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Electrochemical N2 reduction reaction (E‐NRR) has recently gained increasing interest within the scientific community, due to the ongoing energy crisis and pursuit of process sustainability. In this scenario, emerging lithium‐mediated (Li‐m) strategies are obtaining promising Faradaic efficiency (FE) and NH3 production rate values. In this work, the Li‐m scenarios are classified and explained toward a more sustainable process. Continuous processes, with a lithium salt and a proton donor in an electrolytic cell, are analyzed and compared with stepwise pathways. Different parameters are summarized in relation to the system stability, for which the importance of a tailored solid electrolyte interphase (SEI) layer emerged. Among stepwise processes, the thermochemical direct nitridation of lithium is discussed together with the recently developed Galvanic Li─N2 cell strategy. [ABSTRACT FROM AUTHOR]

Costs and toxicity concerns are at the center of a heated debate regarding the implementation of perovskite solar cells (PSCs) into commercial products. The first bottleneck could be overcome by eliminating the top metal electrode (generally gold) and the underlying hole transporting material and substituting both with one single thick layer of conductive carbon, as in the so‐called carbon‐based PSCs (C‐PSCs). The second issue, related to the presence of lead, can be tackled by resorting to other perovskite structures based on less toxic metallic components. An interesting case is that of the double perovskite Cs2AgBiBr6, which at present still lacks the outstanding optoelectronic performances of the lead‐based counterparts but is very stable to environmental factors. In this work, the processing of carbon electrodes onto Cs2AgBiBr6‐based C‐PSCs was reported, starting from an additive‐free isopropanol ink of a carbon material obtained from the hydrothermal recycling of waste tires and employing a high‐throughput ultrasonic spray coating method in normal environmental conditions. Through this highly sustainable approach that ensures a valuable step from an end‐of‐life to an end‐of‐waste status for used tires, devices were obtained delivering a record open circuit voltage of 1.293 V, which might in the future represent ultra‐cheap solutions to power the indoor Internet of Things ecosystem. [ABSTRACT FROM AUTHOR]

The article titled "Lithium-Mediated Nitrogen Reduction for Ammonia Synthesis: Reviewing the Gap between Continuous Electrolytic Cells and Stepwise Processes through Galvanic Li-N2 Cells" in Advanced Energy Materials discusses the use of lithium in the production of ammonia and fertilizers using renewable energy. The authors, Federico Bella and his colleagues, present innovative methods and devices that can accelerate the transition to sustainable energy and ecological practices. This research focuses on electrochemical nitrogen reduction and highlights advanced materials and newly developed devices. [Extracted from the article]

Manufactured globally on industrial scale, cyclodextrins (CD) are cyclic oligosaccharides produced by enzymatic conversion of starch. Their typical structure of truncated cone can host a wide variety of guest molecules to create inclusion complexes; indeed, we daily use CD as unseen components of food, cosmetics, textiles and pharmaceutical excipients. The synthesis of active material composites from CD resources can enable or enlarge the effective utilization of these products in the battery industry with some economical as well as environmental benefits. New and simple strategies are here presented for the synthesis of nanostructured silicon and sulfur composite materials with carbonized hyper cross‐linked CD (nanosponges) that show satisfactory performance as high‐capacity electrodes. For the sulfur cathode, the mesoporous carbon host limits polysulfide dissolution and shuttle effects and guarantees stable cycling performance. The embedding of silicon nanoparticles into the carbonized nanosponge allows to achieve high capacity and excellent cycling performance. Moreover, due to the high surface area of the silicon composite, the characteristics at the electrode/electrolyte interface dominate the overall electrochemical reversibility, opening a detailed analysis on the behavior of the material in different electrolytes. We show that the use of commercial LP30 electrolyte causes a larger capacity fade, and this is associated with different solid electrolyte interface layer formation and it is also demonstrated that fluoroethylene carbonate addition can significantly increase the capacity retention and the overall performance of our nanostructured Si/C composite in both ether‐based and LP30 electrolytes. As a result, an integration of the Si/C and S/C composites is proposed to achieve a complete lithiated Si−S cell. [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 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]

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]

Considering the worldwide market of batteries and supercapacitors, the (partial or total) replacement of conventional fossil-derived carbonates with bio-based ones in electrolyte formulations would allow the production of safer and more sustainable devices. In this work, embracing the 7 th principle of green chemistry, glycerol derivatives (namely glycerol carbonate and solketal carbonate) are tested as solvents and additives for electrolyte formulations. Glycerol carbonate is innovatively employed as promising electrolyte solvent for electric double-layer capacitors with excellent performances. On the other hand, a solketal carbonate-laden liquid electrolyte is investigated for potassium-based batteries, showing a rather stable electrochemical behaviour and performance close to those of commercial oil-derived alternatives., (© 2024 The Authors. ChemSusChem published by Wiley-VCH GmbH.)

Manufactured globally on industrial scale, cyclodextrins (CD) are cyclic oligosaccharides produced by enzymatic conversion of starch. Their typical structure of truncated cone can host a wide variety of guest molecules to create inclusion complexes; indeed, we daily use CD as unseen components of food, cosmetics, textiles and pharmaceutical excipients. The synthesis of active material composites from CD resources can enable or enlarge the effective utilization of these products in the battery industry with some economical as well as environmental benefits. New and simple strategies are here presented for the synthesis of nanostructured silicon and sulfur composite materials with carbonized hyper cross-linked CD (nanosponges) that show satisfactory performance as high-capacity electrodes. For the sulfur cathode, the mesoporous carbon host limits polysulfide dissolution and shuttle effects and guarantees stable cycling performance. The embedding of silicon nanoparticles into the carbonized nanosponge allows to achieve high capacity and excellent cycling performance. Moreover, due to the high surface area of the silicon composite, the characteristics at the electrode/electrolyte interface dominate the overall electrochemical reversibility, opening a detailed analysis on the behavior of the material in different electrolytes. We show that the use of commercial LP30 electrolyte causes a larger capacity fade, and this is associated with different solid electrolyte interface layer formation and it is also demonstrated that fluoroethylene carbonate addition can significantly increase the capacity retention and the overall performance of our nanostructured Si/C composite in both ether-based and LP30 electrolytes. As a result, an integration of the Si/C and S/C composites is proposed to achieve a complete lithiated Si-S cell., (© 2021 Wiley-VCH GmbH.)

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.)

Herein it is shown that hydrotalcite-like compounds (HTlcs), doped with a suitably reactive metal, can efficiently act as water oxidation catalysts. As a case study, a ternary HTlc of formula [Zn 0.667 Al 0.306 Ir 0.027 (OH) 2 ]Cl 0.333 ⋅0.6 H 2 O, in which iridium is homogeneously distributed into the octahedral sites of brucite-type sheets, was prepared and tested as a heterogeneous water oxidation catalyst, using NaIO 4 as a sacrificial oxidant. This HTlc showed excellent performance in terms of turnover frequency (up to 113 min -1 ), turnover number (>11 900), stability and recyclability., (© 2016 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.)