"This is the first experiment where we can directly see local structures in three dimensions at atomic-scale resolution — that's never been done before," said Jianwei (John) Miao, a professor of physics and astronomy and a researcher with the California NanoSystems Institute (CNSI) at UCLA.
Miao and his colleagues used a scanning transmission electron microscope to sweep a narrow beam of high-energy electrons over a tiny gold particle only 10 nanometers in diameter (almost 1,000 times smaller than a red blood cell). The nanoparticle contained tens of thousands of individual gold atoms, each about a million times smaller than the width of a human hair. These atoms interact with the electrons passing through the sample, casting shadows that hold information about the nanoparticle's interior structure onto a detector below the microscope.
Miao's team discovered that by taking measurements at 69 different angles, they could combine the data gleaned from each individual shadow into a 3-D reconstruction of the interior of the nanoparticle. Using this method, which is known as electron tomography, Miao's team was able to directly see individual atoms and how they were positioned inside the specific gold nanoparticle.
Presently, X-ray crystallography is the primary method for visualizing 3-D molecular structures at atomic resolutions. However, this method involves measuring many nearly identical samples and averaging the results. X-ray crystallography typically takes an average across trillions of molecules, which causes some information to get lost in the process, Miao said.
"It is like averaging together everyone on Earth to get an idea of what a human being looks like — you completely miss the unique characteristics of each individual," he said.
X-ray crystallography is a powerful technique for revealing the structure of perfect crystals, which are materials with an unbroken honeycomb of perfectly spaced atoms lined up as neatly as books on a shelf. Yet most structures existing in nature are non-crystalline, with structures far less ordered than their crystalline counterparts — picture a rock concert mosh pit rather than soldiers on parade.
"Our current technology is mainly based on crystal structures because we have ways to analyze them," Miao said. "But for non-crystalline structures, no direct experiments have seen atomic structures in three dimensions before."
Probing non-crystalline materials is important because even small variations in structure can greatly alter the electronic properties of a material, Miao noted. The ability to closely examine the inside of a semiconductor, for example, might reveal hidden internal flaws that could affect its performance.
"The three-dimensional atomic resolution of non-crystalline structures remains a major unresolved problem in the physical sciences," he said.
Miao and his colleagues haven't quite cracked the non-crystalline conundrum, but they have shown they can image a structure that isn't perfectly crystalline at a resolution of 2.4 angstroms (the average size of a gold atom is 2.8 angstroms). The gold nanoparticle they measured for their paper turned out to be composed of several different crystal grains, each forming a puzzle piece with atoms aligned in subtly different patterns. A nanostructure with hidden crystalline segments and boundaries inside will behave differently from one made of a single continuous crystal — but other techniques would have been unable to visualize them in three dimensions, Miao said.
Miao's team also found that the small golden blob they studied was in fact shaped like a multi-faceted gem, though slightly squashed on one side from resting on a flat stage inside the gigantic microscope — another small detail that might have been averaged away when using more traditional methods.
This project was inspired by Miao's earlier research, which involved finding ways to minimize the radiation dose administered to patients during CT scans. During a scan, patients must be X-rayed at a variety of angles, and those measurements are combined to give doctors a picture of what's inside the body. Miao found a mathematically more efficient way to obtain similar high-resolution images while taking scans at fewer angles. He later realized that this discovery could benefit scientists probing the insides of nanostructures, not just doctors on the lookout for tumors or fractures.
Nanostructures, like patients, can be damaged if too many scans are administered. A constant bombardment of high-energy electrons can cause the atoms in nanoparticles to be rearranged and the particle itself to change shape. By bringing his medical discovery to his work in materials science and nanoscience, Miao was able to invent a new way to peer inside the field's tiniest structures.
The discovery made by Miao's team may lead to improvements in resolution and image quality for tomography research across many fields, including the study of biological samples.
This research was conducted at CNSI's Electron Imaging Center for NanoMachines and funded by UC Discovery/Tomosoft Technologies. Tomosoft Technologies is a start-up company based on Miao's work.
Other UCLA co-authors included Chris Regan, an assistant professor of physics and astronomy and a CNSI researcher; graduate students Mary Scott, Chien-Chun Chen, Matthew Mecklenburg and Chun Zhu; and postdoctoral scholar Rui Xu. In particular, Chen and Scott played an important role in this work. Peter Ercius and Ulrich Dahmen from the National Center for Electron Microscopy at Lawrence Berkeley National Laboratory are also co-authors.
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Kim DeRose | EurekAlert!
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