The Interaction Between Electrolytes and Sb2O3–based Electrodes in Sodium Batteries: Uncovering Detrimental Effects of Diglyme

Conversion materials are promising to improve the energy density of sodium‐ion‐batteries (NIB). Nevertheless, they suffer from the drawback of phase transitions and pronounced volume changes during cycling, which causes cell instability. When using these types of electrodes, all cell‐components have to be adjusted. In this study, a tremendous influence of the electrolyte solution on Sb$_{2}$O$_{3}$ conversion electrodes for NIBs is discussed. Solutions based on three solvents and solvent combinations established for NIBs, ethylene carbonate/dimethyl carbonate (EC/DMC), EC/DMC+5 % fluoroethylene carbonate (FEC), and diglyme, lead to a massively divergent electrochemical behavior of the same Sb$_{2}$O$_{3}$ electrode. Sb$_{2}$O$_{3}$ demonstrates the highest stability in solutions containing FEC, because this component forms a flexible, protecting surface film that prevent disintegration. One key finding of this work is that electrolyte solutions based on ether solvents like diglyme can remove Sb‐ions from Sb$_{2}$O$_{3}$ during cycling. Diglyme has the ability to coordinate and extract Sb$^{3+}$ during the oxidation of Sb$_{2}$O$_{3}$. This leads to contaminations of all cell components and a strong capacity loss together with an irregular electrochemical signature. Due to its poor reactivity at low potentials, diglyme forms a thin or even no surface layer. Thereby, there are no protecting films on the Sb$_{2}$O$_{3}$ electrodes that can avoid Sb$^{3+}$ ion dissolution. A critical examination of the electrolyte solutions components’ impact is essential to match them with conversion reaction anodes

The Effect of Chlorides on the Performance of DME/Mg[B(HFIP)4_4]2_2 Solutions for Rechargeable Mg Batteries

One of the major issues in developing electrolyte solutions for rechargeable magnesium batteries is understanding the positive effect of chloride anions on Mg deposition-dissolution processes on the anode side, as well as intercalation-deintercalation of Mg$^{2+}$ ions on the cathode side. Our previous results suggested that Cl$^−$ ions are adsorbed on the surface of Mg anodes and Chevrel phase Mg$_x$Mo$_6$S$_8$ cathodes. This creates a surface add-layer that reduces the activation energy for the interfacial Mg ions transportation and related charge transfer, as well as promotes the transport of Mg$^{2+}$ from the solution phase to the Mg anode surface and into the cathodes\u27 host materials. Here, this work further examines the effect of adding chlorides to the state-of-the-art Mg[B(HFIP)$_4$]$_2$/DME electrolyte solution, specifically focusing on reversible magnesium deposition, as well as the performance of Mg cells with benchmark Chevrel phase cathodes. It was observed that the presence of chlorides in these solutions facilitates both Mg deposition, and Mg$^{2+}$ ions intercalation, whereby this effect is more pronounced as the purity level of the solution is lowered

Studies of the Electrochemical Behavior of LiNi0.80Co0.15Al0.05O2 Electrodes Coated with LiAlO2

In this paper, we studied the influence of LiAlO2 coatings of 0.5, 1 and 2 nm thickness prepared by Atomic Layer Deposition onto LiNi0.8Co0.15Al0.05O2 electrodes, on their electrochemical behavior at 30 and 60 degrees C. It was demonstrated that upon cycling, 2 nm LiAlO2 coated electrodes displayed similar to 3 times lower capacity fading and lower voltage hysteresis comparing to bare electrodes. We established a correlation among the thickness of the LiAlO2 coating and parameters of the self-discharge processes at 30 and 60 degrees C. Significant results on the elevated temperature cycling and aging of bare and LiAlO2 coated electrodes at 4.3 V were obtained and analyzed for the first time. By analyzing of X-ray diffraction patterns of bare and 2 nm coated LiNi0.8Co0.15Al0.05O2 electrodes after cycling, we concluded that cycled materials preserved their original structure described by R-3m space group and no additional phases were detected. (c) The Author(s) 2017. Published by ECS. All rights reserved.Peer reviewe

