Controllable self-assembly of CdS@NH2-MIL-125(Ti) heterostructure with enhanced photodegradation efficiency for organic pollutants through synergistic effect
Autor: | Jing-Yi Tan, Cheng Zhang, Cui Penghui, Hang Wang, Na Zhang, Jun-Xia Shi, Jian-Yong Zhang |
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Rok vydání: | 2019 |
Předmět: |
010302 applied physics
Aqueous solution Materials science Scanning electron microscope Mechanical Engineering 02 engineering and technology 021001 nanoscience & nanotechnology Condensed Matter Physics 01 natural sciences chemistry.chemical_compound Adsorption chemistry X-ray photoelectron spectroscopy Chemical engineering Mechanics of Materials 0103 physical sciences Photocatalysis Rhodamine B General Materials Science Nanorod 0210 nano-technology Photodegradation |
Zdroj: | Materials Science in Semiconductor Processing. 97:91-100 |
ISSN: | 1369-8001 |
Popis: | In this work, we employed solvethermal method to assemble highly crystalline NH2-MIL-125(Ti) nanocrystals on the CdS nanorods, forming CdS@NH2-MIL-125(Ti) (S@T-n) heterostructured photocatalyst. The photocatalytic activity, structures and morphology of the composites were characterized by UV–vis diffuse reflectance, powder X-ray diffraction (PXRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), Brunauer–Emmett-Teller (BET), photoluminescence (PL), X-ray photoelectron spectroscopy (XPS). Compared to pristine CdS, the S@T-n composites exhibited enhanced photo-degradation efficiencies for Rhodamine B (RhB), phenol and oxytetracycline (OTC) from aqueous solution under visible-light irradiation. Among them, the S@T-10 composite demonstrated the highest photocatalytic performance, and reached 361.4 times for phenol, and 236 times for OTC of Degussa P-25. The enhancement of photocatalytic activity could be described to the novel heterostructure, which can not only provide abundant surface area for the adsorption and diffusion of organic pollutants, but also efficient visible-light harvesting and interfacial charge separation. The possible photocatalytic mechanism of superoxide (O2 −) and holes (h+) by the electron-spin-resonance (ESR) was also investigated detailed. |
Databáze: | OpenAIRE |
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