Binary vanadium pentoxide carbon-graphene foam composites derived from dark red hibiscus sabdariffa for advanced asymmetric supercapacitor.

The development of advanced electrode materials derived from biomass for the next generation of energy storage devices, such as supercapacitors with high specific energy and specific power coupled with a good cycle stability, is required to meet the high demand for electric vehicles and portable devices. In this study, sustainable binary vanadium pentoxide carbon-graphene foam composites (V2O5@C-R2HS/GF) were synthesized using a solvothermal method. The X-ray diffraction, Raman and FTIR techniques were used to study the structural properties of the composites (V2O5@C-R2HS/20 mg GF and V2O5@C-R2HS/40 mg GF). The SEM micrographs displayed an accordion-like morphology resulting from the graphene foam-modified V2O5@C-R2HS composite. The V2O5@C-R2HS, V2O5@C-R2HS/20 mg GF and V2O5@C-R2HS/40 mg GF composites were evaluated in a three-electrode configuration using 6 M potassium hydroxide (KOH) as an aqueous electrolyte. Furthermore, a two-electrode device was carried out by fabricating an asymmetric device (V2O5@C-R2HS/GF//AC) where V2O5@C-R2HS/20 mg GF was used as a positive electrode and activated carbon (AC) as a negative electrode at a cell voltage of 1.6 V in 6 M KOH. The V2O5@C-R2HS/GF//AC showed a high specific energy and specific power values of 55 W h kg-1 and 707 W kg-1, respectively, at a specific current of 1 A g-1. The asymmetric device presented a good stability test showing 99% capacity retention up to 10 000 cycles and was confirmed by the floating time up to 150 h with specific energy increasing 23.6% after the first 10 h. This article is part of the theme issue 'Bio-derived and bioinspired sustainable advanced materials for emerging technologies (part 2)'.

Effect of porosity enhancing agents on the electrochemical performance of high-energy ultracapacitor electrodes derived from peanut shell waste.

In this study, the synthesis of porous activated carbon nanostructures from peanut (Arachis hypogea) shell waste (PSW) was described using different porosity enhancing agents (PEA) at various mass concentrations via a two-step process. The textural properties obtained were depicted with relatively high specific surface area values of 1457 m2 g-1, 1625 m2 g-1 and 2547 m2 g-1 for KHCO3, K2CO3 and KOH respectively at a mass concentration of 1 to 4 which were complemented by the presence of a blend of micropores, mesopores and macropores. The structural analyses confirmed the successful transformation of the carbon-containing waste into an amorphous and disordered carbonaceous material. The electrochemical performance of the material electrodes was tested in a 2.5 M KNO3 aqueous electrolyte depicted its ability to operate reversibly in both negative and positive potential ranges of 0.90 V. The activated carbon obtained from the carbonized CPSW:PEA with a mass ratio of 1:4 yielded the best electrode performance for all featured PEAs. The porous carbons obtained using KOH activation displayed a higher specific capacitance and the lower equivalent series resistance as compared to others. The remarkable performance further corroborated the findings linked to the textural and structural properties of the material. The assembled device operated in a neutral electrolyte (2.5 M KNO3) at a cell potential of 1.80 V, yielded a ca. 224.3 F g-1 specific capacitance at a specific current of 1 A g-1 with a corresponding specific energy of 25.2 Wh kg-1 and 0.9 kW kg-1 of specific power. This device energy was retained at 17.7 Wh kg-1 when the specific current was quadrupled signifying an excellent supercapacitive retention with a corresponding specific power of 3.6 kW kg-1. These results suggested that peanut shell waste derived activated carbons are promising candidates for high-performance supercapacitors.

A high energy density asymmetric supercapacitor utilizing a nickel phosphate/graphene foam composite as the cathode and carbonized iron cations adsorbed onto polyaniline as the anode.

This work presents the effect of different contents of graphene foam (GF) on the electrochemical capacitance of nickel phosphate Ni3(PO4)2 nano-rods as an electrode material for hybrid electrochemical energy storage device applications. Pristine Ni3(PO4)2 nano-rods and Ni3(PO4)2/GF composites with different GF mass loadings of 30, 60, 90 and 120 mg were synthesised via a hydrothermal method. The electrochemical behavior of pristine Ni3(PO4)2 and Ni3(PO4)2/GF composites were analysed in a three-electrode cell configuration using 6 M KOH electrolyte. The Ni3(PO4)2/90 mg GF composite sample exhibited the highest specific capacity of 48 mA h g-1 at a current density of 0.5 A g-1. The electrochemical behavior of the Ni3(PO4)2/90 mg GF composite was further analysed in a two-electrode hybrid asymmetric device. A hybrid asymmetric device was fabricated with Ni3(PO4)2/90 mg GF as the cathode and carbonized iron cations (Fe3+) adsorbed onto polyaniline (PANI) (C-FP) as the anode material (Ni3(PO4)2/90 mg GF//C-FP) and tested in a wide potential window range of 0.0-1.6 V using 6 M KOH. This hybrid device achieved maximum energy and power densities of 49 W h kg-1 and 499 W kg-1, respectively, at 0.5 A g-1 and had long-term cycling stability.

