The liquid electrolytes in flow batteries provide a bridge to help carry electrons into electrodes, and that changes how chemical engineers think about efficiency.
The way to boost electron transfer in grid-scale batteries is different than researchers had believed, a new study from the University of Michigan has shown.
The findings are a step toward being able to store renewable energy more efficiently.
As governments and utilities around the world roll out intermittent renewable energy sources such as wind and solar, we remain reliant on coal, natural gas and nuclear power plants to provide energy when the wind isn’t blowing and the sun isn’t shining. Grid-scale “flow” batteries are one proposed solution, storing energy for later use. But because they aren’t very efficient, they need to be large and expensive.
In a flow battery, the energy is stored in a pair of “electrolyte” fluids which are kept in tanks and flow through the working part of the battery to store or release energy. An active metal gains or loses electrons from the electrode on either side, depending on whether the battery is charging or discharging. One efficiency bottleneck is how quickly electrons move between the electrodes and the active metal.
“By maximizing the charge transfer, we can reduce the overall cost of flow batteries,” said study first author Harsh Agarwal, a chemical engineering Ph.D. student who works in the lab of Nirala Singh, U-M assistant professor of chemical engineering.
Researchers have been trying different chemical combinations to improve it, but they don’t really know what’s going on at the molecular level. This study, published in Cell Reports Physical Science, is one of the first to explore it.
Researchers had believed that the negatively charged molecular groups from the acids provided more spots for electron transfer to take place on the battery’s negative electrode. The findings from the team co-led by Singh and Bryan Goldsmith, the Dow Corning Assistant Professor of Chemical Engineering, tell a different story. Instead, the acid groups lowered the energy barrier of the electron transfer by serving as a sort of bridge between the active metal in the fluid — vanadium in this case — and the electrode. This helps the vanadium give up its electron.
“Our findings suggest that bridging may play a critical yet underexplored role in other flow battery chemistries employing transition metals,” Singh said. “This discovery is not only relevant to energy storage but also fields of corrosion and electrodeposition.”
The study shows that the reaction rate in flow batteries can be tuned by controlling how well the acid in the liquid electrolyte binds with the active metal.
“Researchers can apply this knowledge to electrolyte engineering or electrocatalyst development, both of which are important disciplines in sustainable energy,” Agarwal said.
Agarwal and Singh measured the reaction rate between the vanadium and electrode for five different acidic electrolytes. To get a clearer picture of the details at the atomic level, the team used a form of quantum mechanical modeling, known as density functional theory, to calculate how well the vanadium-acid combinations bind to the electrode. This part of the study was undertaken by Goldsmith and Jacob Florian, a chemical engineering senior undergraduate student working in the Goldsmith lab.
At Argonne National Laboratory, Agarwal and Singh used X-ray spectroscopy to discover details about how the vanadium ions configured themselves when in contact with different acids. Density functional theory calculations helped interpret the X-ray measurements. The study also provides the first direct experimental verification of how water attaches to vanadium ions.
Materials provided by University of Michigan. Original written by Heather Guenther. Note: Content may be edited for style and length.
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