Structural Behavior of High Durability FRP Helical Screw Piles Installed in Reclaimed Saline Land.

The bearing capacity of fiber-reinforced plastic (FRP) helical screw piles is determined by the lesser of the breaking load at the bolted joint and the resistance provided by the screw tip area. In this study, compression and tensile tests were performed with the number of bolts and edge distance as variables. It showed similar strength when compared to the failure stress derived from material testing. In addition, considering load resistance performance, the optimal screw cross section was obtained through parametric analysis. Considering the structural behavior of the screw, a prediction equation was presented to design the screw cross-section as a tapered cross-section using a theoretical method. As a result of comparing the screw cross-section with the finite element analysis results, it was confirmed that the design stress and analysis stress showed an error of 1.1 MPa and were within the allowable stress of 80 MPa.

Determination of Mechanical Properties of Sand-Coated Carbon Fiber Reinforced Polymer (CFRP) Rebar.

This experimental study investigates the fundamental mechanical characteristics of the carbon fiber-reinforced polymer (CFRP) bars, including the tensile strength, compressive strength, shear strength, and modulus of elasticity of the CFRP bar. The properties need to be accurately determined to understand the behavior of the concrete structures reinforced with CFRP rebars. The CFRP rebar was coated with sand to enhance the adhesive strength of the concrete. Three diameters of CFRP rebar (D10, D12, and D16) were considered in accordance with ASTM provisions. A coefficient, i.e., the ratio of shear strength to tensile strength, was employed to predict the tensile strength of the CFRP rebar specimens. The test results confirm that the tensile strength of CFRP rebar is dependent on its diameter due to the shear lag effect. A coefficient in the range of 0.17 to 0.2 can be used to predict the tensile strength of CFRP rebar using shear strength.

Comparative Evaluation of Flexural Toughness of Steel Fiber-Reinforced Concrete Beams.

Specifications are available to quantify flexural performance of steel-fiber reinforced concrete beams with several parameters. Each specification provides different results. This study comparatively evaluates existing flexural beam test standards that are used to evaluate the flexural toughness of SFRC beam specimens. Two standards, EN-14651 and ASTM C1609, were followed to test SFRC beams under the three-point bending test (3PBT) and the four-point bending test (4PBT), respectively. Both normal tensile strength steel fiber (1200 MPa) and high tensile strength steel fiber (1500 MPa) in high-strength concrete were considered in this study. The reference parameters recommended in the two standards, which include equivalent flexural strength, residual strength, energy absorption capacity, and flexural toughness, were compared based on the tensile strength (normal or high) of the steel fiber in high-strength concrete. The 3PBT and 4PBT results indicate that both standard test methods yield similar results to quantify the flexural performance of SFRC specimens. However, unintended failure modes were observed for both standard test methods. The adopted correlation model shows that the flexural performance of SFRC is similar for 3PBTs and 4PBTs, but the residual strength obtained from the 3PBTs tends to be greater than that obtained from 4PBTs with an increase in the tensile strength of steel fiber.

Programmable Dynamics of Exchange-Biased Domain Wall via Spin-Current-Induced Antiferromagnet Switching.

Magnetic domain wall (DW) motion in perpendicularly magnetized materials is drawing increased attention due to the prospect of new type of information storage devices, such as racetrack memory. To augment the functionalities of DW motion-based devices, it is essential to improve controllability over the DW motion. Other than electric current, which is known to induce unidirectional shifting of a train of DWs, an application of in-plane magnetic field also enables the control of DW dynamics by rotating the DW magnetization and consequently modulating the inherited chiral DW structure. Applying an external bias field, however, is not a viable approach for the miniaturization of the devices as the external field acts globally. Here, the programmable exchange-coupled DW motion in the antiferromagnet (AFM)/ferromagnet (FM) system is demonstrated, where the role of an external in-plane field is replaced by the exchange bias field from AFM layer, enabling the external field-free modulations of DW motions. Interestingly, the direction of the exchange bias field can also be reconfigured by simply injecting spin currents through the device, enabling electrical and programmable operations of the device. Furthermore, the result inspires a prototype DW motion-based device based on the AFM/FM heterostructure, that could be easily integrated in logic devices.

Hierarchically Designed Nitrogen-Doped MoS2/Silicon Oxycarbide Nanoscale Heterostructure as High-Performance Sodium-Ion Battery Anode.

