Hierarchical porous nitrogen-doped carbon (HPNC) nanosheets (NS) have been prepared via simultaneous activation and graphitization of biomass-derived natural silk. The as-obtained HPNC-NS show favorable features for electrochemical energy storage such as high specific surface area (SBET: 2494 m(2)/g), high volume of hierarchical pores (2.28 cm(3)/g), nanosheet structures, rich N-doping (4.7%), and defects. With respect to the multiple synergistic effects of these features, a lithium-ion battery anode and a two-electrode-based supercapacitor have been prepared. A reversible lithium storage capacity of 1865 mA h/g has been reported, which is the highest for N-doped carbon anode materials to the best of our knowledge. The HPNC-NS supercapacitor's electrode in ionic liquid electrolytes exhibit a capacitance of 242 F/g and energy density of 102 W h/kg (48 W h/L), with high cycling life stability (9% loss after 10,000 cycles). Thus, a high-performance Li-ion battery and supercapacitors were successfully assembled for the same electrode material, which was obtained through a one-step and facile large-scale synthesis route. It is promising for next-generation hybrid energy storage and renewable delivery devices.

Nanocomposites of CNTs and Nb2O5 nanocrystals were fabricated exhibiting excellent conductivity, high specific capacitance, and large voltage window, which led to successful fabrication of asymmetric supercapacitors with high energy densities, power densities, and cycling stability.

The research and development of advanced energy-storage systems must meet a large number of requirements, including high energy density, natural abundance of the raw material, low cost and environmental friendliness, and particularly reasonable safety. As the demands of high-performance batteries are continuously increasing, with large-scale energy storage systems and electric mobility equipment, lithium-sulfur batteries have become an attractive candidate for the new generation of high-performance batteries due to their high theoretical capacity (1675 mA h g) and energy density (2600 Wh kg). However, rapid capacity attenuation with poor cycle and rate performances make the batteries far from ideal with respect to real commercial applications. Outstanding breakthroughs and achievements have been made to alleviate these problems in the past ten years. This paper presents an overview of recent advances in lithium-sulfur battery research. We cover the research and development to date on various components of lithium-sulfur batteries, including cathodes, binders, separators, electrolytes, anodes, collectors, and some novel cell configurations. The current trends in materials selection for batteries are reviewed and various choices of cathode, binder, electrolyte, separator, anode, and collector materials are discussed. The current challenges associated with the use of batteries and their materials selection are listed and future perspectives for this class of battery are also discussed.

Nanocomposites consisting of the bimetallic carbide Co(6)Mo(6)C(2) supported on graphitic carbon ((g)C) were synthesized in situ by an anion-exchange method for the first time. The Co(6)Mo(6)C(2)/(g)C nanocomposites were not only chemically stable but also electrochemically stable. The catalyst prepared by loading Pt nanoparticles onto Co(6)Mo(6)C(2)/(g)C was evaluated for the oxygen reduction reaction in acidic solution and showed superior activity and stability in comparison with commercial Pt/C. The higher mass activity of the Pt-Co(6)Mo(6)C(2)/(g)C catalyst indicated that less Pt would be required for the same performance, which in turn would reduce the cost of the fuel cell electrocatalyst. The method reported here will promote broader interest in the further development of other nanostructured materials for real-world applications.

A novel nanocomposite of carbon quantum dots (CQDs) and TiO 2 nanotubes was fabricated and its enhanced photocatalytic and photoelectrochemical properties were demonstrated. Carbon quantum dots were obtained by electrochemical-etching graphite electrodes and TiO 2 nanotubes arrays were prepared by anodization methods. Subsequently, CQDs were assembled on the surface of vertically aligned TiO 2 nanotube arrays (CQDs/TiO 2 nanotubes) and the as-prepared samples were characterized by field-emission scanning electron microscopy, X-ray diffraction, UV-vis diffuse reflectance spectroscopy, photoelectrochemical and photocatalytic measurements. XPS measurement shows the presence of carbon species which come from CQDs. A red shift of light absorption edge and more absorption in the visible light region were observed for the resulting samples from the UV-vis diffuse reflectance spectra. An enhanced photocurrent and photopotential were demonstrated for the CQDs sensitized TiO 2 nanotubes under visible light irradiation and the photocurrent density was 2.7 times larger than that of pristine TiO 2 nanotubes. A solar cell was fabricated for further verifying the sensitization of CQDs over TiO 2 nanotubes. Moreover, the photocatalytic activity of CQDs/TiO 2 nanotubes towards the degradation of methylene blue was demonstrated and about 14% enhanced degradation efficiency was obtained with the presence of CQDs. This work developed a simple method to fabricate CQDs and demonstrated the introduction of CQDs to be a new approach for improving the utilization of visible light for TiO 2 nanotube arrays.

Rechargeable magnesium batteries (rMBs) have been recognized as one of most promising next-generation energy storage devices with high energy and power density. However, the development of rMBs has been hampered by the lack of usable cathode materials with high capacity and cycling stability. Herein, we report an ultra-rapid, cost-effective, and scalable synthesis of ultrathin CuS hierarchical nanosheets by a one-step microwave-assisted preparation. Benefiting from the exceptional structural configuration, when used as the cathode material for rMBs at room temperature, the CuS hierarchical nanosheets deliver a high reversible discharge capacity of 300 mA h g–1 at 20 mA g–1, remarkable rate capability (256.5 mA h g–1 at 50 mA g–1 and 237.5 mA h g–1 at 100 mA g–1), and excellent cycling stability (135 mA h g–1 at 200 mA g–1 over 200 cycles). To date, the obtained excellent electrochemical performances are superior to most results ever reported for cathode materials of rMBs.

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The photovoltage onset reveals the energetics of the donor states, while photovoltage size and reversibility provide information on the charge transfer dynamics of the dopants and their ability to oxidize methanol.