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Francesca M. Toma

Publications and source records attributed to Francesca M. Toma.

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A nanoporous capacitive electrochemical ratchet for continuous ion separations

Directed ion transport in liquid electrolyte solutions underlies many phenomena in Nature and industry. While Nature has devised structures that drive continuous ion flow without Faradaic redox reactions, artificial analogs do not exist. Here we report the first demonstration of an ion pump that drives aqueous ions against a force using a capacitive ratchet mechanism that does not require redox reactions. Modulation of an electric potential between thin metallic layers on either face of a nanoporous alumina wafer immersed in solution resulted in persistent voltages and ionic currents. This occurs due to the non-linear capacitive nature of electric double layers, whose repeated charging and discharging sustains a continuous ion flux. Ratchet driven electrodialysis was demonstrated reaching a 50% decrease in the conductivity of the solution in a dilution cell. These ratchet-based ion pumps can enable continuous desalination and selective ion separation using an electrically powered device with no moving parts.

physics.app-ph

Development of a low flow vapor phase electrochemical reactor without catholyte reliance for CO2 electrolysis to high value carbon products

A continuous CO2 vapor-fed electrochemical cell prototype that performs CO2R with high faradaic efficiency for desired carbon products for up to 72 hours of operation is presented. The cell design facilitates a flow through configuration, capitalizing on gas diffusion electrode (GDE) and membrane electrode architecture (MEA) without requiring a catholyte. We demonstrate stable performance and design adaptability by incorporating various CO2R catalysts and membranes into the cell, investigating lifetime performance and selectivity under established experimental conditions. With an Ag foil and PPO anion exchange membrane, the design achieves an average current density of -30mA/cm2 and FE ~80% for CO obtained over a 12-hour duration. With a Cu-based catalyst, FE ~40% selectivity for ethylene was achieved. The unique geometry and flexibility of the cell provides an adaptive and dynamic GDE electrochemical cell framework, easing future research for novel electro-catalysts on GDE electrodes and MEA/GDE assemblies for enhanced (photo)electrochemical carbon dioxide reduction.

cond-mat.mtrl-sci