Achieving Cycling Stability in Anode of Lithium-Ion Batteries with Silicon-Embedded Titanium Oxynitride Microsphere.

Surface coating approaches for silicon (Si) have demonstrated potential for use as anodes in lithium-ion batteries (LIBs) to address the large volume change and low conductivity of Si. However, the practical application of these approaches remains a challenge because they do not effectively accommodate the pulverization of Si during cycling or require complex processes. Herein, Si-embedded titanium oxynitride (Si-TiON) was proposed and successfully fabricated using a spray-drying process.

A Novel High-Performance TiO /TiO N Coating Material for Silicon Anode in Lithium-Ion Batteries.

Protective surface coatings on Si anodes are promising for improving the electrochemical performance of lithium-ion batteries (LIBs). Nevertheless, most coating materials have severe issues, including low initial coulombic efficiency, structural fracture, morphology control, and complicated synthetic processing. In this study, a multifunctional TiO /TiO N (TTN) formed via a facile and scalable synthetic process is applied as a coating material for Si anodes.

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) in comparison with conventional electrodes, e.g., graphite.

Microscopic evidence of strong interactions between chemical vapor deposited 2D MoS film and SiO growth template.

Two-dimensional MoS film can grow on oxide substrates including AlO and SiO. However, it cannot grow usually on non-oxide substrates such as a bare Si wafer using chemical vapor deposition. To address this issue, we prepared as-synthesized and transferred MoS (AS-MoS and TR-MoS) films on SiO/Si substrates and studied the effect of the SiO layer on the atomic and electronic structure of the MoS films using spherical aberration-corrected scanning transition electron microscopy (STEM) and electron energy loss spectroscopy (EELS).

Correction: Suppression of metal-to-insulator transition using strong interfacial coupling at cubic and orthorhombic perovskite oxide heterointerfaces.

Correction for 'Suppression of metal-to-insulator transition using strong interfacial coupling at cubic and orthorhombic perovskite oxide heterointerfaces' by Woonbae Sohn et al., Nanoscale, 2021, 13, 708-715, DOI: 10.1039/D0NR07545K.

Suppression of metal-to-insulator transition using strong interfacial coupling at cubic and orthorhombic perovskite oxide heterointerfaces.

A quasi-two-dimensional electron gas (2DEG) evolved at the LaAlO3 (LAO)/SrTiO3 (STO) interface has attracted significant attention, because the insertion of perovskite titanates can tune the 2DEG conductivity. However, this depends on the Ti-O-Ti bonding angle and structural symmetry. In this study, we controlled the octahedral tilt of the LAO/CaTiO3 (CTO) interface by heterostructuring it with CTO grown on STO substrates of various thicknesses.

Silver grass-derived activated carbon with coexisting micro-, meso- and macropores as excellent bioanodes for microbial colonization and power generation in sustainable microbial fuel cells.

In this study, highly biocompatible three-dimensional hierarchically porous activated carbon from the low-cost silver grass (Miscanthus sacchariflorus) has been fabricated through a facile carbonization approach and tested it as bioanode in microbial fuel cell (MFC) using Escherichia coli as biocatalyst. This silver grass-derived activated carbon (SGAC) exhibited an unprecedented specific surface area of 3027 m g with the coexistence of several micro-, meso-, and macropores. The synergistic effect from pore structure (macropores - hosting E.

An ionic liquid incorporated in a quasi-solid-state electrolyte for high-temperature supercapacitor applications.

An ionic liquid (IL) incorporated in a quasi-solid-state electrolyte (ILQSE) is prepared using 1-ethyl-3-methylimidazolium tetrafluoroborate (EMIBF) and poly (ethylene glycol dimethacrylayte) (PEGDMA) for high-temperature application of supercapacitors. The prepared ILQSE displays a thermal stability up to 150 °C and the supercapacitors exhibit a specific capacitance of 134 F g.

Improved pseudocapacitive charge storage in highly ordered mesoporous TiO/carbon nanocomposites as high-performance Li-ion hybrid supercapacitor anodes.

A Li-ion hybrid supercapacitor (Li-HSCs), an integrated system of a Li-ion battery and a supercapacitor, is an important energy-storage device because of its outstanding energy and power as well as long-term cycle life. In this work, we propose an attractive material (a mesoporous anatase titanium dioxide/carbon hybrid material, m-TiO-C) as a rapid and stable Li storage anode material for Li-HSCs. m-TiO-C exhibits high specific capacity (∼198 mA h g at 0.

Magnéli Phase Titanium Oxide as a Novel Anode Material for Potassium-Ion Batteries.

