Search Results (126)

High-nickel (Ni) ternary lithium-ion batteries (LIBs) are widely used in low-pressure environments such as in the aviation industry, but their attribute of high energy density poses significant fire hazards, especially under low pressure where thermal runaway behavior is complex, thus requiring relevant experiments. This study investigates the thermal runaway characteristics of LiNi_0.8Mn_0.1Co_0.1O₂ (NCM811) 18650 LIBs at different states of charge (SOCs) (75%, 100%) under various ambient pressures (101 kPa, 80 kPa, 60 kPa, 40 kPa). The results show that, as the pressure is decreased from 101 kPa to 40 kPa, the onset time of thermal runaway is extended by 28.2 s for 75% SOC and by 40.8 s for 100% SOC; accordingly, the onset temperature of thermal runaway increases by 19.3 °C for 75% SOC and by 33.5 °C for 100% SOC; the maximum surface temperature decreases by 70.8 °C for 75% SOC and by 68.2 °C for 100% SOC. The cell mass loss and loss rate slightly decrease with reduced pressure. However, ambient pressure has little impact on the time and temperature of venting as well as the voltage drop time. SEM/EDS analysis verifies that electrolyte evaporates faster under low pressure. Furthermore, the oxygen concentration is lower under low pressure, which consequently leads to a delay in thermal runaway. This study contributes to understanding thermal runaway characteristics of high-Ni ternary LIBs and provides guidance for their safe application in low-pressure aviation environments. Full article

Lithium–sulfur batteries (LSBs) have attracted widespread attention due to their high theoretical energy density and low cost. However, their development has been constrained by the shuttle effect of lithium polysulfides and their slow reaction kinetics. In this work, a nitrogen/oxygen dual-doped porous carbon (N/O-PC) was synthesized by annealing the precursor of zeolitic imidazolate framework-8 grown in situ on MWCNTs (ZIF-8/MWCNTs). Then, the N/O-PC composite served as an efficient host for LSBs through chemical adsorption and providing catalytic conversion sites of polysulfides. Moreover, the interconnected porous carbon-based structure facilitates electron and ion transfer. Thus, the S/N/O-PC cathode exhibits high cycling stability (a stable capacity of 685.9 mA h g⁻¹ at 0.2 C after 100 cycles). It also demonstrates excellent rate performance with discharge capacities of 1018.2, 890.2, 775.1, 722.7, 640.4, and 579.6 mAh g⁻¹ at 0.2, 0.5, 1.0, 2.0, 3.0, and 5.0 C, respectively. This work provides an effective strategy for designing and developing high energy density, long cycle life LSBs. Full article

As modern society continues to advance, the depletion of non-renewable energy sources (such as natural gas and petroleum) exacerbates environmental and energy issues. The development of green, environmentally friendly energy storage and conversion systems is imperative. The energy density of commercial lithium-ion batteries is approaching its theoretical limit, and even so, it struggles to meet the rapidly growing market demand. Lithium–oxygen batteries have garnered significant attention from researchers due to their exceptionally high theoretical energy density. However, challenges such as poor electrolyte stability, short cycle life, low discharge capacity, and high overpotential arise from the sluggish kinetics of the oxygen reduction reaction (ORR) during discharge and the oxygen evolution reaction (OER) during charging. This article elucidates the fundamental principles of lithium–oxygen batteries, analyzes the primary issues currently faced, and summarizes recent research advancements in air cathodes and anodes. Additionally, it proposes future directions and efforts for the development of lithium–air batteries. Full article

Understanding the thermal runaway mechanism of lithium-ion batteries under low pressure and low temperature is paramount for their application and transportation in the aviation industry. This work investigated the coupling effects of ambient pressure (100 kPa, 70 kPa, 40 kPa) and ambient temperature (−15 °C, 0 °C, 25 °C) on thermal behaviors in an altitude temperature chamber. The experimental results indicate that lowering ambient pressure and temperature could attenuate the thermal runaway intensity, which is mainly attributable to the reduction in oxygen concentration and the increase in heat loss. Such a dual effect leads to the maximum temperature decreasing from 811.9 °C to 667.5 °C, and the maximum temperature rate declines up to 2.6 times. Correspondingly, the whole thermal runaway process is deferred, the total time increases from 370 s to 503 s, and the time interval, Δt, from safety venting gains by 32.3% as the ambient pressure and temperature decrease. This work delivers an in-depth understanding of the thermal characteristics under low pressure and low temperature and provides meritorious guidance for the safety of cell transportation in aviation. Full article

