Rechargeable lithium, sodium and aluminium metal-based batteries are among the most versatile platforms for high-energy, cost-effective electrochemical energy storage. Non-uniform metal deposition and dendrite formation on the negative electrode during repeated cycles of charge and discharge are major hurdles to commercialization of energy-storage devices based on each of these chemistries. A long-held view is that unstable electrodeposition is a consequence of inherent characteristics of these metals and their inability to form uniform electrodeposits on surfaces with inevitable defects. We report on electrodeposition of lithium in simple liquid electrolytes and in nanoporous solids infused with liquid electrolytes. We find that simple liquid electrolytes reinforced with halogenated salt blends exhibit stable long-term cycling at room temperature, often with no signs of deposition instabilities over hundreds of cycles of charge and discharge and thousands of operating hours. We rationalize these observations with the help of surface energy data for the electrolyte/lithium interface and impedance analysis of the interface during different stages of cell operation. Our findings provide support for an important recent theoretical prediction that the surface mobility of lithium is significantly enhanced in the presence of lithium halide salts. Our results also show that a high electrolyte modulus is unnecessary for stable electrodeposition of lithium.

Stable lithium electrodeposition in liquid and nanoporous solid electrolytes

Lithium-ion batteries (LIBs) with liquid electrolytes and microporous polyolefin separator membranes are ubiquitous. Though not necessarily an active component in a cell, the separator plays a key role in ion transport and influences rate performance, cell life and safety. As our understanding of separator properties and the interactions between the separator and the electrolyte deepens, it becomes evident that there are opportunities for improving separators to help meet the greater demands that new applications place on LIB technology. Here, we review the impact of the separator structure and chemistry on LIB performance, assess characterization techniques relevant for understanding structure–performance relationships in separator membranes, and provide an outlook on next-generation separator technology. Insights from this Review indicate that LIB performance can be improved by taking into account the interplay of the separator with its surroundings and indicate that, in the future, separators will be designed to play a more active role in LIB operation. Current and emerging characterization techniques will play an important role in guiding this evolution in separator technology. Separators are an essential part of current lithium-ion batteries. Vanessa Wood and co-workers review the properties of separators, discuss their relationship with battery performance and survey the techniques for characterizing separators.

Characterization and performance evaluation of lithium-ion battery separators

As the most widely used energy storage device in consumer electronic and electric vehicle fields, lithium ion battery (LIB) is closely related to our daily lives, on which its safety is of paramount importance. LIB is a typical multidisciplinary product. A tiny single cell is composed of both organic and inorganic materials in multi scale. In addition, its relatively closure property made it difficult to be studied on line, let alone in the battery pack or system level. Safety, often manifested by stability on abuse, including mechanical, electrical and thermal abuses, is a quite complicated issue of LIB. Safety has to be guaranteed in large scale application. Here, safety issues related to key materials and cell design techniques will be reviewed. Key materials, including cathode, anode, electrolyte and separator, are the fundamental of the battery. Cell design and fabrication techniques also have significant influence on the cell’s electrochemical and safety performances. Here, we will summarize the thermal runaway process in single cell level, and some recent advances on battery materials and cell design.

/pdf/safety-issues-in-lithium-ion-batteries-materials-and-cell-27j92y2xih.pdf

Safety Issues in Lithium Ion Batteries: Materials and Cell Design

https://publikationen.bibliothek.kit.edu/1000077359/6843166

Comparative study of imide-based Li salts as electrolyte additives for Li-ion batteries

Microplasmas are low-temperature plasmas that feature microscale dimensions and a unique high-energy-density and a nonequilibrium reactive environment, which makes them promising for the fabrication of advanced nanomaterials and devices for diverse applications. Here, recent microplasma applications are examined, spanning from high-throughput, printing-technology-compatible synthesis of nanocrystalline particles of common materials types, to water purification and optoelectronic devices. Microplasmas combined with gaseous and/or liquid media at low temperatures and atmospheric pressure open new ways to form advanced functional materials and devices. Specific examples include gas-phase, substrate-free, plasma-liquid, and surface-supported synthesis of metallic, semiconducting, metal oxide, and carbon-based nanomaterials. Representative applications of microplasmas of particular importance to materials science and technology include light sources for multipurpose, efficient VUV/UV light sources for photochemical materials processing and spectroscopic materials analysis, surface disinfection, water purification, active electromagnetic devices based on artificial microplasma optical materials, and other devices and systems including the plasma transistor. The current limitations and future opportunities for microplasma applications in materials related fields are highlighted.

