Biomineralization of mesoporous silica and metal nanoparticle/mesoporous silica nanohybrids by chemo-enzymatically prepared peptides

I. Hsiu Chen, Ting Yuan Lee, Yu Chao Tseng, Jhih Han Liou, Jeng Shiung Jan

研究成果: Article同行評審

1 引文 斯高帕斯(Scopus)

摘要

We report the feasibility of using chemo-enzymatically prepared peptides, oligo(L-lysine-co-L-tyrosine) (oligoKY) and oligo(L-lysine-co-L-phenylalanine) (oligoKF) for sequentially mediated growth of metal nanoparticles (NPs) and/or silica mineralization. This approach is easy to handle, environmentally benign, and economical as compared to other tedious and multiple-step peptide synthesis approaches. Colloidal stable silica/peptide particles with various sizes between 150 and 430 nm can be simply fabricated by tuning silica precursor concentration via peptide-mediated silica mineralization. Mesoporous silica with pore sizes mostly between 2 and 8 nm can be obtained by replication of sheet-like peptide nano-assemblies. In addition, Au NP/silica and Ag NP/silica nanohybrids can be prepared by peptide-mediated nucleation of metal NPs onto silica/peptide colloidal particles. Silver/palladium (AgPd) alloy-based silica nanohybrids were also prepared via galvanic replacement reaction. The experimental data revealed that these nanohybrids showed reliable and enhanced catalytic activities in reducing 4-nitrophenol, which are primarily dictated by the surface area/size of metal NPs and the accessibility to metal NPs, as well as the mass transfer of chemicals in the porous network. This study demonstrated that chemo-enzymatic polymerization is a promising approach to design peptide materials with designated building blocks for specific applications.

原文English
文章編號125753
期刊Colloids and Surfaces A: Physicochemical and Engineering Aspects
610
DOIs
出版狀態Published - 2021 二月 5

All Science Journal Classification (ASJC) codes

  • 表面和介面
  • 物理與理論化學
  • 膠體和表面化學

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