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Prolonging charge-separation states by doping lanthanide-ions into {001}/{101} facets-coexposed TiO_2 nanosheets for enhancing photocatalytic H_2 evolution 被引量:10
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作者 Yongan Zhu Zhenyi Zhang +2 位作者 Na Lu Ruinian Hua Bin Dong 《Chinese Journal of Catalysis》 SCIE EI CAS CSCD 北大核心 2019年第3期413-423,共11页
Ultrathin TiO2 nanosheets with coexposed {001}/{101} facets have attracted considerable attention because of their high photocatalytic activity. However, the charge-separated states in the TiO2 nanosheets must be exte... Ultrathin TiO2 nanosheets with coexposed {001}/{101} facets have attracted considerable attention because of their high photocatalytic activity. However, the charge-separated states in the TiO2 nanosheets must be extended to further enhance their photocatalytic activity for H2 evolution. Herein, we present a successful attempt to selectively dope lanthanide ions into the {101} facets of ultrathin TiO2 nanosheets with coexposed {001}/{101} facets through a facile one-step solvothermal method. The lanthanide doping slightly extended the light-harvesting region and markedly improved the charge-separated states of the TiO2 nanosheets as evidenced by UV-vis absorption and steady-state/transient photoluminescence spectra. Upon simulated sunlight irradiation, we observed a 4.2-fold enhancement in the photocatalytic H2 evolution activity of optimal Yb3+-doped TiO2 nanosheets compared to that of their undoped counterparts. Furthermore, when Pt nanoparticles were used as cocatalysts to reduce the H2 overpotential in this system, the photocatalytic activity enhancement factor increased to 8.5. By combining these results with those of control experiments, we confirmed that the extended charge-separated states play the main role in the enhancement of the photocatalytic H2 evolution activity of lanthanide-doped TiO2 nanosheets with coexposed {001}/{101} facets. 展开更多
关键词 Photocatalysis H2 evolution Lanthanide ion doping TiO2 coexposed facets {001} facets NANOSHEETS
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