Oxygen reduction reaction (ORR) and oxygen evolutionc reaction (OER) are important chemical reactions for a rechargeable lithium–oxygen battery (LOB). Recently, high-entropy alloys and oxides have attracted much attention because they showed good electrocatalytic performance for oxygen evolution reaction (OER) and/or oxygen reduction reaction (ORR). In this study, we aimed to synthesize and characterize CoSn(OH)₆ and two types of high-entropy perovskite hydroxides, that is, (Co_0.2Cu_0.2Fe_0.2Mn_0.2Mg_0.2)Sn(OH)₆ (CCFMMSOH) and (Co_0.2Cu_0.2Fe_0.2Mn_0.2Ni_0.2)Sn(OH)₆ (CCFMNSOH). TEM observation and XRD measurements revealed that the high-entropy hydroxides CCFMMSOH and CCFMNSOH had cubic crystals with sides of approximately 150–200 nm and crystal structures similar to those of perovskite-type CSOH. LSV measurement results showed that the high-entropy hydroxides CCFMMSOH and CCFMNSOH showed bifunctional catalytic functions for the ORR and OER. CCFMNSOH showed better catalytic performance than CCFMMSOH. Full article

Using silicon/reduced graphene oxide (Si/rGO) composites as lithium-ion battery (LIB) anodes can effectively buffer the volumetric expansion and shrinkage of Si. Herein, we designed and prepared Si/rGO-b with a sandwiched structure, formed by a duple combination of ammonia-modified silicon (m-Si) nanoparticles (NP) with graphene oxide (GO). In the first composite process of m-Si and GO, a core–shell structure of primal Si/rGO-b (p-Si/rGO-b) was formed. The amino groups on the m-Si surface can not only hybridize with the GO surface to fix the Si particles, but also form covalent chemical bonds with the remaining carboxyl groups of rGO to enhance the stability of the composite. During the electrochemical reaction, the oxygen on the m-Si surface reacts with lithium ions (Li⁺) to form Li₂O, which is a component of the solid–electrolyte interphase (SEI) and is beneficial to buffering the volume expansion of Si. Then, the p-Si/rGO-b recombines with GO again to finally form a sandwiched structure of Si/rGO-b. Covalent chemical bonds are formed between the rGO layers to tightly fix the p-Si/rGO-b, and the conductive network formed by the reintroduced rGO improves the conductivity of the Si/rGO-b composite. When used as an electrode, the Si/rGO-b composite exhibits excellent cycling performance (operated stably for more than 800 cycles at a high-capacity retention rate of 82.4%) and a superior rate capability (300 mA h/g at 5 A/g). After cycling, tiny cracks formed in some areas of the electrode surface, with an expansion rate of only 27.4%. The duple combination of rGO and the unique sandwiched structure presented here demonstrate great effectiveness in improving the electrochemical performance of alloy-type anodes. Full article

High-nickel ternary materials are currently the most promising lithium battery cathode materials due to their development and application potential. Nevertheless, these materials encounter challenges like cation mixing, lattice oxygen loss, interfacial reactions, and microcracks. These issues are exacerbated at high voltages, compromising their cyclic stability and safety. In this study, we successfully prepared Nb⁵⁺-doped high-nickel ternary cathode materials via a high-temperature solid-phase method. We investigated the impact of Nb⁵⁺ doping on the microstructure and electrochemical properties of LiNi_0.88Co_0.05Mn_0.07O₂ ternary cathode materials by varying the amount of Nb₂O₅ added. The experimental results suggest that Nb⁵⁺ doping does not alter the crystal structure but modifies the particle morphology, yielding radially distributed, elongated, rod-like structures. This morphology effectively mitigates the anisotropic volume changes during cycling, thereby bolstering the material’s cyclic stability. The material exhibits a discharge capacity of 224.4 mAh g⁻¹ at 0.1C and 200.3 mAh g⁻¹ at 1C, within a voltage range of 2.7 V–4.5 V. Following 100 cycles at 1C, the capacity retention rate maintains a high level of 92.9%, highlighting the material’s remarkable capacity retention and cyclic stability under high-voltage conditions. The enhancement of cyclic stability is primarily due to the synergistic effects caused by Nb⁵⁺ doping. Nb⁵⁺ modifies the particle morphology, thereby mitigating the formation of microcracks. The formation of high-energy Nb-O bonds prevents oxygen precipitation at high voltages, minimizes the irreversibility of the H2–H3 phase transition, and thereby enhances the stability of the composite material at high voltages. Full article

