Browse
Submit Data
Databases
API
Help

Dataset Information

49 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Fabrication of the Ni-NiCl₂ Composite Cathode Material for Fast-Response Thermal Batteries.

ABSTRACT: Thermal batteries with a high power density and rapid activation time are crucial for improving the fast response ability of sophisticated weapons. In this study, an Ni-NiCl₂ composite was prepared via hydrogen reduction and employed as a cathode material. Discharge tests on a battery assembled using the fabricated composite revealed that its initial internal resistance decreased and the activation time reduced. Notably, the Ni-NiCl₂ cathode increased the energy output by 47% (from 6.76 to 9.94 Wh in NiCl₂ and Ni-NiCl₂, respectively) with a cut-off voltage of 25 V; the power density of the novel battery system reached 11.4 kW/kg. The excellent performance of the thermal battery benefited from the high electrode potential and low internal resistance of Ni-NiCl₂. This study contributes to the development of high-performance electrode materials for next-generation thermal battery-related technologies.

SUBMITTER: Tian Q

PROVIDER: S-EPMC8165393 | biostudies-literature | 2021

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Fabrication of the Ni-NiCl2 Composite Cathode Material for Fast-Response Thermal Batteries.

Tian Qianqiu Q Wang Jiajun J Xiang Wendi W Zhao Jun J Guo Hao H Hu Jing J Han Xiaopeng X Hu Wenbin W

Frontiers in chemistry 20210517

Thermal batteries with a high power density and rapid activation time are crucial for improving the fast response ability of sophisticated weapons. In this study, an Ni-NiCl2 composite was prepared via hydrogen reduction and employed as a cathode material. Discharge tests on a battery assembled using the fabricated composite revealed that its initial internal resistance decreased and the activation time reduced. Notably, the Ni-NiCl2 cathode increased the energy outp ...[more]

PMID: 34079790

Similar Datasets

Sulfate-Containing Composite Based on Ni-Rich Layered Oxide LiNi0.8Mn0.1Co0.1O2 as High-Performance Cathode Material for Li-ion Batteries.

Project description:Composite positive electrode materials (1-x) LiNi0.8Mn0.1Co0.1O2∙xLi2SO4 (x = 0.002-0.005) for Li-ion batteries have been synthesized via conventional hydroxide or carbonate coprecipitation routes with subsequent high-temperature lithiation in either air or oxygen atmosphere. A comparative study of the materials prepared from transition metal sulfates (i.e., containing sulfur) and acetates (i.e., sulfur-free) with powder X-ray diffraction, electron diffraction, high angle annular dark field transmission electron microscopy, energy-dispersive X-ray spectroscopy, and electron energy loss spectroscopy revealed that the sulfur-containing species occur as amorphous Li2SO4 at the grain boundaries and intergranular contacts of the primary NMC811 crystallites. This results in a noticeable enhancement of rate capability and capacity retention over prolonged charge/discharge cycling compared to their sulfur-free analogs. The improvement is attributed to suppressing the high voltage phase transition and the associated accumulation of anti-site disorder upon cycling and improving the secondary agglomerates' mechanical integrity by increasing interfacial fracture toughness through linking primary NMC811 particles with soft Li2SO4 binder, as demonstrated with nanoindentation experiments. As the synthesis of the (1-x) LiNi0.8Mn0.1Co0.1O2∙xLi2SO4 composites do not require additional operational steps to introduce sulfur, these electrode materials might demonstrate high potential for commercialization.

| S-EPMC7759786 | biostudies-literature

Fabrication and Characterization of a Composite Ni-SDC Fuel Cell Cathode Reinforced by Ni Foam.

