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The objective of this study is to optimize the performance of a graphitized carbon xerogel doped with graphene oxide (GXGO) as cathode for sodium dual-ion batteries. Carbon xerogels are synthetic materials produced in large amounts, with well-controlled chemistry, porosity and structure, by a simple and fast microwave process that has been scaled-up. The intercalation of PF6− anions from various NaPF6 salt-based electrolytes in a GXGO-based cathode is investigated by considering the influence of the upper cut-off voltage (UCOV) and of the electrolyte on the electrochemical parameters. The best results were attained in an electrolyte with a 2.0 M NaPF6 concentration in EC : EMC carbonate solvent mixture with added FEC, at a UCOV of 5.0 V. GXGO cathode provides a discharge capacity of 47 mAh g−1 after 2500 cycles with a coulombic efficiency of 97 %. Moreover, it shows great cycling stability and capacity retention of essentially 100 % after the initial cycles.

In recent years, the research on lithium-ion batteries (LIBs) to improve their lifetime, efficiency and energy density has led to the use of silicon-based materials as a promising anode alternative to graphite. Specifically, crystalline silicon (cSi) and silicon carbide (SiC) obtained from deposition or reduction processes (e.g., magnesiothermal reduction) stand out for their electrochemical properties. However, the synthesis routes proposed until now have limitations that make them difficult to afford or operate on a large scale. For this reason, in this work, carbon-silicon (C-Si) hybrid materials synthesized through an efficient route are evaluated as the potential precursor for the obtention of both cSi and SiC species in a single material. The feasibility and influence of the magnesiothermal reduction process were evaluated, and materials with 10 wt.% of reduced Si and 10-26 wt.% of SiC were obtained. Both species play a role in the improvement of the performance of silicon-based materials as anodes in lithium-ion batteries. In comparison with materials obtained by the reduction of silica gels and composites, the reduced C-Si hybrid gels stand out thanks to the homogeneous distribution and stability of the species developed.

A detailed study of the intercalation/de-intercalation mechanisms of PF6− anions in a graphite cathode of sodium dual-ion batteries is carried out by cyclic voltammetry. The influence of the continuous anion intercalation/de-intercalation on the graphite structure is investigated by ex-situ XRD after cycling. It was concluded that the intercalation/de-intercalation occurs through a combination of diffusion-controlled and pseudocapacitive mechanisms. Initially, the contribution of the diffusion-controlled is significant, specifically at the highest voltage and at the lowest scan rates which agrees with the slow kinetic of this mechanism and its usual prevalence in carbon materials with a graphitic structure. However, the continuous anion intercalation/de-intercalation causes some deterioration of the graphite structural order, even from the initial cycles, as it was demonstrated by the evolution of the crystalline parameters, interlayer spacing, d002, and crystallite size, Lc. This deterioration hinders the diffusion-controlled anion intercalation/de-intercalation and, as a consequence, the pseudocapacitive becomes the main mechanism along cycling. Therefore, since graphite is capable of intercalating PF6− anions at high voltages through a capacitive mechanism, with its consequent rapid kinetics, this carbon material is an excellent candidate for using as cathode in high power sodium dual-ion batteries, in which, kinetically fast mechanisms are required.

The electrochemical intercalation of PF6− anions into graphitic nanomaterials of renewable origin with different degrees of structural order to be subsequently used as cathodes for sodium dual-ion batteries is herein investigated for the first time. Overall, the electrochemical performance of the biogas-derived carbon nanofibers depends on their graphitic structure, specifically on crystallite height which was found to be the determining parameter for the scope of electrochemical intercalation of PF6− anions into these nanomaterials.

The reduction of CO2 emissions is an urgent need that is acknowledged worldwide. Amino-silica sorbents are one of the most promising adsorbents for capturing CO2 from several gas streams due to their excellent textural properties and reversible reactions with CO2. However, gas streams also contain impurities that can affect the retention of CO2 by such sorbents. This study focuses on the effect of the presence of mercury in the gas stream on a series of amino sorbents developed for CO2 capture. Amino-silica adsorbents were functionalized by grafting with aminopropyl-trimethoxysilane (AP) or trimethoxysilylpropyl-diethylenetriamine (DT) and by impregnation with polyethyleneimine (PEI) or tetraethylenepentamine (TEPA). A double functionalization route that combines grafting and impregnation was also assayed. The effect of mercury on the CO2 adsorption capacity of the sorbents was evaluated in a fixed reactor at 40 °C. The double-functionalized adsorbents showed high CO2 uptakes with CO2 adsorption capacities of 5–6 mmol CO2/g (0.15 bar CO2, 40 °C). In addition, their CO2 adsorption capacity was maintained over several cycles. It was established that the presence of mercury undermined the CO2 adsorption capacity of the adsorbents by just 3–16%, demonstrating in general the good selectivity of these materials for CO2, an essential requirement for avoiding the accumulation of mercury during the regeneration process of the solid sorbent and the consequent environmental and technological problems that might ensue.

