Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Influence of Mo addition on the structural and electrochemical performance of Ni-rich cathode material for lithium-ion batteries.

ABSTRACT: Molybdenum modified LiNi0.84Co0.11Mn0.05O2 cathode with different doping concentrations (0-5 wt.%) is successfully prepared and its electrochemical performances are investigated. It is demonstrated that molybdenum in LiNi0.84Co0.11Mn0.05O2 has a positive effect on structural stability and extraordinary electrochemical performances, including improved long-term cycling and high-rate capability. Among all samples, the 1 wt. % molybdenum LiNi0.84Co0.11Mn0.05O2 delivers superior initial discharge capacity of 205 mAh g-1 (0.1?C), cycling stability of 89.5% (0.5?C) and rate capability of 165 mAh g-1 (2?C) compared to those of others. Therefore, we can conclude that the 1 wt. % molybdenum is an effective strategy for Ni-rich LiNi0.84Co0.11Mn0.05O2 cathode used in lithium ion batteries.

SUBMITTER: Sattar T

PROVIDER: S-EPMC7244510 | biostudies-literature | 2020 May

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Influence of Mo addition on the structural and electrochemical performance of Ni-rich cathode material for lithium-ion batteries.

Sattar Tahir T Lee Seung-Hwan SH Jin Bong-Soo BS Kim Hyun-Soo HS

Scientific reports 20200522 1

Molybdenum modified LiNi0.84Co0.11Mn0.05O2 cathode with different doping concentrations (0-5 wt.%) is successfully prepared and its electrochemical performances are investigated. It is demonstrated that molybdenum in LiNi0.84Co0.11Mn0.05O2 has a positive effect on structural stability and extraordinary electrochemical performances, including improved long-term cycling and high-rate capability. Among all sampl ...[more]

PMID: 32444645

Similar Datasets

Dual function Li-reactive coating from residual lithium on Ni-rich NCM cathode material for Lithium-ion batteries.

Project description:In this study, lithium phosphate (Li3PO4) is coated on the surface of Ni-rich LiNi0.91Co0.06Mn0.03O2 cathode material to enhance its cyclability and rate performance. The process is carried-out by achieving dual benefits, reduction of residual lithium compounds by converting them into Li3PO4 coating material. The 0.1 mol.% Li3PO4 (LiP) sample exhibits a capacity retention of 82% while the pristine NCM shows only 68.1% after 100 cycles. In addition, the LiP-0.1 NCM delivers high discharge capacities (161.9 mAh g-1 at 3C, 144.3 mAh g-1 at 4C and 94.6 mAh g-1 at 5C) as compared to the pristine NCM (129.3 mAh g-1 at 3C, 67.4 mAh g-1 at 4C and 33.4 mAh g-1 at 5C) in the voltage range of 3.0-4.3 V. In addition, the irreversible phase transition has also suppressed in the coated sample which is confirmed by cyclic voltammetry. Our study suggests that Li3PO4 coating reduces the polarization and acts as protecting layer between the electrode and electrolyte that results in the superior electrochemical performance.

| S-EPMC8452671 | biostudies-literature

Ni-Rich Layered Oxide with Preferred Orientation (110) Plane as a Stable Cathode Material for High-Energy Lithium-Ion Batteries.

Project description:The cathode, a crucial constituent part of Li-ion batteries, determines the output voltage and integral energy density of batteries to a great extent. Among them, Ni-rich LiNixCoyMnzO2 (x + y + z = 1, x ≥ 0.6) layered transition metal oxides possess a higher capacity and lower cost as compared to LiCoO2, which have stimulated widespread interests. However, the wide application of Ni-rich cathodes is seriously hampered by their poor diffusion dynamics and severe voltage drops. To moderate these problems, a nanobrick Ni-rich layered LiNi0.6Co0.2Mn0.2O2 cathode with a preferred orientation (110) facet was designed and successfully synthesized via a modified co-precipitation route. The galvanostatic intermittent titration technique (GITT) and electrochemical impedance spectroscopy (EIS) analysis of LiNi0.6Co0.2Mn0.2O2 reveal its superior kinetic performance endowing outstanding rate performance and long-term cycle stability, especially the voltage drop being as small as 67.7 mV at a current density of 0.5 C for 200 cycles. Due to its unique architecture, dramatically shortened ion/electron diffusion distance, and more unimpeded Li-ion transmission pathways, the current nanostructured LiNi0.6Co0.2Mn0.2O2 cathode enhances the Li-ion diffusion dynamics and suppresses the voltage drop, thus resulting in superior electrochemical performance.

| S-EPMC7764293 | biostudies-literature

Upcycling Real Waste Mixed Lithium-Ion Batteries by Simultaneous Production of rGO and Lithium-Manganese-Rich Cathode Material.

