Issue 10, 2013

Size-controlled synthesis and characterization of CoPt nanoparticles using protein shells

Abstract

Nanostructured magnetic materials such as iron oxide and bimetallic nanoparticles can be potentially applied to a variety of fields, including electronics and nanomedicine. To develop these applications, it is important to control their particle size which affects their magnetic properties. In particular, it is a major challenge to synthesize small-sized nanoparticles with high reproducibility. In this study, we synthesized cobalt–platinum nanoparticles (CoPt NPs) in an ambient solution phase using PepA, a bacterial aminopeptidase, as a protein shell, and investigated the physicochemical and magnetic properties of NPs with and without encapsulating proteins. The size of CoPt NPs encapsulated by PepA was stringently controlled from 1.1 to 2.8 nm, and their magnetic property was related to the size. The CoPt NPs with the diameter of 1.1 nm showed a superparamagnetic behavior only at low temperatures, while 2.1 and 2.8 nm CoPt NPs were ferromagnetic below the blocking temperature. PepA had no deleterious effects on the coercivity of CoPt NPs, as evidenced by the marginal effect of PepA on the coercivity of CoPt NPs. This study demonstrated that the particle size and magnetic property of CoPt NPs can be controlled by using PepA as a protein shell. Encapsulation by PepA will aid the development of multifunctional magnetic materials, since the biocompatibility and modification capability of PepA can be synergistically combined with the advanced functionalities of CoPt NPs.

Graphical abstract: Size-controlled synthesis and characterization of CoPt nanoparticles using protein shells

Supplementary files

Article information

Article type
Paper
Submitted
22 Oct 2012
Accepted
03 Jan 2013
First published
08 Jan 2013

J. Mater. Chem. B, 2013,1, 1453-1460

Size-controlled synthesis and characterization of CoPt nanoparticles using protein shells

B. H. San, S. Lee, S. H. Moh, J. Park, J. H. Lee, H. Hwang and K. K. Kim, J. Mater. Chem. B, 2013, 1, 1453 DOI: 10.1039/C2TB00290F

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