High-Power and Large-Area Anodes for Safe Lithium-Metal Batteries.

The lithium deposited via the complex electrochemical heterogeneous lithium deposition reaction (LDR) process on a lithium foil-based anode (LFA) forms a high-aspect-ratio shape whenever the reaction kinetics reach its limit, threatening battery safety. Thereby, a research strategy that boosts the LDR kinetics is needed to construct a high-power and safe lithium metal anode. In this study, the kinetic limitations of the LDR process on LFA are elucidated through operando and ex situ observations using in-depth electrochemical analyses. In addition, ultra-thin (≈0.5 µm) and high modulus (≥19 GPa) double-walled carbon nanotube (DWNT) membranes with different surface properties are designed to catalyze high-safety LDRs. The oxygen-functionalized DWNT membranes introduced on the LFA top surface simultaneously induce multitudinous lithium nuclei, leading to film-like lithium deposition even at a high current density of 20 mA cm-2. More importantly, the layer-by-layer assembly of the oxygen-functionalized and pristine DWNT membranes results in different surface energies between the top and bottom surfaces, enabling selective surface LDRs underneath the high-modulus bilayer membranes. The protective LDR on the bilayer-covered LFA guarantees an invulnerable cycling process in large-area pouch cells at high current densities for more than 1000 cycles, demonstrating the practicability of LFA in a conventional liquid electrolyte system.

Hierarchically Nanoporous 3D Assembly Composed of Functionalized Onion-Like Graphitic Carbon Nanospheres for Anode-Minimized Li Metal Batteries.

Despite the recent attention for Li metal anode (LMA) with high theoretical specific capacity of ≈3860 mA h g-1 , it suffers from not enough practical energy densities and safety concerns originating from the excessive metal load, which is essential to compensate for the loss of Li sources resulting from their poor coulombic efficiencies (CEs). Therefore, the development of high-performance LMA is needed to realize anode-minimized Li metal batteries (LMBs). In this study, high-performance LMAs are produced by introducing a hierarchically nanoporous assembly (HNA) composed of functionalized onion-like graphitic carbon building blocks, several nanometers in diameter, as a catalytic scaffold for Li-metal storage. The HNA-based electrodes lead to a high Li ion concentration in the nanoporous structure, showing a high CE of ≈99.1%, high rate capability of 12 mA cm-2 , and a stable cycling behavior of more than 750 cycles. In addition, anode-minimized LMBs are achieved using a HNA that has limited Li content (≈0.13 mg cm-2 ), corresponding to 6.5% of the cathode material (commercial NCM622 (≈2 mg cm-2 )). The LMBs demonstrate a feasible electrochemical performance with high energy and power densities of ≈510 Wh kgelectrode -1 and ≈2760 W kgelectrode -1 , respectively, for more than 100 cycles.

Electrolyte-Dependent Sodium Ion Transport Behaviors in Hard Carbon Anode.

A comprehensive study is conducted on hard carbon (HC) series samples by tuning the graphitic local microstructures systematically as an anode for SIBs in both carbonate- (CBE) and glyme-based electrolytes (GBE). The results reveal more detailed charge storage characters of HCs on the LVP section. 1) The LVP capacity is closely related to the prismatic surface area to the basal plane as well as the bulk density, regardless of electrolyte systems. 2) The glyme-sodium ion complex can facilitate sodium ion delivery into the internal closed pores of the HCs along with not well-ordered graphitic structures. 3) The glyme-mediated sodium ion-storage behavior causes significant decreases in both surface film resistance and charge transfer resistance, leading to enhanced rate capability. 4) The LVP originates from the formation of pseudo-metallic sodium nanoclusters, which are the same in a CBE and GBE. These results provide insight into the sodium ion-storage behaviors of HCs, particularly on the interrelationship between graphitic local microstructures and electrolyte systems. In addition, a high-performance HC anode with a plateau capacity of ≈300 mA h g-1 is designed based on the information, and its workability is demonstrated in a full-cell SIB device.

Anode-Free Sodium Metal Batteries Based on Nanohybrid Core-Shell Templates.