Molybedenum disulfide (MoS2) is regarded as a promising anode material for next-generation sodium-ion batteries (SIBs) owing to its high theoretical capacity. However, its low conductivity, large volume changes, and undesirable phase transformation hinder its practical applications. In this study, we synthesize a hierarchically designed core-shell heterostructure based on nitrogen-doped MoS2/C and silicon oxycarbide (SiOC) (N-MoS2/C@SiOC) via the facile pyrolysis of a suspension of an N-MoS2/polyfurfural precursor in silicone oil. The in situ nitrogen doping in a two-dimensional MoS2 structure with carbon incorporation leads to the enlargement of the interlayer spacing and enhancement of the electronic conductivity and mechanical stability, which allows the facile, highly reversible insertion and extraction of sodium ions upon cycling. Further, the nanoscale SiOC shell with surface capacitive reactivity provides a conductive pathway, preventing unfavorable side reactions at the electrode/electrolyte interface and acting as a structure-reinforcing buffer against severe volume expansion issues. As a result, the N-MoS2/C@SiOC composite exhibits high reversible capacity (540.7 mAh g-1), high-capacity retention (>100% after 200 cycles), and excellent rate capability up to 10 A g-1. The simple hierarchical core-shell design strategy developed in this study allows for the fabrication of high-performance metal sulfide anodes as well as other high-capacity anode materials for energy storage applications.

Shear Strengthening of High Strength Concrete Beams That Contain Hooked-End Steel Fiber.

Steel fiber has been used successfully in concrete mixtures to control volumetric changes, including shrinkage. However, the feasibility of the use of steel fiber has been restricted to nonstructural construction, such as 'slab on ground'. Recently, researchers have attempted to expand the applications of steel fiber to replace structural reinforcement (rebar) and have shown promising results in its substitution for shear reinforcement. Few studies have been conducted to ensure the feasibility of using steel fiber in structural components, however. This experimental study was designed to investigate the shear performance of steel fiber-reinforced concrete beams using the tensile strength of steel fiber and the shear span-to-depth ratio as variables. The experimental results indicate that the tensile strength of steel fiber significantly affects the shear strength of steel fiber-reinforced concrete beams, regardless of the shear span-to-depth ratio, and that steel fiber can play a role in shear reinforcement of concrete beams.

Bifunctional Surface Coating of LiNbO3 on High-Ni Layered Cathode Materials for Lithium-Ion Batteries.

High-Ni cathode materials with a layered structure generally suffer from structural instability induced by a highly reactive Ni component, especially at the surface. Crystalline LiNbO3, with excellent thermal stability and ionic conductivity, has the potential to considerably enhance the interfacial stability of these cathode materials. By optimizing the crystalline coating of bifunctional LiNbO3 on a high-Ni cathode material, we are able to improve cycle performance and rate capability by minimizing the direct exposure of Ni with electrolytes. Since a LiNbO3 coating layer directly affects electrochemical performance, we also focus on the correlation of LiNbO3 crystallinity with electrochemical behaviors of Li+ in the cathode materials. We show that the Li+ conducting behaviors are closely related to the crystallinity of LiNbO3. Highly crystalline LiNbO3 effectively suppresses the structural changes of the cathode materials by facilitating strain relaxation induced by repeated Li+ intercalation and deintercalation into and from the host structure. Moreover, it offers strong enhancement in mechanical and thermal stabilities at elevated temperatures above 60 °C. In this regard, this research provides a practical solution for successfully utilizing high-Ni layered cathode materials in commercial LIBs.

Selective TiO2 Nanolayer Coating by Polydopamine Modification for Highly Stable Ni-Rich Layered Oxides.

Ni-rich layered oxides are promising cathode materials for developing high-energy lithium-ion batteries. To overcome the major challenge of surface degradation, a TiO2 surface coating based on polydopamine (PDA) modification was investigated in this study. The PDA precoating layer had abundant OH catechol groups, which attracted Ti(OEt)4 molecules in ethanol solvent and contributed towards obtaining a uniform TiO2 nanolayer after calcination. Owing to the uniform coating of the TiO2 nanolayer, TiO2 -coated PDA-LiNi0.6 Co0.2 Mn0.2 O2 (TiO2 -PNCM) displayed an excellent electrochemical stability during cycling under high voltage (3.0-4.5 V vs. Li+ /Li), during which the cathode material undergoes a highly oxidative charge process. In addition, TiO2 -PNCM exhibited excellent cyclability at elevated temperature (60 °C) compared with the bare NCM. The surface degradation of the Ni-rich cathode material, which is accelerated under harsh cycling conditions, was effectively suppressed after the formation of an ultra-thin TiO2 coating layer.

