Scientists at the U.S. Department of Energy's Brookhaven National Laboratory have developed a general approach for combining different types of nanoparticles to produce large-scale composite materials.
The approach takes advantage of the attractive pairing of complementary strands of synthetic DNA—based on the molecule that carries the genetic code in its sequence of matched bases known by the letters A, T, G, and C. After coating the nanoparticles with a chemically standardized "construction platform" and adding extender molecules to which DNA can easily bind, the scientists attach complementary lab-designed DNA strands to the two different kinds of nanoparticles they want to link up. The natural pairing of the matching strands then "self-assembles" the particles into a three-dimensional array consisting of billions of particles. Varying the length of the DNA linkers, their surface density on particles, and other factors gives scientists the ability to control and optimize different types of newly formed materials and their properties.
"Our study demonstrates that DNA-driven assembly methods enable the by-design creation of large-scale 'superlattice' nanocomposites from a broad range of nanocomponents now available—including magnetic, catalytic, and fluorescent nanoparticles," said Brookhaven physicist Oleg Gang, who led the research at the Lab's Center for Functional Nanomaterials (CFN). "This advance builds on our previous work with simpler systems, where we demonstrated that pairing nanoparticles with different functions can affect the individual particles' performance, and it offers routes for the fabrication of new materials with combined, enhanced, or even brand new functions."
Pairing up dissimilar particles presents many challenges the scientists investigated in the work leading to this paper. To understand the fundamental aspects of various newly formed materials they used a wide range of techniques, including x-ray scattering studies at Brookhaven's National Synchrotron Light Source (NSLS) and spectroscopy and electron microcopy at the CFN.
They also investigated how the DNA-pairing mechanism and other intrinsic physical forces, such as magnetic attraction among particles, might compete during the assembly process. For example, magnetic particles tend to clump to form aggregates that can hinder the binding of DNA from another type of particle. "We show that shorter DNA strands are more effective at competing against magnetic attraction," Gang said.
For the particular composite of gold and magnetic nanoparticles they created, the scientists discovered that applying an external magnetic field could "switch" the material's phase and affect the ordering of the particles. "This was just a demonstration that it can be done, but it could have an application—perhaps magnetic switches, or materials that might be able to change shape on demand," said Zhang.
The third fundamental factor the scientists explored was how the particles were ordered in the superlattice arrays: Does one type of particle always occupy the same position relative to the other type—like boys and girls sitting in alternating seats in a movie theater—or are they interspersed more randomly? "This is what we call a compositional order, which is important for example for quantum dots because their optical properties—e.g., their ability to glow—depend on how many gold nanoparticles are in the surrounding environment," said Gang. "If you have compositional disorder, the optical properties would be different." In the experiments, increasing the thickness of the soft DNA shells around the particles increased compositional disorder.
These fundamental principles give scientists a framework for designing new materials. The specific conditions required for a particular application will be dependent on the particles being used, Zhang emphasized, but the general assembly approach would be the same.
This story is reprinted from material from Brookhaven National Laboratory, with editorial changes made by Materials Today. The views expressed in this article do not necessarily represent those of Elsevier. Link to original source.