Recently, K-ion batteries (KIBs) have attracted attention for potential applications in next-generation energy storage devices principally on the account of their abundancy and lower cost. Herein, for the first time, we report an anatase TiO-derived Magnéli phase TiO as a novel anode material for KIBs. We incorporate pristine carbon nanotube (CNT) on the TiO host materials due to the low electronic conductivity of the host materials.

The effect of ILs as co-salts in electrolytes for high voltage supercapacitors.

Ionic liquids (ILs) which have electrical stability are attractive materials to enhance the potential window of electrolyte. According to the potential window is extended, available voltage for supercapacitor is broaden. In this study, the addition of ILs which is 1-ethyl-3-methylimidazolium tetrafluoroborate (EMIBF4) and 1-ethyl-3-methylimidazolium bis(trifluoromethylesulfonyl) imide (EMITFSI) as co-salts, to a supercapacitor electrolyte increases the ionic conductivity and stability of it due to inhibition of electrolyte decomposition.

Lithium-Sulfur Capacitors.

Although many existing hybrid energy storage systems demonstrate promising electrochemical performances, imbalances between the energies and kinetics of the two electrodes must be resolved to allow their widespread commercialization. As such, the development of a new class of energy storage systems is a particular challenge, since future systems will require a single device to provide both a high gravimetric energy and a high power density. In this context, we herein report the design of novel lithium-sulfur capacitors.

A new general approach to synthesizing filled and yolk-shell structured metal oxide microspheres by applying a carbonaceous template.

New mechanisms were found for the formation of metal oxide microspheres with yolk-shell and filled structures by applying carbonaceous template microspheres with high porosity. Repeated impregnation first adopted to achieve a high loading rate of metal precursor in the carbonaceous template provided the breakthrough. The carbonaceous template with an appropriate loading rate of the metal precursor produced metal oxide microspheres with filled and yolk-shell structure depending on the ramping rate and oxygen concentration during the post-treatment process.

Multimodal porous carbon derived from ionic liquids: correlation between pore sizes and ionic clusters.

In this proof of concept study on the synthesis of ionic liquid (IL)-derived multimodal porous carbon using ionic clusters of different sizes as porogens, the carbonization behaviors of binary IL mixtures of 1-ethyl-3-methylimidazolium dicyanamide (EMIM-dca) and 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (EMIM-TfN) were systematically investigated to demonstrate the formation of multimodal porous carbons with hierarchical structures originating from the ionic cluster porogens. The multimodal porous structures of the resulting IL-derived porous carbons were characterized based on the quenched solid density functional theory, and the role of the ionic clusters as porogens is discussed. From the viewpoint of green and sustainable chemistry, the IL-based synthesis using ionic clusters as porogens is a simple, effective, and sustainable technique for synthesizing multimodal porous carbons with hierarchical structures.

Multi-functionalized herringbone carbon nanofiber for anodes of lithium ion batteries.

Herringbone carbon nanofibers (HCNFs) are prepared for use as anode materials in lithium-ion batteries (LIBs). HCNFs are prepared using a Ni-Fe catalyst and subsequently multi-functionalized with oxygen using the Hummers' method, and then with both oxygen and nitrogen-containing 2-ureido-4[1H]pyrimidinone (UHP) moieties, which endow the HCNFs with the ability to form quadruple hydrogen bonds (QHBs). The as-prepared HCNFs are, on average, 13 μm in length and 100 nm in diameter, with a highly graphitic structure.

A study of the effects of synthesis conditions on LiFeO/carbon nanotube composites.

LiFeO/carbon nanotube (LFO/CNT) composites composed of sub-micron sized LFO and a nanocarbon with high electrical conductivity were successfully synthesized for the use as lithium ion predoping source in lithium ion cells. The phase of LFO in the composite was found to be very sensitive to the synthesis conditions, such as the heat treatment temperature, type of lithium salt, and physical state of the precursors (powder or pellet), due to the carbothermic reduction of FeO by CNTs during high temperature solid state reaction. Under optimized synthesis conditions, LFO/CNT composites could be synthesized without the formation of impurities.

Graphene-Selenium Hybrid Microballs as Cathode Materials for High-performance Lithium-Selenium Secondary Battery Applications.

In this study, graphene-selenium hybrid microballs (G-SeHMs) are prepared in one step by aerosol microdroplet drying using a commercial spray dryer, which represents a simple, scalable continuous process, and the potential of the G-SeHMs thus prepared is investigated for use as cathode material in applications of lithium-selenium secondary batteries. These morphologically unique graphene microballs filled with Se particles exhibited good electrochemical properties, such as high initial specific capacity (642 mA h g(-1) at 0.1 C, corresponding to Se electrochemical utilisation as high as 95.

