4.7 Article

Carbon-carbon supercapacitors: Beyond the average pore size or how electrolyte confinement and inaccessible pores affect the capacitance

期刊

JOURNAL OF CHEMICAL PHYSICS
卷 155, 期 18, 页码 -

出版社

AIP Publishing
DOI: 10.1063/5.0065150

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资金

  1. European Research Council (ERC) under the European Unions Horizon 2020 research and innovation program [714581]
  2. CALMIP supercomputing center [P17037]

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In this study, molecular simulations were used to demonstrate that carbon electrodes with a more ordered structure and a well defined pore size exhibit higher capacitance compared to those with a more disordered structure and a broader pore size distribution. This is attributed to the larger quantities and higher confinement of ions adsorbed in the ordered carbon, which favor better charge separation. This work opens the door to computationally tractable screening strategies for supercapacitors.
Carbon-carbon supercapacitors are high power electrochemical energy storage systems, which store energy through reversible ion adsorption at the electrode-electrolyte interface. Due to the complex structure of the porous carbons used as electrodes, extracting structure-property relationships in these systems remains a challenge. In this work, we conduct molecular simulations of two model supercapacitors based on nanoporous electrodes with the same average pore size, a property often used when comparing porous materials, but different morphologies. We show that the carbon with the more ordered structure, and a well defined pore size, has a much higher capacitance than the carbon with the more disordered structure and a broader pore size distribution. We analyze the structure of the confined electrolyte and show that the ions adsorbed in the ordered carbon are present in larger quantities and are also more confined than for the disordered carbon. Both aspects favor a better charge separation and thus a larger capacitance. In addition, the disordered electrodes contain a significant amount of carbon atoms, which are never in contact with the electrolyte, carry a close to zero charge, and are thus not involved in the charge storage. The total quantities of adsorbed ions and degrees of confinement do not change much with the applied potential, and as such, this work opens the door to computationally tractable screening strategies.

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