Highly Selective and Reversible Detection of Simulated Breath Hydrogen Sulfide Using Fe-Doped CuO Hollow Spheres: Enhanced Surface Redox Reaction by Multi-Valent Catalysts.

The precise and reversible detection of hydrogen sulfide (H2 S) at high humidity condition, a malodorous and harmful volatile sulfur compound, is essential for the self-assessment of oral diseases, halitosis, and asthma. However, the selective and reversible detection of trace concentrations of H2 S (≈0.1 ppm) in high humidity conditions (exhaled breath) is challenging because of irreversible H2 S adsorption/desorption at the surface of chemiresistors. The study reports the synthesis of Fe-doped CuO hollow spheres as H2 S gas-sensing materials via spray pyrolysis. 4 at.% of Fe-doped CuO hollow spheres exhibit high selectivity (response ratio ≥ 34.4) over interference gas (ethanol, 1 ppm) and reversible sensing characteristics (100% recovery) to 0.1 ppm of H2 S under high humidity (relative humidity 80%) at 175 °C. The effect of multi-valent transition metal ion doping into CuO on sensor reversibility is confirmed through the enhancement of recovery kinetics by doping 4 at.% of Ti- or Nb ions into CuO sensors. Mechanistic details of these excellent H2 S sensing characteristics are also investigated by analyzing the redox reactions and the catalytic activity change of the Fe-doped CuO sensing materials. The selective and reversible detection of H2 S using the Fe-doped CuO sensor suggested in this work opens a new possibility for halitosis self-monitoring.

Scalable Dry Process for Fabricating a Na Superionic Conductor-Type Solid Electrolyte Sheet.

The cost reduction and mass production of oxide-based solid electrolytes are critical for the commercialization of all-solid-state batteries. In this study, an environmentally friendly, low-cost, and high-density oxide-based Na superionic conductor-type solid electrolyte sheet was fabricated via a dry process without the use of any solvent. The polytetrafluoroethylene (PTFE), used as a binder, was transformed into thin thread-like structures via shear force, resulting in a flexible solid electrolyte sheet. The solid electrolyte powder quantity was limited to 50 wt % for fabricating a uniform green sheet via the wet process. However, when the dry process was employed for green sheet fabrication, the solid electrolyte powder quantity could be increased to values exceeding 95 wt %. Therefore, the green sheets produced by using the dry process demonstrated a higher density than those fabricated by using the wet process. The binder content and particle size affected the ionic conductivity of a solid electrolyte sheet fabricated via a dry process. The sheet obtained via the blending of 3 wt % PTFE binder with a solid electrolyte powder, finely ground using a planetary ball mill, which exhibited the highest total ionic conductivity of 1.03 mS cm-1.

Synergistic Integration of Machine Learning with Microstructure/Composition-Designed SnO2 and WO3 Breath Sensors.

A high-performance semiconductor metal oxide gas sensing strategy is proposed for efficient sensor-based disease prediction by integrating a machine learning methodology with complementary sensor arrays composed of SnO2- and WO3-based sensors. The six sensors, including SnO2- and WO3-based sensors and neural network algorithms, were used to measure gas mixtures. The six constituent sensors were subjected to acetone and hydrogen environments to monitor the effect of diet and/or irritable bowel syndrome (IBS) under the interference of ethanol. The SnO2- and WO3-based sensors suffer from poor discrimination ability if sensors (a single sensor or multiple sensors) within the same group (SnO2- or WO3-based) are separately applied, even when deep learning is applied to enhance the sensing operation. However, hybrid integration is proven to be effective in discerning acetone from hydrogen even in a two-sensor configuration through the synergistic contribution of supervised learning, i.e., neural network approaches involving deep neural networks (DNNs) and convolutional neural networks (CNNs). DNN-based numeric data and CNN-based image data can be exploited for discriminating acetone and hydrogen, with the aim of predicting the status of an exercise-driven diet and IBS. The ramifications of the proposed hybrid sensor combinations and machine learning for the high-performance breath sensor domain are discussed.

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.

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.

Field-induced orientational switching produces vertically aligned Ti3C2Tx MXene nanosheets.

