AI Article Synopsis

  • Experimental studies have indicated that the choice of electrolyte solvents affects ion transport and specific capacitance in microporous carbons, but the structure-property relationships are not well understood.
  • Researchers utilized in situ small angle neutron scattering (SANS) to investigate how organic electrolyte ions are adsorbed in carbon pores of varying sizes, using a 1 M solution of TEATFB salt in deuterated acetonitrile.
  • The study found that even though smaller carbon pores are not fully wet by the solvent, ion sorption increases in these pores with applied potential—suggesting that electrowetting phenomena play a significant role, which could explain certain characteristics observed in cyclic voltammetry curves.

Article Abstract

Experimental studies showed the impact of the electrolyte solvents on both the ion transport and the specific capacitance of microporous carbons. However, the related structure-property relationships remain largely unclear and the reported results are inconsistent. The details of the interactions of the charged carbon pore walls with electrolyte ions and solvent molecules at a subnanometer scale are still largely unknown. Here for the first time we utilize in situ small angle neutron scattering (SANS) to reveal the electroadsorption of organic electrolyte ions in carbon pores of different sizes. A 1 M solution of tetraethylammonium tetrafluoroborate (TEATFB) salt in deuterated acetonitrile (d-AN) was used in an activated carbon with the pore size distribution similar to that of the carbons used in commercial double layer capacitors. In spite of the incomplete wetting of the smallest carbon pores by the d-AN, we observed enhanced ion sorption in subnanometer pores under the applied potential. Such results suggest the visible impact of electrowetting phenomena counterbalancing the high energy of the carbon/electrolyte interface in small pores. This behavior may explain the characteristic butterfly wing shape of the cyclic voltammetry curve that demonstrates higher specific capacitance at higher applied potentials, when the smallest pores become more accessible to electrolyte. Our study outlines a general methodology for studying various organic salts-solvent-carbon combinations.

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Source
http://dx.doi.org/10.1021/nn406077nDOI Listing

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