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Electrochemical CO2 reduction offers a method to use renewable electricity to convert CO2 into CO and other carbon-based chemical building blocks. While nearly all studies rely on a CO2 feed, we show herein that aqueous bicarbonate solutions can also be electrochemically converted into CO gas at meaningful rates in a flow cell. We achieved this result in a flow cell containing a bipolar membrane (BPM) and a silver nanoparticle catalyst on a porous carbon support. Electrolysis upon a N2-saturated 3.0-M potassium bicarbonate electrolyte solution yields CO with a faradaic efficiency (F.E.CO) of 81% at 25 mA cm-2 and 37% at 100 mA cm-2. This output is comparable to the analogous experiment where the electrolyte is saturated with gaseous CO2 (faradaic efficiency for CO is 78% at 25 mA cm-2 and 35% at 100 mA cm-2). The H+ flux from the BPM is critical to this chemistry in that it reacts with the bicarbonate feed to generate CO2, which is then reduced to CO at the gas diffusion electrode. These results are important in that they show that the addition of gaseous CO2 to bicarbonate electrolytes is not necessary in order to obtain reduced carbon products with a flow cell architecture. This process offers a means of using electrolysis to bypass the thermally-intensive step of extracting CO2 from bicarbonate solutions generated in carbon capture schemes.
Organic molecular hole-transport materials (HTMs) are appealing for the scalable manufacture of perovskite solar cells (PSCs) because they are easier to reproducibly prepare in high purity than polymeric and inorganic HTMs. There is also a need to co
Following some recent unexpected hints of neutron production in setups like high-voltage atmospheric discharges and plasma discharges in electrolytic cells, we present a measurement of the neutron flux in a configuration similar to the latter. We use
Generator-collector experiments offer insights into the mechanisms of electrochemical reactions by correlating the product and generator currents. Most commonly, these experiments are performed using a rotating ring-disk electrode (RRDE). We develope
Our recent paper on the Search for Neutron Flux Generation in a Plasma Discharge Electrolytic Cell [1] has as main goal the validation of the experiment in Ref.[2]. As a follow-up, Ref.[3] moves a set of objections on our procedure and presents argum
A one dimensional (1-D), isothermal model for a direct methanol fuel cell (DMFC) is presented. This model accounts for the kinetics of the multi-step methanol oxidation reaction at the anode. Diffusion and crossover of methanol are modeled and the mi