Anode-free sodium metal batteries (AF-SMBs) can deliver high energy and enormous power, but their cycle lives are still insufficient for them to be practical as a power source in modern electronic devices and/or grid systems. In this study, a nanohybrid template based on high aspect-ratio silver nanofibers and nitrogen-rich carbon thin layers as a core-shell structure is designed to improve the Coulombic efficiency (CE) and cycling performance of AF-SMBs. The catalytic nanohybrid templates dramatically reduce the voltage overshooting caused by metal nucleation to one-fifth that of a bare Al foil electrode (≈6 mV vs ≈30 mV), and high average CE values of >99% are achieved over a wide range of current rates from 0.2 to 8 mA cm-2 . Moreover, exceptionally long cycle lives for more than 1600 cycles and an additional 1500 cycles are achieved with a highly stable CE of >99.9%. These results show that AF-SMBs are feasible with the nanohybrid electrode system.

Pyrolytic Carbon Nanosheets for Ultrafast and Ultrastable Sodium-Ion Storage.

Na-ion cointercalation in the graphite host structure in a glyme-based electrolyte represents a new possibility for using carbon-based materials (CMs) as anodes for Na-ion storage. However, local microstructures and nanoscale morphological features in CMs affect their electrochemical performances; they require intensive studies to achieve high levels of Na-ion storage performances. Here, pyrolytic carbon nanosheets (PCNs) composed of multitudinous graphitic nanocrystals are prepared from renewable bioresources by heating. In particular, PCN-2800 prepared by heating at 2800 °C has a distinctive sp2 carbon bonding nature, crystalline domain size of ≈44.2 Å, and high electrical conductivity of ≈320 S cm-1 , presenting significantly high rate capability at 600 C (60 A g-1 ) and stable cycling behaviors over 40 000 cycles as an anode for Na-ion storage. The results of this study show the unusual graphitization behaviors of a char-type carbon precursor and exceptionally high rate and cycling performances of the resulting graphitic material, PCN-2800, even surpassing those of supercapacitors.

Tin Sulfide-Based Nanohybrid for High-Performance Anode of Sodium-Ion Batteries.

Nanohybrid anode materials for Na-ion batteries (NIBs) based on conversion and/or alloying reactions can provide significantly improved energy and power characteristics, while suffering from low Coulombic efficiency and unfavorable voltage properties. An NIB paper-type nanohybrid anode (PNA) based on tin sulfide nanoparticles and acid-treated multiwalled carbon nanotubes is reported. In 1 m NaPF6 dissolved in diethylene glycol dimethyl ether as an electrolyte, the above PNA shows a high reversible capacity of ≈1200 mAh g-1 and a large voltage plateau corresponding to a capacity of ≈550 mAh g-1 in the low-voltage region of ≈0.1 V versus Na+ /Na, exhibiting high rate capabilities at a current rate of 1 A g-1 and good cycling performance over 250 cycles. In addition, the PNA exhibits a high first Coulombic efficiency of ≈90%, achieving values above 99% during subsequent cycles. Furthermore, the feasibility of PNA usage is demonstrated by full-cell tests with a reported cathode, which results in high specific energy and power values of ≈256 Wh kg-1 and 471 W kg-1 , respectively, with stable cycling.

Free-standing nitrogen-doped reduced graphene oxide anode for lithium-ion batteries.

Graphenes have been considered suitable candidate materials for electrodes of energy storage devices such as lithium-ion batteries (LIBs) because of their outstanding mechanical, thermal and electrical properties. However, there are problems when using these carbon materials for electrodes because of their low electrochemical performance. In this work, to improve the electrochemical performances of graphenes, free-standing nitrogen-doped reduced graphene oxides (FNRGOs) were prepared as an anode for LIBs using a facile vacuum filtration method and thermal annealing at different temperatures. X-ray diffraction and X-ray photoelectron spectroscopy were employed to characterize the prepared samples, and then their electrochemical performance was investigated by galvanostatic charge/discharge (GCD) tests. GCD tests revealed that FNRGO prepared from thermal annealing at 500 degrees C exhibited good initial reversible capacity (502 mA h/g at 50 mA/g (0.14 C)) and enhanced cycle stability (capacity retention of 90.5% after 50th cycles at 100 mA/g (0.27 C), which demonstrated that FNRGOs were suitable candidates as anodes for LIBs.

Synergistic effects of alkylated graphene oxide on the properties of polypropylene-based carbon nanocomposites.

