<p>The residual antibiotics in the water environment pose a great threat to the ecological environment and human life safety. However, an effective and environmentally friendly method for degrading antibiotics is still lacking. Herein, a novel Bi<sub>2</sub>WO<sub>6</sub> catalyst with optimized morphology and abundant crystal defects was designed to remove tetracycline. The experimental results showed that the generation of grain boundaries and dislocations were induced through the epitaxial growth method, which endowed Bi<sub>2</sub>WO<sub>6</sub> with rapid separation and transfer of photoinduced electrons. Moreover, the specific surface area and light adsorption capacity of optimized catalyst (0.5Bi-Bi) were significantly improved. As a result, 0.5Bi-Bi exhibited the excellent photocatalytic performance, which degraded 90.78% of TC within 40&#xa0;min under visible light illumination. Meanwhile, the synthesized 0.5Bi–Bi catalyst has robust photocatalytic stability and sustainability. The capture experiment proved that ⋅O<sub>2</sub><sup>−</sup> was the prime active substance, and a possible mechanism of photodegradation of TC was proposed.</p> Graphical Abstract <p></p>

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Constructing Bi2WO6 with Abundant Crystal Defects for High-Efficiency Photocatalytic Degradation of Tetracycline

  • Lan Zhang,
  • Zhipeng Zou,
  • Na Li,
  • Cong Tan,
  • Baofei Hao,
  • Huizhong Ma

摘要

The residual antibiotics in the water environment pose a great threat to the ecological environment and human life safety. However, an effective and environmentally friendly method for degrading antibiotics is still lacking. Herein, a novel Bi2WO6 catalyst with optimized morphology and abundant crystal defects was designed to remove tetracycline. The experimental results showed that the generation of grain boundaries and dislocations were induced through the epitaxial growth method, which endowed Bi2WO6 with rapid separation and transfer of photoinduced electrons. Moreover, the specific surface area and light adsorption capacity of optimized catalyst (0.5Bi-Bi) were significantly improved. As a result, 0.5Bi-Bi exhibited the excellent photocatalytic performance, which degraded 90.78% of TC within 40 min under visible light illumination. Meanwhile, the synthesized 0.5Bi–Bi catalyst has robust photocatalytic stability and sustainability. The capture experiment proved that ⋅O2 was the prime active substance, and a possible mechanism of photodegradation of TC was proposed.

Graphical Abstract