Correction: A high energy density asymmetric supercapacitor utilizing a nickel phosphate/graphene foam composite as the cathode and carbonized iron cations adsorbed onto polyaniline as the anode.

[This corrects the article DOI: 10.1039/C7RA12028A.].

Green and scalable synthesis of 3D porous carbons microstructures as electrode materials for high rate capability supercapacitors.

Porous carbon nanostructures have long been studied because of their importance in many natural phenomena and their use in numerous applications. A more recent development is the ability to produce porous carbon materials with tuneable properties for electrochemical applications, which has enabled new research directions towards the production of suitable carbon materials for energy storage applications. Thus, this work explores the activation of carbon from polyaniline (PANI) using a less-corrosive potassium carbonate (K2CO3) salt, with different mass ratios of PANI and the activating agent (K2CO3 as compared to commonly used KOH). The obtained activated carbon exhibits a specific surface area (SSA) of up to ∼1700 m2 g-1 for a carbon derived PANI : K2CO3 ratio of 1 : 6. Moreover, the prepared samples were tested as electrode materials for supercapacitors with the results showing excellent electrical double layer capacitor behavior. Charge storage was still excellent for scan rates of up to 2000 mV s-1, and a capacitance retention of 70% at a very high specific current of 50 A g-1 was observed. Furthermore, the fabricated device can deliver an energy density of 25 W h kg-1 at a specific current of 0.625 A g-1 and a power density of 260 W kg-1 in 1-ethyl-3-methylimidazolium bistrifluorosulfonylimide (EMIM-TFSI) ionic liquid, with excellent rate capability after cycling for 16 000 cycles at 3.0 V with ∼98% efficiency. These results are promising and demonstrate the electrode's potential for energy storage, leading to the conclusion that K2CO3 is a very good alternative to corrosive activation agents such as KOH in order to achieve high electrochemical performance.

Doping a semiconductor to create an unconventional metal.

Landau-Fermi liquid theory, with its pivotal assertion that electrons in metals can be simply understood as independent particles with effective masses replacing the free electron mass, has been astonishingly successful. This is true despite the Coulomb interactions an electron experiences from the host crystal lattice, lattice defects and the other approximately 10(22) cm(-3) electrons. An important extension to the theory accounts for the behaviour of doped semiconductors. Because little in the vast literature on materials contradicts Fermi liquid theory and its extensions, exceptions have attracted great attention, and they include the high-temperature superconductors, silicon-based field-effect transistors that host two-dimensional metals, and certain rare-earth compounds at the threshold of magnetism. The origin of the non-Fermi liquid behaviour in all of these systems remains controversial. Here we report that an entirely different and exceedingly simple class of materials-doped small-bandgap semiconductors near a metal-insulator transition-can also display a non-Fermi liquid state. Remarkably, a modest magnetic field functions as a switch which restores the ordinary disordered Fermi liquid. Our data suggest that we have found a physical realization of the only mathematically rigorous route to a non-Fermi liquid, namely the 'undercompensated Kondo effect', where there are too few mobile electrons to compensate for the spins of unpaired electrons localized on impurity atoms.

Magnetoresistance from quantum interference effects in ferromagnets

The desire to maximize the sensitivity of read/write heads (and thus the information density) of magnetic storage devices has stimulated interest in the discovery and design of new magnetic materials exhibiting magnetoresistance. Recent discoveries include the 'colossal' magnetoresistance in the manganites and the enhanced magnetoresistance in low-carrier-density ferromagnets. An important feature of these systems is that the electrons involved in electrical conduction are different from those responsible for the magnetism. The latter are localized and act as scattering sites for the mobile electrons, and it is the field tuning of the scattering strength that ultimately gives rise to the observed magnetoresistance. Here we argue that magnetoresistance can arise by a different mechanism in certain ferromagnets--quantum interference effects rather than simple scattering. The ferromagnets in question are disordered, low-carrier-density magnets where the same electrons are responsible for both the magnetic properties and electrical conduction. The resulting magnetoresistance is positive (that is, the resistance increases in response to an applied magnetic field) and only weakly temperature-dependent below the Curie point.