Exploring electrolysis for energy storage
Research team creates electrolytic flow cell to produce alcohols from carboxylic acids
SUMMARY:
A research team developed a flow-type polymer electrolyte cell for power storage. The cell reduces oxalic acid (OX) to glycolic acid, which has a higher volumetric energy-storage capacity than hydrogen gas. Newly fabricated TiO2 cathode enhanced the speed and efficiency of OX reduction. This competitive energy-storage device could be used to balance out the fluctuations in renewable power supplies.
A Kyushu University research
team realized continuous electrochemical synthesis of an alcoholic
compound from a carboxylic acid using a polymer electrolyte alcohol
electrosynthesis cell, which enables direct power charge into alcoholic
compound.
Interest in renewable energy continues to
burgeon. Many renewables, though, can be frustratingly intermittent --
when the sun stops shining, or the wind stops blowing, the power
flickers. The fluctuating supply can be partly smoothed-out by energy
storage during peak production times. However, storing electricity is
not without its challenges either.
Recently, a team at the International Institute for Carbon-Neutral
Energy Research (I2CNER), within southern Japan's Kyushu University,
created a device to store energy in chemical form through continuous
electrolysis.
The researchers noted that glycolic acid (GC) has a much greater energy capacity than hydrogen, one of the more popular energy-storage chemicals. GC can be produced by four-electron reduction of oxalic acid (OX), a widely available carboxylic acid. As described in their publication in Scientific Reports, the team devised an electrolytic cell based on a novel membrane-electrode assembly. Sandwiched between two electrodes are an iridium oxide-based anode and a titanium dioxide (TiO2)-coated titanium (Ti) cathode, linked by a polymer membrane.
"Flow-type systems are very important for energy storage with liquid-phase reaction," study lead author Masaaki Sadakiyo explains. "Most electrolyzers producing alcohols operate a batch process, which is not suitable for this purpose. In our device, by using a solid polymer electrolyte in direct contact with the electrodes, we can run the reaction as a continuous flow without addition of impurities (e.g. electrolytes). The OX solution can effectively be thought of as a flowable electron pool."
Another key consideration is the cathode design. The cathodic reaction is catalyzed by anatase TiO2. To ensure a solid connection between catalyst and cathode, the team "grew" TiO2 directly on Ti in the form of a mesh or felt. Electron microscope images show the TiO2 as a wispy fuzz, clinging to the outside of the Ti rods like a coating of fresh snow. In fact, its job is to catalyze the electro-reduction of OX to GC. Meanwhile, at the anode, water is oxidized to oxygen.
The team found that the reaction accelerated at higher temperatures. However, turning the heat up too high encouraged an unwanted by-process -- the conversion of water to hydrogen. The ideal balance between these two effects was at 60°C. At this temperature, the device could be further optimized by slowing the flow of reactants, while increasing the amount of surface area available for the reaction.
Interestingly, even the texture of the fuzzy TiO2 catalyst made a major difference. When TiO2 was prepared as a "felt," by growing it on thinner and more densely packed Ti rods, the reaction occurred faster than on the "mesh" -- probably because of the greater surface area. The felt also discouraged hydrogen production, by blanketing the Ti surface more snugly than the mesh, preventing the exposure of bare Ti.
"In the right conditions, our cell converts nearly 100% of OX, which we find very encouraging," co-author Miho Yamauchi says. "We calculate that the maximum volumetric energy capacity of the GC solution is around 50 times that of hydrogen gas. To be clear, the energy efficiency, as opposed to capacity, still lags behind other technologies. However, this is a promising first step to a new method for storing excess current."
The researchers noted that glycolic acid (GC) has a much greater energy capacity than hydrogen, one of the more popular energy-storage chemicals. GC can be produced by four-electron reduction of oxalic acid (OX), a widely available carboxylic acid. As described in their publication in Scientific Reports, the team devised an electrolytic cell based on a novel membrane-electrode assembly. Sandwiched between two electrodes are an iridium oxide-based anode and a titanium dioxide (TiO2)-coated titanium (Ti) cathode, linked by a polymer membrane.
"Flow-type systems are very important for energy storage with liquid-phase reaction," study lead author Masaaki Sadakiyo explains. "Most electrolyzers producing alcohols operate a batch process, which is not suitable for this purpose. In our device, by using a solid polymer electrolyte in direct contact with the electrodes, we can run the reaction as a continuous flow without addition of impurities (e.g. electrolytes). The OX solution can effectively be thought of as a flowable electron pool."
Another key consideration is the cathode design. The cathodic reaction is catalyzed by anatase TiO2. To ensure a solid connection between catalyst and cathode, the team "grew" TiO2 directly on Ti in the form of a mesh or felt. Electron microscope images show the TiO2 as a wispy fuzz, clinging to the outside of the Ti rods like a coating of fresh snow. In fact, its job is to catalyze the electro-reduction of OX to GC. Meanwhile, at the anode, water is oxidized to oxygen.
The team found that the reaction accelerated at higher temperatures. However, turning the heat up too high encouraged an unwanted by-process -- the conversion of water to hydrogen. The ideal balance between these two effects was at 60°C. At this temperature, the device could be further optimized by slowing the flow of reactants, while increasing the amount of surface area available for the reaction.
Interestingly, even the texture of the fuzzy TiO2 catalyst made a major difference. When TiO2 was prepared as a "felt," by growing it on thinner and more densely packed Ti rods, the reaction occurred faster than on the "mesh" -- probably because of the greater surface area. The felt also discouraged hydrogen production, by blanketing the Ti surface more snugly than the mesh, preventing the exposure of bare Ti.
"In the right conditions, our cell converts nearly 100% of OX, which we find very encouraging," co-author Miho Yamauchi says. "We calculate that the maximum volumetric energy capacity of the GC solution is around 50 times that of hydrogen gas. To be clear, the energy efficiency, as opposed to capacity, still lags behind other technologies. However, this is a promising first step to a new method for storing excess current."
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