Synergistic Combination of Dual Clays in Multilayered Nanocomposites for Enhanced Flame Retardant Properties.

In an effort to reduce the flammability of synthetic polymeric materials such as cotton fabrics and polyurethane foam (PUF), hybrid nanocoatings are prepared by layer-by-layer assembly. Multilayered nanocomposites of a cationic polyelectrolyte, poly(diallyldimethylammonium chloride) (PDDA), are paired with two kinds of clay nanoplatelets, montmorillonite (MMT) and vermiculite (VMT). The physical properties such as thickness and mass and thermal behaviors in clay-based nanocoatings with and without incorporation of tris buffer are compared to assess the effectiveness of amine salts on flame retardant (FR) performances. A PDDA-tris/VMT-MMT system, in which tris buffer is introduced into the cationic PDDA aqueous solution, produces a thicker and heavier coating. Three different systems, including PDDA/MMT, PDDA/VMT-MMT, and PDDA-tris/VMT-MMT, result in conformal coating, retaining the weave structure of the fabrics after being exposed to a vertical and horizontal flame test, while the uncoated sample is completely burned out. The synergistic effects of dual clay-based hybrid nanocoatings are greatly improved by adding amine salts. Cone calorimetry reveals that the PDDA-tris/VMT-MMT-coated PUF eliminates a second peak heat release rate and significantly reduces other FR performances, compared to those obtained from the clay-based multilayer films with no amine salts added. Ten bilayers of PDDA-tris/VMT-MMT (≈250 nm thick) maintain the shape of foam after exposure to a butane torch flame for 12 s. As for practical use of these nanocomposites in real fire disasters, spray-assisted PDDA-tris/VMT-MMT multilayers on woods exhibit high resistance over flammability. Improved fire resistance in PDDA-tris/VMT-MMT is believed to be due to the enhanced char yield through the addition of tris buffer that promotes the deposition of more clay particles while retaining a highly ordered deposition of a densely packed nanobrick wall structure. This work demonstrates the ability to impart significant fire resistance to synthetic polymer materials in a fully renewable nanocoating that uses environmentally benign chemistry.

Construction of Nickel Molybdenum Sulfide/Black Phosphorous 3D Hierarchical Structure Toward High Performance Supercapacitor Electrodes.

Supercapacitors (SCs) with outstanding versatility have a lot of potential applications in next-generation electronics. However, their practical uses are limited by their short working potential window and ultralow-specific capacity. Herein, the facile one-step in-situ hydrothermal synthesis is employed for the construction of a NiMo3 S4 /BP (black phosphorous) hybrid with a 3D hierarchical structure. After optimization, the NiMo3 S4 /BP hybrid displays a high specific capacitance of 830 F/g at 1 A/g compared to the pristine NiMo3 S4 electrode. The fabricated NiMo3 S4 /BP//NiCo2 S4 /Ti3 C2 Tx asymmetric supercapacitor exhibits a better specific capacitance of 120 F/g at 0.5 A/g, which also demonstrates a high energy density of 54 Wh/kg at 1148.53 W/kg and good cycle stability with capacity retention of 86% and 97% of Coulombic efficiency after 6000 cycles. Further from the DFT simulations, the hybrid NiMo3 S4 /BP structure shows higher conductivity and quantum capacitance, which demonstrate greater charge storage capability, due to enhanced electronic states near the Fermi level. The lower diffusion energy barrier for the electrolyte K+ ions in the hybrid structure is facilitated by improved charge transfer performance for the hybrid NiMo3 S4 /BP. This work highlights the potential significance of hybrid nanoarchitectonics and compositional tunability as an emerging method for improving the charge storage capabilities of active electrodes.

Synthesis of Iron Sulfide Nanocrystals Encapsulated in Highly Porous Carbon-Coated CNT Microsphere as Anode Materials for Sodium-Ion Batteries.