The Influence of Steel Fiber Tensile Strengths and Aspect Ratios on the Fracture Properties of High-Strength Concrete.

Steel fiber embedded in concrete serves to reduce crack development and prevent crack growth at the macroscopic level of the concrete matrix. Steel fiber-reinforced concrete (SFRC) with high compressive concrete strength is affected primarily by the dimensions, shape, content, aspect ratio, and tensile strength of the embedded steel fiber. In this study, double-ended hook steel fiber was used in SFRC with a concrete compressive strength of 80 MPa. This fiber was used for the study variables with two aspect ratios (64, 80) and tensile strength values up to 1600 MPa. The flexural performance of the SFRC specimens was evaluated using crack mouth open displacement tests, and the test results were compared with code provisions. A modified reinforcement index was also used to quantify the flexural performance based on comparisons with fracture energy.

Unveiling the mechanism of sodium ion storage for needle-shaped ZnxCo3-xO4 nanosticks as anode materials.

The interest in the development of micro-nanostructured metal oxides has been increasing recently because of their advantages as electrode materials in energy storage applications. In this study, dandelion-like ZnxCo3-xO4 microspheres assembled with porous needle-shaped nanosticks were synthesized by co-precipitation followed by a post-annealing treatment. The open space between neighboring nanosticks enables easy infiltration of the electrolyte; therefore, each nanostick is surrounded by the electrolyte solution, which ensures proper utilization of the active material during the electrochemical reaction. The dandelion-like ZnxCo3-xO4 hierarchical microspheres exhibit a greatly improved electrochemical performance with a high capacity and good cyclability as anodes for sodium-ion batteries (SIBs). A high initial reversible capacity of 612 mA h g-1 (at 35 mA g-1, ∼0.04C) is obtained and a capacity of 349 mA h g-1 is retained after 200 cycles. Meanwhile, the electrode shows a high rate performance with a capacity of 246 mA h g-1 at 2.0C-rate. The conversion of ZnxCo3-xO4 with Na is followed by ex situ X-ray absorption spectroscopy (XAS) and transmission electron microscopy (TEM) in different sodiation/de-sodiation states during electrochemical cycling. These analyses reveal that Na insertion/extraction is followed by complete reduction/oxidation of both metallic cobalt and zinc. The development of metallic Co and Zn after complete discharge and the formation of Co3O4 and ZnO when the electrode was fully recharged were identified by ex situ TEM analysis. In addition, the ZnxCo3-xO4 anode demonstrates feasible operation in a full cell by pairing with a NaNi2/3Bi1/3O2 cathode, affording a sodium-ion battery with an average working voltage of 2.6 V.

Correction: Coaxial-nanostructured MnFe2O4 nanoparticles on polydopamine-coated MWCNT for anode materials in rechargeable batteries.

Correction for 'Coaxial-nanostructured MnFe2O4 nanoparticles on polydopamine-coated MWCNT for anode materials in rechargeable batteries' by Hyeongwoo Kim et al., Nanoscale, 2018, 10, 18949-18960.

Conducting Polymer Coating on a High-Voltage Cathode Based on Soft Chemistry Approach toward Improving Battery Performance.

The surface of a 5 V class LiNi0.5Mn1.5O4 particle is modified with poly(3,4-ethylenedioxythiophene) (PEDOT) conducting polymer by utilizing the hydrophobic characteristics of the 3,4-ethylenedioxythiophene (EDOT) monomer and the tail group of cetyl trimethyl ammonium bromide (CTAB) surfactants, in addition to the electrostatic attraction between cationic CTAB surfactant and cathode materials with a negative ζ potential in aqueous solution. With this novel concept, we design and prepare a uniform EDOT monomer layer on the cathode materials, and chemical polymerization of the EDOT coating layer is then carried out to achieve PEDOT-coated cathode materials via a simple one-pot preparation process. This uniform conducting polymer layer provides notable improvement in the power characteristics of electrodes, and stable electrochemical performance can be obtained especially at severe operating conditions such as the fully charged state and elevated temperatures owing to the successful suppression of the side reaction between the oxide particle and the electrolyte as well as the suppression of Mn dissolution from the oxide material.

Coaxial-nanostructured MnFe2O4 nanoparticles on polydopamine-coated MWCNT for anode materials in rechargeable batteries.

