Towards High-Performance Supercapacitor Electrodes via Achieving 3D Cross-Network and Favorable Surface Chemistry.

Transition metal phosphides/phosphates (TMPs) are considered appealing electrode materials in energy-related fields, especially in supercapacitors. However, the dilemma of inadequate electrode kinetics and dimensional unreliability evoked by a huge volume variation during cycling significantly plagues their progress. To mitigate this issue, in this work, a 3D cross-network in situ assembled via self-derived N-doped carbon hybrid Ni-Co-P/POx 2D sheets is fabricated. Particularly, high-Fermi-level N-doped carbon well confines Ni-Co-P/POx nanoparticles at the molecular level, and N-doping leads to redistribution of spin/electron density in the carbon skeleton, effectively regulating the electron environment of nearby Ni-Co-based moieties, resulting in a relatively lower surface work function, as known via experimental and Kelvin probe force microscopy (KPFM) results, which favors electron flee from the electrode surface and facilitates electron transport toward a rapid supercapacitor response. Moreover, the well-defined 3D cross-network architectures featured with in-plane pores and interconnected with each other can provide more ion/electron transfer pathways and 2D sheets with excellent surface chemistry available for sustainable ion/electron mobility, synergistically affording the favorable electrode kinetics. Accordingly, the resultant Ni-Co-P/POx@NC electrode shows admirable specific capacitance, excellent rate survivability, and long-term cyclability. The as-assembled asymmetric device exhibits remarkable energy and power outputs (48.5 Wh kg-1 and 7500 W kg-1), superior to many reported devices. Furthermore, our devices possess the prominent ability to power a commercial electronic thermometer for 1560 s at least, showcasing superb application prospects.

Graphene Quantum Dots Pinned on Nanosheets-Assembled NiCo-LDH Hollow Micro-Tunnels: Toward High-Performance Pouch-Type Supercapacitor via the Regulated Electron Localization.

A combined delicate micro-/nano-architecture and corresponding surface modification at the nanometer level can co-tailor the physicochemical properties to realize an advanced supercapacitor electrode material. Herein, nanosheets-assembled nickel-cobalt-layered double hydroxide (NiCo-LDH) hollow micro-tunnels strongly coupled with higher-Fermi-level graphene quantum dots (GQDs) are reported. The unique hollow structure endows the electrolyte accessible to more electroactive sites, while 2D nanosheets have excellent surface chemistry, which favors rapid ion/electron transfer, synergistically resulting in more super-capacitive activities. The experimental and density functional theory calculations recognize that such a precise decoration generally tunes the charge density distribution at the near-surface due to the Fermi-level difference of two components, thus regulating the electron localization, while decorating with conductive GQDs co-improves the charge mobility, affording superior capacitive response and electrode integrity. The as-acquired GQDs@LDH-2 electrode yields excellent capacitance reaching ≈1628 F g-1 at 1 A g-1 and durable cycling longevity (86.2% capacitive retention after 8000 cycles). When coupled with reduced graphene oxide-based negative electrode, the hybrid device unveils an impressive energy/power density (46 Wh kg-1 / 7440 W kg-1 ); moreover, a flexible pouch-type supercapacitor can be constructed based on this hybrid system, which holds high mechanical properties and stable energy and power output at various situations, showcasing superb application prospects.

Preparation of Lithium Titanate/Reduced Graphene Oxide Composites with Three-Dimensional "Fishnet-Like" Conductive Structure via a Gas-Foaming Method for High-Rate Lithium-Ion Batteries.

With use of ammonium chloride (NH4Cl) as the pore-forming agent, three-dimensional (3D) "fishnet-like" lithium titanate/reduced graphene oxide (LTO/G) composites with hierarchical porous structure are prepared via a gas-foaming method. Scanning electron microscopy and transmission electron microscopy images show that, in the composite prepared with the NH4Cl concentration of 1 mg mL-1 (1-LTO/G), LTO particles with sizes of 50-100 nm disperse homogeneously on the 3D "fishnet-like" graphene. The nitrogen-sorption analyses reveal the existence of micro-/mesopores, which is attributed to the introduction of NH4Cl into the gap between the graphene sheets that further decomposes into gases and produces hierarchical pores during the thermal treatment process. The loose and porous structure of 1-LTO/G composites enables the better penetration of electrolytes, providing more rapid diffusion channels for lithium ion. As a result, the 1-LTO/G electrode delivers an ultrahigh specific capacity of 176.6 mA h g-1 at a rate of 1 C. Even at 3 and 10 C, the specific capacity can reach 167.5 and 142.9 mA h g-1, respectively. Moreover, the 1-LTO/G electrode shows excellent cycle performance with 95.4% capacity retention at 10 C after 100 cycles. The results demonstrate that the LTO/G composite with these properties is one of the most promising anode materials for lithium-ion batteries.