Highly porous carbon materials with a rationally designed pore structure can be utilized as reservoirs for metal or nonmetal components. The use of small-sized metal or metal compound nanoparticles, completely encapsulated by carbon materials, has attracted significant attention as an effective approach to enhancing sodium ion storage properties. These materials have the ability to mitigate structural collapse caused by volume expansion during the charging process, enable short ion transport length, and prevent polysulfide elution. In this study, a concept of highly porous carbon-coated carbon nanotube (CNT) porous microspheres, which serve as excellent reservoir materials is suggested and a porous microsphere is developed by encapsulating iron sulfide nanocrystals within the highly porous carbon-coated CNTs using a sulfidation process. Furthermore, various sulfidation processes to determine the optimal method for achieving complete encapsulation are investigated by comparing the morphologies of diverse iron sulfide-carbon composites. The fully encapsulated structure, combined with the porous carbon, provides ample space to accommodate the significant volume changes during cycling. As a result, the porous iron sulfide-carbon-CNT composite microspheres exhibited outstanding cycling stability (293 mA h g-1 over 600 cycles at 1 A g-1 ) and remarkable rate capability (100 mA h g-1 at 5 A g-1 ).

Hollow porous carbon nanospheres containing polar cobalt sulfide (Co9S8) nanocrystals as electrocatalytic interlayers for the reutilization of polysulfide in lithium-sulfur batteries.

HYPOTHESIS: The introduction of functional interlayers for efficient anchoring of lithium polysulfides has received significant attention worldwide. EXPERIMENTS: A facile wet-chemical method was adopted to obtain hollow porous carbon nanospheres (HPCNSs) impregnated with metallic and polar cobalt sulfide (Co9S8) nanocrystals (abbreviated as "Co9S8@HPCNS"). The prepared nanocrystals were employed as electrocatalytic interlayers via separator coating for the efficient capture and reutilization of polysulfide species in Li-S batteries. The HPCNSs were synthesized via the polymerization method followed by carbonization and template removal. The Co9S8 nanocrystals were impregnated inside the HPCNSs, followed by heat treatment in a reducing atmosphere. FINDINGS: The porous structure of the CNS enables the efficient percolation of the electrolyte, in addition to accommodating unwanted volume fluctuations during redox processes. Furthermore, the metallic Co9S8 nanocrystals improve the electronic conductivity and enhance the polarity of the CNS towards the polysulfide. Correspondingly, the Li-S cells featuring Co9S8@HPCNS as electrocatalytic interlayers and regular sulfur (S) electrodes display improved electrochemical performance such as reasonable rate performance and prolonged cycling stability at different current rates (0.1, 0.5, and 1.0 C). Therefore, we anticipate that the rational design strategy proposed herein will provide significant insights into the synthesis of advanced materials for various energy storage applications.

In situ crystal reconstruction strategy-based highly efficient air-processed inorganic CsPbI2Br perovskite photovoltaics for indoor, outdoor, and switching applications.

All-inorganic CsPbI2Br (CPIB) perovskite has gained strong attention due to their favorable optoelectronic properties for photovoltaics. However, solution-processed CPIB films suffer from poor morphology due to the rapid crystallization process, which must be resolved for desirable photovoltaic performance. We introduced phenethylammonium iodide (PEAI) as an additive into a perovskite precursor that effectively controls the crystallization kinetics to construct the preferred quality α-CPIB film under ambient conditions. Various photophysical and structural characterization studies were performed to investigate the microstructural, morphological, and optoelectronic properties of the CPIB and PEAI-assisted perovskite films. We found that PEAI plays a vital role in decreasing pinholes, ensuring precise crystal growth, enhancing the crystallinity, improving the uniformity, and tailoring the film morphology by retarding the crystallization process, resulting in an improved device performance. The device based on the optimized PEAI additive (0.8 mg) achieved a respectably high power conversion efficiency (PCE) of 17.40% compared to the CPIB perovskite solar cell (PSC; 15.75%). Moreover, the CPIB + 0.8 mg PEAI PSC retained ∼87.25% of its original PCE, whereas the CPIB device retained ∼66.90% of the initial PCE after aging in a dry box at constant heating (85 °C) over 720 h, which revealed high thermal stability. Furthermore, the indoor photovoltaic performance under light-emitting diode (LED) lighting conditions (3200 K, 1000 lux) was investigated, and the CPIB + 0.8 mg PEAI PSC showed a promising PCE of 26.73% compared to the CPIB device (19.68%). In addition, we developed a switching function by employing the optimized PSC under LED lighting conditions, demonstrating the practical application of constructed indoor PSCs.