MnFe2O4@PDA-coated MWCNT coaxial nanocables are successfully designed via a simple one-pot process by utilizing the adhesion property of polydopamine (PDA) with cations in aqueous solutions and employing a modified co-precipitation synthesis at a low temperature. The incorporation of the PDA coating layer on the MWCNT leads to the well-dispersed state of the MWCNTs in the aqueous solution due to the hydrophilic functional group of the PDA coating layer. In addition, the catechol-based functional group of the PDA coating layer effectively anchors the Mn and Fe ions from the aqueous solution before the co-precipitation process, eventually resulting in the preferential and homogeneous formation of MnFe2O4 nanoparticles on the MWCNT. The final MnFe2O4@PDA-coated MWCNT electrode exhibits excellent power characteristics such as a high rate capacity of around of 367 mA h g-1 at a 5C-rate condition (= 4585 mA g-1). Cycling tests reveal that the stable performance of the MnFe2O4@PDA-coated MWCNT electrode persists even after 350 cycles.

Investigation of Thermal Stability of P2-NaxCoO2 Cathode Materials for Sodium Ion Batteries Using Real-Time Electron Microscopy.

Here, we take advantage of in situ transmission electron microscopy (TEM) to investigate the thermal stability of P2-type NaxCoO2 cathode materials for sodium ion batteries, which are promising candidates for next-generation lithium ion batteries. A double-tilt TEM heating holder was used to directly characterize the changes in the morphology and the crystallographic and electronic structures of the materials with increase in temperature. The electron diffraction patterns and the electron energy loss spectra demonstrated the presence of cobalt oxides (Co3O4, CoO) and even metallic cobalt (Co) at higher temperatures as a result of reduction of Co ions and loss of oxygen. The bright-field TEM images revealed that the surface of NaxCoO2 becomes porous at high temperatures. Higher cutoff voltages result in degrading thermal stability of NaxCoO2. The observations herein provide a valuable insight that thermal stability is one of the important factors to be considered in addition to the electrochemical properties when developing new electrode materials for novel battery systems.

Study on the Electrochemical Reaction Mechanism of NiFe2O4 as a High-Performance Anode for Li-Ion Batteries.

Nickel ferrite (NiFe2O4) has been previously shown to have a promising electrochemical performance for lithium-ion batteries (LIBs) as an anode material. However, associated electrochemical processes, along with structural changes, during conversion reactions are hardly studied. Nanocrystalline NiFe2O4 was synthesized with the aid of a simple citric acid assisted sol-gel method and tested as a negative electrode for LIBs. After 100 cycles at a constant current density of 0.5 A g-1 (about a 0.5 C-rate), the synthesized NiFe2O4 electrode provided a stable reversible capacity of 786 mAh g-1 with a capacity retention greater than 85%. The NiFe2O4 electrode achieved a specific capacity of 365 mAh g-1 when cycled at a current density of 10 A g-1 (about a 10 C-rate). At such a high current density, this is an outstanding capacity for NiFe2O4 nanoparticles as an anode. Ex-situ X-ray diffraction (XRD) and X-ray absorption spectroscopy (XAS) were employed at different potential states during the cell operation to elucidate the conversion process of a NiFe2O4 anode and the capacity contribution from either Ni or Fe. Investigation reveals that the lithium extraction reaction does not fully agree with the previously reported one and is found to be a hindered oxidation of metallic nickel to nickel oxide in the applied potential window. Our findings suggest that iron is participating in an electrochemical reaction with full reversibility and forms iron oxide in the fully charged state, while nickel is found to be the cause of partial irreversible capacity where it exists in both metallic nickel and nickel oxide phases.

Hygral Behavior of Superabsorbent Polymers with Various Particle Sizes and Cross-Linking Densities.

This study focuses on investigating the effects of particle size and cross-linking density on the hygral behavior of superabsorbent polymers (SAPs), which are increasingly used as an internal curing material for high-performance concrete. Four SAPs with different mean particle diameters and cross-linking densities were tested under controlled wetting and drying conditions to measure free absorption and desorption kinetics. Absorption capacities of SAPs under actual mixing conditions were additionally measured and verified by means of mortar flow and semi-adiabatic hydration heat measurements. In addition, the effects of SAP type and dosage (i.e., 0.2, 0.4, and 0.6% by mass of cement) on the mechanical properties of hardened mortar were assessed. The results indicated that: (1) the absorption capacity increased with decreased cross-linking density and increased particle size under both load-free and mixing conditions; and (2) the greater the cross-linking density and the lower the particle size, the shorter the desorption time. It was also confirmed that while the early-age mechanical properties were more related with the gel strength of swollen SAP, the later-age mechanical properties were more affected by the water retention capacity and spatial distribution of SAP in the matrix.