Supramolecule-Inspired Fabrication of Carbon Nanoparticles In Situ Anchored Graphene Nanosheets Material for High-Performance Supercapacitors.

The remarkable electrochemical performance of graphene-based materials has drawn a tremendous amount of attention for their application in supercapacitors. Inspired by supramolecular chemistry, the supramolecular hydrogel is prepared by linking ß-cyclodextrin to graphene oxide (GO). The carbon nanoparticles-anchored graphene nanosheets are then assembled after the hydrothermal reduction and carbonization of the supramolecular hydrogels; here, the ß-cyclodextrin is carbonized to carbon nanoparticles that are uniformly anchored on the graphene nanosheets. Transmission electron microscopy reveals that carbon nanoparticles with several nanometers are uniformly anchored on both sides of graphene nanosheets, and X-ray diffraction spectra demonstrate that the interlayer spacing of graphene is enlarged due to the anchored nanoparticles among the graphene nanosheets. The as-prepared carbon nanoparticles-anchored graphene nanosheets material (C/r-GO-1:3) possesses a high specific capacitance (310.8 F g-1, 0.5 A g-1), superior rate capability (242.5 F g-1, 10 A g-1), and excellent cycle stability (almost 100% after 10 000 cycles, at the scan rate of 50 mV s-1). The outstanding electrochemical performance of the resulting C/r-GO-1:3 is mainly attributed to (i) the presence of the carbon nanoparticles, (ii) the enlarged interlayer spacing of the graphene sheets, and (iii) the accelerated ion transport rates toward the interior of the electrode material. The supramolecule-inspired approach for the synthesis of high-performance carbon nanoparticles-modified graphene sheets material is promising for future application in graphene-based energy storage devices.

Performance of Solid Oxide Fuel Cell With La and Cr Co-doped SrTiO3 as Anode.

The La0.3Sr0.55Ti0.9Cr0.1O3-δ (LSTC10) anode material was synthesized by citric acid-nitrate process. The yttria-stabilized zirconia (YSZ) electrolyte-supported cell was fabricated by screen printing method using LSTC10 as anode and (La0.75Sr0.25)0.95MnO3-δ (LSM) as cathode. The electrochemical performance of cell was tested by using dry hydrogen as fuel and air as oxidant in the temperature range of 800-900 °C. At 900 °C, the open circuit voltage (OCV) and the maximum power density of cell are 1.08 V and 13.0 mW·cm-2, respectively. The microstructures of cell after performance testing were investigated by scanning electron microscope (SEM). The results show that the anode and cathode films are porous and closely attached to the YSZ electrolyte. LSTC10 is believed to be a kind of potential solid oxide fuel cell (SOFC) anode material.

Effect of activated carbon fiber anode structure and electrolysis conditions on electrochemical degradation of dye wastewater.

The alizarin red S (ARS) in simulated dye wastewater was electrochemically oxidized using an activated carbon fiber (ACF) felt as an anode. The influence of electrolytic conditions and anode structure on the dye degradation was investigated. The results indicated that initial pH, current density and supporting electrolyte type all played an important role in the dye degradation. The chemical oxygen demand (COD) removal efficiency of dye solution in neutral or alkaline medium was about 74% after 60 min of electrolysis, which was higher than that in acidic medium. Increasing current density would lead to a corresponding increase in the dye removal. The addition of NaCl could also improve the treatment effect by enhancing the COD removal efficiency 10.3%. For ACF anodes, larger specific surface area and higher mesopore percentage could ensure more effective electrochemical degradation of dye. The data showed that the color removal efficiency increased from 54.2 to 83.9% with the specific surface area of ACF anodes increasing correspondingly from 894 to 1,682 m(2)/g.