Controllable Synthesis of Carbon Yolk-Shell Microsphere and Application of Metal Compound-Carbon Yolk-Shell as Effective Anode Material for Alkali-Ion Batteries.

Recently, nanostructured carbon materials, such as hollow-, yolk-, and core-shell-configuration, have attracted attention in various fields owing to their unique physical and chemical properties. Among them, yolk-shell structured carbon is considered as a noteworthy material for energy storage due to its fast electron transfer, structural robustness, and plentiful active reaction sites. However, the difficulty of the synthesis for controllable carbon yolk-shell has been raised as a limitation. In this study, novel synthesis strategy of nanostructured carbon yolk-shell microspheres that enable to control morphology and size of the yolk part is proposed for the first time. To apply in the appropriate field, cobalt compounds-carbon yolk-shell composites are applied as the anode of alkali-ion batteries and exhibit superior electrochemical performances to those of core-shell structures owing to their unique structural merits. Co3 O4 -C hollow yolk-shell as a lithium-ion battery anode exhibits a long cycling lifetime (619 mA h g-1 for 400 cycles at 2 A g-1 ) and excellent rate capability (286 mA h g-1 at 10 A g-1 ). The discharge capacities of CoSe2 -C hollow yolk-shell as sodium- and potassium-ion battery anodes at the 200th cycle are 311 mA h g-1 at 0.5 A g-1 and 268 mA h g-1 at 0.2 A g-1 , respectively.

Porous Microspheres Comprising CoSe2 Nanorods Coated with N-Doped Graphitic C and Polydopamine-Derived C as Anodes for Long-Lived Na-Ion Batteries.

Metal-organic framework-templated nitrogen-doped graphitic carbon (NGC) and polydopamine-derived carbon (PDA-derived C)-double coated one-dimensional CoSe2 nanorods supported highly porous three-dimensional microspheres are introduced as anodes for excellent Na-ion batteries, particularly with long-lived cycle under carbonate-based electrolyte system. The microspheres uniformly composed of ZIF-67 polyhedrons and polystyrene nanobeads (ϕ = 40 nm) are synthesized using the facile spray pyrolysis technique, followed by the selenization process (P-CoSe2@NGC NR). Further, the PDA-derived C-coated microspheres are obtained using a solution-based coating approach and the subsequent carbonization process (P-CoSe2@PDA-C NR). The rational synthesis approach benefited from the synergistic effects of dual carbon coating, resulting in a highly conductive and porous nanostructure that could facilitate rapid diffusion of charge species along with efficient electrolyte infiltration and effectively channelize the volume stress. Consequently, the prepared nanostructure exhibits extraordinary electrochemical performance, particularly the ultra-long cycle life stability. For instance, the advanced anode has a discharge capacity of 291 (1000th cycle, average capacity decay of 0.017%) and 142 mAh g-1 (5000th cycle, average capacity decay of 0.011%) at a current density of 0.5 and 2.0 A g-1, respectively.

Recent Advances in Layered Metal-Oxide Cathodes for Application in Potassium-Ion Batteries.