Project description:High-temperature fuel cells (namely, molten carbonate and solid oxide; MCFCs and SOFCs) require the cathode to be designed to maximize oxygen catalytic reduction, oxygen ion transport, electrical conductivity, and gas transport. This then leads to the optimization of the volume fraction and morphology of phases, as they are a pathway for electrons, ions, and gases to be continuous and self-interpenetrating. Apart from the functional properties, the cathode must be mechanically stable to prevent cracking during fuel cell assembly and operation. The manufacturing process of the composite cathode was optimized to meet such requirements in this research work. The tape casting technique and further firing process were used to fabricate the cathodes. The slurry for the green tape was composed of nickel (Ni), cerium oxide doped with samarium oxide (SDC), water (solvent), and an organic binder (which becomes pore space after firing). Each of these elements is necessary for the effective transport of specific species: electrons, oxygen, ions, and gas particles, respectively. Moreover, the nickel foam was embedded into the powder-based structure to improve mechanical strength. The study involved many technological issues, such as the effect of the SDC fraction on the cathode microstructure, mechanical strength, and chemical stability at high temperatures, and also involved environmental issues.

| S-EPMC9319338 | biostudies-literature

Tunnel/Layer Composite Na0.44MnO2 Cathode Material with Enhanced Structural Stability via Cobalt Doping for Sodium-Ion Batteries.

Project description:Sodium-ion batteries (SIBs) are the most promising alternative to lithium-ion batteries (LIBs) due to their low cost and environmental friendliness; therefore, enhancing the performance of SIBs' components is crucial. Although most of the studies have focused on single-phase cathode electrodes, these materials have difficulty in meeting the requirements in practice. At this point, composite materials show superior performance due to balancing different structures and are offered as an alternative to single-phase cathodes. In this study, we synthesized a Na0.44MnO2/Na0.7MnO2.05 composite material in a single step with cobalt substitution. Changes in the crystal structure and the physical and electrochemical properties of the composite and bare structures were studied. We report that even if the initial capacity is slightly lower, the rate and cyclic performance of the 1% Co-substituted composite sample (CO10) are superior to the undoped Na0.44MnO2 (NMO) and 5% Co-substituted (CO50) samples after 100 cycles. The results show that with the composite cathode phase transformations are suppressed, structural degradation is prevented, and better battery performance is achieved.

| S-EPMC10399157 | biostudies-literature

High-Ni cathode material improved with Zr for stable cycling of Li-ion rechargeable batteries.

Project description:The Zr solvent solution method, which allows primary and secondary particles of LiNi0.90Co0.05Mn0.05O2 (NCM) to be uniformly doped with Zr and simultaneously to be coated with an Li2ZrO3 layer, is introduced in this paper. For Zr doped NCM, which is formed using the Zr solvent solution method (L-NCM), most of the pinholes inside the precursor disappear owing to the diffusion of the Zr dopant solution compared with Zr-doped NCM, which is formed using the dry solid mixing method from the (Ni0.90Co0.05Mn0.05)(OH)2 precursor and the Zr source (S-NCM), and Li2ZrO3 is formed at the pinhole sites. The mechanical strength of the powder is enhanced by the removal of the pinholes by the formation of Li2ZrO3 resulting from diffusion of the solvent during the mixing process, which provides protection from cracking. The coating layer functions as a protective layer during the washing process for removing the residual Li. The electrochemical performance is improved by the synergetic effects of suitable coatings and the enhanced structural stability. The capacity-retentions for 2032 coin cells are 86.08%, 92.12%, and 96.85% at the 50th cycle for pristine NCM, S-NCM, and L-NCM, respectively. The superiority of the liquid mixing method is demonstrated for 18 650 full cells. In the 300th cycle in the voltage range of 2.8-4.35 V, the capacity-retentions for S-NCM and L-NCM are 77.72% and 81.95%, respectively.

| S-EPMC9055541 | biostudies-literature

Outstanding Electrochemical Performance of Ni-Rich Concentration-Gradient Cathode Material LiNi0.9Co0.083Mn0.017O2 for Lithium-Ion Batteries.

