Manipulating spin polarization of titanium dioxide for efficient photocatalysis

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作者
Lun Pan
Minhua Ai
Chenyu Huang
Li Yin
Xiang Liu
Rongrong Zhang
Songbo Wang
Zheng Jiang
Xiangwen Zhang
Ji-Jun Zou
Wenbo Mi
机构
[1] Tianjin University,Key Laboratory for Green Chemical Technology of the Ministry of Education, School of Chemical Engineering and Technology
[2] Collaborative Innovative Center of Chemical Science and Engineering (Tianjin),Tianjin Key Laboratory of Low Dimensional Materials Physics and Preparation Technology, School of Science
[3] Tianjin University,Tianjin Key Laboratory of Brine Chemical Engineering and Resource Eco
[4] Tianjin University of Science & Technology,utilization, College of Chemical Engineering and Materials Science
[5] Chinese Academy of Sciences,Shanghai Synchrotron Radiation Facility, Shanghai Institute of Applied Physics
[6] Chinese Academy of Science,Shanghai Synchrotron Radiation Facility, Zhangjiang Lab, Shanghai Advanced Research Institute
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摘要
Photocatalysis has been regarded as a promising strategy for hydrogen production and high-value-added chemicals synthesis, in which the activity of photocatalyst depends significantly on their electronic structures, however the effect of electron spin polarization has been rarely considered. Here we report a controllable method to manipulate its electron spin polarization by tuning the concentration of Ti vacancies. The characterizations confirm the emergence of spatial spin polarization among Ti-defected TiO2, which promotes the efficiency of charge separation and surface reaction via the parallel alignment of electron spin orientation. Specifically, Ti0.936O2, possessing intensive spin polarization, performs 20-fold increased photocatalytic hydrogen evolution and 8-fold increased phenol photodegradation rates, compared with stoichiometric TiO2. Notably, we further observed the positive effect of external magnetic fields on photocatalytic activity of spin-polarized TiO2, attributed to the enhanced electron-spin parallel alignment. This work may create the opportunity for tailoring the spin-dependent electronic structures in metal oxides.
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