To meet future energy demands, currently, dominant lithium-ion batteries (LIBs) must be supported by abundant and cost-effective alternative battery materials. Potassium-ion batteries (KIBs) are promising alternatives to LIBs because KIB materials are abundant and because KIBs exhibit intercalation chemistry like LIBs and comparable energy densities. In pursuit of superior batteries, designing and developing highly efficient electrode materials are indispensable for meeting the requirements of large-scale energy storage applications. Despite using graphite anodes in KIBs instead of in sodium-ion batteries (NIBs), developing suitable KIB cathodes is extremely challenging and has attracted considerable research attention. Among the various cathode materials, layered metal oxides have attracted considerable interest owing to their tunable stoichiometry, high specific capacity, and structural stability. Therefore, the recent progress in layered metal-oxide cathodes is comprehensively reviewed for application to KIBs and the fundamental material design, classification, phase transitions, preparation techniques, and corresponding electrochemical performance of KIBs are presented. Furthermore, the challenges and opportunities associated with developing layered oxide cathode materials are presented for practical application to KIBs.

Nanofibers Comprising Interconnected Chain-Like Hollow N-Doped C Nanocages as 3D Free-Standing Cathodes for Li-S Batteries with Super-High Sulfur Content and Lean Electrolyte/Sulfur Ratio.

The development of a suitable cathode host that withstands high sulfur content/loading and low electrolyte/sulfur (E/S) ratio is particularly important for practically sustainable Li-S batteries. Herein, a facile approach is utilized to prepare free-standing 3D cathode substrates comprising nitrogen-doped carbon (N-C) scaffold and metal-organic framework derived interconnected chain-like hollow N-C nanocages, forming a highly porous N-C nanofiber (HP-N-CNF) framework. The N-C skeleton provides highly conductive pathways for fast lithium ion/electron diffusion. The hollow interconnected N-C nanocages not only offer enough space to absorb a high volume of active material but also effectively channelize severe volume stress during the electrochemical performance. The Li-S cell utilizing HP-N-CNF as cathode host displays exceptional battery parameters with high effective sulfur content (83.2 wt%), ultrahigh sulfur loading (14.3 mg cm-2 ), and low E/S ratio (6.8 µL mg-1 ). The Li-S cell exhibits a maximum areal capacity of 12.2 mAh cm-2 which stabilizes at ≈5.5 mAh cm-2 after the 130th cycle at 0.05 C-rate and is well above the theoretical threshold. Therefore, the proposed unique nanostructure synthesis approach would open new frontiers for developing more realistic and sustainable host materials with feasible battery parameters for various energy storage applications.

Morphological and Electrochemical Properties of ZnMn2O4 Nanopowders and Their Aggregated Microspheres Prepared by Simple Spray Drying Process.

Phase-pure ZnMn2O4 nanopowders and their aggregated microsphere powders for use as anode material in lithium-ion batteries were obtained by a simple spray drying process using zinc and manganese salts as precursors, followed by citric acid post-annealing at different temperatures. X-ray diffraction (XRD) analysis indicated that phase-pure ZnMn2O4 powders were obtained even at a low post-annealing temperature of 400 °C. The post-annealed powders were transformed into nanopowders by simple milling process, using agate mortar. The mean particle sizes of the ZnMn2O4 powders post-treated at 600 and 800 °C were found to be 43 and 85 nm, respectively, as determined by TEM observation. To provide practical utilization, the nanopowders were transformed into aggregated microspheres consisting of ZnMn2O4 nanoparticles by a second spray drying process. Based on the systematic analysis, the optimum post-annealing temperature required to obtain ZnMn2O4 nanopowders with high capacity and good cycle performance was found to be 800 °C. Moreover, aggregated ZnMn2O4 microsphere showed improved cycle stability. The discharge capacities of the aggregated microsphere consisting of ZnMn2O4 nanoparticles post-treated at 800 °C were 1235, 821, and 687 mA h g-1 for the 1st, 2nd, and 100th cycles at a high current density of 2.0 A g-1, respectively. The capacity retention measured after the second cycle was 84%.

