Nanoporous supercapacitors attract much attention as green energy storage devices with remarkable cyclability and high power and energy densities. However, their use in high-frequency applications is limited by relatively slow charging processes, while accelerating charging without compromising the energy storage still remains a challenging task. Here, we study in detail the charging and discharging behavior of nanoporous supercapacitors with narrow pores, which provide exceptionally high capacitances and stored energy densities. We scrutinize the dynamic modes of charging, revealing, in particular, a transient formation of crowded and dilute ionic-liquid phases inside the pores, which leads to co-ion trapping and correspondingly slow charging. We show how trapping can be circumvented by applying a slow voltage sweep, and we demonstrate that it can accelerate the overall charging process considerably if the sweep rate is chosen appropriately. While one might be tempted to apply a similar strategy to discharging, we find that the best discharge rates are obtained when the voltage is switched off in a step-like fashion, whereby the optimal charge and discharge times differ a few-fold. We unveil the scaling laws for such optimal quantities, which allow one to predict quantitatively the charging behavior for realistically long pores. On the basis of our findings, we propose an optimal charge-discharge cycle and elaborate on optimization strategies.

ESPResSo is an extensible simulation package for research on soft matter. This versatile molecular dynamics program was originally developed for coarse-grained simulations of charged systems [Limbach et al., Comput. Phys. Commun. 174, 704 (2006)]. The scope of the software has since broadened considerably: ESPResSo can now be used to simulate systems with length scales spanning from the molecular to the colloidal. Examples include, self-propelled particles in active matter, membranes in biological systems, and the aggregation of soot particles in process engineering. ESPResSo also includes solvers for hydrodynamic and electrokinetic problems, both on the continuum and on the explicit particle level. Since our last description of version 3.

Nanoporous carbon-based supercapacitors store electricity through adsorption of ions from the electrolyte at the surface of the electrodes. Room temperature ionic liquids, which show the largest ion concentrations among organic liquid electrolytes, should in principle yield larger capacitances. Here we show by using electrochemical measurements that the capacitance is not significantly affected when switching from a pure ionic liquid to a conventional organic electrolyte using the same ionic species. By performing additional molecular dynamics simulations, we interpret this result as an increasing difficulty of separating ions of opposite charges when they are more concentrated, i.e. in the absence of a solvent which screens the Coulombic interactions. The charging mechanism consistently changes with ion concentration, switching from counter-ion adsorption in the diluted organic electrolyte to ion exchange in the pure ionic liquid. Contrarily to the capacitance, in-pore diffusion coefficients largely depend on the composition, with a noticeable slowing of the dynamics in the pure ionic liquid.Supercapacitors are a promising electrochemical energy storage technology. They may be separated into two families of devices, depending on the electricity storage mechanism, i.e. the electric double-layer capacitors (EDLCs) and pseudocapacitors. 1 . In EDLCs, the charge is stored by a simple process of ion adsorption at the surface of the electrodes, even if at the microscopic scale complex mechanisms are at play. The most prominently employed electrode materials are porous carbons with high accessible surface area. Research and development of such EDLCs is being driven by demand from emerging applications which require efficient energy storage, notably renewable energy, 2 electric vehicles, 3 and smartgrid management. 4,5 Currently, commercial supercapacitors have energy densities on the order of 5 W h kg −1 . 5 There is a large ongoing interest in the design of electrolytes with improved performance over the traditional organic liquids, such as acetonitrile-based electrolytes. Room temperature ionic liquids (RTILs) have raised a lot of interest due to their high window of electrochemical stability, 6 high thermal stability, 7 and low toxicity. 8 RTILs are also highly tunable, and there are many possible combinations available which is beneficial as they can be selected to match specific electrodes. 9 However, when used as a pure electrolyte in EDLCs with highly microporous carbon electrodes, they suffer from high viscosity and poor conductivity. 10 Superconcentrated electrolytes, which are highly-concentrated mixtures of RTILs and organic solvents, may offer a good compromise for these target properties, while keeping most of the RTIL benefits. They are therefore considered as promising alternatives in EDLCs.A difficulty for choosing the optimal electrolyte is that the ions they contain adsorb inside electrified nanoporous carbon electrodes, in which the structure changes significantly due to strong electric field and co...

Electrolyte-filled subnanometre pores exhibit exciting physics and play an increasingly important role in science and technology. In supercapacitors, for instance, ultranarrow pores provide excellent capacitive characteristics. However, ions experience difficulties in entering and leaving such pores, which slows down charging and discharging processes. In an earlier work we showed for a simple model that a slow voltage sweep charges ultranarrow pores quicker than an abrupt voltage step. A slowly applied voltage avoids ionic clogging and co-ion trapping—a problem known to occur when the applied potential is varied too quickly—causing sluggish dynamics. Herein, we verify this finding experimentally. Guided by theoretical considerations, we also develop a non-linear voltage sweep and demonstrate, with molecular dynamics simulations, that it can charge a nanopore even faster than the corresponding optimized linear sweep. For discharging we find, with simulations and in experiments, that if we reverse the applied potential and then sweep it to zero, the pores lose their charge much quicker than they do for a short-circuited discharge over their internal resistance. Our findings open up opportunities to greatly accelerate charging and discharging of subnanometre pores without compromising the capacitive characteristics, improving their importance for energy storage, capacitive deionization, and electrochemical heat harvesting.

We introduce a hierarchy of generic coarse-grained models of ionic liquids of increasing complexity. We use them in molecular dynamics simulations to study the differential capacitance of a capacitor consisting of an ionic liquid between two planar electrodes. The primary goal is to explain the complex dependence of the differential capacitance Cd on the electrode potential U in simple terms, e.g. in terms of the size and valency of the ions. For this purpose we introduce the symmetric model A, which qualitatively reproduces the Cd(U) dependence predicted by the mean-field theory but also reveals strong quantitative deviations. We further introduce size asymmetry in model A by increasing the cation size. In model B we vary the cation valency, keeping the sizes of both ions constant. We show that simultaneous increases in size and valency may compensate for each other, leading to a Cd(U) very similar to that for the symmetric case. We interpret distinct features in Cd(U) on the basis of the density profiles of the ions and charge density profiles. We focus on the first two ion layers at the electrode, and demonstrate that the polarization of the ionic liquid proceeds through replacement of one ion type by the other, in contrast to the simple increase in ion concentrations typical for dilute systems. The understanding gained for the simple models serves as a reference for interpretation of complex effects of ion size, valency and shape. This is carried through in part II (a separate article) where we show how the planar shape of ions in model C brings new features to the Cd(U) curve and also to the polarization mechanism.