Sodium metal is one of the ideal anodes for high-performance rechargeable batteries because of its high specific capacity (~ 1166 mAh·g⁻¹), low reduction potential (−2.71 V compared to standard hydrogen electrodes), and low cost. However, the unstable solid electrolyte interphase, uncontrolled dendrite growth, and inevitable volume expansion hinder the practical application of sodium metal anodes. At present, many strategies have been developed to achieve stable sodium metal anodes. Here, we systematically summarize the latest strategies adopted in interface engineering, current collector design, and the emerging methods to improve the reaction kinetics of sodium deposition processes. First, the strategies of constructing protective layers are reviewed, including inorganic, organic, and mixed protective layers through electrolyte additives or pretreatments. Then, the classification of metal-based, carbon-based, and composite porous frames is discussed, including their function in reducing local deposition current density and the effect of introducing sodiophilic sites. Third, the recent progress of alloys, nanoparticles, and single atoms in improving Na deposition kinetics is systematically reviewed. Finally, the future research direction and the prospect of high-performance sodium metal batteries are proposed.

The electrical energy that can be harnessed from the salinity difference across the sea water and river water interface can be one of the sustainable and clean energy resources of the future. This energy can be harnessed via the nanofluidic channels that selectively permeate ions. The selective diffusion of cations and anions can produce electricity through reverse electrodialysis. Two-dimensional (2D) materials are a class of nanomaterials that hold great promise in this field. Several breakthrough works have been previously published which demonstrate the high electrical power densities of 2D membranes. The ion transportation can be either through the nano-sized in-plane pores or interlayer spacings of 2D materials. This review article highlights the progress in 2D materials for salinity gradient power generation. Several types of 2D membranes with various nano-architectures are discussed in this review article. These include atom-thick 2D membranes with nanopores, 2D lamellar membranes, 2D lamellar membranes with nanopores, 2D/one-dimensional (1D), and 2D/2D hybrid membranes. The fabrication techniques, physical characteristics, ion transportation properties, and the osmotic power generation of these 2D membranes are elaborated in this review article. Finally, we overview the future research direction in this area. It is envisioned that the research on 2D materials can make practical salinity gradient power generation one step closer to reality.

Lithium-rich oxide compounds have been recognized as promising cathode materials for high performance Li-ion batteries, owing to their high specific capacity. However, it remains a great challenge to achieve the fully reversible anionic redox reactions to realize high capacity, high stability, and low voltage hysteresis for lithium-rich cathode materials. Therefore, it is critically important to comprehensively understand and control the anionic redox chemistry of lithium-rich cathode materials, including atomic structure design, and nano-scale materials engineering technologies. Herein, we summarize the recent research progress of lithium-rich cathode materials with a focus on redox chemistry. Particularly, we highlight the oxygen-based redox reactions in lithium-rich metal oxides, with critical views of designing next generation oxygen redox lithium cathode materials. Furthermore, we purposed the most promising strategies for improving the performances of lithium-rich cathode materials with a technology-spectrum from the atomic scale to nano-scale.

The rapid development of portable, foldable, and wearable electronic devices requires flexible energy storage systems. Sodium-ion capacitors (SICs) combining the high energy of batteries and the high power of supercapacitors are promising solutions. However, the lack of flexible and durable electrode materials that allow fast and reversible Na⁺ storage hinders the development of flexible SICs. Herein, we report a high-capacity, free-standing and flexible Sb₂S₃/Ti₃C₂T_x composite film for fast and stable sodium storage. In this hybrid nano-architecture, the Sb₂S₃ nanowires uniformly anchored between Ti₃C₂T_x nanosheets not only act as sodium storage reservoirs but also pillar the two-dimensional (2D) Ti₃C₂T_x to form three-dimensional (3D) channels benefiting for electrolyte penetration. Meanwhile, the highly conductive Ti₃C₂T_x nanosheets provide rapid electron transport pathways, confine the volume expansion of Sb₂S₃ during sodiation, and restrain the dissolution of discharged sodium polysulfides through physical constraint and chemical absorption. Owing to the synergistic effects of the one-dimensional (1D) Sb₂S₃ nanowires and 2D MXenes, the resultant composite anodes exhibit outstanding rate performance (553 mAh·g⁻¹ at 2 A·g⁻¹) and cycle stability in sodium-ion batteries. Moreover, the flexible SICs using Sb₂S₃/Ti₃C₂T_x anodes and active carbon/reduced graphene oxide (AC/rGO) paper cathodes deliver a superior energy and power density in comparison with previously reported devices, as well as an excellent cycling performance with a high capacity retention of 82.78% after 5,000 cycles. This work sheds light on the design of next-generation low-cost, flexible and fast-charging energy storage devices.