/pdf/microplasmas-for-advanced-materials-and-devices-2iz3yxotk8.pdf

Microplasmas for Advanced Materials and Devices

For a better understanding of the adsorption behavior of alkylcarbonate-based electrolytes on graphite electrodes and Celgard separator for Li-ion batteries applications, the interface parameters are determined by contact angle and surface tension measurements. The correlation between these parameters and chemical compositions made of alkyl carbonate with a varying nature of lithium salts (LiPF6 and LiTFSI) and volume fractions of binary and ternary mixtures containing propylene carbonate (PC), ethylene carbonate (EC), and dimethyl carbonate (DMC) is investigated. From the obtained contact angle and surface tension (γL) values for each liquid, the dispersive and polar components of the surface tension (γLd and γLp) of the electrolyte and interfacial free energy between the solid and liquid (γSL) were then calculated using the Young’s equation. The variation of contact angle (θ) and the surface tension, as well as the work of adhesion (WA) of binary PC/DMC mixtures on PP, PE, and PET model surfaces were al...

Interfacial Properties of LiTFSI and LiPF6-Based Electrolytes in Binary and Ternary Mixtures of Alkylcarbonates on Graphite Electrodes and Celgard Separator

In theory, animal signals are designed to optimize transmission across a specific habitat. However, sexual signals characteristics often reflect habitat quality, a feature that does not necessarily match habitat structure. Besides, many species exploit a particular habitat for breeding so that the growth of sexual signals can depend on the additive effects of breeding and non-breeding habitats. We combined field and experimental data to investigate the relative effect of terrestrial and aquatic habitat on the development of sexual ornaments in the palmate newt, Triturus helveticus. This species exploits a large ecological range of habitats. Like many amphibians, it spends the breeding season in water and the rest of year on land. We tested the influence of terrestrial (forest cover) and aquatic habitat variables (turbidity, organic matter, pH, nitrate and chloride) on male sexual morphology. Neither terrestrial nor aquatic habitat variables accounted for body size variation. In contrast, the size of male sexual traits decreased with water turbidity, suggesting that the expression of visual signals matched the local conditions of signal transmission. We provide experimental evidence that this pattern is not caused by reduced foraging efficiency in turbid water. We propose alternative mechanisms to account for the relationship between turbidity and visual sexual signals, and discuss the consequences of small scale environmental variation on mate choice.

Water Turbidity Affects the Development of Sexual Morphology in the Palmate Newt

The aim of this work is to test the wettability enhancement of a low-wetting and low-cost commercial polymer separator by cold microplasma treatments. Liquid and gas ammonia are tested as precursors in a pulsed microreactor at low pressure. Two modes of plasma producing are used, i.e., with and without bias. Optical emission spectroscopy, contact angle technique, and cycling tests are performed to characterize the process and the separator. Best results are obtained with liquid ammonia precursor without bias (contact angle between water and a polyethylene separator being 10° ± 2° compared to 111° ± 2° without any treatment). Cycling tests of lithium half-cells incorporating plasma-treated separator show drastic improvements to capacity retention at high rates (after 100 cycles at a 2C rate, the discharge capacity of a Li4Ti5O12 is almost three times higher, i.e., 38 mA h g−1 and 113 mA h g−1 with an untreated separator and a treated one, respectively).

Surface properties enhancement of battery separator by micro-plasma treatments

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Papers

Interfacial Properties of LiTFSI and LiPF6-Based Electrolytes in Binary and Ternary Mixtures of Alkylcarbonates on Graphite Electrodes and Celgard Separator

Water Turbidity Affects the Development of Sexual Morphology in the Palmate Newt

Surface properties enhancement of battery separator by micro-plasma treatments