Polypropylene (PP)/carbon black (CB)-alkylated graphene oxide (AGO) hybrid nanocomposites were prepared via solution process and the synergistic effects of AGO on the properties of the PP/CB nanocomposites were investigated. AGO at a content of only 0.2 wt% formed an overlapped network structure in the PP matrix and affected the electrical, thermal and mechanical properties of the PP/CB nanocomposites. Specifically, PP/CB (5 wt%)-AGO (0.2 wt%) nanocomposites exhibited an electrical percolation threshold at lower CB contents than the PP/CB nanocomposites did, and the sheet resistance was decreased to 2.3 x 10(7) omega/sq. The thermal degradation temperature and recrystallization temperature of the PP/CB (10 wt%) nanocomposites were increased by 11.3 and 1.6 degrees C, respectively, by the addition of 0.2 wt% AGO. In addition, the Young's modulus of the PP/CB (10 wt%) nanocomposite was increased from 438.1 to 540.1 MPa.

Silver nanowire catalysts on carbon nanotubes-incorporated bacterial cellulose membrane electrodes for oxygen reduction reaction.

Silver nanowires have unique electrical, thermal and optical properties, which support their potential application in numerous fields including catalysis, electronics, optoelectronics, sensing, and surface-enhanced spectroscopy. Especially, their application such as catalysts for alkaline fuel cells (AFCs) have attracted much interest because of their superior electrical conductivity over that of any metal and their lower cost compared to Pt. In this study, multiwalled carbon nanotubes (MWCNTs)-incorporated bacterial cellulose (BC) membrane electrode with silver nanowire catalyst was prepared. First, acid-treated MWCNTs were incorporated into BC membranes and then freeze-dried after solvent exchange to tert-butanol in order to maintain the 3D-network macroporous structure. Second, silver nanowires synthesized by polyol process were introduced onto the surface of the MWCNTs-incorporated BC membrane through easy vacuum filtration. Finally, thermal treatment was carried out to confirm the effect of the PVP on the silver nanowire catalysts toward oxygen reduction reaction. The electrode with thermally treated silver nanowire had great electrocatalytic activity compared with non-treated one. These results suggest that the MWCNTs-incorporated BC electrode with silver nanowire catalysts after thermal treatment could be potentially used in cathodes of AFCs.

Amorphous carbon nanotube/MnO2/graphene oxide ternary composite electrodes for electrochemical capacitors.

Ternary composites of amorphous carbon nanotube/MnO2/graphene oxide (a-CNT/MnO2/GO) were synthesized by a facile direct redox reaction between potassium permanganate and a-CNT, which was prepared by anodic aluminum oxide template method following co-filtration with GO. Needle-like, 100-nm-thick, MnO2 crystals were homogeneously coated on the a-CNT surface, which was then covered with GO. The electrochemical performance of the resulting MnO2-coated a-CNTs exhibited a specific capacitance of 473 F/g at a scan rate of 5 mV/s, and excellent charge/discharge stability after 500 cycles.

Nanocomposites of polystyrene/polystyrene-grafted graphene oxides synthesized by in-situ bulk polymerization.

In this study, polystyrene-grafted graphene oxide (GO-g-PS) nanocomposites with different PS chain lengths were prepared by in-situ polymerization, and their reinforcing effect on the PS matrix was investigated. The glass transition (T(g)) and the thermal degradation (T(d)) temperatures of the PS/GO-g-PS nanocomposites were increased up to 2.8 degrees C and 23.9 degrees C, respectively. The addition of only 0.1 wt% of the GO-g-PS to the PS/GO-g-PS nanocomposites increased the tensile strength and Young's modulus by around 20.5% and 71.4%, respectively. These results showed that the thermal and mechanical properties of the PS/GO-g-PS nanocomposites gradually improved with increasing length of the PS chain grafted onto the GO surface. These differences in reinforcing effects were attributed to differences in interfacial interaction between the graphene and PS matrix.

Revisiting Lithium- and Sodium-Ion Storage in Hard Carbon Anodes.