The porous architectures of oxygen cathodes are highly desired for high-capacity lithium–oxygen batteries (LOBs) to support cathodic catalysts and provide accommodation for discharge products. However, controllable porosity is still a challenge for laminated cathodes with cathode materials and binders, since polymer binders usually shield the active sites of catalysts and block the pores of cathodes. In addition, polymer binders such as poly(vinylidene fluoride) (PVDF) are not stable under the nucleophilic attack of intermediate product superoxide radicals in the oxygen electrochemical environment. The parasitic reactions and blocking effect of binders deteriorate and then quickly shut down the operation of LOBs. Herein, the present work proposes a binder-free three-dimensional (3D) porous graphene (PG) cathode for LOBs, which is prepared by the self-assembly and the chemical reduction of GO with triblock copolymer soft templates (Pluronic F127). The interconnected mesoporous architecture of resultant 3D PG cathodes achieved an ultrahigh capacity of 10,300 mAh g⁻¹ for LOBs. Further, the cathodic catalysts ruthenium (Ru) and manganese dioxide (MnO₂) were, respectively, loaded onto the inner surface of PG cathodes to lower the polarization and enhance the cycling performance of LOBs. This work provides an effective way to fabricate free-standing 3D porous oxygen cathodes for high-performance LOBs. Full article

The biaxially-oriented PA56/512 has excellent mechanical strength, extensibility and water–oxygen barrier properties and has broad application prospects in green packaging, lithium battery diaphragm and medical equipment materials. The correlation between the aggregation structure evolution and macroscopic comprehensive properties of copolymer PA56/512 under biaxial stretching has been demonstrated in this work. The structure of the random copolymerization sequence was characterized by ¹³C Nuclear magnetic resonance (NMR). The typical isodimorphism behavior of the co-crystallization system of PA56/512 and its BOPA-56/512 films was revealed by differential scanning calorimetry (DSC) and X-ray diffraction (XRD) tests. And the aggregation structure, including the hydrogen bond arrangement, crystal structure and crystal morphology of PA56/512 before and after biaxial stretching, was investigated by XRD, Fourier-transform infrared spectroscopy (FTIR) and polarized optical microscopy (POM) tests. Furthermore, the effect of the biaxially-oriented stretching process on the mechanical properties of PA56/512 has been demonstrated. In addition, a deep insight into the influence of the structure on the crystallization process and physical–mechanical performance has been presented. The lowest melting point at a 512 content of 60 mol% is regarded as a “eutectic” point of the isodimorphism system. Due to the high disorder of the structural units in the polymer chain, the transition degree of the folded chain (gauche conformation) is relatively lowest when it is straightened to form an extended chain (trans conformation) during biaxially-oriented stretching, and part of the folded chain can be retained. This explains why biaxially stretched PA56/512 has high strength, outstanding toughness and excellent barrier properties at the pseudo-eutectic point. In this study, using the unique multi-scale aggregation structure characteristics of a heterohomodymite polyamide at the pseudo-eutectic point, combined with the new material design scheme and the idea of biaxial-stretching processing, a new idea for customized design of high-performance multifunctional polyamide synthetic materials is provided. Full article

Lithium-ion batteries (LIBs) remain the cornerstone of EV technology due to their exceptional energy density. The selection of cathode materials is a decisive factor in LIB technology, profoundly influencing performance, energy density, and lifespan. Among these materials, nickel-rich NCM cathodes have gained significant attention due to their high specific capacity and cost-effectiveness, making them a preferred choice for EV energy storage. However, the transition from the laboratory-scale to industrial-scale production of NMC-811 cathode material presents challenges, particularly in optimizing the oxidation process of Ni²⁺ ions. This paper addresses the challenges of transitioning NMC-811 cathode material production from a lab scale to a pilot scale, with its high nickel content requiring specialized oxidation processes. The important point emphasized in this transition process is how to produce cathode materials on a pilot scale, but show results equivalent to the laboratory scale. Several optimization variations are carried out, namely, the optimization of the heating rate and the calcination and sintering temperatures, as well as oxygen variations. These two aspects are important for large-scale production. This paper discusses strategies for successful pilot-scale production, laying the foundation for industrial-scale manufacturing. Additionally, NMC-811 cathodes are incorporated into 18650 cylindrical cells, advancing the adoption of high-performance cathode materials. Full article

Ni-rich layered cathodes are deemed as a potential candidate for high-energy-density lithium-ion batteries, but their high sensitivity to air during storage and poor thermal stability are a vital challenge for large-scale applications. In this paper, distinguished from the conventional surface modification and ion doping, an effective solid-solution strategy was proposed to strengthen the surface and structural stability of Ni-rich layered cathodes by introducing Li₂MnO₃. The structural analysis results indicate that the formation of Li₂CO₃ inert layers on Ni-rich layered cathodes during storage in air is responsible for the increased electrode interfacial impedance, thereby leading to the severe deterioration of electrochemical performance. The introduction of Li₂MnO₃ can reduce the surface reactivity of Ni-rich cathode materials, playing a certain suppression effect on the formation of surface Li₂CO₃ layer and the deterioration of electrochemical performances. Additionally, the thermal analysis results show that the heat release of Ni-rich cathodes strongly depends on the charge of states, and Li₂MnO₃ can suppress oxygen release and significantly enhance the thermal stability of Ni-rich layered cathodes. This work provides a method to improving the storage performance and thermal stability of Ni-rich cathode materials. Full article

