Search Results (61)

This study focuses on the structural and electrochemical behavior of the compound ZnLaFeO₄ as a negative electrode material for nickel–metal hydride (Ni-MH) batteries. The material was synthesized by a sol–gel hydrothermal method to assess the influence of lanthanum doping on the ZnFe₂O₄ spinel structure. X-ray diffraction revealed the formation of a dominant LaFeO₃ perovskite phase, with ZnFe₂O₄ and La₂O₃ as secondary phases. SEM analysis showed agglomerated grains with an irregular morphology. Electrochemical characterization at room temperature and a discharge rate of C/10 (full charge in 10 h) revealed a maximum discharge capacity of 106 mAhg⁻¹. Although La³⁺ doping modified the microstructure and slowed the activation process, the electrode exhibited stable cycling with moderate polarization behavior. The decrease in capacity during cycling is due mainly to higher internal resistance. These results highlight the potential and limitations of La-doped spinel ferrites as alternative negative electrodes for Ni-MH systems. Full article

Next-generation recycling technologies must be urgently innovated to tackle huge volumes of spent batteries, photovoltaic panels or printed circuit boards (WPCBs). Current e-waste recycling industrial technology is dominated by traditional recycling technologies. Herein, ionic liquids (ILs), deep eutectic solvents (DESs) and promising oxidizing additives that can overcome some traditional recycling methods of metal ions from e-waste, used in our works from last year, are presented. The unique chemical environments of ILs and DESs, with the application of low-temperature extraction procedures, are important environmental aspects known as “Green Methods”. A closed-loop system for recycling zinc and manganese from the “black mass” (BM) of waste, Zn-MnO₂ batteries, is presented. The leaching process achieves a high efficiency and distribution ratio using the composition of two solvents (Cyanex 272 + diethyl phosphite (DPh)) for Zn(II) extraction. High extraction efficiency with 100% zinc and manganese recovery is also achieved using DESs (cholinum chloride/lactic acid, 1:2, DES 1, and cholinum chloride/malonic acid, 1:1, DES 2). New, greener recycling approaches to metal extraction from the BM of spent Li-ion batteries are presented with ILs ([N_8,8,8,1][Cl], (Aliquat 336), [P_6,6,6,14][Cl], [P_6,6,6,14][SCN] and [Benzet][TCM]) eight DESs, Cyanex 272 and D2EHPA. A high extraction efficiency of Li(I) (41–92 wt%) and Ni(II) (37–52 wt%) using (Cyanex 272 + DPh) is obtained. The recovery of Ni(II) and Cd(II) from the BM of spent Ni-Cd batteries is also demonstrated. The extraction efficiency of DES 1 and DES 2, contrary to ILs ([P_6,6,6,14][Cl] and [P_6,6,6,14][SCN]), is at the level of 30 wt% for Ni(II) and 100 wt% for Cd(II). In this mini-review, the option to use ILs, DESs and Cyanex 272 for the recovery of valuable metals from end-of-life WPCBs is presented. Next-generation recycling technologies, in contrast to the extraction of metals from acidic leachate preceded by thermal pre-treatment or from solid material only after thermal pre-treatment, have been developed with ILs and DESs using the ABS method, as well as Cyanex 272 (only after the thermal pre-treatment of WPCBs), with a process efficiency of 60–100 wt%. In this process, four new ILs are used: didecyldimethylammonium propionate, [N_10,10,1,1][C₂H₅COO], didecylmethylammonium hydrogen sulphate, [N_10,10,1,H][HSO₄], didecyldimethylammonium dihydrogen phosphate, [N_10,10,1,1][H₂PO₄], and tetrabutylphosphonium dihydrogen phosphate, [P_4,4,4,4][H₂PO₄]. The extraction of Cu(II), Ag(I) and other metals such as Al(III), Fe(II) and Zn(II) from solid WPCBs is demonstrated. Various additives are used during the extraction processes. The Analyst 800 atomic absorption spectrometer (FAAS) is used for the determination of metal content in the solid BM. The ICP-OES method is used for metal analysis. The obtained results describe the possible application of ILs and DESs as environmental media for upcycling spent electronic wastes. Full article

