Rich surface hydroxyl design for nanostructured TiO2 and its hole-trapping effect

• Published in: Chemical engineering journal (Lausanne, Switzerland : 1996) Switzerland : 1996), 2020-11, Vol.400, p.125909, Article 125909
• Main Authors: Xiao, Shi-Tian, Wu, Si-Ming, Dong, Yu, Liu, Jia-Wen, Wang, Li-Ying, Wu, Lu, Zhang, Yue-Xing, Tian, Ge, Janiak, Christoph, Shalom, Menny, Wang, Yi-Tian, Li, Yuan-Zhou, Jia, Ruo-Kun, Bahnemann, Detlef W., Yang, Xiao-Yu
• Format: Article
• Language: English
• Subjects: Directed catalysis; Hierarchical structure; Hydrogen production from seawater; Surface hydroxyl; Titanium oxide
• ISSN: 1385-8947; 1873-3212
• DOI: 10.1016/j.cej.2020.125909

•TiO2 with rich surface hydroxyl species (Ti-OH) has been designed using ionic liquid.•The directed charge transport mechanism of rich Ti-OH have been investigated.•The rich Ti-OH greatly enhance performances in photocatalysis and energy storage. The surface hydroxyl groups in TiO2 are crucial to many of its practical applications, but their controlled synthesis represents still a challenge. Herein, nanostructured TiO2 with rich surface hydroxyl species groups and high crystallinity (TiO2-OH) by high-temperature calcination have been developed by using the ionic liquid. Experimental measurements and theoretical calculations show a strong surface hydroxyl signal of two-dimensional 1H TQ-SQ MAS NMR, as well as clear changes of the charge density of TiO2 with the rich surface hydroxyl species. Moreover, the rich surface hydroxyl species groups in TiO2 not only significantly enhance its performances involving photogenerated current, photocatalysis and energy strorage but also show a bright future on marine applications because of its high activity and stability in simulation seawater. The characteristics and mechanism have been proposed to clarify the generation of surface hydroxyl species of TiO2 and the correponding directed hole-trapping at an atomic-/nanoscale.