Electrochemical Performance of Na3V2(PO4)2F3 Electrode Material in a Symmetric Cell.

A NASICON-based Na3V2(PO4)2F3 (NVPF) cathode material is reported herein as a potential symmetric cell electrode material. The symmetric cell was active from 0 to 3.5 V and showed a capacity of 85 mAh/g at 0.1 C. With cycling, the NVPF symmetric cell showed a very long and stable cycle life, having a capacity retention of 61% after 1000 cycles at 1 C. The diffusion coefficient calculated from cyclic voltammetry (CV) and the galvanostatic intermittent titration technique (GITT) was found to be ~10-9-10-11, suggesting a smooth diffusion of Na+ in the NVPF symmetric cell. The electrochemical impedance spectroscopy (EIS) carried out during cycling showed increases in bulk resistance, solid electrolyte interphase (SEI) resistance, and charge transfer resistance with the number of cycles, explaining the origin of capacity fade in the NVPF symmetric cell. Finally, the postmortem analysis of the symmetric cell after 1000 cycles at a 1 C rate indicated that the intercalation/de-intercalation of sodium into/from the host structure occurred without any major structural destabilization in both the cathode and anode. However, there was slight distortion in the cathode structure observed, which resulted in capacity loss of the symmetric cell. The promising electrochemical performance of NVPF in the symmetric cell makes it attractive for developing long-life and cost-effective batteries.

High Na+ Mobility in rGO Wrapped High Aspect Ratio 1D SbSe Nano Structure Renders Better Electrochemical Na+ Battery Performance.

We chose to understand the cyclic instability and rate instability issues in the promising class of Na+ conversion and alloying anodes with Sb2 Se3 as a typical example. We employ a synthetic strategy that ensures efficient rGO (reduced graphene oxide) wrapping over Sb2 Se3 material. By utilization of the minimum weight of additive (5 wt.% of rGO), we achieved a commendable performance with a reversible capacity of 550 mAh g-1 at a specific current of 100 mA g-1 and an impressive rate performance with 100 % capacity retention after high current cycling involving a 2 Ag-1 intermediate current step. The electrochemical galvanostatic intermittent titration technique (GITT) has been employed for the first time to draw a rationale between the enhanced performance and the increased mobility in the rGO wrapped composite (Sb2 Se3 -rGO) compared to bare Sb2 Se3 . GITT analysis reveals higher Na+ diffusion coefficients (approx. 30 fold higher) in the case of Sb2 Se3 -rGO as compared to bare Sb2 Se3 throughout the operating voltage window. For Sb2 Se3 -rGO the diffusion coefficients in the range of 8.0×10-15  cm2 s-1 to 2.2×10-12  cm2 s-1 were observed, while in case of bare Sb2 Se3 the diffusion coefficients in the range of 1.6×10-15  cm2 s-1 to 9.4×10-15  cm2 s-1 were observed.

Determining phase transitions of layered oxides via electrochemical and crystallographic analysis.

The chemical diffusion coefficient in LiNi1/3Mn1/3Co1/3O2 was determined via the galvanostatic intermittent titration technique in the voltage range 3 to 4.2 V. Calculated diffusion coefficients in these layered oxide cathodes during charging and discharging reach a minimum at the open-circuit voltage of 3.8 V and 3.7 V vs. Li/Li+, respectively. The observed minima of the chemical diffusion coefficients indicate a phase transition in this voltage range. The unit cell parameters of LiNi1/3Mn1/3Co1/3O2 cathodes were determined at different lithiation states using ex situ crystallographic analysis. It was shown that the unit cell parameter variation correlates well with the observed values for chemical diffusion in NMC cathodes; with a notable change in absolute values in the same voltage range. We relate the observed variation in unit cell parameters to the nickel conversion into the trivalent state, which is Jahn-Teller active, and to the re-arrangement of lithium ions and vacancies.

An Efficient Methodology Combining K-Means Machine Learning and Electrochemical Modelling for the Determination of Ionic Diffusivity and Kinetic Properties in Battery Electrodes.

This paper presents an innovative and efficient methodology for the determination of the solid-state diffusion coefficient in electrode materials with phase transitions for which the assumption of applying the well-known formula from the work of Weppner et al. is not satisfied. This methodology includes a k-means machine learning screening of Galvanostatic Intermittent Titration Technique (GITT) steps, whose outcomes feed a physics-informed algorithm, the latter involving a pseudo-two-dimensional (P2D) electrochemical model for carrying out the numerical simulations. This methodology enables determining, for all of the 47 steps of the GITT characterization, the dependency of the Na+ diffusion coefficient as well as the reaction rate constant during the sodiation of an NVPF electrode to vary between 9 × 10-18 and 6.8 × 10-16 m2·s-1 and between 2.7 × 10-14 and 1.5 × 10-12 m2.5·mol-0.5·s-1, respectively. This methodology, also validated in this paper, is (a) innovative since it presents for the first time the successful application of unsupervised machine learning via k-means clustering for the categorization of GITT steps according to their characteristics in terms of voltage; (b) efficient given the considerable reduction in the number of iterations required with an average number of iterations equal to 8, and given the fact the entire experimental duration of each step should not be simulated anymore and hence can be simply restricted to the part with current and a small part of the rest period; (c) generically applicable since the methodology and its physics-informed algorithm only rely on "if" and "else" statements, i.e., no particular module/toolbox is required, which enables its replication and implementation for electrochemical models written in any programming language.

Sheet-Like Stacking SnS2/rGO Heterostructures as Ultrastable Anodes for Lithium-Ion Batteries.

