Battery-Type-Behavior-Retention Ni(OH)2-rGO Composite for an Ultrahigh-Specific-Capacity Asymmetric Electrochemical Capacitor Electrode.

Nanosized battery-type materials applied in electrochemical capacitors can effectively reduce a series of problems caused by low conductivity and large volume changes. However, this approach will lead to the charging and discharging process being dominated by capacitive behavior, resulting in a serious decline in the specific capacity of the material. By controlling the material particles to an appropriate size and a suitable number of nanosheet layers, the battery-type behavior can be retained to maintain a large capacity. Here, Ni(OH)2, which is a typical battery-type material, is grown on the surface of reduced graphene oxide to prepare a composite electrode. By controlling the dosage of the nickel source, the composite material with an appropriate Ni(OH)2 nanosheet size and a suitable number of layers was prepared. The high-capacity electrode material was obtained by retaining the battery-type behavior. The prepared electrode had a specific capacity of 397.22 mA h g-1 at 2 A g-1. After the current density was increased to 20 A g-1, the retention rate was as high as 84%. The prepared asymmetric electrochemical capacitor had an energy density of 30.91 W h kg-1 at a power density of 1319.86 W kg-1 and the retention rate could reach 79% after 20,000 cycles. We advocate an optimization strategy that retains the battery-type behavior of electrode materials by increasing the size of nanosheets and the number of layers, which can significantly improve the energy density while combining the advantage of the high rate capability of the electrochemical capacitor.

Polyethylene Oxide as a Multifunctional Binder for High-Performance Ternary Layered Cathodes.

Nickel cobalt manganese ternary cathode materials are some of the most promising cathode materials in lithium-ion batteries, due to their high specific capacity, low cost, etc. However, they do have a few disadvantages, such as an unstable cycle performance and a poor rate performance. In this work, polyethylene oxide (PEO) with high ionic conductance and flexibility was utilized as a multifunctional binder to improve the electrochemical performance of LiNi0.6Co0.2Mn0.2O2 cathode materials. Scanning electron microscopy showed that the addition of PEO can greatly improve the adhesion of the electrode components and simultaneously enhance the integrity of the electrode. Thus, the PEO-based electrode (20 wt% PEO in PEO/PVDF) shows a high electronic conductivity of 19.8 S/cm, which is around 15,000 times that of the pristine PVDF-based electrode. Moreover, the PEO-based electrode exhibits better cycling stability and rate performance, i.e., the capacity increases from 131.1 mAh/g to 147.3 mAh/g at 2 C with 20 wt% PEO addition. Electrochemical impedance measurements further indicate that the addition of the PEO binder can reduce the electrode resistance and protect the LiNi0.6Co0.2Mn0.2O2 cathode materials from the liquid electrolyte attack. This work offers a simple yet effective method to improve the cycling performance of the ternary cathode materials by adding an appropriate amount of PEO as a binder in the electrode fabrication process.

Localized Electrons Enhanced Ion Transport for Ultrafast Electrochemical Energy Storage.

The rate-determining process for electrochemical energy storage is largely determined by ion transport occurring in the electrode materials. Apart from decreasing the distance of ion diffusion, the enhancement of ionic mobility is crucial for ion transport. Here, a localized electron enhanced ion transport mechanism to promote ion mobility for ultrafast energy storage is proposed. Theoretical calculations and analysis reveal that highly localized electrons can be induced by intrinsic defects, and the migration barrier of ions can be obviously reduced. Consistently, experiment results reveal that this mechanism leads to an enhancement of Li/Na ion diffusivity by two orders of magnitude. At high mass loading of 10 mg cm-2 and high rate of 10C, a reversible energy storage capacity up to 190 mAh g-1 is achieved, which is ten times greater than achievable by commercial crystals with comparable dimensions.

Well-constructed silicon-based materials as high-performance lithium-ion battery anodes.

Silicon has been considered as one of the most promising anode material alternates for next-generation lithium-ion batteries, because of its high theoretical capacity, environmental friendliness, high safety, low cost, etc. Nevertheless, silicon-based anode materials (especially bulk silicon) suffer from severe capacity fading resulting from their low intrinsic electrical conductivity and great volume variation during lithiation/delithiation processes. To address this challenge, a few special constructions from nanostructures to anchored, flexible, sandwich, core-shell, porous and even integrated structures, have been well designed and fabricated to effectively improve the cycling performance of silicon-based anodes. In view of the fast development of silicon-based anode materials, we summarize their recent progress in structural design principles, preparation methods, morphological characteristics and electrochemical performance by highlighting the material structure. We also point out the associated problems and challenges faced by these anodes and introduce some feasible strategies to further boost their electrochemical performance. Furthermore, we give a few suggestions relating to the developing trends to better mature their practical applications in next-generation lithium-ion batteries.

Low-current field-assisted assembly of copper nanoparticles for current collectors.

Current collectors are essential features of batteries and many other electronic devices being responsible for efficient charge transport to active electrode materials. Three-dimensional (3D), high surface area current collectors considerably improve the performance of cathodes and anodes in batteries, but their technological implementation is impeded by the complexity of their preparation, which needs to be simple, fast, and energy efficient. Here we demonstrate that field-stimulated assembly of ∼3 nm copper nanoparticles (NPs) enables the preparation of porous Cu NP films. The use of NP dispersions enables 30× reduction of the deposition current for making functional 3D coatings. In addition to high surface area, lattice-to-lattice connectivity in the self-assembly of NPs in 3D structures enables fast charge transport. The mesoscale dimensions of out-of-plane features and the spacing between them in Cu films made by field-stimulated self-assembly of NPs provides promising morphology for current collection in lithium ion batteries (LIBs). Half-cell electrochemical models based on self-assembled films show improved specific capacity, total capacity, and cycling performance compared to traditional flat and other 3D current collectors. While integration of active electrode material into the 3D topography of the current collector needs to be improved, this study indicates that self-assembled NP films represent a viable manufacturing approach for 3D electrodes.