Doped MXenes—A new paradigm in 2D systems: Synthesis, properties and applications

Since 2011, 2D transition metal carbides, carbonitrides and nitrides known as MXenes have gained huge attention due to their attractive chemical and electronic properties. The diverse functionalities of MXenes make them a promising candidate for multitude of applications. Recently, doping MXene with metallic and non-metallic elements has emerged as an exciting new approach to endow new properties to this 2D systems, opening a new paradigm of theoretical and experimental studies. In this review, we present a comprehensive overview on the recent progress in this emerging field of doped MXenes. We compare the different doping strategies; techniques used for their characterization and discuss the enhanced properties. The distinct advantages of doping in applications such as electrocatalysis, energy storage, photovoltaics, electronics, photonics, environmental remediation, sensors, and biomedical applications is elaborated. Additionally, theoretical developments in the field of electrocatalysis, energy storage, photovoltaics, and electronics are explored to provide key specific advantages of doping along with the underlying mechanisms. Lastly, we present the advantages and challenges of doped MXenes to take this thriving field forward

Doped MXenes—A new paradigm in 2D systems: Synthesis, properties and applications

Since 2011, 2D transition metal carbides, carbonitrides and nitrides known as MXenes have gained huge attention due to their attractive chemical and electronic properties. The diverse functionalities of MXenes make them a promising candidate for multitude of applications. Recently, doping MXene with metallic and non-metallic elements has emerged as an exciting new approach to endow new properties to this 2D systems, opening a new paradigm of theoretical and experimental studies. In this review, we present a comprehensive overview on the recent progress in this emerging field of doped MXenes. We compare the different doping strategies; techniques used for their characterization and discuss the enhanced properties. The distinct advantages of doping in applications such as electrocatalysis, energy storage, photovoltaics, electronics, photonics, environmental remediation, sensors, and biomedical applications is elaborated. Additionally, theoretical developments in the field of electrocatalysis, energy storage, photovoltaics, and electronics are explored to provide key specific advantages of doping along with the underlying mechanisms. Lastly, we present the advantages and challenges of doped MXenes to take this thriving field forward

A practical perspective on the potential of rechargeable Mg batteries

Emerging energy storage systems based on abundant and cost-effective materials are key to overcome the global energy and climate crisis of the 21st century. Rechargeable Magnesium Batteries (RMB), based on Earth-abundant magnesium, can provide a cheap and environmentally responsible alternative to the benchmark Li-ion technology, especially for large energy storage applications. Currently, RMB technology is the subject of intense research efforts at laboratory scale. However, these emerging approaches must be placed in a real-world perspective to ensure that they satisfy key technological requirements. In an attempt to bridge the gap between laboratory advancements and industrial development demands, herein, we report the first non-aqueous multilayer RMB pouch cell prototypes and propose a roadmap for a new advanced RMB chemistry. Through this work, we aim to show the great unrealized potential of RMBs.This work was funded by European Union's Horizon 2020 research and innovation program under the FET Proactive call with grant agreement no 824066 via the “E-MAGIC” project

A practical perspective on the potential of rechargeable Mg batteries

Emerging energy storage systems based on abundant and cost-effective materials are key to overcome the global energy and climate crisis of the 21st century. Rechargeable Magnesium Batteries (RMB), based on Earth-abundant magnesium, can provide a cheap and environmentally responsible alternative to the benchmark Li-ion technology, especially for large energy storage applications. Currently, RMB technology is the subject of intense research efforts at laboratory scale. However, these emerging approaches must be placed in a real-world perspective to ensure that they satisfy key technological requirements. In an attempt to bridge the gap between laboratory advancements and industrial development demands, herein, we report the first non-aqueous multilayer RMB pouch cell prototypes and propose a roadmap for a new advanced RMB chemistry. Through this work, we aim to show the great unrealized potential of RMBs