The widespread, worldwide utilisation of alkaline batteries requires development of proper recycling methods for used batteries, which are considered both as a secondary source of valuable metals and as a threat to the environment (may contain toxic substances). As many separation methods of metal ions from battery leachates are based on the use of substances that require complex synthesis or are not eco-safe, new materials suitable for this purpose are systematically sought. Therefore, in this study, the results of the separation of Ni(II), Zn(II) and Mn(II) ions from alkaline battery leachates using polymer materials (PMs) impregnated with easily synthesised, “green” deep eutectic solvents (DESs) or with ionic liquids (ILs) were presented. Additionally, PMs surface wettability were determined and their chemical compositions were analysed using the Fourier transform infrared spectroscopy–attenuated total reflectance (FTIR–ATR) method. Among all PMs synthesised, materials containing DESs (composed of Aliquat 336 or Cyphos IL 101 and diacetamide) performed best in the separation of Ni(II) ions (removal of 93.42% and 80.86%). The application of DES-based PMs for the separation of metal ions from battery leachates is in line with green chemistry principles, and such materials can potentially be used in the processing of e-waste. Full article

Metal sulfides are promising anode candidates for sodium–ion batteries (SIBs) due to their high theoretical capacities. However, their practical application is limited by significant volume extension and sluggish Na⁺ diffusion during cycling, which lead to rapid capacity degradation and poor long-term stability. In this work, we report the rational design of a hollow triple-shelled high-entropy sulfide (NaFeZnCoNiMn)₉S₈, synthesized through sequential templating method under hydrothermal conditions. Transmission electron microscopy confirms its well-defined three-shelled architecture. The inter-shell voids effectively buffer Na⁺ insertion/desertion-induced volume extension, while the tailored high-entropy matrix enhances electronic conductivity and accelerates Na⁺ transport. This synergistic design yields outstanding performance, including a high initial Coulombic efficiency (ICE) of 94.1% at 0.1 A g⁻¹, low charge-transfer resistance (0.32~2.54 Ω), fast Na⁺ diffusion efficiency (10^−8.5–10^−10.5 cm² s⁻¹), and reversible capacity of 582.6 mAh g⁻¹ after 1600 cycles at 1 A g⁻¹ with 91.2% capacity retention. These results demonstrate the potential of high-entropy, multi-shelled architectures as a robust platform for next-generation durable SIB anodes. Full article

Zeolite Battery Research Africa (ZEBRA) batteries (Na-NiCl₂ solid electrolyte batteries, SEBs) have commercial applications in energy storage due to their low costs and recyclability, long lifetime, and high safety. In commercial ZEBRA batteries, Ni electrode and beta’’-alumina solid electrolyte (BASE) have a more than 70% share of the overall cell material costs. Na-ZnCl₂ all-liquid batteries (ALBs), which replace Ni with abundant and low-cost Zn and BASE electrolyte with molten salt electrolyte, could reduce costs and provide a longer lifetime and higher safety, making their application in grid storage promising. However, compared to SEBs, ALBs are in an early development stage, particularly for their molten salt electrolytes, which have a significant effect on the battery performance. Physical and chemical properties of the salt electrolyte like melting temperatures and solubilities of electrode materials (i.e., Na and Zn metal) are vital for the molten salt electrolyte selection and battery cell design and optimization. In this work, the binary and ternary phase diagrams of salt mixtures containing NaCl, CaCl₂, BaCl₂, SrCl₂, and KCl, obtained via FactSage simulation and DSC measurements, as well as the solubilities of electrode materials (Na and Zn metals), are presented and used for the selection of the molten salt electrolyte. Moreover, various criteria, considered for the selection of the molten salt electrolyte, include high electromotive force (EMF) for suitable electrochemical properties, low melting temperature for large charge/discharge range, low solubilities of electrode materials for low self-discharge, low material costs, and high material abundance for easy scale-up. Based on these criteria, the NaCl-CaCl₂-BaCl₂ and NaCl-SrCl₂-KCl salt mixtures are selected as the two most promising ALB molten salt electrolytes and suggested to be tested in the ALB demonstrators currently under development. Full article

