Researchers tailor catalyst microenvironments to enhance CO2 electroreduction to multicarbon products
A promising route for turning CO2 emissions into a fuel feedstock is the process of electrochemical reduction (e.g., earlier post). However, to be commercially viable, the process needs to be improved to yield a higher amount of desirable carbon-rich products.
Now, as reported in the journal Nature Energy, researchers at Lawrence Berkeley National Laboratory (Berkeley Lab) have improved the process’ selectivity by developing a new approach to modify the surface of the copper catalysts used to assist the reaction.
Although we know copper is the best catalyst for this reaction, it doesn’t give high selectivity to the desired products. Our group has found that you can do various tricks with the local environment of the catalyst to provide that selectivity.—Alexis Bell, a faculty senior scientist in Berkeley Lab’s Chemical Sciences Division and professor of chemical engineering at UC Berkeley
In previous studies, the researchers had established the precise conditions that gave the best electrical and chemical environment for creating commercially interesting carbon-rich products. But those conditions are contrary to those that naturally occur in a typical fuel cell, which uses a water-based conductive material.
To pinpoint a design that could be used in the aqueous environment of fuel cells, Bell and his team, as part of the Department of Energy’s Liquid Sunlight Alliance Energy Innovation Hub (LiSA) project, turned to thin layers of ionomers, polymers that allow certain charged molecules (ions) to pass through while excluding others. As a result of their highly selective chemistry, they are uniquely suited to have a strong influence on the microenvironment.
Schematic of a two-layer coating of films, called ionomers, on top of a copper surface. The negatively charged ionomer, Nafion, raises the pH near the surface. The positively charged ionomer, Sustainion, more strongly attracts CO2. These effects combined with a pulsed voltage result in substantially enhanced rates of CO2 conversion to valuable carbon-rich products. (Credit: Berkeley Lab)
Chanyeon Kim, a postdoctoral researcher in Bell’s group and the lead author on the paper, proposed to coat the surface of the copper catalyst with two common ionomers, Nafion and Sustainion. Doing so, the team hypothesized, should modify the environment—including the pH and amounts of water and CO2—in the catalyst’s immediate vicinity in a way that would steer the reaction to generate carbon-rich products that can be readily converted to useful chemicals and liquid fuels.
The researchers applied a thin layer of each ionomer, as well as a bilayer of both ionomers, to copper films supported by a polymer material, forming membranes that they could insert near one end of a hand-sized electrochemical cell. While feeding CO2 into the cell and applying a voltage, they measured the total current flowing through the cell. Then they measured the gases and liquids that collected in adjoining reservoirs during the reaction. For the two-layer case, they found that carbon-rich products accounted for 80% of the energy consumed by the reaction—up from 60% in the uncoated situation.
This sandwich coating gives the best of both worlds: high product selectivity and high activity.—Alexis Bell
The bilayered surface favored not only carbon-rich products, but at the same time generated a strong electrical current, indicating increased activity.
The researchers concluded that the improved reaction was a consequence of the high CO2 concentration that built up in the coating layer immediately on top of the copper. Additionally, negatively charged molecules that piled up in the region between the two ionomers created a low local acidity. That combination countered the concentration trade-off that tends to occur in the absence of the ionomer films.
To increase the reaction efficiency even further, the researchers turned to a technique that had been demonstrated before, without ionomer films, as another way to increase CO2 and pH: pulsing the voltage. By using a pulsed voltage with the bilayer ionomer coating, the researchers achieved a 250% increase in carbon-rich products compared to uncoated copper and a static voltage.
While some researchers have focused their work on developing new catalysts, catalyst discovery does not consider the operating conditions. Controlling the environment at the catalyst’s surface is a new and different approach.
Rather than coming up with a brand new catalyst, we’ve taken what we know about the kinetics of a reaction and used that knowledge to guide our thinking about how to change the environment at the catalyst site.—Adam Weber, a senior staff scientist in Berkeley Lab’s Energy Technologies Area and a co-author
The next step is to scale up production of the coated catalyst. The Berkeley Lab team’s initial experiments involved small, flat model systems, which are far simpler to work with compared with the high-area, porous structures necessary for commercial applications.
Although coating a flat surface is not difficult, a commercial approach might involve coating tiny copper spheres, noted Bell. Adding a second coating becomes challenging. One possibility is to mix and deposit the two coatings together in a solvent and hope that they separate as the solvent evaporates.
This work was supported by the DOE Office of Science.
Kim, C., Bui, J.C., Luo, X. et al. (2021) “Tailored catalyst microenvironments for CO2 electroreduction to multicarbon products on copper using bilayer ionomer coatings.” Nat Energy 6, 1026–1034 doi: 10.1038/s41560-021-00920-8