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Making a consistency with the objectives of circular economy, herein, waste pistachios shells were utilized for the development of hydrogen evolution reaction (HER) and oxygen reduction reaction (ORR) electrocatalysts which are the key bottleneck in the technological evolution of electrolyzers and fuel cells, respectively. As an alternative to scarce and expensive platinum-group-metal (PGM) electrocatalysts, metal nitrogen carbons (MNCs) are emerging as a promising candidate for both aforementioned electrocatalysis where iron and nickel are the metal of choice for ORR and HER, respectively. Therefore, FeNCs and NiNCs were fabricated utilizing inedible pistachio shells as a low-cost biosource of carbon. The steps involved in the fabrication of electrocatalyst were correlated with electrochemical performance in alkaline media. Encouraging onset potential of ~ 0.88 V vs RHE with a possibility of a 2 + 2 reaction pathway was observed in pyrolyzed and ball-milled FeNC. However, HF etching for template removal slightly affected the kinetics and eventually resulted in a relatively higher yield of peroxide. In parallel, the pyrolyzed NiNC demonstrated a lower HER overpotential of ~ 0.4 V vs RHE at − 10 mA cm−2. Nevertheless, acid washing adversely affected the HER performance and consequently, very high overpotential was witnessed.

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The aim of this paper is to demonstrate lithium metal battery cells assembled with high potential cathodes produced by sustainable processes. Specifically, LiNi0.5Mn1.5O4 (LMNO) electrodes were fabricated using two different water-processable binders: pullulan (PU) or the bifunctional electronically conductive poly(3,4-ethylenedioxythiophene)-poly(styrene sulfonate) (PEDOT:PSS). The cell performance was evaluated by voltammetric and galvanostatic charge/discharge cycles at different C-rates with 1M LiPF6 in 1:1 (v:v) ethylene carbonate (EC):dimethyl carbonate (DMC) (LP30) electrolyte and compared to that of cells assembled with LMNO featuring poly(vinylidene difluoride) (PVdF). At C/10, the specific capacity of LMNO-PEDOT:PSS and LMNO-PU were, respectively, 130 mAh g−1 and 127 mAh g−1, slightly higher than that of LMNO-PVdF (124 mAh g−1). While the capacity retention at higher C-rates and under repeated cycling of LMNO-PU and LMNO-PVdF electrodes was similar, LMNO-PEDOT:PSS featured superior performance. Indeed, lithium metal cells assembled with PEDOT:PSS featured a capacity retention of 100% over 200 cycles carried out at C/1 and with a high cut-off voltage of 5 V. Overall, this work demonstrates that both the water-processable binders are a valuable alternative to PVdF. In addition, the use of PEDOT:PSS significantly improves the cycle life of the cell, even when high-voltage cathodes are used, therefore demonstrating the feasibility of the production of a green lithium metal battery that can exhibit a specific energy of 400 Wh kg−1, evaluated at the electrode material level. Our work further demonstrates the importance of the use of functional binders in electrode manufacturing.

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The electrochemical behaviour of steel, copper, and titanium current collectors was studied in aqueous solutions of lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) at various concentrations, from 0.5 up to 20 m. As the concentration of the electrolyte increases, the electrochemical window of water stability widens according to the “water-in-salt” concept. The metal grids have been studied electrochemically, both under anodic and cathodic conditions, by means of cyclic voltammetry and chronoamperometry. Subsequently, a microscopic analysis with SEM and compositional analysis with XPS was carried out to evaluate the surface modifications following electrochemical stress. We found that copper is not very suitable for this kind of application, while titanium and steel showed interesting behaviour and large electrochemical window.

In this paper, nitrogen doped carbon materials with mesopores 4–8 nm‐wide and a high surface area of ca.1100 m2 g−1 were synthesized according to an innovative hard template method. Sucrose was used as carbon source and propylamine functionalized silica acted as both nitrogen source and templating agent. The novel doped carbons were compared with mesoporous carbons featuring similar texture properties (pore size and surface area) but obtained by the pyrolysis of sucrose or 1,10‐phenantholine and employing non‐functionalized silica as a templating agent. The interest of this investigation is to understand how doping occurs when a functionalized silica is employed, and whether the nitrogen doping remains a surface property or it is extended also to the bulk of the material, influencing the morphological and the electrical properties of the resulting carbon. X‐ray photoemission spectroscopy, elemental analysis, and EDX confirmed the doping action of the functionalized silica and the electrochemical characterization allowed to compare the different performances as supercapacitor materials.