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Whereas the commercialization of dye‐sensitized solar cells (DSSCs) is finally proceeding taking advantage of their low cost and tunable optical features, such as colour and transparency for both indoor and building‐integrated applications, the corresponding aqueous counterpart is still at its infancy. As the TiO2 electrode is a fundamental component for hybrid solar cells, this work investigates the effect of different molecular (α‐terpineol, propylene carbonate) and polymeric (polyethylene oxide, polyethylene glycol, carboxymethyl cellulose and xanthan gum) additives that can be introduced into a commercial TiO2 paste for for screen‐printing (or doctor blade). Among all, the addition of polyethylene glycol leads to the best cell performances, with markedly increased short‐circuit current density (+18 %) and power conversion efficiency (+48 %) with respect to the pristine (commercial) counterpart. When further explored at different concentration levels, electrodes fabricated from polyethylene glycol‐based pastes show different morphologies, thicknesses and performances, which are investigated through (photo)electrochemical, structural, physical‐chemical and microscopic techniques. [ABSTRACT FROM AUTHOR]

In the present work, the preparation and characterization of quasi-solid polymer electrolyte membranes based on methacrylic monomers and oligomers, with the addition of organic plasticizers and lithium salt, are described. Noticeable improvements in the mechanical properties by reinforcement with natural cellulose hand-sheets or nanoscale microfibrillated cellulose fibers are also demonstrated. The ionic conductivity of the various prepared membranes is very high, with average values approaching 10-3 S cm-1 at ambient temperature. The electrochemical stability window is wide (anodic breakdown voltages > 4.5 V vs. Li in all the cases) along with good cyclability in lithium cells at ambient temperature. The galvanostatic cycling tests are conducted by constructing laboratory-scale lithium cells using LiFePO4 as cathode and lithium metal as anode with the selected polymer electrolyte membrane as the electrolyte separator. The results obtained demonstrate that UV induced radical photo-polymerization is a well suited method for an easy and rapid preparation of easy tunable quasi-solid polymer electrolyte membranes for energy storage devices. [ABSTRACT FROM AUTHOR]

Carbon capture is amongst the key emerging technologies for the mitigation of greenhouse gases (GHG) pollution. Several materials as adsorbents for CO2 and other gases are being developed, which often involve using complex and expensive fabrication techniques. In this work, we suggest a sound, easy and cheap route for the production of nitrogen-doped carbon materials for CO2 capture by pyrolysis of electrospun poly(acrylonitrile) (PAN) fibers. PAN fibers are generally processed following specific heat treatments involving up to three steps (to get complete graphitization), one of these being stabilization, during which PAN fibers are oxidized and stretched in the 200–300 °C temperature range. The effect of stabilization temperature on the chemical structure of the carbon nanofibers is investigated herein to ascertain the possible implication of incomplete conversion/condensation of nitrile groups to form pyridine moieties on the CO2 adsorption capacity. The materials were tested in the pure CO2 atmosphere at 20 °C achieving 18.3% of maximum weight increase (equivalent to an uptake of 4.16 mmol g−1), proving the effectiveness of a high stabilization temperature as route for the improvement of CO2 uptake. [ABSTRACT FROM AUTHOR]

Keywords: aqueous electrolyte; dye-sensitized solar cell; polyethylene glycol; screen printing; TiO2 EN aqueous electrolyte dye-sensitized solar cell polyethylene glycol screen printing TiO2 6459 6459 1 12/21/20 20201217 NES 201217 B The Cover Feature b shows a modern building powered by aqueous solar cells, placed both indoors and outdoors. Aqueous electrolyte, dye-sensitized solar cell, polyethylene glycol, screen printing, TiO2. [Extracted from the article]

Graphene is a new generation material, which finds potential and practical applications in a vast range of research areas. It has unrivalled characteristics, chiefly in terms of electronic conductivity, mechanical robustness and large surface area, which allow the attainment of outstanding performances in the material science field. Some unneglectable issues, such as the high cost of production at high quality and corresponding scarce availability in large amounts necessary for mass scale distribution, slow down graphene widespread utilization; however, in the last decade both basic academic and applied industrial materials research have achieved remarkable breakthroughs thanks to the implementation of graphene and related 1D derivatives. In this work, after briefly recalling the main characteristics of graphene, we present an extensive overview of the most recent advances in the development of the Li-ion battery anodes granted by the use of neat and engineered graphene and related 1D materials. Being far from totally exhaustive, due to the immense scientific production in the field yearly, we chiefly focus here on the role of graphene in materials modification for performance enhancement in both half and full lithium-based cells and give some insights on related promising perspectives. [ABSTRACT FROM AUTHOR]

