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Duke chemist Ivan Moreno-Hernandez (left) and his Ph.D. student Avery Vigil (right) use a technique called liquid phase electron microscopy to watch chemical processes in action. Credit: Photo by Justin Cook.

Nanoscale Movies Shed Light on One Barrier to a Clean Energy Future

Research could dramatically extend the lifetime of devices needed to turn hydrogen green

It might look like little more than a dark speck, but this tiny crystal of ruthenium dioxide -- shown here in the process of corroding -- could be one of the keys to a clean energy future: It turns water into hydrogen. Using nanoscale imaging techniques, Duke researchers are trying to understand why these catalysts break down and lose activity over time. Credit: Avery Vigil, Duke chemistry
It might look like little more than a dark speck, but this tiny crystal of ruthenium dioxide -- shown here in the process of corroding -- could be one of the keys to a clean energy future: It turns water into hydrogen. Using nanoscale imaging techniques, Duke researchers are trying to understand why these catalysts break down and lose activity over time. Credit: Avery Vigil, Duke chemistry

Part of the trouble is electrolyzers require rare metal catalysts to function, and these are prone to corrosion. They’re not the same after a year of operation as they were in the beginning.

In a study published April 10 in the Journal of the American Chemical Society, Moreno-Hernandez and his Ph.D. student Avery Vigil used a technique called liquid phase transmission electron microscopy to study the complex chemical reactions that go on between these catalysts and their environment that cause them to decay.

You might remember from high school that to make hydrogen gas, an electrolyzer splits water into its constituent hydrogen and oxygen molecules. For the current study, the team focused on a catalyst called ruthenium dioxide that speeds up the oxygen half of the reaction, since that’s the bottleneck in the process.

“We essentially put these materials through a stress test,” Vigil said.

They zapped nanocrystals of ruthenium dioxide with high-energy radiation, and then watched the changes wrought by the acidic environment inside the cell.

To take pictures of such tiny objects, they used a transmission electron microscope, which shoots a beam of electrons through nanocrystals suspended inside a super-thin pocket of liquid to create time-lapse images of the chemistry taking place at 10 frames per second.

The result: desktop-worthy close-ups of virus-sized crystals, more than a thousand times finer than a human hair, as they get oxidized and dissolve into the acidic liquid around them.

“We're actually able to see the process of this catalyst breaking down with nanoscale resolution,” Moreno-Hernandez said.

Over the course of five minutes, the crystals broke down fast enough to “render a real device useless in a matter of hours,” Vigil said.

Zooming in hundreds of thousands of times, the videos reveal subtle defects in the crystals’ 3D shapes that create areas of strain, causing some to break down faster than others.

By minimizing such imperfections, the researchers say it could one day be possible to design renewable energy devices that last two to three times longer than they currently do.

“So instead of being stable for, say, two years, an electrolyzer could last six years. That could have a massive impact on renewable technologies,” Moreno-Hernandez said.

Advocates of hydrogen power say it could help wean us off fossil fuels, but a key ingredient in its production tends to break down. New imaging research could help explain why, and help extend the lifetime of devices needed to turn hydrogen green. Photo by Justin Cook.

This research was supported by grants from the National Science Foundation (DGE-2139754, ECCS-2025064, ECCS-2025064).

CITATION: "Dissolution Heterogeneity Observed in Anisotropic Ruthenium Dioxide Nanocrystals via Liquid-Phase Transmission Electron Microscopy," S. Avery Vigil, Ivan A. Moreno-Hernandez. Journal of the American Chemical Society, April 10, 2024. https://doi.org/10.1021/jacs.3c13709