Improved nanomaterials: Understanding surface structure of quantum dots will aid design of new solar devices
- Date:
- November 20, 2014
- Source:
- University of Oregon
- Summary:
- A potential path to identify imperfections and improve the quality of nanomaterials for use in next-generation solar cells has just emerged.
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A potential path to identify imperfections and improve the quality of nanomaterials for use in next-generation solar cells has emerged from a collaboration of University of Oregon and industry researchers.
To increase light-harvesting efficiency of solar cells beyond silicon's limit of about 29 percent, manufacturers have used layers of chemically synthesized semiconductor nanocrystals. Properties of quantum dots that are produced are manipulated by controlling the synthetic process and surface chemical structure.
This process, however, creates imperfections at the surface-forming trap states that limit device performance. Until recently, improvements in production quality have relied on feedback provided by traditional characterization techniques that probe average properties of large numbers of quantum dots.
"We want to use these materials in real devices, but they are not yet optimized," said co-author Christian F. Gervasi, a UO doctoral student.
In their study, detailed in the Journal of Physical Chemistry Letters, researchers investigated electronic states of lead sulfide nanocrystals. By using a specially designed scanning tunneling microscope, researchers created atomic-scale maps of the density of states in individual nanocrystals. This allowed them to pinpoint the energies and localization of charge traps associated with defects in the nanocrystal surface structure that are detrimental to electron propagation.
The microscope was designed in the lab of co-author George V. Nazin, a professor in the UO Department of Chemistry and Biochemistry. Its use was described in a previous paper in the same journal, in which Nazin's lab members were able to visualize the internal structures of electronic waves trapped by external electrostatic charges in carbon nanotubes.
"This technology is really cool," said Peter Palomaki, senior scientist for Voxtel Nanophotonics and co-author on the new paper. "When you really dig down into the science at a very fundamental level, this problem has always been an open-ended question. This paper is just the tip of the iceberg in terms of being able to understand what's going on."
The insight, he said, should help manufacturers tweak their synthesis of nanocrystals used in a variety of electronic devices. Co-author Thomas Allen, also a senior scientist at Voxtel, agreed. The project began after Allen heard Gervasi and Nazin discussing the microscope's capabilities.
"We wanted to see what the microscope could accomplish, and it turns out that it gives us a lot of information about the trap states and the depths of trap states in our quantum dots," said Allen, who joined Voxtel after completing the Industrial Internship Program in the UO's Materials Science Institute. "The information will help us fine-tune the ligand chemistry to make better devices for photovoltaics, detectors and sensors."
The trap states seen by the microscope in this project may explain why nanoparticle-based solar cells have not yet been commercialized, Nazin said.
"Nanoparticles are not always stable. It is a fundamental problem. When you synthesize something at this scale you don't necessarily get the same structure for all of the quantum dots. Working at the atomic scale can produce large variations in the electronic states. Our tool allows us to see these states directly and allow us to provide feedback on the materials."
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Materials provided by University of Oregon. Note: Content may be edited for style and length.
Journal Reference:
- Dmitry A. Kislitsyn, Christian F. Gervasi, Thomas Allen, Peter K. B. Palomaki, Jason D. Hackley, Ryuichiro Maruyama, George V. Nazin. Spatial Mapping of Sub-Bandgap States Induced by Local Nonstoichiometry in Individual Lead Sulfide Nanocrystals. The Journal of Physical Chemistry Letters, 2014; 5 (21): 3701 DOI: 10.1021/jz5019465
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