(Left) Tiny crystals are imaged with a scanning electron microscope, distinguishing the individual building blocks, which consist of spherical polystyrene beads. (Right) Larger crystals are imaged with a regular iPhone camera, revealing bright colors similar to naturally occurring opals. Image: Theodore Hueckel, Sacanna Lab at NYU.
(Left) Tiny crystals are imaged with a scanning electron microscope, distinguishing the individual building blocks, which consist of spherical polystyrene beads. (Right) Larger crystals are imaged with a regular iPhone camera, revealing bright colors similar to naturally occurring opals. Image: Theodore Hueckel, Sacanna Lab at NYU.

Using just electrostatic charge, common microparticles can spontaneously organize themselves into highly ordered crystalline materials – the equivalent of table salt or opals – according to a new study led by chemists at New York University (NYU) and reported in a paper in Nature.

"Our research shines new light on self-assembly processes that could be used to manufacture new functional materials," said Stefano Sacanna, associate professor of chemistry at NYU and the paper's senior author.

Self-assembly is a process in which tiny particles recognize each other and bind in a predetermined manner. These particles come together spontaneously, often after a triggering event or a change in conditions, and can assemble into something useful.

One approach to programming particles to assemble in a particular manner is to coat them with DNA strands, which instruct the particles on how and where to bind with one another. However, because this approach requires a considerable amount of DNA, it can be expensive and is limited to making very small samples.

In this study, the researchers took a different approach to self-assembly using a much simpler method. Instead of using DNA, they used electrostatic charge.

The process is similar to what happens when you mix salt into a pot of water, Sacanna explained. When salt is added to water, the tiny crystals dissolve into negatively charged chlorine ions and positively charged sodium ions. When the water evaporates, the positively and negatively charged particles recombine into salt crystals.

"Instead of using atomic ions like those in salt, we used colloidal particles, which are thousands of times bigger. When we mix the colloidal particles together under the right conditions, they behave like atomic ions and self-assemble into crystals," said Sacanna.

This process allows for making large quantities of materials. "Using the particles' natural surface charge, we managed to avoid doing any of the surface chemistry typically required for such elaborate assembly, allowing us to easily create large volumes of crystals," said Theodore Hueckel, postdoctoral researcher at NYU and the paper's first author.

In addition to creating salt-like colloidal materials, the researchers used self-assembly to create colloidal materials that mimic gemstones – in particular, opals. Opals are iridescent and colorful, a result of their inner crystalline microstructure and its interaction with light. In the lab, the researchers created test-tube gemstones that possessed a remarkably similar inner microstructure to natural opals.

"If you take a highly magnified image of an opal, you will see the same tiny spherical building blocks lined up in a regular fashion," said Hueckel.

Using electrostatic charge for self-assembly not only allows researchers to mimic materials found in nature, but also to go beyond what naturally occurs. For instance, adjusting the size and shape of the positively and negatively charged particles should allow for a wide range of different crystalline structures.

"We're inspired by nature's ionic crystals, but we believe we'll move beyond their structural complexity by utilizing all of the design elements uniquely available to colloidal building blocks," said Hueckel.

This story is adapted from material from New York University, with editorial changes made by Materials Today. The views expressed in this article do not necessarily represent those of Elsevier. Link to original source.