4.6 Article

Influences from solvents on charge storage in titanium carbide MXenes

Journal

NATURE ENERGY
Volume 4, Issue 3, Pages 241-248

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/s41560-019-0339-9

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Funding

  1. Fluid Interface Reactions, Structures, and Transport (FIRST) Center, an Energy Frontier Research Center (EFRC) - US Department of Energy, Office of Science, and Office of Basic Energy Sciences
  2. NSF [DMR-1508249]

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Pseudocapacitive energy storage in supercapacitor electrodes differs significantly from the electrical double-layer mechanism of porous carbon materials, which requires a change from conventional thinking when choosing appropriate electrolytes. Here we show how simply changing the solvent of an electrolyte system can drastically influence the pseudocapacitive charge storage of the two-dimensional titanium carbide, Ti3C2 (a representative member of the MXene family). Measurements of the charge stored by Ti3C2 in lithium-containing electrolytes with nitrile-, carbonate- and sulfoxide-based solvents show that the use of a carbonate solvent doubles the charge stored by Ti3C2 when compared with the other solvent systems. We find that the chemical nature of the electrolyte solvent has a profound effect on the arrangement of molecules/ions in Ti3C2, which correlates directly to the total charge being stored. Having nearly completely desolvated lithium ions in Ti3C2 for the carbonate-based electrolyte leads to high volumetric capacitance at high charge-discharge rates, demonstrating the importance of considering all aspects of an electrochemical system during development.

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