We investigate how systematically increasing the accuracy of various molecular dynamics modeling techniques influences the structure and capacitance of ionic liquid electric double layers (EDLs). The techniques probed concern long-range electrostatic interactions, electrode charging (constant charge versus constant potential conditions), and electrolyte polarizability. Our simulations are performed on a quasi-two-dimensional, or slab-like, model capacitor, which is composed of a polarizable ionic liquid electrolyte, [EMIM][BF4], interfaced between two graphite electrodes. To ensure an accurate representation of EDL differential capacitance, we derive new fluctuation formulas that resolve the differential capacitance as a function of electrode charge or electrode potential. The magnitude of differential capacitance shows sensitivity to different long-range electrostatic summation techniques, while the shape of differential capacitance is affected by charging technique and the polarizability of the electrolyte. For long-range summation techniques, errors in magnitude can be mitigated by employing two-dimensional or corrected three dimensional electrostatic summations, which led to electric fields that conform to those of a classical electrostatic parallel plate capacitor. With respect to charging, the changes in shape are a result of ions in the Stern layer (i.e., ions at the electrode surface) having a higher electrostatic affinity to constant potential electrodes than to constant charge electrodes. For electrolyte polarizability, shape changes originate from induced dipoles that soften the interaction of Stern layer ions with the electrode. The softening is traced to ion correlations vertical to the electrode surface that induce dipoles that oppose double layer formation. In general, our analysis indicates an accuracy dependent differential capacitance profile that transitions from the characteristic camel shape with coarser representations to a more diffuse profile with finer representations.
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14 May 2016
Research Article|
May 12 2016
Evaluation of molecular dynamics simulation methods for ionic liquid electric double layers Available to Purchase
Justin B. Haskins;
Justin B. Haskins
a)
1AMA Inc., Thermal Protection Materials Branch,
NASA Ames Research Center
, MS N234-1, Moffett Field, California 94035, USA
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John W. Lawson
John W. Lawson
2Thermal Protection Materials Branch,
NASA Ames Research Center
, MS N234-1, Moffett Field, California 94035, USA
Search for other works by this author on:
Justin B. Haskins
1,a)
John W. Lawson
2
1AMA Inc., Thermal Protection Materials Branch,
NASA Ames Research Center
, MS N234-1, Moffett Field, California 94035, USA
2Thermal Protection Materials Branch,
NASA Ames Research Center
, MS N234-1, Moffett Field, California 94035, USA
a)
Electronic mail: [email protected]
J. Chem. Phys. 144, 184707 (2016)
Article history
Received:
February 11 2016
Accepted:
April 26 2016
Citation
Justin B. Haskins, John W. Lawson; Evaluation of molecular dynamics simulation methods for ionic liquid electric double layers. J. Chem. Phys. 14 May 2016; 144 (18): 184707. https://doi.org/10.1063/1.4948938
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