Thermal synthesis of conversion-type bismuth fluoride cathodes for high-energy-density Li-ion batteries

Towards enhancement of the energy density of Li-ion batteries, BiF3 has recently attracted considerable attention as a compelling conversion-type cathode material due to its high theoretical capacity of 302 mAh g−1, average discharge voltage of ca. 3.0 V vs. Li+/Li, the low theoretical volume change of ca. 1.7% upon lithiation, and an intrinsically high oxidative stability. Here we report a facile and scalable synthesis of phase-pure and highly crystalline orthorhombic BiF3via thermal decomposition of bismuth(III) trifluoroacetate at T = 300 °C under inert atmosphere. The electrochemical measurements of BiF3 in both carbonate (LiPF6-EC/DMC)- and ionic liquid-based (LiFSI-Pyr1,4TFSI) Li-ion electrolytes demonstrated that ionic liquids improve the cyclic stability of BiF3. In particular, BiF3 in 4.3 M LiFSI-Pyr1,4TFSI shows a high initial capacity of 208 mA g−1 and capacity retention of ca. 50% over at least 80 cycles at a current density of 30 mA g−1.

Achieving long cycle life for all-solid-state rechargeable Li-I2 battery by a confined dissolution strategy

Rechargeable Li-I2 battery has attracted considerable attentions due to its high theoretical capacity, low cost and environment-friendliness. Dissolution of polyiodides are required to facilitate the electrochemical redox reaction of the I2 cathode, which would lead to a harmful shuttle effect. All-solid-state Li-I2 battery totally avoids the polyiodides shuttle in a liquid system. However, the insoluble discharge product at the conventional solid interface results in a sluggish electrochemical reaction and poor rechargeability. In this work, by adopting a well-designed hybrid electrolyte composed of a dispersion layer and a blocking layer, we successfully promote a new polyiodides chemistry and localize the polyiodides dissolution within a limited space near the cathode. Owing to this confined dissolution strategy, a rechargeable and highly reversible all-solid-state Li-I2 battery is demonstrated and shows a long-term life of over 9000 cycles at 1C with a capacity retention of 84.1%.

Heterostructure Fe2O3 nanorods@imine-based covalent organic framework for long-cycling and high-rate lithium storage

Fe2O3 as anode for lithium-ion batteries has attracted intense attention because of its high theoretical capacity, natural abundance and good safety. However, the inferior cycling stability, low-rate performance and limited...

Binder-free three-dimensional interconnected CuV2O5•nH2O nest as cathodes for high-loading aqueous zinc-ion batteries

In large-scale energy storage applications, aqueous zinc ion batteries (ZIBs) with low cost, safety, high theoretical capacity, and environmentally friendly have wide application prospects. In the reported cathode materials, the...

High Performance Lithium Ion Electrolyte Based on a Three-dimensional Holey Graphene Frameworks Cross-linked with Polymer

Metallic lithium based batteries hold great promise for next generation high-performance lithium ion batteries mainly due to its with extremely high theoretical capacity of 3860 mAh g-1 and low redox potential...

A Strategic Approach to Use Upcycled Si Nanomaterials for Stable Operation of Lithium-Ion Batteries

Silicon, as a promising next-generation anode material, has drawn special attention from industries due to its high theoretical capacity (around 3600 mAh g−1) in comparison with conventional electrodes, e.g., graphite. However, the fast capacity fading resulted by a large volume change hinders the pragmatic use of Si anodes for lithium ion batteries. In this work, we propose an efficient strategy to improve the cyclability of upcycled Si nanomaterials through a simple battery operation protocol. When the utilization degree of Si electrodes was decreased, the electrode deformation was significantly alleviated. This directly led to an excellent electrochemical performance over 100 cycles. In addition, the average charge (delithation) voltage was shifted to a lower voltage, when the utilization degree of electrodes was controlled. These results demonstrated that our strategic approach would be an effective way to enhance the electrochemical performance of Si anodes and improve the cost-effectiveness of scaling-up the decent nanostructured Si material.

