Energy Extraction from Capacitive Mixing: Experimental and Computational Analysis of Chemical Aspects

The double-layer expansion at the interfaces of charged electrodes when a concentrated salt solution (molar concentration Csalt) is replaced by a diluted solution (Cfresh), produces an increase of the cell voltage. Experiments and simulations were performed in order to study the effect of several va...

Full description

Bibliographic Details
Main Authors: Cabrera, J.N (Author), González, G.A (Author), Lizarraga, L. (Author), Negri, R.M (Author)
Format: Article
Language:English
Published: IOP Publishing Ltd 2022
Subjects:
Online Access:View Fulltext in Publisher
LEADER 02446nam a2200337Ia 4500
001 10.1149-1945-7111-ac613e
008 220510s2022 CNT 000 0 und d
020 |a 00134651 (ISSN) 
245 1 0 |a Energy Extraction from Capacitive Mixing: Experimental and Computational Analysis of Chemical Aspects 
260 0 |b IOP Publishing Ltd  |c 2022 
856 |z View Fulltext in Publisher  |u https://doi.org/10.1149/1945-7111/ac613e 
520 3 |a The double-layer expansion at the interfaces of charged electrodes when a concentrated salt solution (molar concentration Csalt) is replaced by a diluted solution (Cfresh), produces an increase of the cell voltage. Experiments and simulations were performed in order to study the effect of several variables on the obtained transient voltage, V(t), and the rising of voltage at equilibrium, Δφeq. Carbon electrodes were prepared and characterized by cyclic voltammetry, amperometry, and N2-adsorption isotherms. The experimental results and finite elements simulations show that the shape of V(t) is influenced by the diffusion coefficients of the ions. On the other hand, experiments and simulations indicate that Δφeqpresent a Nernstian-like dependence with the dilution coefficient, Cdil= Csalt/Cfresh, while is independent of the initial charge and charging time. Quantitative features are interpreted by proposing a partial blocking of the electrodes for the dilution process, associated to irreversible incorporation of solution into the porous, presenting a model to estimate the blocking degree. Finally, cycles of charging-dilution-work-concentration were performed, extracting energies in the order of 100 μJ cm-2, which are in agreement with the model equations as function of Csalt and Cfresh. © 2022 Electrochemical Society Inc.. All rights reserved. 
650 0 4 |a Chemical analysis 
650 0 4 |a Chemical aspects 
650 0 4 |a Computational analysis 
650 0 4 |a Cyclic voltammetry 
650 0 4 |a Diluted solutions 
650 0 4 |a Double layers 
650 0 4 |a Electrodes 
650 0 4 |a Energy extraction 
650 0 4 |a Experimental analysis 
650 0 4 |a Fresh produce 
650 0 4 |a Layer expansion 
650 0 4 |a Molar concentration 
650 0 4 |a Molar ratio 
650 0 4 |a Salt solution 
700 1 |a Cabrera, J.N.  |e author 
700 1 |a González, G.A.  |e author 
700 1 |a Lizarraga, L.  |e author 
700 1 |a Negri, R.M.  |e author 
773 |t Journal of the Electrochemical Society