Recently, Prussian blue and its analogues (PBAs) have attracted tremendous attention as cathode materials for sodium-ion batteries because of their good cycling performance, low cost, and environmental friendliness. However, they still suffer from kinetic problems associated with the solid-state diffusion of sodium ions during charge and discharge processes, which leads to low specific capacity and poor rate performances. In this work, novel sodium iron hexacyanoferrate nanospheres with a hierarchical hollow architecture have been fabricated as cathode material for sodium-ion batteries by a facile template method. Due to the unique hollow sphere morphology, sodium iron hexacyanoferrate nanospheres can provide large numbers of active sites and high diffusion dynamics for sodium ions, thus delivering a high specific capacity (142 mAh/g), a superior rate capability, and an excellent cycling stability. Furthermore, the sodium insertion/extraction mechanism has been studied by in situ X-ray diffraction, which provides further insight into the crystal structure change of the sodium iron hexacyanoferrate nanosphere cathode material during charge and discharge processes.

Faceted crystals with exposed highly reactive planes have attracted intensive investigations for applications. Herein, we demonstrate a general synthetic method to prepare mesocrystal Co₃O₄ with predominantly exposed {111} reactive facets by the in situ thermal decomposition from Co(OH)₂ nanoplatelets. The mesocrystal feature was identified by field emission scanning electron microscopy, transmission electron microscopy, selected area electron diffraction, and N₂ isotherm analyses. When applied as anode material in lithium-ion batteries, mesocrystal Co₃O₄ nanoplatelets delivered a high specific capacity and an outstanding high rate performance. The superior electrochemical performance should be ascribed to the predominantly exposed {111} active facets and highly accessible surfaces. This synthetic strategy could be extended to prepare other mesocrystal functional nanomaterials.

Silicon has been recognized as the most promising anode material for high capacity lithium ion batteries. However, large volume variations during charge and discharge result in pulverization of Si electrodes and fast capacity loss on cycling. This drawback of Si electrodes can be overcome by combination with well-organized graphene foam. In this work, hierarchical three-dimensional carbon-coated mesoporous Si nanospheres@graphene foam (C@Si@GF) nanoarchitectures were successfully synthesized by a thermal bubble ejection assisted chemical-vapor-deposition and magnesiothermic reduction method. The morphology and structure of the as-prepared nanocomposites were characterized by field emission scanning electron microscopy, transmission electron microscopy and Raman spectroscopy. When employed as anode materials in lithium ion batteries, C@Si@GF nanocomposites exhibited superior electrochemical performance including a high specific capacity of 1, 200 mAh/g at the current density of 1 A/g, excellent high rate capabilities and an outstanding cyclability. Post-mortem analyses identified that the morphology of 3D C@Si@GF electrodes after 200 cycles was well maintained. The synergistic effects arising from the combination of mesoporous Si nanospheres and graphene foam nanoarchitectures may address the intractable pulverization problem of Si electrode.

A nanocomposite of CoO and a mesoporous carbon (CMK-3) has been studied as a cathode catalyst for lithium-oxygen batteries in alkyl carbonate electrolytes. The morphology and structure of the as-prepared nanocomposite were characterized by field emission scanning electron microscopy, transmission electron microscopy and high resolution transmission electron microscopy. The electrochemical properties of the mesoporous CoO/CMK-3 nanocomposite as a cathode catalyst in lithium-oxygen batteries were studied using galvanostatic charge-discharge methods. The reaction products on the cathode were analyzed by Fourier transform infrared spectroscopy. The CoO/CMK-3 nanocomposite exhibited better capacity retention than bare mesoporous CMK-3 carbon, Super-P carbon or CoO/Super-P nanocomposite. The synergistic effects arising from the combination of CoO nanoparticles and the mesoporous carbon nanoarchitecture may be responsible for the optimum catalytic performance in lithium-oxygen batteries.