Project description:The direct synthesis of high-value products from end-of-life Li-ion batteries (LIBs), avoiding the complex and costly separation of the different elements, can be reached through a competitive recycling strategy. Here, we propose the simultaneous synthesis of reduced graphene oxide (rGO) and lithium-manganese-rich (Li1.2Mn0.55Ni0.15Co0.1O2 - LMR) cathode material from end-of-life LIBs. The electrode powder recovered after LIBs mechanical pretreatment was directly subjected to the Hummers' method. This way, quantitative extraction of the target metals (Co, Ni, Mn) and oxidation of graphite to graphene oxide (GO) were simultaneously achieved, and a Mn-rich metal solution resulted after GO filtration, owing to the use of KMnO4 as an oxidizing agent. This solution, which would routinely constitute a heavy-metal liquid waste, was directly employed for the synthesis of Li1.2Mn0.55Ni0.15Co0.1O2 cathode material. XPS measurements demonstrate the presence in the synthesized LMR of Cu2+, SO4 2-, and SiO4 4- impurities, which were previously proposed as effective doping species and can thus explain the improved electrochemical performance of recovered LMR. The GO recovered by filtration was reduced to rGO by using ascorbic acid. To evaluate the role of graphite lithiation/delithiation during battery cycling on rGO production, the implemented synthesis procedure was replicated starting from commercial graphite and from the graphite recovered by a consolidated acidic-reductive leaching procedure for metals extraction. Raman and XPS analysis disclosed that cyclic lithiation/delithiation of graphite during battery life cycle facilitates the graphite exfoliation and thus significantly increases conversion to rGO.

| S-EPMC8493547 | biostudies-literature

Li2SnO3 as a Cathode Material for Lithium-ion Batteries: Defects, Lithium Ion Diffusion and Dopants.

Project description:Tin-based oxide Li2SnO3 has attracted considerable interest as a promising cathode material for potential use in rechargeable lithium batteries due to its high- capacity. Static atomistic scale simulations are employed to provide insights into the defect chemistry, doping behaviour and lithium diffusion paths in Li2SnO3. The most favourable intrinsic defect type is Li Frenkel (0.75?eV/defect). The formation of anti-site defect, in which Li and Sn ions exchange their positions is 0.78?eV/defect, very close to the Li Frenkel. The present calculations confirm the cation intermixing found experimentally in Li2SnO3. Long range lithium diffusion paths via vacancy mechanisms were examined and it is confirmed that the lowest activation energy migration path is along the c-axis plane with the overall activation energy of 0.61?eV. Subvalent doping by Al on the Sn site is energetically favourable and is proposed to be an efficient way to increase the Li content in Li2SnO3. The electronic structure calculations show that the introduction of Al will not introduce levels in the band gap.

| S-EPMC6105723 | biostudies-literature

Dependence of structure and temperature for lithium-rich layered-spinel microspheres cathode material of lithium ion batteries.

Project description:Homogeneous lithium-rich layered-spinel 0.5Li2MnO3·0.5LiMn1/3Ni1/3Co1/3O2 microspheres (~1 μm) are successfully prepared by a solvothermal method and subsequent high-temperature calcinations process. The effects of temperature on the structure and performance of the as-prepared cathode material are systemically studied by X-ray diffraction (XRD), scanning electron microscope (SEM), transmission electron microscope (TEM), galvanostatical charge/discharge and electrochemical impedance spectra. The results show that a spinel Li4Mn5O12 component can be controllably introduced into the lithium-rich layered material at 750°C. Besides, it has been found that the obtained layered-spinel cathode material represents excellent electrochemical characteristics. For example, it can deliver a high initial discharge capacity of 289.6 mAh g(-1) between 2.0 V and 4.6 V at a rate of 0.1 C at room temperature, and a discharge capacity of 144.9 mAh g(-1) at 5 C and 122.8 mAh g(-1) even at 10 C. In addition, the retention of the capacity is still as high as 88% after 200 cycles, while only 79.9% for the single-phase layered material. The excellent electrochemical performance of the as-prepared cathode material can probably be attributed to the hybrid structures combining a fast Li-ion diffusion rate of 3D spinel Li4Mn5O12 phase and a high capacity of the layered Li-Mn-Ni-Co-O component.

| S-EPMC4325327 | biostudies-other

Nano-Crystalline Li1.2Mn0.6Ni0.2O? 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 (Li1.2Mn0.6Ni0.2O?)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

Graphene wrapped ordered LiNi0.5Mn1.5O4 nanorods as promising cathode material for lithium-ion batteries.

