiments demonstrated that photogenerated electrons are the responsible for the reductive dechlorinaton of 4-chlorophenol to phenol. To avoid the oxidative degradation of 4-chlorophenol by holes and ensure sufficient electrons to reductively dechlorinate the substrate, moderate scavengers were required in the reaction system and dissolved oxygen, which might deplete electron on TiO 2 , also should be removed. With the optimal scavengers, the conversion efficiency of 4-chlorophenol (4-CP) achieved 97.5% and the selectivity for phenol was 92.5%, which were much higher than that of commercial TiO 2 P25.