Project description:The full-concentrationgradient LiNi0.9Co0.083Mn0.017O2 (CG-LNCM), consisting of core Ni-rich LiNi0.93Co0.07O2, transition zone LiNi1-x-yCoxMnyO2, and outmost shell LiNi1/3Co1/3Mn1/3O2 was prepared by a facile co-precipitation method and high-temperature calcination. CG-LNCM was then investigated with an X-ray diffractometer, ascanning electron microscope, a transmission electron microscope, and electrochemical measurements. The results demonstrate that CG-LNCM has a lower cation mixing of Li+ and Ni2+ and larger Li+ diffusion coefficients than concentration-constant LiNi0.9Co0.083Mn0.017O2 (CC-LNCM). CG-LNCM presents a higher capacity and a better rate of capability and cyclability than CC-LNCM. CG-LNCM and CC-LNCM show initial discharge capacities of 221.2 and 212.5 mAh g-1 at 0.2C (40 mA g-1) with corresponding residual discharge capacities of 177.3 and 156.1 mAh g-1 after 80 cycles, respectively. Even at high current rates of 2C and 5C, CG-LNCM exhibits high discharge capacities of 165.1 and 149.1 mAh g-1 after 100 cycles, respectively, while the residual discharge capacities of CC-LNCM are as low as 148.8 and 117.9 mAh g-1 at 2C and 5C after 100 cycles, respectively. The significantly improved electrochemical performance of CG-LNCM is attributed to its concentration-gradient microstructure and the composition distribution of concentration-gradient LiNi0.9Co0.083Mn0.017O2. The special concentration-gradient design and the facile synthesis are favorable for massive manufacturing of high-performance Ni-rich ternary cathode materials for lithium-ion batteries.

| S-EPMC10142341 | biostudies-literature

Enabling high energy lithium metal batteries via single-crystal Ni-rich cathode material co-doping strategy.

Project description:High-capacity Ni-rich layered oxides are promising cathode materials for secondary lithium-based battery systems. However, their structural instability detrimentally affects the battery performance during cell cycling. Here, we report an Al/Zr co-doped single-crystalline LiNi0.88Co0.09Mn0.03O2 (SNCM) cathode material to circumvent the instability issue. We found that soluble Al ions are adequately incorporated in the SNCM lattice while the less soluble Zr ions are prone to aggregate in the outer SNCM surface layer. The synergistic effect of Al/Zr co-doping in SNCM lattice improve the Li-ion mobility, relief the internal strain, and suppress the Li/Ni cation mixing upon cycling at high cut-off voltage. These features improve the cathode rate capability and structural stabilization during prolonged cell cycling. In particular, the Zr-rich surface enables the formation of stable cathode-electrolyte interphase, which prevent SNCM from unwanted reactions with the non-aqueous fluorinated liquid electrolyte solution and avoid Ni dissolution. To prove the practical application of the Al/Zr co-doped SNCM, we assembled a 10.8 Ah pouch cell (using a 100 μm thick Li metal anode) capable of delivering initial specific energy of 504.5 Wh kg-1 at 0.1 C and 25 °C.

| S-EPMC9050889 | biostudies-literature

Vanadium Pentoxide-Based Composite Synthesized Using Microwave Water Plasma for Cathode Material in Rechargeable Magnesium Batteries.

Project description:Multivalent cation rechargeable batteries are expected to perform well as high-capacity storage devices. Rechargeable magnesium batteries have an advantage in terms of resource utilization and safety. Here, we report on sulfur-doped vanadium pentoxide (S-V₂O₅) as a potential material for the cathodes of such a battery; S-V₂O₅ showed a specific capacity of 300 mAh·g-1. S-V₂O₅ was prepared by a method using a low-temperature plasma generated by carbon felt and a 2.45 GHz microwave generator. This study investigates the ability of S-V₂O₅ to achieve high capacity when added to metal oxide. The highest recorded capacity (420 mAh·g-1) was reached with MnO₂ added to composite SMn-V₂O₅, which has a higher proportion of included sulfur than found in S-V₂O₅. Results from transmission electron microscopy, energy-dispersive X-ray spectroscopy, Micro-Raman spectroscopy, and X-ray photoelectron spectroscopy show that the bulk of the SMn-V₂O₅ was the orthorhombic V₂O₅ structure; the surface was a xerogel-like V₂O₅ and a solid solution of MnO₂ and sulfur.