SnS2-based materials have attracted considerable attention in energy storage and conversion owing to their high lithium activity and theoretical capacity. However, the practical application is severely limited by the low coulombic efficiency and short cycle life due to irreversible side reactions, low conductivity, and serious pulverization in the discharge/charge process. In this study, sheet-like stacking SnS2/reduced graphene oxide (rGO) heterostructures were developed using a facile solvothermal method. It was found that the composites between SnS2 nanoplates and rGO nanosheets are closely coupled through van der Waals interactions, providing efficient electron/ion paths to ensure high electrical conductivity and sufficient buffer space to alleviate volume expansion. Therefore, the SnS2/rGO heterostructure anode can obtain a high capacity of 840 mA h g-1 after 120 cycles at a current density of 200 mA g-1 and maintain a capacity of 450 mA h g-1 after 1000 cycles at 1000 mA g-1. In situ X-ray diffraction tests showed that SnS2/rGO undergoes typical initial intercalation, conversion, and subsequent alloying reactions during the first discharge, and most of the reactions are dealloying/alloying in the subsequent cycles. The galvanostatic intermittent titration technique showed that the diffusion of lithium ions in the SnS2/rGO heterostructures is faster in the intercalation and conversion reactions than in the alloying reactions. These observations help to clarify the reaction mechanism and ion diffusion behavior in the SnS2 anode materials, thus providing valuable insights for improving the energy efficiency of lithium-ion batteries.

Transition Metal Phthalocyanines as Redox Mediators in Li-O2 Batteries: A Combined Experimental and Theoretical Study of the Influence of 3d Electrons in Redox Mediation.

Redox mediation is an innovative strategy for ensuring efficient energy harvesting from metal-oxygen systems. This work presents a systematic exploratory analysis of first-row transition-metal phthalocyanines as solution-state redox mediators for lithium-oxygen batteries. Our findings, based on experiment and theory, convincingly demonstrate that d5 (Mn), d7 (Co), and d8 (Ni) configurations function better compared to d6 (Fe) and d9 (Cu) in redox mediation of the discharge step. The d10 configuration (Zn) and non-d analogues (Mg) do not show any redox mediation because of the inability of binding with oxygen. The solution-state discharge product, transition-metal bound Li2O2, undergoes dissociation and oxidation in the charging step of the battery, thus confirming a bifunctional redox mediation. Apart from the reaction pathways predicted based on thermodynamic considerations, density functional theory calculations also reveal interesting effects of electrochemical perturbation on the redox mediation mechanisms and the role of the transition-metal center.

Hybrid integral transform analysis of supercooled droplets solidification.

The freezing phenomena in supercooled liquid droplets are important for many engineering applications. For instance, a theoretical model of this phenomenon can offer insights for tailoring surface coatings and for achieving icephobicity to reduce ice adhesion and accretion. In this work, a mathematical model and hybrid numerical-analytical solutions are developed for the freezing of a supercooled droplet immersed in a cold air stream, subjected to the three main transport phenomena at the interface between the droplet and the surroundings: convective heat transfer, convective mass transfer and thermal radiation. Error-controlled hybrid solutions are obtained through the extension of the generalized integral transform technique to the transient partial differential formulation of this moving boundary heat transfer problem. The nonlinear boundary condition for the interface temperature is directly accounted for by the choice of a nonlinear eigenfunction expansion base. Also, the nonlinear equation of motion for the freezing front is solved together with the ordinary differential system for the integral transformed temperatures. After comparisons of the solution with previously reported numerical and experimental results, the influence of the related physical parameters on the droplet temperatures and freezing time is critically analysed.

Modeling VOCs emission/sorption with variable operating parameters and general boundary conditions.

An integrated model of VOCs emission/sorption from/on dry building materials with a general boundary condition, variable air exchange rate and inlet concentration is developed. An analytical solution is obtained by using the generalized integral transform technique. Good agreements are obtained between the present model and the experimental data. The effects of environmental conditions on the emission are investigated. The emission from two surfaces can increase the concentration of hexanal in the air and decrease the initial emission rate at x=δ with the increase in mass transfer coefficient at x=0. Periodical inlet concentration can lead to the periodic variation of materials between a source and a sink. Ventilation can keep the concentration in the air at a low level and help to decrease the concentration of hexanal in materials. The present model is capable of simulating indoor air quality due to the VOCs emission and sorption.

Unraveling the Degradation Process of LiNi0.8Co0.15Al0.05O2 Electrodes in Commercial Lithium Ion Batteries by Electronic Structure Investigations.

The degradation of LiNi0.8Co0.15Al0.05O2 (LNCAO) is reflected by the electrochemical performance in the fatigued state and correlated with the redox behavior of these cathodes. The detailed electrochemical performance of these samples is investigated by galvanostatic and voltammetric cycling as well as with the galvanostatic intermittent titration technique (GITT). Near-edge X-ray absorption fine structure (NEXAFS) spectroscopy was used to investigate the oxidation state of all three materials at the Ni L2,3, O K, and Co L2,3 edges at five different states of charge. Surface and more bulklike properties are distinguished by total electron yield (TEY) and fluorescence yield (FY) measurements. The electrochemical investigations revealed that the changes in the cell performance of the differently aged materials can be explained by considering the reaction kinetics of the intercalation/deintercalation process. The failure of the redox process of oxygen and nickel at low voltages leads to a significant decrease of the reaction rates in the fatigued cathodes. The accompanied cyclic voltammogram (CV) peaks appear as two peaks because of the local minimum of the reaction rate, although it is one peak in the CV of the calendarically aged LNCAO. The absence of the oxidation/reduction process at low voltages can be traced back to changes in the surface morphology (formation of a NiO-like structure). Further consequences of these material changes are overpotentials, which lead to capacity losses of up to 30% (cycled with a C/3 rate).