Lithium-ion batteries (LIBs) are fundamental for the energetic transition necessary to contrast climate change. The characteristics of cathode active materials (CAMs) strongly influence the cell performance, so improved CAMs need to be developed. Currently, Li(Ni_0.8Mn_0.1Co_0.1)O₂ (NMC811) is state-of-the-art among the cathodic active materials. The aim of this work is the optimization of the procedure to produce NMC811: two different syntheses were investigated, the co-precipitation and the self-combustion methods. For a better understanding of the synthesis conditions, three different types of atmospheres were tested during the calcination phase: air (partially oxidizing), oxygen (totally oxidizing), and nitrogen (non-oxidizing). The synthesized oxides were characterized by X-ray Powder Diffraction (XRPD), Scanning Electron Microscopy (SEM), Energy Dispersive X-ray (EDX), Inductively Coupled Plasma (ICP), and Particle Size Distribution (PSD). The most promising materials were tested in a half-cell set up to verify the electrochemical performances. The procedure followed during this study is depicted in the graphical abstract. The oxidizing atmospheric conditions turned out to be the most appropriate to produce NMC811 with good electrochemical properties. Full article

Nitrogen and sulfur co-doped graphene-like carbon nanosheets (CNSs) with a two-dimensional structure are prepared by using methylene blue as a carbon source and expanded vermiculite as a template. After static negative pressure adsorption, high-temperature calcination, and etching in a vacuum oven, they are embedded in the limited space of the vermiculite template. The addition of an appropriate number of mixed elements can improve the performance of a battery. Via scanning electron microscopy, it is found that the prepared nitrogen–sulfur-co-doped carbon nanosheets exhibit a thin yarn shape. The XPS results show that there are four elements of C, N, O, and S in the carbon materials (CNS-600, CNS-700, CNS-800, CNS-900) prepared at different temperatures, and the N atom content shows a gradually decreasing trend. It is mainly doped into a graphene-like network in four ways (graphite nitrogen, pyridine nitrogen, pyrrole nitrogen, and pyridine nitrogen oxide), while the S element shows an increasing trend, mainly in the form of thiophene S and sulfur, which is covalently linked to oxygen. The results show that CNS-700 has a discharge-specific capacity of 460 mAh/g at a current density of 0.1 A/g, and it can still maintain a specific capacity of 200 mAh/g at a current density of 2 A/g. The assembled lithium-ion capacitor has excellent energy density and power density, with a maximum power density of 20,000 W/kg. Full article

Lithium–air batteries (LABs) have a theoretically high energy density. However, LABs have some issues, such as low energy efficiency, short life cycle, and high overpotential in charge–discharge cycles. To solve these issues electrocatalytic materials were developed for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER), which significantly affect battery performance. In this study, we aimed to synthesize electrocatalytic N-doped carbon-based composite materials with solution plasma (SP) using Co or Ni as electrodes from organic solvents containing cup-stacked carbon nanotubes (CSCNTs), iron (II) phthalocyanine (FePc), and N-nethyl-2-pyrrolidinone (NMP). The synthesized N-doped carbon-based composite materials were characterized by transmission electron microscopy (TEM), X-ray diffraction (XRD), Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS). TEM observation and XPS measurements revealed that the synthesized carbon materials contained elemental N, Fe, and electrode-derived Co or Ni, leading to the successful synthesis of N-doped carbon-based composite materials. The electrocatalytic activity for ORR of the synthesized carbon-based composite materials was also evaluated using electrochemical measurements. The electrochemical measurements demonstrated that the electrocatalytic performance for ORR of N-doped carbon-based composite material including Fe and Co showed superiority to that of N-doped carbon-based composite material including Fe and Ni. The difference in the electrocatalytic performance for ORR is discussed regarding the difference in the specific surface area and the presence ratio of chemical bonding species. Full article

Molybdenum trioxide is an abundant natural, low-cost, and environmentally friendly material that has gained considerable attention from many researchers in a variety of high-impact applications. It is an attractive inorganic oxide that has been widely studied because of its layered structure, which results in intercalation ability through tetrahedral/octahedral holes and extension channels and leads to superior charge transfer. Shape-related properties such as high specific capacities, the presence of exposed active sites on the oxygen-rich structure, and its natural tendency to oxygen vacancy that leads to a high ionic conductivity are also attractive to technological applications. Due to its chemistry with multiple valence states, high thermal and chemical stability, high reduction potential, and electrochemical activity, many studies have focused on the development of molybdenum oxide-based systems in the last few years. Thus, this article aims to briefly review the latest advances in technological applications of MoO₃ and MoO₃-based materials in gas sensors, lithium-ion batteries, and water pollution treatment using adsorption and photocatalysis techniques, presenting the most relevant and new information on heterostructures, metal doping, and non-stoichiometric MoO_3−x. Full article