Developing efficient bifunctional oxygen reduction (ORR) and oxygen evolution (OER) electrocatalysts is critical for renewable energy technologies. Noble metal catalysts face limitations in cost, scarcity, and bifunctional compatibility. Herein, we report the synthesis of nickel nanoparticles encapsulated in nitrogen-doped carbon nanosheets (Ni@NC-T) via a solvothermal polymerization and pyrolysis process using a Ni-hexamine coordination framework (NiHMT) as a precursor. The Ni@NC-900 catalyst exhibits superior ORR and OER activity under alkaline conditions, with an ORR performance (half-wave potential = 0.86 V) comparable to commercial Pt/C and an OER overpotential of only 430 mV at 10 mA cm⁻². Structural analysis indicates that the hierarchical porous structure and high specific surface area (409 m² g⁻¹) of Ni@NC-900 facilitate the exposure of active sites and enhance mass transport. The surface-doped nitrogen species, predominantly in the form of pyridinic N and graphitic N, promote electron transfer during the ORR. Furthermore, its application as a bifunctional cathode in rechargeable zinc-air batteries results in a high power density of 137 mW cm⁻², surpassing the performance levels of many existing carbon-based bifunctional catalysts. This work highlights a facile strategy for the fabrication of transition metal-based catalysts encapsulated in MOF-derived carbon matrices, with promising potential for energy storage and conversion devices. Full article

Researchers are developing innovative electrode materials with high energy and power densities worldwide for effectual energy storage systems. Transition metal dichalcogenides (TMDs) are arranged in two dimensions (2D) and have shown great promise as materials for photoelectrochemical activity and supercapacitor batteries. This study reports on the fabrication of WS₂@NiCoS and WS₂@NiCoS@ZnS hybrid nano-architectures through a simple hydrothermal approach. Because of the strong interfacial contact between the two materials, the resultant hierarchical hybrids have tunable porosity nanopetal decorated morphologies, rich exposed active edge sites, and high intrinsic activity. The specific capacities of the hybrid supercapacitors built using WS₂@NiCoS and WS₂@NiCoS@ZnS electrodes are 784.38 C g⁻¹ and 1211.58 C g⁻¹ or 2019.3 F g⁻¹, respectively, when performed at 2 A g⁻¹ using a three-electrode setup. Furthermore, an asymmetric device (WS₂@NiCoS@ZnS//AC) shows a high specific capacity of 190.5 C g⁻¹, an energy density of 49.47 Wh kg^−1, and a power density of 1212.30 W kg⁻¹. Regarding the photoelectrochemical activity, the WS₂@NiCoS@ZnS catalyst exhibits noteworthy characteristics. Our findings pave the way for further in-depth research into the use of composite materials doped with WS₂ as systematic energy-generating devices of the future. Full article

Prussian blue analogs (PBAs) are appealing cathode materials for sodium-ion batteries because of their low material cost, facile synthesis methods, rigid open framework, and high theoretical capacity. However, the poor electrical conductivity, unavoidable presence of [Fe(CN)₆] vacancies and crystalline water within the framework, and phase transition during charge–discharge result in inferior electrochemical performance, particularly in terms of rate capability and cycling stability. Here, cobalt-free PBAs are synthesized using a facile and economic co-precipitation method at room temperature, and their sodium-ion storage performance is boosted due to the reduced crystalline water content and improved electrical conductivity via the high-entropy and component stoichiometry tuning strategies, leading to enhanced initial Coulombic efficiency (ICE), specific capacity, cycling stability, and rate capability. The optimized HE-HCF of Fe_0.60Mn_0.10-hexacyanoferrate (referred to as Fe_0.60Mn_0.10-HCF), with the chemical formula Na_1.156Fe_0.599Mn_0.095Ni_0.092Cu_0.109Zn_0.105 [Fe(CN)₆]_0.724·3.11H₂O, displays the most appealing electrochemical performance of an ICE of 100%, a specific capacity of around 115 and 90 mAh·g⁻¹ at 0.1 and 1.0 A·g⁻¹, with 66.7% capacity retention observed after 1000 cycles and around 61.4% capacity retention with a 40-fold increase in specific current. We expect that our findings could provide reference strategies for the design of SIB cathode materials with superior electrochemical performance. Full article

