Pu Hu

Nickel Disulfide–Graphene Nanosheets Composites with Improved Electrochemical Performance for Sodium Ion Battery

Nickel disulfide-graphene nanosheets (NiS2-GNS) composites were successfully synthesized via a simple and mild hydrothermal method. It was revealed by scanning electron microscopy and transmission electron microscopy images that the spherical NiS2 nanoparticles with a diameter of 200-300 nm were uniformly dispersed on graphene nanosheets. Na(+) electrochemical storage properties including cycling performance and high-rate capability of NiS2-GNS composites were investigated, demonstrating a superior reversible capacity of 407 mAh g(-1) with the capacity retention of 77% over 200 cycles at a current density of 0.1 C. Furthermore, even at a large current density of 2 C, a high capacity of 168 mAh g(-1) can still remain, which is much higher than that of pristine NiS2 materials. The enhancement in electrochemical properties might be attributed to the synergetic effect endowed by high conductivity of graphene and novel structure of the electrode material. Combined with the advantages of low cost and environmental benignity, NiS2-GNS composite would be a potential anode material for sodium ion batteries.

Compatible interface design of CoO-based Li-O 2 battery cathodes with long-cycling stability

Lithium-oxygen batteries with high theoretical energy densities have great potential. Recent studies have focused on different cathode architecture design to address poor cycling performance, while the impact of interface stability on cathode side has been barely reported. In this study, we introduce CoO mesoporous spheres into cathode, where the growth of crystalline discharge products (Li2O2) is directly observed on the CoO surface from aberration-corrected STEM. This CoO based cathode demonstrates more than 300 discharge/charge cycles with excessive lithium anode. Under deep discharge/charge, CoO cathode exhibited superior cycle performance than that of Co3O4 with similar nanostructure. This improved cycle performance can be ascribed to a more favorable adsorption configuration of Li2O2 intermediates (LiO2) on CoO surface, which is demonstrated through DFT calculation. The favorable adsorption of LiO2 plays an important role in the enhanced cycle performance, which reduced the contact of LiO2 to carbon materials and further alleviated the side reactions during charge process. This compatible interface design may provide an effective approach in protecting carbon-based cathodes in metal-oxygen batteries.

Taichi-inspired rigid-flexible coupling cellulose-supported solid polymer electrolyte for high-performance lithium batteries

Inspired by Taichi, we proposed rigid-flexible coupling concept and herein developed a highly promising solid polymer electrolyte comprised of poly (ethylene oxide), poly (cyano acrylate), lithium bis(oxalate)borate and robust cellulose nonwoven. Our investigation revealed that this new class solid polymer electrolyte possessed comprehensive properties in high mechanical integrity strength, sufficient ionic conductivity (3 × 10−4 S cm−1) at 60°C and improved dimensional thermostability (up to 160°C). In addition, the lithium iron phosphate (LiFePO4)/lithium (Li) cell using such solid polymer electrolyte displayed superior rate capacity (up to 6 C) and stable cycle performance at 80°C. Furthermore, the LiFePO4/Li battery could also operate very well even at an elevated temperature of 160°C, thus improving enhanced safety performance of lithium batteries. The use of this solid polymer electrolyte mitigates the safety risk and widens the operation temperature range of lithium batteries. Thus, this fascinating study demonstrates a proof of concept of the use of rigid-flexible coupling solid polymer electrolyte toward practical lithium battery applications with improved reliability and safety.

Rigid-Flexible Coupling High Ionic Conductivity Polymer Electrolyte for an Enhanced Performance of LiMn2O4/Graphite Battery at Elevated Temperature

LiMn2O4-based batteries exhibit severe capacity fading during cycling or storage in LiPF6-based liquid electrolytes, especially at elevated temperatures. Herein, a novel rigid-flexible gel polymer electrolyte is introduced to enhance the cyclability of LiMn2O4/graphite battery at elevated temperature. The polymer electrolyte consists of a robust natural cellulose skeletal incorporated with soft segment poly(ethyl α-cyanoacrylate). The introduction of the cellulose effectively overcomes the drawback of poor mechanical integrity of the gel polymer electrolyte. Density functional theory (DFT) calculation demonstrates that the poly(ethyl α-cyanoacrylate) matrices effectively dissociate the lithium salt to facilitate ionic transport and thus has a higher ionic conductivity at room temperature. Ionic conductivity of the gel polymer electrolyte is 3.3 × 10(-3) S cm(-1) at room temperature. The gel polymer electrolyte remarkably improves the cycling performance of LiMn2O4-based batteries, especially at elevated temperatures. The capacity retention after the 100th cycle is 82% at 55 °C, which is much higher than that of liquid electrolyte (1 M LiPF6 in carbonate solvents). The polymer electrolyte can significantly suppress the dissolution of Mn(2+) from surface of LiMn2O4 because of strong interaction energy of Mn(2+) with PECA, which was investigated by DFT calculation.

Ultrafast Alkaline Ni/Zn Battery Based on Ni-Foam-Supported Ni3S2 Nanosheets

Self-supported Ni3S2 ultrathin nanosheets were in situ formed by direct sulfurization of commercially available nickel foam using thioacetamide as sulfur source under hydrothermal process. The morphology and structure of the as-obtained sample were analyzed by using XRD, XPS, SEM, and TEM, revealing that an ultrathin nanosheets Ni3S2 were grown on the surface of Ni form. The as-obtained Ni3S2/Ni composite with uniform architecture was used as cathode material for alkaline Ni/Zn battery, which delivered high capacity of 125 mAh g(-1) after 100 cycles with no obvious capacity fading, extraordinary rate capability (68 mAh g(-1) at the current density of 5.0 A g(-1)), and high operating voltage (1.75 V).