Rational Design of Perforated Bimetallic (Ni, Mo) Sulfides/N-doped Graphitic Carbon Composite Microspheres as Anode Materials for Superior Na-Ion Batteries.

Highly conductive 3D ordered mesoporous Ni7 S6 -MoS2 /N-doped graphitic carbon (NGC) composite (P-NiMoS/C) microspheres are prepared as anode materials for Na-ion batteries. The rationally designed nanostructure comprises stable Ni7 S6 - and MoS2 -phases along with the homogeneously distributed ordered mesopores (ϕ = 50 nm) over the external and internal structures generated through thermal decomposition of polystyrene nanobeads (ϕ = 100 nm). Therefore, the P-NiMoS/C microspheres deliver initial discharge capacities of 662, 419, 373, 300, 231, 181, and 146 mA h g-1 at current densities of 0.5, 1, 2, 4, 6, 8, and 10 A g-1 , respectively. Furthermore, P-NiMoS/C exhibits a stable discharge capacity of 444 mA h g-1 at the end of the 150th cycle at a current density of 0.5 A g-1 , indicating higher cycling stability than the filled, that is, non-mesoporous, Ni3 S2 -MoS2 /NGC (F-NiMoS/C) microspheres and filled carbon-free Ni3 S2 -MoS2 (F-NiMoS) microspheres. The superior electrochemical performance of P-NiMoS/C microspheres is attributed to the rapid Na+ ion diffusion, alleviation of severe volume stress during prolonged cycling, and higher electrical conductivity of NGC, which results in fast charge transfer during the redox processes. The results in the present study can provide fundamental knowledge for the development of multicomponent, porous, and highly conductive anodes for various applications.

Porous SnO2/C Nanofiber Anodes and LiFePO4/C Nanofiber Cathodes with a Wrinkle Structure for Stretchable Lithium Polymer Batteries with High Electrochemical Performance.

Stretchable lithium batteries have attracted considerable attention as components in future electronic devices, such as wearable devices, sensors, and body-attachment healthcare devices. However, several challenges still exist in the bid to obtain excellent electrochemical properties for stretchable batteries. Here, a unique stretchable lithium full-cell battery is designed using 1D nanofiber active materials, stretchable gel polymer electrolyte, and wrinkle structure electrodes. A SnO2/C nanofiber anode and a LiFePO4/C nanofiber cathode introduce meso- and micropores for lithium-ion diffusion and electrolyte penetration. The stretchable full-cell consists of an elastic poly(dimethylsiloxane) (PDMS) wrapping film, SnO2/C and LiFePO4/C nanofiber electrodes with a wrinkle structure fixed on the PDMS wrapping film by an adhesive polymer, and a gel polymer electrolyte. The specific capacity of the stretchable full-battery is maintained at 128.3 mAh g-1 (capacity retention of 92%) even after a 30% strain, as compared with 136.8 mAh g-1 before strain. The energy densities are 458.8 Wh kg-1 in the released state and 423.4 Wh kg-1 in the stretched state (based on the electrode), respectively. The high capacity and stability in the stretched state demonstrate the potential of the stretchable battery to overcome its limitations.

Golden Bristlegrass-Like Hierarchical Graphene Nanofibers Entangled with N-Doped CNTs Containing CoSe2 Nanocrystals at Each Node as Anodes for High-Rate Sodium-Ion Batteries.

