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

authored by
S.-T. Xiao, S.-M. Wu, Y. Dong, J.-W. Liu, L.-Y. Wang, L. Wu, Y.-X. Zhang, G. Tian, C. Janiak, M. Shalom, Y.-T. Wang, Y.-Z. Li, R.-K. Jia, D.W. Bahnemann, X.-Y. Yang
Abstract

The surface hydroxyl groups in TiO

2 are crucial to many of its practical applications, but their controlled synthesis represents still a challenge. Herein, nanostructured TiO

2 with rich surface hydroxyl species groups and high crystallinity (TiO

2-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 TiO

2 with the rich surface hydroxyl species. Moreover, the rich surface hydroxyl species groups in TiO

2 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 TiO

2 and the correponding directed hole-trapping at an atomic-/nanoscale.

Organisation(s)
Institute of Technical Chemistry
External Organisation(s)
Wuhan University of Technology
Sun Yat-Sen University
Chinese Academy of Sciences (CAS)
Hubei University
Harvard University
Heinrich-Heine-Universität Düsseldorf
Ben-Gurion University of the Negev
Northeast Electric Power University (NEEPU)
Saint Petersburg State University
Qingdao University
Type
Article
Journal
Chemical engineering journal
Volume
400
ISSN
1385-8947
Publication date
15.11.2020
Publication status
Published
Peer reviewed
Yes
ASJC Scopus subject areas
General Chemistry, Environmental Chemistry, General Chemical Engineering, Industrial and Manufacturing Engineering
Sustainable Development Goals
SDG 7 - Affordable and Clean Energy, SDG 14 - Life Below Water
Electronic version(s)
https://doi.org/10.1016/j.cej.2020.125909 (Access: Closed)