A smartphone display that can produce moving, holographic 3D images will need to be able to twist the light it emits. Now, researchers at the University of Michigan and the Ben-Gurion University of the Negev have discovered a way to mass-produce spiral semiconductors that can take that important, light-coiling step.
Researchers a U-M unveiled some of the first holographic images in 1962, made by coaxing waves of light to form an array of bright and dark spots in space. This creates a static illusion of a material object. To make these frozen waves, the researchers encoded images onto a material that could control the direction—or polarization—polarization) and the timing—or phase—of the fluctuations within the electromagnetic waves.
The new semiconductor helices created by the U-M-led team offer that level of control over light in a format that could work in the pixels of displays. They can be incorporated into other semiconductor devices to vary the polarization, phase and color of light emitted by the different pixels, each of them made from the precisely designed semiconductor helices. This could one day enable moving holograms, projected by smartphones and other screens.
Until now, making semiconductors spirals with sufficiently strong twist—reminiscent of nanoscale fusilli pasta—was a difficult prospect because the twisted state is unnatural to semiconductor materials. They usually form sheets or wires. But Nicholas Kotov, Joseph B. and Florence V. Cejka Professor of Chemical Engineering and his team have found a way to guide the attachment of small semiconductor nanoparticles to each other with help from some of nature’s twisted structures: proteins and DNA.
“Amino acids are the quintessential building blocks of proteins,” said Wenchun Feng, a post-doctoral research fellow in Kotov’s lab and the lead author of a newly published paper on the work. “The direction of the spiral of proteins is determined by the geometrical property of amino acids. We found that a common amino acid, cysteine, working together in large numbers, can twist not only proteins but also semiconductors.”
The team coated nanoparticles made out of cadmium telluride, a semiconductor capable of emitting light, with cysteine. Cysteine comes in two forms that are mirror images of one another like our hands are, so it is known as a “chiral” molecule. They observed the nanoparticles spontaneously self-assembling into semiconductor “tornados” following the rightward or leftward chirality of the amino acid.
The team was surprised by the high fidelity of this self-assembly process and the strength of the twist. Nearly all—98 percent—of semiconductor helices had the same twisting direction and indeed looked like nanoscale fusilli. Some organic molecules can form natural spirals, too, but the light-twisting ability of semiconductor helices made by Kotov and colleagues is at least five times stronger.
When they shone light through the semiconductors, they recorded the photons swirling through them. Through a combination of experiments and computer simulations, the researchers developed design principles and methods for engineering the optical properties of the semiconductor helices for the different colors in future holography devices.
One of the unexpected consequences of this technology-driven project was getting a peek into mysteries surrounding how life may have arisen on Earth and why many biological molecules reliably follow either a clockwise or counterclockwise spiral. Kotov suggests that amino acids, which are known to form spontaneously in space dust, may have assembled nanoparticles into spirals that twisted the light from the early stars, serving as stable inorganic templates for organic molecules and particles to follow the same pattern.
The work is described in a paper in Science Advances titled, “Assembly of mesoscale helices with near-unity enantiomeric excess and light-matter interactions for chiral semiconductors.”
The central part of this work was supported by the NSF project “Energy- and Cost-Efficient Manufacturing Employing Nanoparticles” (NSF 1463474). Partial support came from the Center for Photonic and Multiscale Nanomaterials, funded by the NSF Materials Research Science and Engineering Center program (DMR-1120923), as well as NSF projects 1403777 and 1411014. The analytical electron microscope (provided by NSF grant DMR-9871177) used in this work is part of the University of Michigan’s Michigan Center for Materials Characterization.
Written by Wenchun Feng and Kate McAlpine.