WashU Expert: Scaling Up the Circular Economy

BYLINE: Leah Shaffer

Newswise — Electrolysis can resemble a modern version of alchemy. Start with one compound, run it through an electrochemical process and end up with an entirely different mix of chemicals. One can’t turn straw into gold, but humans have used water electrolysis to generate hydrogen fuel from water broken into its separate parts. Similar processes can be applied to carbon dioxide. After all, if the world has excess carbon dioxide; why not turn it into something more useful?

Such is the mission for Lauren and Lee Fixel Distinguished Professor Feng Jiao, a researcher in energy, environmental and chemical engineering at the McKelvey School of Engineering at Washington University in St. Louis. In a recent commentary in Nature Chemical Engineering, Jiao outlined the steps ahead to bring CO and CO₂ electrolysis to the big time.

The challenge: “How we can go from lab-sized device to a scale which is relevant to commercialization?” Jiao asked.

The electrolysis device that that Jiao is talking about converts carbon waste gas into other materials. It looks like a stack of hard metallic plates encased in a cage. The top plate serves as a cathode, the bottom plate is the anode and in between are layers of separators that tease apart the chemical elements and run the electrochemistry that changes its component parts into platform chemicals such as carbon monoxide, formate or formic acid, methanol, ethylene and acetate or acetic acid. These products can be used in manufacturing to create food, fuel, intermediary chemicals or new synthetic materials that all can be fed back into the same manufacturing system — the “circular” part of the so-called circular economy — or broken down into harmless components.

“It’s a device for chemical transformation, chemical manufacturing,” he said.

Going big

Jiao has learned more as he has co-founded an electrolysis startup, Lectrolyst, that includes Gregory Hutchings and Bradie Crandall, co-authors on his commentary piece.

As they looked into the challenge of commercialization, they’ve identified key obstacles in the research. One is finding the “Goldilocks zone” for compression. Too much compression in the stack damages the components, Jiao said, but with too little compression, gases and chemicals can leak.

Along the way, they also must manage the system’s temperature. The bigger it gets, the more challenging it becomes to regulate temperature. Using modeling tools, the team can start to identify the best cell configurations, flow patterns and flow rate to find the sweet spot of temperature control — all while keeping costs down.

They want to design the system to make “a high purity and highly concentrated product stream,” but one that also will “allow us to minimize separation costs.”

Finally, there’s the transport challenge, which relates to how the various elements flow through the system. Small systems have uniform flow, but as they get bigger, they lose that uniformity.

It’s a balancing act, Jiao said. Researchers are working to find an optimized stack to deal with increasing flow and pressure distribution, while also delivering a reaction that doesn’t throw the system out of whack.

There are engineering challenges, but the toughest challenge will be after they sort these kinks. The United States could quickly be left behind as other countries have invested heavily in this type of technology. Taking it big requires government and industry support.

“Europe and Asia are ramping up investment in electrolyzer manufacturing and demonstration projects, underscoring that electrolyzer scale-up is now a global race,” the authors wrote.

“Commitments to long-term government support is essential for building the investor confidence needed for private fundraising efforts,” they said. “In addition, ensuring emerging technologies achieve commercial deployment allows a nation to recoup on its initial investment in earlier-stage development.”

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Crandall, B.S., Hutchings, G.S. & Jiao, F. Stack-level challenges for CO and CO2 electrolysis. Nat Chem Eng (2026). https://doi.org/10.1038/s44286-026-00378-z

This work was supported by the Gates Foundation (INV-051757). F.J. thanks the National Science Foundation (award numbers 2330245 and 2535871).