Golden bristlegrass-like unique nanostructures comprising reduced graphene oxide (rGO) matrixed nanofibers entangled with bamboo-like N-doped carbon nanotubes (CNTs) containing CoSe2 nanocrystals at each node (denoted as N-CNT/rGO/CoSe2 NF) are designed as anodes for high-rate sodium-ion batteries (SIBs). Bamboo-like N-doped CNTs (N-CNTs) are successfully generated on the rGO matrixed nanofiber surface, between rGO sheets and mesopores, and interconnected chemically with homogeneously distributed rGO sheets. The defects in the N-CNTs formed by a simple etching process allow the complete phase conversion of Co into CoSe2 through the efficient penetration of H2 Se gas inside the CNT walls. The N-CNTs bridge the vertical defects for electron transfer in the rGO sheet layers and increase the distance between the rGO sheets during cycles. The discharge capacity of N-CNT/rGO/CoSe2 NF after the 10 000th cycle at an extremely high current density of 10 A g-1 is 264 mA h g-1 , and the capacity retention measured at the 100th cycle is 89%. N-CNT/rGO/CoSe2 NF has final discharge capacities of 395, 363, 328, 304, 283, 263, 246, 223, 197, 171, and 151 mA h g-1 at current densities of 1, 2, 4, 6, 8, 10, 12, 14, 16, 18, and 20 A g-1 , respectively.

Hierarchically Well-Developed Porous Graphene Nanofibers Comprising N-Doped Graphitic C-Coated Cobalt Oxide Hollow Nanospheres As Anodes for High-Rate Li-Ion Batteries.

Hierarchically well-developed porous graphene nanofibers comprising N-doped graphitic C (NGC)-coated cobalt oxide hollow nanospheres are introduced as anodes for high-rate Li-ion batteries. For this, three strategies, comprising the Kirkendall effect, metal-organic frameworks, and compositing with highly conductive C, are applied to the 1D architecture. In particular, NGC layers are coated on cobalt oxide hollow nanospheres as a primary transport path of electrons followed by graphene-nanonetwork-constituting nanofibers as a continuous and secondary electron transport path. Superior cycling performance is achieved, as the unique nanostructure delivers a discharge capacity of 823 mAh g-1 after 500 cycles at 3.0 A g-1 with a low decay rate of 0.092% per cycle. The rate capability is also noteworthy as the structure exhibits high discharge capacities of 1035, 929, 847, 787, 747, 703, 672, 650, 625, 610, 570, 537, 475, 422, 294, and 222 mAh g-1 at current densities of 0.5, 1.5, 3, 5, 7, 10, 12, 15, 18, 20, 25, 30, 40, 50, 80, and 100 A g-1 , respectively. In view of the highly efficient Li+ ion/electron diffusion and high structural stability, the present nanostructuring strategy has a huge potential in opening new frontiers for high-rate and long-lived stable energy storage systems.

Facile and scalable synthesis of silicon nanowires from waste rice husk silica by the molten salt process.

Designing nanostructured silicon, such as in the form of nanoparticles, wires, and porous structures, for high-performance Li-ion electrodes, has progressed significantly. These approaches have largely overcome the capacity fading of silicon electrodes from volume expansion during lithiation/de-lithiation. However, they involve high costs, complex processes, and hazardous precursors. Herein, we propose an electrochemical fabrication of silicon nanowires from waste rice husks via a molten salt process based on electrodeoxidation. The addition of NiO as an electric conductor improved the production efficiency and created pores in the nanowires after washing. The electrically produced high-purity silicon yielded high capacity, and the nanowires provided sufficient free volume to accommodate silicon electrode expansion, resulting in improved cycle life. The converted silicon nanowires from the molten salt process will help develop sustainable energy storage materials.

Dataset on the effect of carbon sources on the morphology and crystallite size of Fe/C composite microspheres prepared by the spray drying process.

The data presented in this manuscript showed the effect of the carbon sources on the morphology and crystallite size of Fe/C composite microspheres obtained after reduction of the as spray-dried powders. Each morphology, phase, and crystalline size of powders obtained after spray-drying and subsequent heat-treatment were investigated.

Porous Hybrid Nanofibers Comprising ZnSe/CoSe2/Carbon with Uniformly Distributed Pores as Anodes for High-Performance Sodium-Ion Batteries.

