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Noble metal-titania hybrid nanoparticle clusters and the interaction to proteins for photo-catalysis in aqueous environments
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Noble metal-titania hybrid nanoparticle clusters and the interaction to proteins for photo-catalysis in aqueous environments

Tung-Yu Tsai, Hong-Li Wang, Yi-Chen Chen, Wei-Chang Chang, Je-Wei Chang, Shih-Yuan LuDe-Hao Tsai
Journal of Colloid and Interface Science, 卷.490, 頁碼.802-811
03/2017

摘要

Aerosol Colloid Gas-phase Nanoparticle P25 Photocatalysis Self-assembly Silver Stability Titania Electronic Optical and Magnetic Materials Biomaterials Surfaces Coatings and Films Colloid and Surface Chemistry
We report a systematic study of the controlled synthesis of new hybrid spherical TiO 2 nanoparticle cluster (TiO 2 -NPC) homogeneously decorated with noble metal nanoparticles (NPs) by gas-phase evaporation-induced self-assembly. Silver NP (AgNP) was used as the representative noble metal NP. The degradation of methyl blue (MB) in the aqueous solution was chosen as the representative system for the study of photocatalysis, which were tested and evaluated with respect to irradiation conditions and the presence of bovine serum albumin (BSA). The results show that particle size and chemical composition of the hybrid nanostructure were tunable by choosing the suitable concentration of precursors. The photocatalytic activity of AgNP-decorated TiO 2 -NPC was strongly affected by the light irradiation and the ligand-nanoparticle interfacial interaction. The presence of BSA influenced molecular conjugation to the surface of the hybrid nanostructure. Under conditions of simultaneous competitive adsorption of MB and BSA, the combination of AgNPs improved the photocatalytic activity of the TiO 2 -NPC-based catalysts. Our work describes a prototype methodology to fabricate TiO 2 -NPC homogeneously decorated with noble metal NPs with well-controlled material properties. The mechanistic understanding developed in this study can be useful for the future optimization of material properties of hybrid nanostructures versus interfacial interactions with the surrounding molecules.

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