Electrical energy can be obtained from the controlled mixing of fresh (river) and saline (sea) water. Existing technologies such as pressure retarded osmosis and reverse electrodialysis make use of ion-exchange membranes which must be crossed by either the water or the ions. Recently a new physical principle has been experimentally demonstrated, which allows extraction of electrical energy without making use of membranes, based on the temporary storage of ions inside two porous electrodes kept at different electrical potentials, and the repeatable expansion/contraction of the electrostatic double layers formed inside the electrodes upon changing the salt concentration [D. Brogioli, Phys. Rev. Lett., 2009, 103, 058501]. To make further investigations and to improve the energy recovery, we developed a simple prototype cell of much larger dimensions. Because of the larger dimensions (thus higher currents), testing is more facile, while this design can be the basis for further scaling-up of this technology. In order to reduce the internal resistance of the cell, the electrodes are no longer placed side-by-side, but parallel to one another, separated only by a 250 μm-thick open spacer channel to form a “sandwich”-like flow cell. In a lab-scale experimental stack consisting of 8 such cells (with outer dimensions 6 × 6 × 1 cm3) we extract about 2 J per charging/discharging cycle in 500 mM/1 mM NaCl salt solution, an amount which is 20 times higher per cycle per unit electrode mass than previously obtained. The extracted energy increases with the operating voltage, in line with predictions of the Gouy-Chapman-Stern model for double layer formation.

Brogioli, D., Zhao, R., Biesheuvel, P. (2011). A prototype cell for extracting energy from a water salinity difference by means of double layer expansion in nanoporous carbon electrodes. ENERGY & ENVIRONMENTAL SCIENCE, 4(3), 772-777 [10.1039/C0EE00524J].

A prototype cell for extracting energy from a water salinity difference by means of double layer expansion in nanoporous carbon electrodes

BROGIOLI, DORIANO COSTANTINO
;
2011

Abstract

Electrical energy can be obtained from the controlled mixing of fresh (river) and saline (sea) water. Existing technologies such as pressure retarded osmosis and reverse electrodialysis make use of ion-exchange membranes which must be crossed by either the water or the ions. Recently a new physical principle has been experimentally demonstrated, which allows extraction of electrical energy without making use of membranes, based on the temporary storage of ions inside two porous electrodes kept at different electrical potentials, and the repeatable expansion/contraction of the electrostatic double layers formed inside the electrodes upon changing the salt concentration [D. Brogioli, Phys. Rev. Lett., 2009, 103, 058501]. To make further investigations and to improve the energy recovery, we developed a simple prototype cell of much larger dimensions. Because of the larger dimensions (thus higher currents), testing is more facile, while this design can be the basis for further scaling-up of this technology. In order to reduce the internal resistance of the cell, the electrodes are no longer placed side-by-side, but parallel to one another, separated only by a 250 μm-thick open spacer channel to form a “sandwich”-like flow cell. In a lab-scale experimental stack consisting of 8 such cells (with outer dimensions 6 × 6 × 1 cm3) we extract about 2 J per charging/discharging cycle in 500 mM/1 mM NaCl salt solution, an amount which is 20 times higher per cycle per unit electrode mass than previously obtained. The extracted energy increases with the operating voltage, in line with predictions of the Gouy-Chapman-Stern model for double layer formation.
Articolo in rivista - Articolo scientifico
Renewable energy; energy from salinity difference
English
2011
4
3
772
777
open
Brogioli, D., Zhao, R., Biesheuvel, P. (2011). A prototype cell for extracting energy from a water salinity difference by means of double layer expansion in nanoporous carbon electrodes. ENERGY & ENVIRONMENTAL SCIENCE, 4(3), 772-777 [10.1039/C0EE00524J].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10281/30733
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