4.8 Article

Self-Doping Based Facet Junctions and Oxygen Vacancies in Ferroelectric Bi3TiXNb2-XO9 Nanosheets for Boosting Photocatalytic Degradation and Antibacterial Activity

期刊

ACS APPLIED MATERIALS & INTERFACES
卷 14, 期 46, 页码 51819-51834

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acsami.2c12026

关键词

self-doping; facet junction; oxygen vacancies; charge separation; photocatalysis

资金

  1. National Natural Science Foundation of China
  2. Natural Science Foundation of Shaanxi Province
  3. [51602185]
  4. [51702201]
  5. [51961007]
  6. [2022JM-182]

向作者/读者索取更多资源

This study proposes a self-doping strategy to regulate the crystal facet exposure ratio in ferroelectric nanosheets, optimizing its facet junction effect. The Ti1.05 sample exhibits the most efficient charge-carrier separation and transportation, outperforming Ti0.95 and Ti1.00. It also shows superior performance in the photodegradation of organic dye and antibiotic molecules, as well as antibacterial activity under visible light.
Constructing facet junction in semiconductor photocatalysts has been demonstrated as an effective method to promote charge-carrier separation and suppress carrier recombination. Herein, we proposed a novel but facile self-doping strategy to regulate the crystal facet exposure ratio in ferroelectric Bi3TixNb2-xO9 single-crystalline nanosheets, thereby optimizing its facet junction effect. Through tuning the atomic ratio of Ti and Nb, the exposure ratio of {001} and {110} crystal planes in Bi3TixNb2-xO9 nanosheets can be delicately modulated, and more {110} facets were exposed with the increase of the Ti/Nb atomic ratio as evidenced by the X-ray diffraction and scanning electron microscopy results. A facet junction between {110} and {001} crystal planes was verified based on the density functional theory calculation and photodeposition experiment results. Photogenerated electrons tend to accumulate in {110}, while holes gathered in {001} crystal planes. Owing to the optimal facet junction effect, the sample of Ti1.05 shows the most efficient charge-carrier separation and transportation compared to Ti0.95 and Ti1.00 as supported by the photoluminescence, surface photovoltage, photoelectrochemistry, and electron paramagnetic resonance (EPR) results. In addition, the oxygen vacancy arising from the inequivalent substitution of Nb5+ by Ti4+ as proved by X-ray photoelectron spectroscopy and EPR results and the enhanced ferroelectricity supported by P-E loops can also assist charge-carrier separation and migration. Benefiting from these properties, Ti1.05 outperformed Ti0.95 and Ti1.00 in the photodegradation of organic dye and antibiotic molecules. Meanwhile, the excellent antibacterial activity of Ti1.05 under visible light was also demonstrated by the Escherichia coli sterilization experiment. This work not only presents a novel pathway to adjust the facet junction but also provides new deep insights into the crystal facet engineering in ferroelectrics as photocatalysts.

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