Controlling the orientation of two-dimensional materials is essential to optimize or tune their functional properties. In particular, aligning MXene, a two-dimensional carbide and/or nitride material, has recently received much attention due to its high conductivity and high-density surface functional group properties that can easily vary based on its arranged directions. However, erecting 2D materials vertically can be challenging, given their thinness of few nanometres. Here, vertical alignment of Ti3C2Tx MXene sheets is achieved by applying an in-plane electric field, which is directly observed using polarised optical microscopy and scanning electron microscopy. The electric field-induced vertical alignment parallel to the applied alternating-current field is demonstrated to be reversible in the absence of a field, back to a random orientation distribution. Interdigitated electrodes with uniaxially aligned MXene nanosheets are demonstrated. These can be further modulated to achieve various patterns using diversified electrode substrates. Anisotropic electrical conductivity is also observed in the uniaxially aligned MXene nanosheet film, which is quite different from the randomly oriented ones. The proposed orientation-controlling technique demonstrates potential for many applications including sensors, membranes, polarisers, and general energy applications.

A Novel High-Performance TiO2-x /TiO1-y Ny 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 TiO2- x /TiO1- y Ny (TTN) formed via a facile and scalable synthetic process is applied as a coating material for Si anodes. A thin layer of amorphous TiO2 is uniformly coated onto Si nanoparticles by a simple sol-gel method and then converted into a two phase TiO2- x /TiO1- y Ny via nitridation. The lithiated TiO2-x provides high ionic and electrical conductivity, while TiO1-y Ny can improve mechanical strength that alleviates volume change of Si to address capacity fading issue. Owing to these synergetic advantages, TiO2- x /TiO1- y Ny -coated Si (Si@TTN) exhibits excellent electrochemical properties, including a high charge capacity of 1650 mA h g-1 at 0.1 A g-1 and 84% capacity retention after 100 cycles at 1 A g-1 . Moreover, a significantly enhanced rate performance can be achieved at a high current density. This investigation presents a facile and effective coating material to use as the high-capacity silicon anode in the emerging Si anode technology in LIBs.

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%.

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. TiON can be uniformly coated on the Si surface via self-assembly, which can enhance the Si utilization and electrode stability. This is because TiON exhibits high mechanical strength and electrical conductivity, allowing it to act as a rigid and electrically conductive matrix. As a result, the Si-TiON electrodes delivered an initial reversible capacity of 1663 mA h g-1 with remarkably enhanced capacity retention and rate performance.

Yolk-Shell-Structured Nanospheres with Goat Pupil-Like S-Doped SnSe Yolk and Hollow Carbon-Shell Configuration as Anode Material for Sodium-Ion Storage.

Rationally nanostructured electrode materials exhibit excellent sodium-ion storage performance. In particular, yolk-shell configurations of metal chalcogenide@void@C are introduced in various synthetic strategies for use as superior anode materials. Herein, yolk-shell-structured nanospheres, with goat pupil-like configuration of S-doped SnSe yolks and hollow carbon shells, are synthesized by salt-infiltration and a simple post-treatment procedure. Impressively, the co-infiltration of thiourea and selenium oxide enables the doping of sulfur into SnSe (SnSeS) and carbon shells, as well as the formation of a goat pupil-like yolk-shell architecture. High-reactivity thiourea-derived H2 S gas forms nanocrystals inside the carbon nanospheres. The nanocrystals act as seeds for the crystal growth of SnSeS through Ostwald ripening. The unique yolk-shell structure and composition with a heterointerface provide not only structural stability but also fast electrode reaction kinetics during repeated cycling. The SnSeS@C electrode shows an excellent cycle life (186 mA h g-1 for 1000 cycles at 0.5 A g-1 ) and rate capability (112 mA h g-1 at 5.0 A g-1 ).

Boosting the Electrochemical Performance of V2 O3 by Anchoring on Carbon Nanotube Microspheres with Macrovoids for Ultrafast and Long-Life Aqueous Zinc-Ion Batteries.

