摘要
With the progress of society and the development of medical care, the abuse of antibiotics has become an environmental problem that cannot be ignored. In this work, a significant improvement in photocatalytic efficiency for tetracycline degradation was achieved through the design of a direct Z-scheme heterojunction In 2 S 3 /MIL-101(Fe), realized by precisely controlling the in situ growth of In 2 S 3 nanoblocks on octahedral MIL-101(Fe). MIL-101(Fe) and In 2 S 3 generate a strong built-in electric field to facilitate the efficient transfer and separation of photoexcited carriers. Furthermore, the enhanced specific surface area of In 2 S 3 /MIL-101(Fe) offers more active sites for catalytic reactions. Simulated sunlight-driven photocatalytic degradation experiments of tetracycline hydrochloride (TC) demonstrated a significant enhancement in the performance of the heterojunction photocatalyst. It achieved an 82.2% TC removal efficiency with a degradation rate constant of 0.0113 min −1 , representing 3.05 times and 4.52 times the performance of pure In 2 S 3 and MIL-101(Fe) materials, respectively. This study offers valuable insights into the design of efficient and stable metal-organic framework (MOF)-based heterojunction photocatalysts and holds promising potential for the remediation of antibiotic pollution.
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