Because of its low concentration, its unique physico-chemical properties and the analytical difficulties associated with its measurement, the determination of mercury species in solids is not an easy task. Thermal desorption (HgTPD) is an attractive option for the identification of mercury species in solids due to its simplicity and accessibility. However, there are still issues that need to be solved for it to reach its full potential. One such issue is the availability of reference materials that will reproduce real mercury associations. The novelty of this study is the use of six uncommon mercury minerals, taken from around the world, and a sphalerite sample to expand the data base of reference materials for mercury speciation by thermal desorption at programmed temperature. In addition, by using such materials, a number of matrix effects can be ascertained. Different mercury associations were identified depending on the temperature of desorption, thereby validating the thermal desorption as a reliable technique for mercury speciation in solid samples and as a consequence improving the knowledge of the geochemistry of mercury in the environment.

This research is focused in the missing link between the specific surface area of carbons surface and their electrochemical capacitance. Current protocols used for the characterization of carbons applied in supercapacitors electrodes induce inconsistencies in the values of the interfacial capacitance (in F m−2), which is hindering the optimization of supercapacitors. The constraints of both the physisorption of N2 at 77 K and the standard methods used for the isotherm analysis frequently lead to a misleading picture of the porosity. Moreover, the specific surface area of carbons loses their meaning when the supercapacitor operates with organic electrolytes and ionic liquids and the actual surface involved in charge storage has to be assessed by molecular probes suiting the critical dimensions of the ions. In the case of certain carbons such as graphene type-materials, the voltage-driven mechanism may facilitate the access of electrolyte ions to spaces between carbon layers, providing a larger area than that estimated by gas adsorption. Finally, the morphological and porous features of carbons can be extremely modified when they are processed in electrodes. Due to their impact, all these issues should not be neglected and the characterization protocols must be adapted for this specific application of carbons.

Helical-ribbon carbon nanofibers produced on an industrial scale were successfully converted in highly functionalized graphene nanoplatelets by using a slight modification of the Hummers oxidation method. The duration of the oxidative process severely affected the interlayer spacing in the resulting nanoplatelets and, consequently, they showed very different exfoliation behavior. Therefore, it was possible to obtain a variety of graphene-related products through their ultrasonication or thermal treatments such as exfoliation-reduction by flash-pyrolysis in air at temperatures between 400 and 1000 °C or standard activation with CO2 at 800 °C. Detailed comparison of the functionalized carbon nanoplatelets, graphene oxides, reduced graphene oxides and activated carbon nanoplatelets reveals the wide spectrum of their properties with specific surface areas in the range of 4–500 m2 g−1, oxygen content from 38 to 5 wt% and different structural ordering. This study also underlines the impact of the structural, textural and chemical changes experienced by the carbon nanofibers along the various processes on the performance as supercapacitor electrodes. This preliminary study, based on cyclic voltammetry in 2 M H2SO4 aqueous electrolyte, is a summary of the strengths and weaknesses of the different graphene-related materials for this application. The helical-ribbon carbon nanofibers displayed only 10 F g−1, the capacitance of the functionalized graphene nanoplatelets greatly rose to 104 F g−1 with clear contributions from pseudocapacitance. Values around 100–120 F g−1 were found for the graphene oxides and activated graphene nanoplatelets although a marked resistive character is detected. Flash-pyrolysis at 1000 °C leads to lower capacitance (79 F g−1) but much quicker charge propagation. Among all these materials, the lower-cost functionalized graphene nanoplatelets displayed the better behavior for aqueous supercapacitors.

The results obtained for binder-free electrodes made of carbon monoliths with narrow micropore size distributions confirm that the specific capacitance in the electrolyte (C2H5)4NBF4/acetonitrile does not depend significantly on the micropore size and support the foregoing constant result of 0.094 ± 0.011 F m−2.