The performance of electrical double layer capacitors (EDLCs), also known as supercapacitors, which are composed of porous electrodes and ionic liquid electrolytes, depends largely on the structure and dynamics of molecules/ions at the electrode–electrolyte interfaces. Immobilization of ions on the electrode surface and diffusivity of ions in the middle of the pores are two important phenomena influencing the performance of supercapacitors. In recent years, porous carbon or metal carbide derived electrodes and ionic liquid electrolytes, either in the neat state or mixed with organic solvents, were used to improve the energy and power density of supercapacitors. The molecular/ionic level predictive understanding of ion immobilization and movement inside the pores can be achieved, in principle, using molecular dynamics (MD) simulations. This calls for experimental techniques capable of validating MD predictions and providing directions for future MD studies. Neutron scattering techniques, particularly quasi-elastic neutron scattering (QENS), uniquely provide information directly comparable with MD simulation results. This includes electrolytes confined in electrode materials, due to high penetrative power of neutrons and their high sensitivity to hydrogen-bearing species. This study reviews recent research where QENS, together with electrochemical measurements and molecular dynamics simulations, has been employed to explore complex electrode/electrolyte systems, which is critical for developing predictive understanding of the charge storage mechanism in supercapacitors.
Osti, Naresh C. and Mamontov, Eugene. "Microscopic dynamics in room-temperature ionic liquids confined in materials for supercapacitor applications." Sustainable Energy & Fuels, vol. 4, no. 4, Jan. 2020. https://doi.org/10.1039/c9se00829b
@article{osti_1657986,
author = {Osti, Naresh C. and Mamontov, Eugene},
title = {Microscopic dynamics in room-temperature ionic liquids confined in materials for supercapacitor applications},
annote = {The performance of electrical double layer capacitors (EDLCs), also known as supercapacitors, which are composed of porous electrodes and ionic liquid electrolytes, depends largely on the structure and dynamics of molecules/ions at the electrode–electrolyte interfaces. Immobilization of ions on the electrode surface and diffusivity of ions in the middle of the pores are two important phenomena influencing the performance of supercapacitors. In recent years, porous carbon or metal carbide derived electrodes and ionic liquid electrolytes, either in the neat state or mixed with organic solvents, were used to improve the energy and power density of supercapacitors. The molecular/ionic level predictive understanding of ion immobilization and movement inside the pores can be achieved, in principle, using molecular dynamics (MD) simulations. This calls for experimental techniques capable of validating MD predictions and providing directions for future MD studies. Neutron scattering techniques, particularly quasi-elastic neutron scattering (QENS), uniquely provide information directly comparable with MD simulation results. This includes electrolytes confined in electrode materials, due to high penetrative power of neutrons and their high sensitivity to hydrogen-bearing species. This study reviews recent research where QENS, together with electrochemical measurements and molecular dynamics simulations, has been employed to explore complex electrode/electrolyte systems, which is critical for developing predictive understanding of the charge storage mechanism in supercapacitors.},
doi = {10.1039/c9se00829b},
url = {https://www.osti.gov/biblio/1657986},
journal = {Sustainable Energy & Fuels},
issn = {ISSN 2398-4902},
number = {4},
volume = {4},
place = {United States},
publisher = {Royal Society of Chemistry},
year = {2020},
month = {01}}
Energy Frontier Research Centers (EFRC) (United States). Fluid Interface Reactions, Structures and Transport Center (FIRST); Oak Ridge National Laboratory (ORNL), Oak Ridge, TN (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22)
Grant/Contract Number:
AC05-00OR22725
OSTI ID:
1657986
Alternate ID(s):
OSTI ID: 1597150
Journal Information:
Sustainable Energy & Fuels, Journal Name: Sustainable Energy & Fuels Journal Issue: 4 Vol. 4; ISSN 2398-4902
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