Preparation of Electrode Materials Based on Carbon Cloth via Hydrothermal Method and Their Application in Supercapacitors

Supercapacitors have the unique advantages of high power density, fast charge and discharge rates, long cycle life, high safety, and reliability, and are increasingly being used for applications including automobiles, rail transit, communication equipment, digital electronics, and aerospace equipment. The supercapacitor industry is currently in a stage of rapid development; great breakthroughs have also been made in improving the performance of supercapacitors and the expansion of their application. Electrode technology is the core of supercapacitors. Transition-metal compounds have a relatively high theoretical capacity and have received widespread attention as electrode materials for supercapacitors. In addition, there is a synergistic effect between the different components of various electrode composite materials. Due to their superior electrochemical performance, supercapacitors are receiving increasing research attention. Flexible supercapacitors have been hailed for their good plasticity, resulting in a development boom. This review article mainly outlines the development process of various electrode materials, including carbon materials, conductive polymers, metal compounds, and composite materials, as well as flexible electrode materials based on carbon cloth.

Zn Metal Anodes for Zn-Ion Batteries in Mild Aqueous Electrolytes: Challenges and Strategies

Over the past few years, rechargeable aqueous Zn-ion batteries have garnered significant interest as potential alternatives for lithium-ion batteries because of their low cost, high theoretical capacity, low redox potential, and environmentally friendliness. However, several constraints associated with Zn metal anodes, such as the growth of Zn dendrites, occurrence of side reactions, and hydrogen evolution during repeated stripping/plating processes result in poor cycling life and low Coulombic efficiency, which severely impede further advancements in this technology. Despite recent efforts and impressive breakthroughs, the origin of these fundamental obstacles remains unclear and no successful strategy that can address these issues has been developed yet to realize the practical applications of rechargeable aqueous Zn-ion batteries. In this review, we have discussed various issues associated with the use of Zn metal anodes in mildly acidic aqueous electrolytes. Various strategies, including the shielding of the Zn surface, regulating the Zn deposition behavior, creating a uniform electric field, and controlling the surface energy of Zn metal anodes to repress the growth of Zn dendrites and the occurrence of side reactions, proposed to overcome the limitations of Zn metal anodes have also been discussed. Finally, the future perspectives of Zn anodes and possible design strategies for developing highly stable Zn anodes in mildly acidic aqueous environments have been discussed.

Fabrication of Phosphorus-Doped Cobalt Silicate with Improved Electrochemical Properties

The development of electrode materials for supercapacitors (SCs) is greatly desired, and this still poses an immense challenge for researchers. Cobalt silicate (Co2SiO4, denoted as CoSi) with a high theoretical capacity is deemed to be one of the sustainable electrode materials for SCs. However, its achieved electrochemical properties are still not satisfying. Herein, the phosphorus (P)-doped cobalt silicate, denoted as PCoSi, is synthesized by a calcining strategy. The PCoSi exhibits 1D nanobelts with a specific surface area of 46 m2∙g−1, and it can significantly improve the electrochemical properties of CoSi. As a supercapacitor’s (SC’s) electrode, the specific capacitance of PCoSi attains 434 F∙g−1 at 0.5 A∙g−1, which is much higher than the value of CoSi (244 F∙g−1 at 0.5 A∙g−1). The synergy between the composition and structure endows PCoSi with attractive electrochemical properties. This work provides a novel strategy to improve the electrochemical performances of transition metal silicates.

MOF-Derived ZnS Nanodots/Ti3C2Tx MXene Hybrids Boosting Superior Lithium Storage Performance

ZnS has great potentials as an anode for lithium storage because of its high theoretical capacity and resource abundance; however, the large volume expansion accompanied with structural collapse and low conductivity of ZnS cause severe capacity fading and inferior rate capability during lithium storage. Herein, 0D-2D ZnS nanodots/Ti3C2Tx MXene hybrids are prepared by anchoring ZnS nanodots on Ti3C2Tx MXene nanosheets through coordination modulation between MXene and MOF precursor (ZIF-8) followed with sulfidation. The MXene substrate coupled with the ZnS nanodots can synergistically accommodate volume variation of ZnS over charge–discharge to realize stable cyclability. As revealed by XPS characterizations and DFT calculations, the strong interfacial interaction between ZnS nanodots and MXene nanosheets can boost fast electron/lithium-ion transfer to achieve excellent electrochemical activity and kinetics for lithium storage. Thereby, the as-prepared ZnS nanodots/MXene hybrid exhibits a high capacity of 726.8 mAh g−1 at 30 mA g−1, superior cyclic stability (462.8 mAh g−1 after 1000 cycles at 0.5 A g−1), and excellent rate performance. The present results provide new insights into the understanding of the lithium storage mechanism of ZnS and the revealing of the effects of interfacial interaction on lithium storage performance enhancement.