PHILADELPHIA — When semiconductor nanorods are exposed to light, they blink in a seemingly random pattern. By clustering nanorods together, physicists at the University of Pennsylvania have shown that their combined “on” time is increased dramatically providing new insight into this mysterious blinking behavior.
The research was conducted by associate professor Marija Drndic’s group, including graduate student Siying Wang and postdoctorial fellows Claudia Querner and Tali Dadosh, all of the Department of Physics and Astronomy in Penn’s School of Arts and Sciences. They collaborated with Catherine Crouch of Swarthmore College and Dmitry Novikov of New York University’s School of Medicine.
Their research was published in the journal Nature Communications.
When provided with energy, whether in the form of light, electricity or certain chemicals, many semiconductors emit light. This principle is at work in light-emitting diodes, or LEDs, which are found in any number of consumer electronics.
At the macro scale, this electroluminescence is consistent; LED light bulbs, for example, can shine for years with a fraction of the energy used by even compact-fluorescent bulbs. But when semiconductors are shrunk down to nanometer size, instead of shining steadily, they turn “on” and “off” in an unpredictable fashion, switching between emitting light and being dark for variable lengths of time. For the decade since this was observed, many research groups around the world have sought to uncover the mechanism of this phenomenon, which is still not completely understood.
“If you put nanorods together, if each one blinks in rare short bursts, you would think the maximum ‘on’ time for the group will not be much bigger than that for one nanorod, since their bursts mostly don’t overlap,” Novikov said. “What we see are greatly prolonged ‘on’ bursts when nanorods are very close together, as if they help each other to keep shining, or ‘burning.’”
Drndic’s group demonstrated this by depositing cadmium selenide nanorods onto a substrate, shining a blue laser on them, then taking video under an optical microscope to observe the red light the nanorods then emitted. While that technique provided data on how long each cluster was “on,” the team needed to use transmission electron microscopy, or TEM, to distinguish each individual, 5-nanometer rod and measure the size of each cluster.
A set of gold gridlines allowed the researchers to label and locate individual nanorod clusters. Wang then accurately overlaid about a thousand stitched-together TEM images with the luminescence data that she took with the optical microscope. The researchers observed the “campfire effect” in clusters as small as two and as large as 110, when the cluster effectively took on macroscale properties and stopped blinking entirely.
While the exact mechanism that causes this prolonged luminescence can’t yet be pinpointed, Drndic’s team’s findings support the idea that interactions between electrons in the cluster are at the root of the effect.
“By moving from one end of a nanorod to the other, or otherwise changing position, we hypothesize that electrons in one rod can influence those in neighboring rods in ways that enhance the other rods’ ability to give off light,” Crouch said. “We hope our findings will give insight into these nanoscale interactions, as well as helping guide future work to understand blinking in single nanoparticles.”
As nanorods can be an order of magnitude smaller than a cell, but can emit a signal that can be relatively easily seen under a microscope, they have been long considered as potential biomarkers. Their inconsistent pattern of illumination, however, has limited their usefulness.
“Biologists use semiconductor nanocrystals as fluorescent labels. One significant disadvantage is that they blink,” Drndic said. “If the emission time could be extended to many minutes it makes them much more usable. With further development of the synthesis, perhaps clusters could be designed as improved labels.”
Future research will use more ordered nanorod assemblies and controlled inter-particle separations to further study the details of particle interactions.
This research was supported by the National Science Foundation.
Contact: Evan Lerner email@example.com 215-573-6604 University of Pennsylvania