Aqueous zinc ion batteries (AZIBs) have received a lot of attention in electrochemical energy storage systems for their low cost, environmental compatibility, and good safety. However, cathode materials still face poor material stability and conductivity, which cause poor reversibility and poor rate performance in AZIBs. Herein, a heterogeneous structure combined with cation pre-intercalation strategies was used to prepare a novel CaV₆O₁₆·3H₂O@Ni_0.24V₂O₅·nH₂O material (CaNiVO) for high-performance Zn storage. Excellent energy storage performance was achieved via the wide interlayer conductive network originating from the interlayer-embedded metal ions and heterointerfaces of the two-phase CaNiVO. Furthermore, this unique structure further showed excellent structural stability and led to fast electron/ion transport dynamics. Benefiting from the heterogeneous structure and cation pre-intercalation strategies, the CaNiVO electrodes showed an impressive specific capacity of 334.7 mAh g⁻¹ at 0.1 A g⁻¹ and a rate performance of 110.3 mAh g⁻¹ at 2 A g⁻¹. Therefore, this paper provides a feasible strategy for designing and optimizing cathode materials with superior Zn ion storage performance. Full article

The recycling and recovery of value-added secondary raw materials such as spent Zn/C batteries is crucial to reduce the environmental impact of wastes and to achieve cost-effective and sustainable processing technologies. The aim of this work is to fabricate reduced graphene oxide (rGO)-based sorbents with a desulfurization capability using recycled graphite from spent Zn/C batteries as raw material. Recycled graphite was obtained from a black mass recovered from the dismantling of spent batteries by a hydrometallurgical process. Graphene oxide (GO) obtained by the Tour’s method was comparable to that obtained from pure graphite. rGO-based sorbents were prepared by doping obtained GO with NiO and ZnO precursors by a hydrothermal route with a final annealing step. Recycled graphite along with the obtained GO, intermediate (rGO-NiO-ZnO) and final composites (rGO-NiO-ZnO-400) were characterized by Wavelength Dispersive X-ray Fluorescence (WDXRF) and X-ray diffraction (XRD) that corroborated the removal of metal impurities from the starting material as well as the presence of NiO- and ZnO-doped reduced graphene oxide. The performance of the prepared composites was evaluated by sulfidation tests under different conditions. The results revealed that the proposed rGO-NiO-ZnO composite present a desulfurization capability similar to that of commercial sorbents which constitutes a competitive alternative to syngas cleaning. Full article

This study aims to optimize the Environmental Life Cycle Assessment (LCA) and Life Cycle Cost (LCC) of NiZn batteries using Pareto Optimization (PO) and Multi-objective Particle Swarm Optimization (MOPSO), which combine Pareto optimization and genetic algorithms (GA). The optimization focuses on the raw material acquisition phase and the end-of-life phase of NiZn batteries to improve their sustainability Key Performance Indicators (KPIs). The optimization methodology, programmed in MATLAB, is based on a formulation model of LCC and the environmental LCA, using data available from the Ecoinvent database, the OpenLCA software (V1.11.0), and other public databases. Results provide insights about the best combination of countries for acquiring raw materials to manufacture NiZn and for disposing of the waste of NiZn batteries that cannot be recycled. These results were automatically linked to some sustainability KPIs, such as global warming and capital costs, being replicable in case of data updates or changes in production or recycling locations, which were initially considered at Paris (France) and Krefeld (Germany), respectively. These results provided by an AI model were validated by using a sensitivity analysis and the Analytical Hierarchy Process (AHP) through an expert panel. The sensitivity analysis ensures the robustness of mathematical parameters and future variations in the market; on the other hand, the AHP validates the Artificial Intelligence (AI) results with interactions of human factors. Further developments should also consider the manufacturing and use phases in the optimization model. Full article