In article number 1802438, Freddy Kleitz, Claudio Gerbaldi and co‐workers report a new anode material for high‐performing and long‐lasting Li‐ion batteries, which is built from an innovative 2D/3D nanostructure design. The active material consists of exfoliated graphene‐wrapped mesoporous mixed metal oxide microspheres, obtained through a simple spray‐drying procedure. Such electrode material provides significantly improved specific capacity with unprecedented reversible cycling stability over 3000 charge/discharge cycles. [ABSTRACT FROM AUTHOR]

Exfoliated graphene‐wrapped mesoporous Cu‐Ni oxide (CNO) nanocast composites are developed using a straightforward nanostructure engineering strategy. The synergistic effect of hierarchical mesoporous CNO nanobuilding blocks that are homogeneously wrapped by graphene nanosheets (GNSs) using a rapid spray drying technique effectively preserves the electroactive species against the volume changes resulting from the charge/discharge process. Owing to the intriguing structural/morphological features arising from the caging effect of exfoliated graphene sheets, these 3D/2D CNO@GNS nanocomposite microspheres are promising as high‐performance Li‐ion battery anode materials. They exhibit unprecedented electrochemical behavior, such as high reversible specific capacity (initial discharge capacities exceeding 1700 mAh g−1 at low 0.1 mA g−1, stable 850 and 730 mAh g−1 at 1 and 5 mA g−1 after 800 and 1300 cycles, respectively, and higher than 400 mAh g−1 at very high current density of 10 mA g−1 after more than 2000 cycles), excellent coulombic efficiency and long‐term stability (more than 3000 cycles with >55% capacity retention) at high current density that are remarkable compared to most transition metal oxides and nanocomposites prepared by conventional techniques. This simple, yet innovative, material design is inspiring to develop advanced conversion materials for Li‐ion batteries or other energy storage devices. High‐performance exfoliated graphene‐wrapped mesoporous mixed oxide nanocomposites are synthesized using a straightforward nanostructure engineering strategy. They show significantly improved specific capacity with unprecedented reversible cycling stability exceeding 3000 charge/discharge cycles even at very high current regimes (up to effective 1280 mA) and, thus, can be used as superior alternative anodes in the next generation of high‐performing and long‐lasting Li‐ion batteries. [ABSTRACT FROM AUTHOR]

Unveiling the CuFeO 2 surface properties for adsorption and activation of CO 2. [Display omitted] • CuFeO 2 photo-catalyze the carbon dioxide reduction to formic acid. • Effects of surface oxygen vacancies on the adsorption and the activation of CO 2. • CO 2 adsorption on CuFeO 2 surfaces calculated by DFT. • Role of Cu and Fe for the effective CO 2 adsorption. The recycling of CO 2 back into chemicals via photo-electrochemical cells represents a viable route to mitigate the global climate crisis of current days. In this paper we focus on the copper-iron delafossite oxide, CuFeO 2 , which has been proven to have suitable physico-chemical properties to photo-catalyze the carbon dioxide reduction to formic acid. The specific electronic and structural features that allow activating the highly stable CO 2 molecule are dissected by exploiting state-of-the art first principles methods. The effects of surface oxygen vacancies as well as the different roles of copper and iron on the adsorption and the activation of carbon dioxide at the CuFeO 2 most stable surface are analyzed. These results highlight the key role of oxygen defects in favoring the CO 2 adsorption and in promoting the formation of a radical anion CO 2 − or a carbonate-like adsorbate so providing the scientific grounds for implementing new rational design strategies and improving the performances of CuFeO 2 -based photoelectrodes for CO 2 reduction. [ABSTRACT FROM AUTHOR]

