Manipulating spin polarization of titanium dioxide for efficient photocatalysis

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...

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Veröffentlicht in:Nature communications 2020-01, Vol.11 (1), p.418-418, Article 418
Hauptverfasser: Pan, Lun, Ai, Minhua, Huang, Chenyu, Yin, Li, Liu, Xiang, Zhang, Rongrong, Wang, Songbo, Jiang, Zheng, Zhang, Xiangwen, Zou, Ji-Jun, Mi, Wenbo
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Sprache:eng
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Zusammenfassung: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 TiO 2 , which promotes the efficiency of charge separation and surface reaction via the parallel alignment of electron spin orientation. Specifically, Ti 0.936 O 2 , possessing intensive spin polarization, performs 20-fold increased photocatalytic hydrogen evolution and 8-fold increased phenol photodegradation rates, compared with stoichiometric TiO 2 . Notably, we further observed the positive effect of external magnetic fields on photocatalytic activity of spin-polarized TiO 2 , attributed to the enhanced electron-spin parallel alignment. This work may create the opportunity for tailoring the spin-dependent electronic structures in metal oxides. Photocatalyst activity depends significantly on the material’s electronic structures. Here, authors manipulate the electron spin polarization of TiO 2 by tuning the concentration of Ti vacancies and show improved photocatalytic activities.
ISSN:2041-1723
2041-1723
DOI:10.1038/s41467-020-14333-w