Zinc-ion batteries (ZIBs) are next-generation energy storage systems with high safety and environmental friendliness because they can be operated in aqueous systems. However, the search for electrode materials with ideal nanostructures and compositions for aqueous ZIBs is in progress. Herein, the synthesis of porous microspheres, consisting of V2 O3 anchored on entangled carbon nanotubes (p-V2 O3 -CNT) and their application as cathode for ZIBs is reported. From various analyses, it is revealed that V2 O3 phase disappears after the initial charge process, and Zn3+ x (OH)2+3 x V2- x O7-3 x ∙2H2 O and zinc vanadate (Zny VOz ) phases undergo zinc-ion intercalation/deintercalation processes from the second cycle. Additionally, the electrochemical performances of p-V2 O3 -CNT, V2 O3 -CNT (without macrovoids), and porous V2 O3 (without CNTs) microspheres are compared to determine the effects of nanostructures and conductive carbonaceous matrix on the zinc-ion storage performance. p-V2 O3 -CNT exhibits a high reversible capacity of 237 mA h g-1 after 5000 cycles at 10 A g-1 . Furthermore, a reversible capacity of 211 mA h g-1 is obtained at an extremely high current density of 50 A g-1 . The macrovoids in V2 O3 nanostructure effectively alleviate the volume changes during cycling, and the entangled CNTs with high electrical conductivity assist in achieving fast electrochemical kinetics.

Carbon-Coated Three-Dimensional MXene/Iron Selenide Ball with Core-Shell Structure for High-Performance Potassium-Ion Batteries.

Two-dimensional (2D) MXenes are promising as electrode materials for energy storage, owing to their high electronic conductivity and low diffusion barrier. Unfortunately, similar to most 2D materials, MXene nanosheets easily restack during the electrode preparation, which degrades the electrochemical performance of MXene-based materials. A novel synthetic strategy is proposed for converting MXene into restacking-inhibited three-dimensional (3D) balls coated with iron selenides and carbon. This strategy involves the preparation of Fe2O3@carbon/MXene microspheres via a facile ultrasonic spray pyrolysis and subsequent selenization process. Such 3D structuring effectively prevents interlayer restacking, increases the surface area, and accelerates ion transport, while maintaining the attractive properties of MXene. Furthermore, combining iron selenides and carbon with 3D MXene balls offers many more sites for ion storage and enhances the structural robustness of the composite balls. The resultant 3D structured microspheres exhibit a high reversible capacity of 410 mAh g-1 after 200 cycles at 0.1 A g-1 in potassium-ion batteries, corresponding to the capacity retention of 97% as calculated based on 100 cycles. Even at a high current density of 5.0 A g-1, the composite exhibits a discharge capacity of 169 mAh g-1.

Magnetic Control and Real-Time Monitoring of Stem Cell Differentiation by the Ligand Nanoassembly.

Native extracellular matrix (ECM) exhibits dynamic change in the ligand position. Herein, the ECM-emulating control and real-time monitoring of stem cell differentiation are demonstrated by ligand nanoassembly. The density of gold nanoassembly presenting cell-adhesive Arg-Gly-Asp (RGD) ligand on Fe3 O4 (magnetite) nanoparticle in nanostructures flexibly grafted to material is changed while keeping macroscale ligand density invariant. The ligand nanoassembly on the Fe3 O4 can be magnetically attracted to mediate rising and falling ligand movements via linker stretching and compression, respectively. High ligand nanoassembly density stimulates integrin ligation to activate the mechanosensing-assisted stem cell differentiation, which is monitored via in situ real-time electrochemical sensing. Magnetic control of rising and falling ligand movements hinders and promotes the adhesion-mediated mechanotransduction and differentiation of stem cells, respectively. These rising and falling ligand states yield the difference in the farthest distance (≈34.6 nm) of the RGD from material surface, thereby dynamically mimicking static long and short flexible linkers, which hinder and promote cell adhesion, respectively. Design of cytocompatible ligand nanoassemblies can be made with combinations of dimensions, shapes, and biomimetic ligands for remotely regulating stem cells for offering novel methodologies to advance regenerative therapies.

Highly Selective Detection of Benzene and Discrimination of Volatile Aromatic Compounds Using Oxide Chemiresistors with Tunable Rh-TiO2 Catalytic Overlayers.