| S-EPMC5452843 | biostudies-other

Nano-Crystalline Li1.2Mn0.6Ni0.2O₂ Prepared via Amorphous Complex Precursor and Its Electrochemical Performances as Cathode Material for Lithium-Ion Batteries.

Project description:An amorphous complex precursor with uniform Mn/Ni cation distribution is attempted for preparing a nano-structured layered Li-rich oxide (Li1.2Mn0.6Ni0.2O₂)cathode material, using diethylenetriaminepentaacetic acid (DTPA) as a chelating agent. The materials are characterized by powder X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and electrochemical tests. The crystal structure of Li-rich materials is found to be closely related to synthesis temperature. As-obtained nano materials sintered at 850 °C for 10 h show an average size of 200 nm with a single crystal phase and good crystallinity. At a current density of 20 mA·g-1, the specific discharge capacity reaches 221 mAh·g-1 for the first cycle and the capacity retention is 81% over 50 cycles. Even at a current density of 1000 mA·g-1, the capacity is as high as 118 mAh·g-1. The enhanced rate capability can be ascribed to the nano-sized morphology and good crystal structure.

| S-EPMC5509272 | biostudies-literature

δ-VOPO4 as a high-voltage cathode material for aqueous zinc-ion batteries.

Project description:Aqueous zinc-ion batteries (AZIBs) with excellent safety, low-cost and environmental friendliness have great application potential in large-scale energy storage systems and thus have received extensive research interest. Layered oxovanadium phosphate dihydrate (VOPO4·2H2O) is an appealing cathode for AZIBs due to the unique layered framework and desirable discharge plateau, but bottlenecked by low operation voltage and unstable cycling. Herein, we propose delta-oxovanadium phosphate (δ-VOPO4) without conventional pre-embedding of metal elements or organics into the structure and paired it into AZIBs for the first time. Consequently, superior to the layered counterpart, δ-VOPO4 exhibits better performance with a prominent discharge voltage of 1.46 V and a higher specific capacity of 122.6 mA h g-1 at 1C (1C = 330 mA g-1), as well as an impressive capacity retention of 90.88 mA h g-1 after 1000 cycles under 10C. By investigation of structure resolution and theoretical calculation, this work well elucidates the structure-function relationship in vanadyl phosphates, offering more chances for exploration of new cathode materials to construct high performance AZIBs.

| S-EPMC10395308 | biostudies-literature

Li1.2Mn0.54Ni0.13Co0.13O2 nanosheets with porous structure as a high-performance cathode material for lithium-ion batteries.

Project description:The morphological and structural optimizations of electrode materials are efficient ways to enhance their electrochemical performance. Herein, we report a facile co-precipitation and subsequent calcination method to fabricate Li1.2Mn0.54Ni0.13Co0.13O2 nanosheets consisting of interconnected primary nanoparticles and open holes through the full thickness. By comparing the nanosheets and the agglomerated nanoparticles, the effects of the morphology and structure on the electrochemical performance are investigated. Specifically, the nanosheets exhibit a discharge capacity of 210 mA h g-1 at 0.5C with a capacity retention of 85% after 100 cycles. The improved electrochemical performance could be attributed to their morphological and structural improvements, which may facilitate sufficient electrolyte contacts, short diffusion paths and good structural integrity during the charge/discharge process. This work provides a feasible approach to fabricate lithium-rich layered oxide cathode materials with 2D morphology and porous structure, and reveals the relationships between their morphology, structure and electrochemical performance.

| S-EPMC9043626 | biostudies-literature