One-Step Catalytic Synthesis of CuO/Cu2O in a Graphitized Porous C Matrix Derived from the Cu-Based Metal-Organic Framework for Li- and Na-Ion Batteries.

The hybrid composite electrode comprising CuO and Cu2O micronanoparticles in a highly graphitized porous C matrix (CuO/Cu2O-GPC) has a rational design and is a favorable approach to increasing the rate capability and reversible capacity of metal oxide negative materials for Li- and Na-ion batteries. CuO/Cu2O-GPC is synthesized through a Cu-based metal-organic framework via a one-step thermal transformation process. The electrochemical performances of the CuO/Cu2O-GPC negative electrode in Li- and Na-ion batteries are systematically studied and exhibit excellent capacities of 887.3 mAh g(-1) at 60 mA g(-1) after 200 cycles in a Li-ion battery and 302.9 mAh g(-1) at 50 mA g(-1) after 200 cycles in a Na-ion battery. The high electrochemical stability was obtained via the rational strategy, mainly owing to the synergy effect of the CuO and Cu2O micronanoparticles and highly graphitized porous C formed by catalytic graphitization of Cu nanoparticles. Owing to the simple one-step thermal transformation process and resulting high electrochemical performance, CuO/Cu2O-GPC is one of the prospective negative active materials for rechargeable Li- and Na-ion batteries.

Layered-Layered-Spinel Cathode Materials Prepared by a High-Energy Ball-Milling Process for Lithium-ion Batteries.

In this work, we report the electrochemical properties of 0.5Li2MnO3·0.25LiNi0.5Co0.2Mn0.3O2·0.25LiNi0.5Mn1.5O4 and 0.333Li2MnO3·0.333LiNi0.5Co0.2Mn0.3O2·0.333LiNi0.5Mn1.5O4 layered-layered-spinel (L*LS) cathode materials prepared by a high-energy ball-milling process. Our L*LS cathode materials can deliver a large and stable capacity of ∼200 mAh g(-1) at high voltages up to 4.9 V, and do not show the anomalous capacity increase upon cycling observed in previously reported three-component cathode materials synthesized with different routes. Furthermore, we have performed synchrotron-based in situ X-ray diffraction measurements and found that there are no significant structural distortions during charge/discharge runs. Lastly, we carry out (opt-type) van der Waals-corrected density functional theory (DFT) calculations to explain the enhanced cycle characteristics and reduced phase transformations in our ball-milled L*LS cathode materials. Our simple synthesis method brings a new perspective on the use of the high-power L*LS cathodes in practical devices.

Carbon-Coated Li4Ti5O12 as Anode Material for Sodium-Ion Batteries.

The surface-coating of carbon was performed on the spinel Li4Ti5O12 materials for the electrochemical sodium insertion in sodium ion battery application. The carbon-coated Li4Ti5O12 was synthesized by using the citric acid sol-gel method. Carbon-coated Li4Ti5O12 exhibits superior cycle performance as well as the rate capability in comparison to the pristine Li4Ti5O12. Electrochemical impedance spectroscopy analyses also reveal that surface modification with carbon suppresses the increase in resistance concerning charge transfer reaction as well as solid electrolyte interface layer formation during cycle test.

Coating lithium titanate with nitrogen-doped carbon by simple refluxing for high-power lithium-ion batteries.

Nitrogen-doped carbon is coated on lithium titanate (Li4Ti5O12, LTO) via a simple chemical refluxing process, using ethylenediamine (EDA) as the carbon and nitrogen source. The process incorporates a carbon coating doped with a relatively high amount of nitrogen to form a conducting network on the LTO matrix. The introduction of N dopants in the carbon matrix leads to a higher density of C vacancies, resulting in improved lithium-ion diffusion. The uniform coating of nitrogen-doped carbon on Li4Ti5O12 (CN-LTO) enhances the electronic conductivity of a CN-LTO electrode and the corresponding electrochemical properties of the cell employing the electrode. The results of our study demonstrate that the CN-LTO anode exhibits higher rate capability and cycling performance over 100 cycles. From the electrochemical tests performed, the specific capacity of CN-LTO electrode at higher rates of 20 and 50 C are found to be 140.7 and 82.3 mAh g(-1), respectively. In addition, the CN-Li4Ti5O12 anode attained higher capacity retention of 100% at 1 C rate after 100 cycles and 92.9% at 10 C rate after 300 cycles.