Synthesis of Reduced Graphene Oxide-Modified LiMn0.75Fe0.25PO4 Microspheres by Salt-Assisted Spray Drying for High-Performance Lithium-Ion Batteries.

Microsized, spherical, three-dimensional (3D) graphene-based composites as electrode materials exhibit improved tap density and electrochemical properties. In this study, we report 3D LiMn0.75Fe0.

Hierarchically structured activated carbon for ultracapacitors.

To resolve the pore-associated bottleneck problem observed in the electrode materials used for ultracapacitors, which inhibits the transport of the electrolyte ions, we designed hierarchically structured activated carbon (HAC) by synthesizing a mesoporous silica template/carbon composite and chemically activating it to simultaneously remove the silica template and increase the pore volume. The resulting HAC had a well-designed, unique porous structure, which allowed for large interfaces for efficient electric double-layer formation. Given the unique characteristics of the HAC, we believe that the developed synthesis strategy provides important insights into the design and fabrication of hierarchical carbon nanostructures.

Template-Free Synthesis of Ruthenium Oxide Nanotubes for High-Performance Electrochemical Capacitors.

One-dimensional, hydrous ruthenium oxide nanotubes (RuO2·1.84H2O) have been successfully achieved using a template-free, microwave-hydrothermal process. These were found to be amorphous in nature and have a large specific surface area of 250 m(2)·g(-1), producing a specific and volumetric capacitance of 511 F·g(-1) and 531 F·cm(-3), respectively, at a discharging current density of 0.

Facile Synthesis of Nb2O5@Carbon Core-Shell Nanocrystals with Controlled Crystalline Structure for High-Power Anodes in Hybrid Supercapacitors.

Hybrid supercapacitors (battery-supercapacitor hybrid devices, HSCs) deliver high energy within seconds (excellent rate capability) with stable cyclability. One of the key limitations in developing high-performance HSCs is imbalance in power capability between the sluggish Faradaic lithium-intercalation anode and rapid non-Faradaic capacitive cathode. To solve this problem, we synthesize Nb2O5@carbon core-shell nanocyrstals (Nb2O5@C NCs) as high-power anode materials with controlled crystalline phases (orthorhombic (T) and pseudohexagonal (TT)) via a facile one-pot synthesis method based on a water-in-oil microemulsion system.

High-Surface-Area Nitrogen-Doped Reduced Graphene Oxide for Electric Double-Layer Capacitors.

A two-step method consisting of solid-state microwave irradiation and heat treatment under NH3 gas was used to prepare nitrogen-doped reduced graphene oxide (N-RGO) with a high specific surface area (1007 m(2)  g(-1) ), high electrical conductivity (1532 S m(-1) ), and low oxygen content (1.5 wt %) for electrical double-layer capacitor applications. The specific capacitance of N-RGO was 291 F g(-1) at a current density of 1 A g(-1) , and a capacitance of 261 F g(-1) was retained at 50 A g(-1) , which indicated a very good rate capability.

Spine-like nanostructured carbon interconnected by graphene for high-performance supercapacitors.

Recent studies on supercapacitors have focused on the development of hierarchical nanostructured carbons by combining two-dimensional graphene and other conductive sp(2) carbons, which differ in dimensionality, to improve their electrochemical performance. Herein, we report a strategy for synthesizing a hierarchical graphene-based carbon material, which we shall refer to as spine-like nanostructured carbon, from a one-dimensional graphitic carbon nanofiber by controlling the local graphene/graphitic structure via an expanding process and a co-solvent exfoliation method. Spine-like nanostructured carbon has a unique hierarchical structure of partially exfoliated graphitic blocks interconnected by thin graphene sheets in the same manner as in the case of ligaments.

The effect of the ionic size of small quaternary ammonium BF₄ salts on electrochemical double layer capacitors.

By varying the cation size of quaternary ammonium salts, approximately 10% higher capacitance was achieved with trimethylethylammonium BF4 and trimethylpropylammonium BF4 relative to tetraethylammonium BF4 using microporous activated carbon (AC) electrodes. The ions carried solvation shells in the bulk electrolytes, but became desolvated within the narrow AC pores when the electrochemical double-layer capacitor was charged to a high potential. The capacitance depended on the size of the cation rather than that of the BF4 anion because the anion is smaller than the quaternary ammonium ions.