| نویسندگان | حیدر رئیسی,افسانه قهاری |
| نشریه | Journal of Molecular Liquids |
| شماره صفحات | 124523-124545 |
| شماره سریال | ۴۰۱ |
| شماره مجلد | ۴۰ |
| ضریب تاثیر (IF) | 3.648 |
| نوع مقاله | Full Paper |
| تاریخ انتشار | ۲۰۲۴ |
| رتبه نشریه | ISI |
| نوع نشریه | چاپی |
| کشور محل چاپ | هلند |
| نمایه نشریه | ISI،JCR،Scopus |
چکیده مقاله
Ionic liquids (ILs), due to their tunable propensities and properties, are discussed as a new class of solvents for
scientific and industrial applications. Developing novel processes and applying ionic liquids further accelerate
the growth of our fundamental and engineering understanding.
In this work, the structure of four ILs, 1-ethyl-3-methylimidazolium tetrafluoroborate formate (Emim+BF4
− )/
chloride (Emim+Cl− )/Nitrate (Emim+NO3
− ), and thiocyanate (Emim+SCN− ) is reported. Then via employing
classical molecular dynamics and well-tempered metadynamics simulations their dynamics are investigated. The
dynamics of ILs are represented by studying mean squared displacements. Additionally, the increased size and
weight of anions interacting with the Emim+ cation cause the dynamics to become slow. Therefore, due to the
higher molecular weight, the BF4
− anion has lower diffusion than any other. Indeed, radial distribution functions
between cations and anions reveal the structural arrangement in ILs. On the other hand, it is unexpectedly found
that a certain amount of ILs are distributed near the electrode surface. Such phenomena occur because of the
relatively strong ionic interactions between cations and anions; also, the π–π stacking between cations and
graphene caused their interactions to become stronger. Furthermore, the atoms in molecules (AIM) analyses
identified several interatomic interactions between the ILs and graphene. The free energy values for the ILs at
their global minima are about ~ -271.79, − 267.93, − 251.37 kJ mol− 1 and ~ -241.98 kJ mol− 1 in systems
Emim+/Cl− , Emim//NO3
− , Emim+/SCN− , and Emim+/BF4
− , respectively. Our findings represent a crucial step
towards interpreting the complex interactions and nanostructures at the electrolyte–electrode interface, which
could be beneficial for designing high-performance supercapacitors in energy storage using carbon electrodes
and IL electrolytes in experiments
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