Volatile aromatic compounds are major air pollutants, and their health impacts should be assessed accurately based on the concentration and composition of gas mixtures. Herein, novel bilayer sensors consisting of a SnO2 sensing layer and three different xRh-TiO2 catalytic overlayers (x = 0.5, 1, and 2 wt%) are designed for the new functionalities such as the selective detection, discrimination, and analysis of benzene, toluene, and p-xylene. The 2Rh-TiO2/SnO2 bilayer sensor shows a high selectivity and response toward ppm- and sub-ppm-levels of benzene over a wide range of sensing temperatures (325-425 °C). An array of 0.5Rh-, 1Rh-, and 2Rh-TiO2/SnO2 sensors exhibits discrimination and composition analyses of aromatic compounds. The conversion of gases into more active species at moderate catalytic activation and the complete oxidation of gases into non-reactive forms by excessive catalytic promotion are proposed as the reasons behind the enhancement and suppression of analyte gases, respectively. Analysis using proton transfer reaction-quadrupole mass spectrometer (PTR-QMS) is performed to verify the above proposals. Although the sensing characteristics exhibit mild moisture interference, bilayer sensors with systematic and tailored control of gas selectivity and response provide new pathways for monitoring aromatic air pollutants and evaluating their health impacts.

Remote Control of Time-Regulated Stretching of Ligand-Presenting Nanocoils In Situ Regulates the Cyclic Adhesion and Differentiation of Stem Cells.

Native extracellular matrix (ECM) can exhibit cyclic nanoscale stretching and shrinking of ligands to regulate complex cell-material interactions. Designing materials that allow cyclic control of changes in intrinsic ligand-presenting nanostructures in situ can emulate ECM dynamicity to regulate cellular adhesion. Unprecedented remote control of rapid, cyclic, and mechanical stretching ("ON") and shrinking ("OFF") of cell-adhesive RGD ligand-presenting magnetic nanocoils on a material surface in five repeated cycles are reported, thereby independently increasing and decreasing ligand pitch in nanocoils, respectively, without modulating ligand-presenting surface area per nanocoil. It is demonstrated that cyclic switching "ON" (ligand nanostretching) facilitates time-regulated integrin ligation, focal adhesion, spreading, YAP/TAZ mechanosensing, and differentiation of viable stem cells, both in vitro and in vivo. Fluorescence resonance energy transfer (FRET) imaging reveals magnetic switching "ON" (stretching) and "OFF" (shrinking) of the nanocoils inside animals. Versatile tuning of physical dimensions and elements of nanocoils by regulating electrodeposition conditions is also demonstrated. The study sheds novel insight into designing materials with connected ligand nanostructures that exhibit nanocoil-specific nano-spaced declustering, which is ineffective in nanowires, to facilitate cell adhesion. This unprecedented, independent, remote, and cytocompatible control of ligand nanopitch is promising for regulating the mechanosensing-mediated differentiation of stem cells in vivo.

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.

Encapsulation of Se into Hierarchically Porous Carbon Microspheres with Optimized Pore Structure for Advanced Na-Se and K-Se Batteries.

Sodium-selenium (Na-Se) and potassium-selenium (K-Se) batteries have emerged as promising energy storage systems with high energy density and low cost. However, major issues such as huge Se volume changes, polyselenide shuttling, and low Se loading need to be overcome. Although many strategies have been developed to resolve these issues, the relationship between the carbon host pore structure and electrochemical performance of Se has not been studied extensively. Here, the effect of the carbon host pore structure on the electrochemical performance of Na-Se and K-Se batteries is investigated. N, S-co-doped hierarchically porous carbon microspheres with different pore structures that can incorporate a large amount of amorphous Se (∼60 wt %) are synthesized by spray pyrolysis and subsequent chemical activation at different temperatures. By optimizing the amount of micropore volume and micropore-to-mesopore ratio, high reversible capacity and cycling stability are achieved for the Se cathode. The optimized cathode delivers a reversible capacity of 445 mA h g-1 after 400 cycles at 0.5C for Na-Se batteries and 436 mA h g-1 after 120 cycles at 0.2C for K-Se batteries. This study marks the importance of developing conductive carbon matrices with delicately designed pore structures for advanced alkali metal-chalcogen battery systems.

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.