Conjugated microporous polymers with excellent electrochemical performance for lithium and sodium storage

Conjugated microporous polymers, which exhibit high specific capacity, superior cycle stability and remarkable rate capability, are explored as high-performance electrode materials for lithium and sodium storage. Their excellent electrochemical performance can be attributed to their conductive frameworks, plentiful redox-active units, high specific surface area and homogeneous microporous structure.

Progress in nitrile-based polymer electrolytes for high performance lithium batteries

Nitrile or cyano-based compounds have aroused interest in high performance battery electrolyte fields due to their unique characteristics such as a high dielectric constant, high anodic oxidization potential and favorable interaction with lithium ions. Particularly, owing to the presence of a unique plastic-crystalline phase, succinonitrile/salt-based solid electrolytes possess an ultra high ionic conductivity of more than 10−3 S cm−1 at room temperature. Herein, recent progress in nitrile-based polymer electrolytes has been reviewed in terms of their potential application in flexible, solid-state or high voltage lithium batteries. Factors affecting the ionic conductivity of nitrile-based electrolytes have also been summarized. We hope that fresh and established researchers can obtain a clear perspective of nitrile based polymer electrolytes and our mini review can spur more extensive interest for the exploration of high performance batteries.

A high-voltage poly(methylethyl α-cyanoacrylate) composite polymer electrolyte for 5 V lithium batteries

High-voltage lithium batteries have attracted increasing attention for large scale energy storage application in electric vehicles, smart grids and other electronic devices. However, a major bottleneck to achieve high-voltage lithium batteries is the anodic voltage stability of electrolytes. Herein, we fabricate a composite polymer electrolyte, comprised of poly(methylethyl α-cyanoacrylate), nonwoven polytetrafluoroethylene and lithium bis(oxalate)borate salt. The composite polymer electrolyte presents a wide electrochemical window, which is explored to address the above-mentioned bottleneck. It is demonstrated that such a composite polymer electrolyte exhibits a higher ionic conductivity (1.24 mS cm−1 at 25 °C), better dimensional thermal resistance (150 °C) and higher ion transference number (0.63) compared to those of commercially available liquid electrolytes with a polypropylene separator. In addition, LiNi0.5Mn1.5O4/Li batteries employing such a composite polymer electrolyte deliver excellent cycling performance and outstanding rate capability. So, it is demonstrated that the poly(methylethyl α-cyanoacrylate) based polymer electrolyte appears to be a promising candidate of high-voltage lithium battery electrolyte towards next generation high energy density batteries.

Single-ion dominantly conducting polyborates towards high performance electrolytes in lithium batteries

A couple of thermally stable polyborate salts, polymeric lithium pentaerythrite borate (PLPB) and polymeric lithium di(trimethylolpropane) borate (PLDB), for applications in lithium ion batteries were synthesized via a facile one-step reaction in aqueous solution. Both the lithium polyborate salts exhibited a high thermal decomposition temperature at about 240 degrees C. Besides, their corresponding single-ion dominantly conducting gel polymer electrolytes of ethylene carbonate (EC) and dimethyl carbonate (DMC) (1 : 1, v/v) swollen PLPB@PVDF-HFP (poly(vinylidenefluoride-co-hexafluoropropene)) and PLDB@PVDF-HFP exhibited favorable ionic conductivity over a wide temperature range, superior electrochemical stability, high lithium ion transference number and Al passivating ability. The Li/LiFePO4 batteries using these single-ion dominantly conducting electrolytes exhibited stable charge-discharge behavior and excellent cycling performance both at room temperature and at elevated temperatures. These superior performances could make this class of gel polymer electrolytes very promising candidates for lithium batteries especially at elevated temperatures.

Boron Substituted Na3V2(P1−xBxO4)3 Cathode Materials with Enhanced Performance for Sodium-Ion Batteries

The development of excellent performance of Na‐ion batteries remains great challenge owing to the poor stability and sluggish kinetics of cathode materials. Herein, B substituted Na3V2P3 –xBxO12 (0 ≤ x ≤ 1) as stable cathode materials for Na‐ion battery is presented. A combined experimental and theoretical investigations on Na3V2P3 –xBxO12 (0 ≤ x ≤ 1) are undertaken to reveal the evolution of crystal and electronic structures and Na storage properties associated with various concentration of B. X‐ray diffraction results indicate that the crystal structure of Na3V2P3 –xBxO12 (0 ≤ x ≤ 1/3) consisted of rhombohedral Na3V2(PO4)3 with tiny shrinkage of crystal lattice. X‐ray absorption spectra and the calculated crystal structures all suggest that the detailed local structural distortion of substituted materials originates from the slight reduction of V–O distances. Na3V2P3‐1/6B1/6O12 significantly enhances the structural stability and electrochemical performance, giving remarkable enhanced capacity of 100 and 70 mAh g−1 when the C‐rate increases to 5 C and 10 C. Spin‐polarized density functional theory (DFT) calculation reveals that, as compared with the pristine Na3V2(PO4)3, the superior electrochemical performance of the substituted materials can be attributed to the emergence of new boundary states near the band gap, lower Na+ diffusion energy barriers, and higher structure stability.