Project description:LiNi0.5Mn1.5O4 nanorods wrapped with graphene nanosheets have been prepared and investigated as high energy and high power cathode material for lithium-ion batteries. The structural characterization by X-ray diffraction, Raman spectroscopy, and Fourier transform infrared spectroscopy indicates the LiNi0.5Mn1.5O4 nanorods prepared from ?-MnO2 nanowires have ordered spinel structure with P4332 space group. The morphological characterization by scanning electron microscopy and transmission electron microscopy reveals that the LiNi0.5Mn1.5O4 nanorods of 100-200 nm in diameter are well dispersed and wrapped in the graphene nanosheets for the composite. Benefiting from the highly conductive matrix provided by graphene nanosheets and one-dimensional nanostructure of the ordered spinel, the composite electrode exhibits superior rate capability and cycling stability. As a result, the LiNi0.5Mn1.5O4-graphene composite electrode delivers reversible capacities of 127.6 and 80.8 mAh g(-1) at 0.1 and 10 C, respectively, and shows 94% capacity retention after 200 cycles at 1 C, greatly outperforming the bare LiNi0.5Mn1.5O4 nanorod cathode. The outstanding performance of the LiNi0.5Mn1.5O4-graphene composite makes it promising as cathode material for developing high energy and high power lithium-ion batteries.

| S-EPMC4493710 | biostudies-literature

Transition metal-doped Ni-rich layered cathode materials for durable Li-ion batteries.

Project description:Doping is a well-known strategy to enhance the electrochemical energy storage performance of layered cathode materials. Many studies on various dopants have been reported; however, a general relationship between the dopants and their effect on the stability of the positive electrode upon prolonged cell cycling has yet to be established. Here, we explore the impact of the oxidation states of various dopants (i.e., Mg2+, Al3+, Ti4+, Ta5+, and Mo6+) on the electrochemical, morphological, and structural properties of a Ni-rich cathode material (i.e., Li[Ni0.91Co0.09]O2). Galvanostatic cycling measurements in pouch-type Li-ion full cells show that cathodes featuring dopants with high oxidation states significantly outperform their undoped counterparts and the dopants with low oxidation states. In particular, Li-ion pouch cells with Ta5+- and Mo6+-doped Li[Ni0.91Co0.09]O2 cathodes retain about 81.5% of their initial specific capacity after 3000 cycles at 200 mA g-1. Furthermore, physicochemical measurements and analyses suggest substantial differences in the grain geometries and crystal lattice structures of the various cathode materials, which contribute to their widely different battery performances and correlate with the oxidation states of their dopants.

| S-EPMC8589951 | biostudies-literature

Synergistic Effects of Surface Coating and Bulk Doping in Ni-Rich Lithium Nickel Cobalt Manganese Oxide Cathode Materials for High-Energy Lithium Ion Batteries.

Project description:Ni-rich layered oxide cathodes are promising candidates to satisfy the increasing energy demand of lithium-ion batteries for automotive applications. Thermal and cycling stability issues originating from increasing Ni contents are addressed by mitigation strategies such as elemental bulk substitution ("doping") and surface coating. Although both approaches separately benefit the cycling stability, there are only few reports investigating the combination of two of such approaches. Herein, the combination of Zr as common dopant in commercial materials with effective Li2 WO4 and WO3 coatings was investigated with special focus on the impact of different material processing conditions on structural parameters and electrochemical performance in nickel-cobalt-manganese (NCM) || graphite cells. Results indicated that the Zr4+ dopant diffusing to the surface during annealing improved the electrochemical performance compared to samples without additional coatings. This work emphasizes the importance to not only investigate the effect of individual dopants or coatings but also the influences between both.

| S-EPMC9300204 | biostudies-literature

Enabling Aqueous Processing of Ni-Rich Layered Oxide Cathode Materials by Addition of Lithium Sulfate.

Project description:Aqueous processing of Ni-rich layered oxide cathode materials is a promising approach to simultaneously decrease electrode manufacturing costs, while bringing environmental benefits by substituting the state-of-the-art (often toxic and costly) organic processing solvents. However, an aqueous environment remains challenging due to the high reactivity of Ni-rich layered oxides towards moisture, leading to lithium leaching and Al current collector corrosion because of the resulting high pH value of the aqueous electrode paste. Herein, a facile method was developed to enable aqueous processing of LiNi0.8 Co0.1 Mn0.1 O2 (NCM811) by the addition of lithium sulfate (Li2 SO4 ) during electrode paste dispersion. The aqueously processed electrodes retained 80 % of their initial capacity after 400 cycles in NCM811||graphite full cells, while electrodes processed without the addition of Li2 SO4 reached 80 % of their capacity after only 200 cycles. Furthermore, with regard to electrochemical performance, aqueously processed electrodes using carbon-coated Al current collector outperformed reference electrodes based on state-of-the-art production processes involving N-methyl-2-pyrrolidone as processing solvent and fluorinated binders. The positive impact on cycle life by the addition of Li2 SO4 stemmed from a formed sulfate coating as well as different surface species, protecting the NCM811 surface against degradation. Results reported herein open a new avenue for the processing of Ni-rich NCM electrodes using more sustainable aqueous routes.

| S-EPMC10107986 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data