Whereas the commercialization of dye-sensitized solar cells (DSSCs) is finally proceeding taking advantage of their low cost and tunable optical features, such as colour and transparency for both indoor and building-integrated applications, the corresponding aqueous counterpart is still at its infancy. As the TiO 2 electrode is a fundamental component for hybrid solar cells, this work investigates the effect of different molecular (α-terpineol, propylene carbonate) and polymeric (polyethylene oxide, polyethylene glycol, carboxymethyl cellulose and xanthan gum) additives that can be introduced into a commercial TiO 2 paste for for screen-printing (or doctor blade). Among all, the addition of polyethylene glycol leads to the best cell performances, with markedly increased short-circuit current density (+18 %) and power conversion efficiency (+48 %) with respect to the pristine (commercial) counterpart. When further explored at different concentration levels, electrodes fabricated from polyethylene glycol-based pastes show different morphologies, thicknesses and performances, which are investigated through (photo)electrochemical, structural, physical-chemical and microscopic techniques., (© 2020 Wiley-VCH GmbH.)

Na-ion batteries (NIBs) are attracting widespread interest as a potentially more convenient alternative to current state-of-the-art Li-ion batteries (LIBs), chiefly for large-scale energy storage from renewables. Developing novel active materials is essential for the deployment of NIBs, especially in terms of negative electrodes that can accommodate the larger sodium ions. We focus on TiO 2 anatase, which has been proposed as a promising anode material for the overall balance of performance, stability and cost. As the exposed crystal facets in different morphologies of nanostructured anatase can affect the electrochemical performances, here we report a theoretical investigation of Na + adsorption and migration through (101), (100) and (001) surface terminations, thus explaining the different activities toward sodiation reported in the literature. Energy barriers computed by means of the CI-NEB method at the DFT+U level of theory show that the (001) surface is the most effective termination for Na + insertion. We also provide a detailed analysis to elucidate that the energy barriers are due to structural modifications of the lattice upon sodiation. From these results we derive new design directions for the development of cheap and effective oxide-based nanostructured electrode materials for advanced NIBs., Competing Interests: There are no conflicts of interest to declare., (This journal is © The Royal Society of Chemistry.)

We report a thorough, multitechnique investigation of the structure and transport properties of a UV-cross-linked polymer electrolyte based on poly(ethylene oxide), tetra(ethylene glycol)dimethyl ether (G4), and lithium bis(trifluoromethane)sulfonimide. The properties of the cross-linked polymer electrolyte are compared to those of a non-cross-linked sample of same composition. The effect of UV-induced cross-linking on the physico/chemical characteristics is evaluated by X-ray diffraction, differential scanning calorimetry, shear rheology, 1 H and 7 Li magic angle spinning nuclear magnetic resonance (NMR) spectroscopy, 19 F and 7 Li pulsed field gradient stimulated echo NMR analyses, electrochemical impedance spectroscopy, and Fourier transform Raman spectroscopy. Comprehensive analysis confirms that UV-induced cross-linking is an effective technique to suppress the crystallinity of the polymer matrix and reduce ion aggregation, yielding improved Li + transport number (>0.5) and ionic conductivity (>0.1 mS cm ?1 ) at ambient temperature, by tailoring the structural/morphological characteristics of the polymer matrix. Finally, the polymer electrolyte allows reversible operation with stable profile for hundreds of cycles upon galvanostatic test at ambient temperature of LiFePO 4 -based lithium-metal cells, which deliver full capacity at 0.05 or 0.1C current rate and keep high rate capabilities up to 1C. This enforces the role of UV-induced cross-linking in achieving excellent electrochemical characteristics, exploiting a practical, easy up-scalable process.

In the challenging scenario of anode materials for sodium-ion batteries, TiO 2 nanotubes could represent a winning choice in terms of cost, scalability of the preparation procedure, and long-term stability upon reversible operation in electrochemical cells. In this work, a detailed physicochemical, computational, and electrochemical characterization is carried out on TiO 2 nanotubes synthesized by varying growth time and heat treatment, viz. the two most significant experimental parameters during preparation. A chemometric approach is proposed to obtain a concrete and solid multivariate analysis of sodium battery electrode materials. Such a statistical approach, combined with prolonged galvanostatic cycling and density functional theory analysis, allows identifying anatase at high growth time as the TiO 2 polymorph of choice as an anode material, thus creating a benchmark for sodium-ion batteries, which currently took the center stage of the research in the field of energy storage systems from renewables., Competing Interests: The authors declare no competing financial interest.