Well-designed porous structured bimetallic ZnSe/CoSe2/carbon composite nanofibers with uniformly distributed pores were prepared as anodes for sodium-ion batteries by electrospinning and subsequent simple heat-treatment processes. Size-controlled polystyrene (PS) nanobeads in the electrospinning solution played a key role in the formation and uniform distribution of pores in the nanofiber structure, after the removal of selected PS nanobeads during the heat-treatment process. The porous ZnSe/CoSe2/C composite nanofibers were able to release severe mechanical stress/strain during discharge-charge cycles, introduce larger contact area between the active materials and the electrolyte, and provide more active sites during cycling. The discharge capacity of porous ZnSe/CoSe2/C composite nanofibers at the 10,000th cycle was 297 mA h g-1, and the capacity retention measured from the second cycle was 81%. The final rate capacities of porous ZnSe/CoSe2/C composite nanofibers were 438, 377, 367, 348, 335, 323, and 303 mA h g-1 at current densities of 0.1, 0.5, 1, 3, 5, 7, and 10 A g-1, respectively. At the higher current densities of 10, 20, and 30 A g-1, the final rate capacities were 310, 222, and 141 mA h g-1, respectively.

Data on hollow NiO nanofibers prepared via electrospinning using camphene and subsequent various heat-treatment temperatures for anodes in lithium ion batteries.

The data presented in this article are related to the research article entitled "New synthesis strategy for hollow NiO nanofibers with interstitial nanovoids prepared via electrospinning using camphene for anodes of lithium-ion batteries" [1]. Hollow NiO nanofibers were prepared by electrospinning process using camphene and subsequent heat-treatment process with various temperatures. The data presented in this manuscript showed the effect of the heat-treatment temperature of the as-spun fibers on the lithium ion storage properties of the hollow NiO nanofibers as anodes for lithium ion batteries. Each FE-SEM image, XRD pattern, cycle, and rate properties of the hollow NiO nanofibers obtained at various heat-treatment temperatures were investigated.

Dataset on the effect of the reaction temperature during spray pyrolysis for the synthesis of the hierarchical yolk-shell CNT-(NiCo)O/C microspheres.

The data presented in this article are related to the research article entitled "Hierarchical yolk-shell CNT-(NiCo)O_C microspheres prepared by one-pot spray pyrolysis as anodes in lithium-ion batteries" (Oh et al., 2019). The data presented in this manuscript showed the effect of the reaction temperature during spray pyrolysis on the obtained microspheres morphology. Each morphology and phase of the microspheres obtained after spray pyrolysis were investigated.

Advances in the synthesis and design of nanostructured materials by aerosol spray processes for efficient energy storage.

The increasing demand for energy storage has motivated the search for highly efficient electrode materials for use in rechargeable batteries with enhanced energy density and longer cycle life. One of the most promising strategies for achieving improved battery performance is altering the architecture of nanostructured materials employed as electrode materials in the energy storage field. Among numerous synthetic methods suggested for the fabrication of nanostructured materials, aerosol spray techniques such as spray pyrolysis, spray drying, and flame spray pyrolysis are reliable, as they are facile, cost-effective, and continuous processes that enable the synthesis of nanostructured electrode materials with desired morphologies and compositions with controlled stoichiometry. The post-treatment of spray-processed powders enables the fabrication of oxide, sulfide, and selenide nanostructures hybridized with carbonaceous materials including amorphous carbon, reduced graphene oxide, carbon nanotubes, etc. In this article, recent progress in the synthesis of nanostructured electrode materials by spray processes and their general formation mechanisms are discussed in detail. A brief introduction to the working principles of each spray process is given first, and synthetic strategies for the design of electrode materials for lithium-ion, sodium-ion, lithium-sulfur, lithium-selenium, and lithium-oxygen batteries are discussed along with some examples. This analysis sheds light on the synthesis of nanostructured materials by spray processes and paves the way toward the design of other novel and advanced nanostructured materials for high performance electrodes in rechargeable batteries of the future.