The galvanostatic lithiation/sodiation voltage profiles of hard carbon anodes are simple, with a sloping drop followed by a plateau. However, a precise understanding of the corresponding redox sites and storage mechanisms is still elusive, which hinders further development in commercial applications. Here, a comprehensive comparison of the lithium- and sodium-ion storage behaviors of hard carbon is conducted, yielding the following key findings: 1) the sloping voltage section is presented by the lithium-ion intercalation in the graphitic lattices of hard carbons, whereas it mainly arises from the chemisorption of sodium ions on their inner surfaces constituting closed pores, even if the graphitic lattices are unoccupied; 2) the redox sites for the plateau capacities are the same as those for the closed pores regardless of the alkali ions; 3) the sodiation plateau capacities are mostly determined by the volume of the available closed pore, whereas the lithiation plateau capacities are primarily affected by the intercalation propensity; and 4) the intercalation preference and the plateau capacity have an inverse correlation. These findings from extensive characterizations and theoretical investigations provide a relatively clear elucidation of the electrochemical footprint of hard carbon anodes in relation to the redox mechanisms and storage sites for lithium and sodium ions, thereby providing a more rational design strategy for constructing better hard carbon anodes.

Enhanced thermal properties of graphene oxide-incorporated polymeric microspheres.

Polystyrene (PS) microspheres coated with graphene oxide (GO) were prepared and the variation of their thermal properties according to the GO loading was examined. The GO content in the PS-GO nanocomposites was controlled by the GO dispersions at various concentrations. The GO was coated onto the surface of the PS microspheres through the strong ionic interaction between polyvinylpyrrolidone and the GO sheet. The thermal properties of the GO incorporated PS microspheres were affected by the GO, which disturbed the chain activity and exhibited effective heat shielding. It also delayed the permeation of oxygen and hindered the escape of volatile degradation products from the PS-GO nanocomposites. In addition, the thermal degradation temperature of the nanocomposites was increased above 15 degrees C and their T(g) was also increased above 4.0 degrees C. PS-GO exhibited higher thermal conductivity (0.173 W/mK) than that of pure PS (0.117 W/mK).

Flexible bio-composites based on silks and celluloses.

Biomaterials have attracted worldwide attention due to the concerns regarding health and the environment. Silk, a natural protein produced by several species of insects, has been examined as a potential material for applications in many biotechnological and biomedical fields. However, regenerated silk fibroin has poor ductility and mechanical properties. Therefore, in this study, silk fibroin-cellulose composite films were prepared in an aqueous system to increase the ductility of regenerated silk fibroin. The morphology of the silk fibroin-cellulose composite film was observed by field emission scanning electron microscopy. The structure of the silk fibroin-cellulose composite films was examined by Fourier transform-infrared spectroscopy. The flexibility was analyzed using a bending test.

Understanding the Effects of Interfacial Lithium Ion Concentration on Lithium Metal Anode.

Despite the development of multidimensional state-of-the-art electrode materials for constructing better lithium metal anodes (LMAs), the key factors influencing the electrochemical performance of LMAs are still poorly understood. Herein, it is demonstrated that the local lithium ion concentration at the interface between the electrode and electrolyte exerts significant influence on the electrochemical performance of LMAs. The local ion concentration is multiplied by introducing pseudocapacitive nanocarbons (PNCs) containing numerous heteroatoms, because PNCs can store large numbers of lithium ions in a pseudocapacitive manner, and promote the formation of an electrochemical double layer. The high interfacial lithium ion concentration induces the formation of lithium-rich inorganic solid-electrolyte-interface layers with high ionic conductivities, and facilitates sustainable and stable supplies of lithium ion charge carriers on the overall active surfaces of the PNCs. Accordingly, the PNC-induced LMA exhibits high Coulombic efficiencies, high rate capabilities, and stable cycling performance.

Morphology and pore characteristics of bacterial cellulose/multiwalled carbon nanotube composite cryogels.

Bacterial cellulose/multiwalled carbon nanotube (MWCNT) composite cryogels were prepared via sol-gel chemistry using epichlorohydrin as a crosslinker. Their morphology and pore characteristics were examined under various conditions. The bacterial cellulose/MWCNT composite cryogels had a macroporous structure that contained mesopores and micropores due to the MWCNTs that were homogeneously incorporated in the macroporous network structure.

Alkylated graphene nanosheet composites with polyaniline nanofibers.