In this study, we synthesized spinel high-entropy oxide (HEO) (Cr_0.2Mn_0.2Co_0.2Ni_0.2Zn_0.2)₃O₄ nanoparticles by a simple solution combustion method. These particles were investigated for their performance as anodes in lithium-ion batteries. The reversible capacity is 132 mAh·g⁻¹ after 100 cycles at a current density of 100 mA·g⁻¹, 107 mAh·g⁻¹ after 1000 cycles at a current density of 1 A g⁻¹, and 96 mAh·g⁻¹ rate capacity at a high current density of 2 A g⁻¹. The outstanding cycle stability under high current densities and remarkable rate performance can be attributed to the stable structure originating from the high entropy of the material. Full article

This paper presents a comprehensive and systematic analysis of the environmental impacts (EI) produced by novel nickel-zinc battery (RNZB) technology, which is a promising alternative for energy storage applications. The paper develops mathematical models for estimating the life cycle environmental impacts of RNZB from cradle to grave, based on an extensive literature review and the ISO standards for life cycle costing and life cycle analysis. The paper uses the ReCiPe 2016 method of life cycle analysis (LCA) to calculate the EI of RNZB in terms of eighteen Midpoint impact categories and three Endpoint impact categories: damage to human health, damage to ecosystem diversity, and damage to resource availability. The paper also compares the EI of RNZB with those of other battery technologies, such as lead-acid and lithium-ion LFP and NMC. The paper applies the models and compares results with those provided by the software openLCA (version 1.11.0), showing its reliability and concluding that NiZn batteries contribute approximately 14 MJ for CED and 0.82 kg CO₂ eq. for global warming per kWh of released energy, placing them between lithium-ion and lead-acid batteries. This study suggests that NiZn battery technology could benefit from using more renewable energy in end-use applications and adopting green recovery technology to reduce environmental impact. Further developments can use these models as objective functions for heuristic optimisation of the EI in the life cycle of RNZB. Full article

The development of low-cost, high-performance oxygen electrocatalysts is of great significance for energy conversion and storage. As a potential substitute for precious metal electrocatalysts, the construction of efficient and cost-effective oxygen electrocatalysts is conducive to promoting the widespread application of zinc–air batteries. Herein, Co_xNi_yMOF nanoparticles encapsulated within a carbon matrix were synthesized and employed as cathode catalysts in zinc–air batteries. Co_0.5Ni_0.5MOF exhibits superior oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) performance and durability. The zinc–air battery assembled with Co_0.5Ni_0.5MOF as the air cathode exhibits a maximum power density of 138.6 mW·cm⁻². These improvements are mainly attributed to the optimized metal composition of the cobalt–nickel alloy, which increases the specific surface area of the material and optimizes its pore structure. Significantly, the optimization of the electronic structure and active sites within the material has led to amplified ORR/OER activity and better zinc–air battery performance. This study underscores the immense promise of Co_0.5Ni_0.5MOF catalysts as feasible substitutes for commercial Pt/C catalysts in zinc–air batteries. Full article

This research investigated the contamination characteristics, sources, and health risks of five metals in soils from two villages named DK and SXC, downstream from a battery industry hub in Xinxiang city, Henan Province, China. The average concentrations of Cd, Pb, Ni, Cu, and Zn in DK were 5.93, 41.31, 71.40, 62.20, and 115.83 mg/kg, respectively, and in SXC were 2.04, 30.41, 41.22, 36.18, and 96.04 mg/kg, respectively. The single factor pollution index (P_i) revealed a consistent descending order of Cd > Cu > Zn > Ni > Pb in DK and SXC. The geo-accumulation index (I_geo) indicated that the Cd pollution in DK was extreme, and in SXC was at a heavy to extreme level. The potential ecological risk index (PERI) indicated that Cd presented a significantly high ecological risk while it was low for other metals. Principal component analysis classified them into the anthropogenic origin of Cd and common mixed origin of others. The elevated levels and pollution load of heavy metals with closer proximity to the battery factory imply that the factory is a probable source of contamination. Overall, the health risks posed by heavy metals were more pronounced for local children compared to adults, with Cd being the primary contributor to both pollution and health risks. This investigation provides a crucial basis for the heavy metal pollution management and related risk prevention in areas affected by electronic waste irrigation. Full article