Increasing the Sodium Metal Electrode Compatibility with the Na3 PS4 Solid-State Electrolyte through Heteroatom Substitution.

Rechargeable batteries are essential to the global shift towards renewable energy sources and their storage. At present, improvements in their safety and sustainability are of great importance as part of global sustainable development goals. A major contender in this shift are rechargeable solid-state sodium batteries, as a low-cost, safe, and sustainable alternative to conventional lithium-ion batteries. Recently, solid-state electrolytes with a high ionic conductivity and low flammability have been developed. However, these still face challenges with the highly reactive sodium metal electrode. The study of these electrolyte-electrode interfaces is challenging from a computational and experimental point of view, but recent advances in molecular dynamics neural-network potentials are finally enabling access to these environments compared to more computationally expensive conventional ab-initio techniques. In this study, heteroatom-substituted Na3 PS3 X1 analogues, where X is sulfur, oxygen, selenium, tellurium, nitrogen, chlorine, and fluorine, are investigated using total-trajectory analysis and neural-network molecular dynamics. It was found that inductive electron-withdrawing and electron-donating effects, alongside differences in heteroatom atomic radius, electronegativity, and valency, influenced the electrolyte reactivity. The Na3 PS3 O1 oxygen analogue was found to have superior chemical stability against the sodium metal electrode, paving the way towards high-performance, long lifetime and reliable rechargeable solid-state sodium batteries.

Molecular Resolution Nanostructure and Dynamics of the Deep Eutectic Solvent-Graphite Interface as a Function of Potential.

Interest in deep eutectic solvents (DESs), particularly for electrochemical applications, has boomed in the past decade because they are more versatile than conventional electrolyte solutions and are low cost, renewable, and non-toxic. The molecular scale lateral nanostructures as a function of potential at the solid-liquid interface-critical design parameters for the use of DESs as electrochemical solvents-are yet to be revealed. In this work, in situ amplitude modulated atomic force microscopy complemented by molecular dynamics simulations is used to probe the Stern and near-surface layers of the archetypal and by far most studied DES, 1:2 choline chloride:urea (reline), at the highly orientated pyrolytic graphite surface as a function of potential, to reveal highly ordered lateral nanostructures with unprecedented molecular resolution. This detail allows identification of choline, chloride, and urea in the Stern layer on graphite, and in some cases their orientations. Images obtained after the potential is switched from negative to positive show the dynamics of the Stern layer response, revealing that several minutes are required to reach equilibrium. These results provide valuable insight into the nanostructure and dynamics of DESs at the solid-liquid interface, with implications for the rational design of DESs for interfacial applications.

The role of hydrogen bond donor and water content on the electrochemical reduction of Ni2+ from solvents - an experimental and modelling study.

Deep Eutectic Solvents (DESs) are hygroscopic liquids composed of a hydrogen bond donor (HBD) and acceptor (HBA). Their physical, chemical and electrochemical properties can be tailored to use them as solvents for different applications, i.e. electrodeposition, catalysis, extraction, etc. This can be done by changing the HBD, as well by adding water. However, the interrelated influence of H2O and HBD on the structure of the electrolyte, and on the behavior of the active species is not fully understood. In this work, we select nickel electrodeposition as a case study and we combine electrochemical techniques (cyclic voltammetry, chronoamperometry) with UV-vis spectroscopy and molecular dynamics to understand the influence of water and HBD on the electrochemical behaviour of DESs. The unique combination of these different experimental and modelling techniques provides new insights into the field. The addition of H2O changes, not only the interactions between the constituents of the liquid, but also the coordination of metal cations, which is reflected in the electrochemical performance of different DESs. More importantly, we show that, in the presence of very little (between 0.1 wt% and 2.8 wt%) and high (>4.5 wt%) water contents, DESs behave differently, and the changes in their electrochemical behavior are caused by both the complexation of metal cations and the electrolyte transport properties.

Water distribution at the electrified interface of deep eutectic solvents.

Deep eutectic solvents (DESs) are a new class of solvents with wider potential window than that of water and high electrochemical stability, making them potential candidates for a wide range of electrochemical systems. However, due to the hygroscopic nature of DESs, the presence of latent water is unavoidable. Therefore, understanding the interfacial structure and the electrosorption and distribution of residual water at the electrified interface is of great importance for the use of these solvents in electrochemical systems. Using atomistic molecular dynamics, we explore the electrosorption and distribution of different amounts of water in 1 : 2 choline chloride-urea DES (Reline) at the electrified graphene interface. We found that both the water distribution and the interfacial structure are sensitive to the electrification of the graphene electrode. As a result, it is found that for moderately charged electrodes, water shows a preferential asymmetric adsorption in the vicinity of the positively charged electrode, partly due to strong intermolecular interactions with anions through hydrogen bonds. In contrast, for highly charged electrodes, water adsorbs at both electrodes due to a strongly enhanced external electrostatic interaction between the electrodes and the water dipoles.

Correction: Water distribution at the electrified interface of deep eutectic solvents.

[This corrects the article DOI: 10.1039/C9NA00331B.].

Atomistic Insight into the Electrochemical Double Layer of Choline Chloride-Urea Deep Eutectic Solvents: Clustered Interfacial Structuring.

Green, stable, and wide electrochemical window deep eutectic solvents (DESs) are ideal candidates for electrochemical systems. However, despite several studies of their bulk properties, their structure and properties under electrified confinement have barely been investigated, which has hindered widespread use of these solvents in electrochemical applications. In this Letter, we explore the electrical double layer structure of 1:2 choline chloride-urea (Reline), with a particular focus on the electrosorption of the hydrogen bond donor on a graphene electrode using atomistic molecular dynamics simulations. We discovered that the interface is composed of a mixed layer of urea and counterions followed by a mixed charged clustered structure of all of the Reline components. This interfacial structuring is strongly dependent on the balance between intermolecular interactions and surface polarization. These results provide new insights into the electrical double layer structure of a new generation of electrolytes whose interfacial structure can be tuned at the molecular level.

Numerical insights into the early stages of nanoscale electrodeposition: nanocluster surface diffusion and aggregative growth.

Fundamental understanding of the early stages of electrodeposition at the nanoscale is key to address the challenges in a wide range of applications. Despite having been studied for decades, a comprehensive understanding of the whole process is still out of reach. In this work, we introduce a novel modelling approach that couples a finite element method (FEM) with a random walk algorithm, to study the early stages of nanocluster formation, aggregation and growth, during electrochemical deposition. This approach takes into account not only electrochemical kinetics and transport of active species, but also the surface diffusion and aggregation of adatoms and small nanoclusters. The simulation results reveal that the relative surface mobility of the nanoclusters compared to that of the adatoms plays a crucial role in the early growth stages. The number of clusters, their size and their size dispersion are influenced more significantly by nanocluster mobility than by the applied overpotential itself. Increasing the overpotential results in shorter induction times and leads to aggregation prevalence at shorter times. A higher mobility results in longer induction times, a delayed transition from nucleation to aggregation prevalence, and as a consequence, a larger surface coverage of smaller clusters with a smaller size dispersion. As a consequence, it is shown that a classical first-order nucleation kinetics equation cannot describe the evolution of the number of clusters with time, N(t), in potentiostatic electrodeposition. Instead, a more accurate representation of N(t) is provided. We show that an evaluation of N(t), which neglects the effect of nanocluster mobility and aggregation, can induce errors of several orders of magnitude in the determination of nucleation rate constants. These findings are extremely important towards evaluating the elementary electrodeposition processes, considering not only adatoms, but also nanoclusters as building blocks.