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Core–Shell Structured Phenolic Polymer@TiO(2) Nanosphere with Enhanced Visible-Light Photocatalytic Efficiency

Core–shell structured TiO(2) is a promising solution to promote the photocatalytic effectiveness in visible light. Compared to metal or semiconductor materials, polymers are rarely used as the core materials for fabricating core–shell TiO(2) materials. A novel core–shell structured polymer@TiO(2) wa...

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Detalles Bibliográficos
Autores principales: Xu, Xiankui, Zhang, Lei, Zhang, Shihua, Wang, Yanpeng, Liu, Baoying, Ren, Yanrong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7153608/
https://www.ncbi.nlm.nih.gov/pubmed/32150857
http://dx.doi.org/10.3390/nano10030467
Descripción
Sumario:Core–shell structured TiO(2) is a promising solution to promote the photocatalytic effectiveness in visible light. Compared to metal or semiconductor materials, polymers are rarely used as the core materials for fabricating core–shell TiO(2) materials. A novel core–shell structured polymer@TiO(2) was developed by using phenolic polymer (PP) colloid nanoparticles as the core material. The PP nanoparticles were synthesized by an enzyme-catalyzed polymerization in water. A subsequent sol–gel and hydrothermal reaction was utilized to cover the TiO(2) shell on the surfaces of PP particles. The thickness of the TiO(2) shell was controlled by the amount of TiO(2) precursor. The covalent connection between PP and TiO(2) was established after the hydrothermal reaction. The core–shell structure allowed the absorption spectra of PP@TiO(2) to extend to the visible-light region. Under visible-light irradiation, the core–shell nanosphere displayed enhanced photocatalytic efficiency for rhodamine B degradation and good recycle stability. The interfacial C–O–Ti bonds and the π-conjugated structures in the PP@TiO(2) nanosphere played a key role in the quick transfer of the excited electrons between PP and TiO(2), which greatly improved the photocatalytic efficiency in visible light.