Engineers Produce ‘How-To’ Guide for Controlling the Structure of Nanoparticles
For Immediate Release
Tiny objects known as nanoparticles are often heralded as holding great potential for future applications in electronics, medicine and other areas. The properties of nanoparticles depend on their size and structure. Now researchers from North Carolina State University have learned how to consistently create hollow, solid and amorphous nanoparticles of nickel phosphide, which has potential uses in the development of solar cells and as catalysts for removing sulfur from fuel. Their work can now serve as a “how-to” guide for other researchers to controllably create hollow, solid and amorphous nanoparticles – in order to determine what special properties they may have.
The study provides a step-by-step analysis of how to create solid or hollow nanoparticles that are all made of the same material. “It’s been known that these structures could be made,” says Dr. Joe Tracy, an assistant professor of material science engineering at NC State and co-author of the paper, “but this research provides us with a comprehensive understanding of nanostructural control during nanoparticle formation, showing how to consistently obtain different structures in the lab.” The study also shows how to create solid nanoparticles that are amorphous, meaning they do not have a crystalline structure.
Tracy explains that there is a great deal of interest in the formation of hollow nanoparticles and amorphous nanoparticles. But for many kinds of nanoparticles, there had previously been no clear understanding of how to control the formation of these structures. As a result of the new study, Tracy says, “nanoparticles with desired structures can be made more consistently, making it easier for researchers to determine their electronic, optical and catalytic properties.” For example, amorphous nanoparticles may be of use in future electronic applications or for nanostructure fabrication. Tracy stresses that while the NC State researchers were able to show how to create hollow nanoparticles and amorphous nanoparticles, they were not able to create nanoparticles that were both hollow and amorphous.
The study could also have implications for many additional types of nanoparticles, not just nickel phosphide. Tracy says that the findings “could provide important insights for further studies to control the structures of many other kinds of nanoparticles, with a wide array of potential applications.” These could include metal oxide, sulfide, selenide and phosphide nanoparticles.
Specifically, the researchers found that they could control whether nickel phosphide nanoparticles would be hollow or solid by adjusting the ratio of phosphorus to nickel reactants when they synthesized the nanoparticles. The researchers found that they could create amorphous solid nanoparticles by controlling the temperature.
The study, “Nickel Phosphide Nanoparticles with Hollow, Solid, and Amorphous Structures,” was co-authored by Tracy, NC State post-doctoral researcher Junwei Wang and NC State Ph.D. student Aaron Johnston-Peck. The research was funded by NC State and the National Science Foundation, and was published online by Chemistry of Materials.
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Note: The study abstract follows.
“Nickel Phosphide Nanoparticles with Hollow, Solid, and Amorphous Structures”
Authors: Junwei Wang, Aaron C. Johnston-Peck, Joe Tracy, North Carolina State University
Published: Online, September 16, 2009, Chemistry of Materials
Abstract: Conversion of unary metal nanoparticles (NPs) upon exposure to O, S, Se, and P precursors usually produces hollow metal oxide, sulfide, selenide, or phosphide NPs through the Kirkendall effect. Here, nanostructural control of mixed-phase Ni2P/Ni12P5 (represented as NixPy) NPs prepared through thermolysis of nickel acetylacetonate using trioctylphosphine (TOP) as a ligand and phosphorous precursor is reported. The P:Ni mole ratio controls the NP size and is the key factor in determining the nanostructure. For P:Ni mole ratios of 1-3, Ni NPs form below 240 °C and subsequently convert to crystalline-hollow NixPy NPs at 300 °C. For higher P:Ni ratios, a Ni-TOP complex forms that requires higher temperatures for NP growth, thus favoring direct formation of NixPy rather than Ni. Consequently, for P:Ni mole ratios greater than 9, amorphous-solid NixPy NPs form at 240 °C and become crystalline-solid NixPy NPs at 300 °C. For intermediate P:Ni mole ratios of ~6, both growth mechanisms give rise to a mixture of hollow and solid NixPy NPs. Similar results have been obtained using tributlyphosphine or triphenyphosphine as the phosphorous source, but trioctylphosphine oxide cannot serve as a phosphorous source.