We demonstrate a simple method to prepare alkylated graphene/polyaniline composites (a-GR/PANI) using solution mixing of exfoliated alkyl Iodododecane treated graphene oxide sheets with polyaniline nanofiber; polyaniline nanofibers (PANI) prepared by using rapid mixing polymerization significantly improve the processibility of polyaniline and its performance in many conventional applications. Also, polyaniline nanofibers exhibit excellent water dispersibility due to their uniform nanofiber morphology. Morphological study using SEM and TEM analysis showed that the fibrous PANI in the composites a-GR/PANI mainly adsorbed onto the surface or intercalated between the graphene sheets, due especially to the good interfacial interaction between the alkylated gaphene and the polyaniline nanofibers. The existence of polyaniline nanofibers on the surface of the garphene and the alkylated graphene sheets was confirmed by using FT-IR, FT-Raman and X-ray diffraction analysis. Due to the good interfacial interaction between the alkylated graphene and the polyanilines nanofibers, the composite (a-GR/PANI) exhibited excellent dispersion stability in DMF compared to the same composite (GR/PANI) without alkylation. The electrical conductivity of the (GR/PANI) composite was 9% higher than that of pure PANI and the same weight percent for the composite after alkylation was 13% higher than that of pure PANI nanofibers.

Adsorption behavior of carbon nanotubes on polystyrene surfaces.

Polystyrene (PS) was prepared using two different polymerization methods (dispersion polymerization and seed polymerization) to investigate the steric stabilizer effect during the adsorption process of carbon nanotubes (CNTs) on the surface of PS microspheres. Experiments with different microsphere diameters and difference types of CNTs were conducted to analyze the curvature effect of the spheres on the adsorption mechanism. The results showed that PS microspheres prepared through dispersion polymerization exhibited preferable adsorption behavior compared to PS spheres prepared through seed polymerization, suggesting that poly(N-vinylpyrrolidone) led to improved adsorption interactions between the CNTs and the PS microspheres in the CNTs dispersion. Additionally, the PS diameter and CNT curvature were examined with respect to the adsorption behavior between the PS microspheres and the CNTs. Multiwalled carbon nanotubes (MWCNTs) were found to be well adsorbed on the surface of PS microspheres measuring 2 microm. However, the MWCNTs were adsorbed much less on the surface of submicron-sized PS microspheres, compared with thinwalled carbon nanotubes (TWCNTs). On the other hand, TWCNTs were found to be suitable for adsorption on submicron-sized PS microspheres. These results also indicate that the curvature of the CNTs and the polymer microspheres are important to the CNT adsorption process.

Stem cell response to multiwalled carbon nanotube-incorporated regenerated silk fibroin films.

Multiwalled carbon nanotubes (MWCNTs) are considered to be the ideal reinforcements for biorelated applications on account of their remarkable structural, mechanical and thermal properties. However, before MWCNTs can be incorporated into new and existing biomedical devices, their toxicity and biocompatibility need to be investigated thoroughly. In this study, regenerated silk fibroin/MWCNT nanocomposite films were prepared using a solvent system with pre-dispersed MWCNTs. Their biocompatibility was examined in vitro using human bone marrow stem cells. Scanning electron microscopy and a WST-1 assay demonstrated that the silk fibroin/MWCN film supported BMSC attachment and growth over 7 days in culture similar to the silk fibroin only film.

Effects of carbon black-carbon nanotube complex fillers on the properties of isotactic polypropylene nanocomposites.

In this study, the reinforcing effects of carbon black (CB) and carbon nanotube (CNT) complex fillers on the properties of isotactic polypropylene (iPP) nanocomposites were investigated using various methods. The surface of the CNTs was modified using a linear alkyl chain in order to create a homogeneous CNT dispersion in the iPP matrix. When the CB content that was incorporated in the iPP matrix increased, the thermal and mechanical properties of the iPP/CB nanocomposites were enhanced. Additionally these enhancements in the properties were similarly induced by introducing a small amount of alkylated CNTs (a-CNTs). In contrast, the CB/a-CNT complex filler was more effective for the iPP nanocomposites than the CB or a-CNT single filler in terms of the thermal stability and the electrical properties. However, the mechanical properties of the CB/a-CNT complex filler incorporated iPP nanocomposites were poorer than the only a-CNT incorporated iPP nanocomposites. Additionally, the complex filler did not overcome the nucleation behavior of the a-CNTs in the re-crystallization of iPP.