Browse
Submit Data
Databases
API
Help

Dataset Information

21 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

High-rate aluminium yolk-shell nanoparticle anode for Li-ion battery with long cycle life and ultrahigh capacity.

ABSTRACT: Alloy-type anodes such as silicon and tin are gaining popularity in rechargeable Li-ion batteries, but their rate/cycling capabilities should be improved. Here by making yolk-shell nanocomposite of aluminium core (30?nm in diameter) and TiO2 shell (?3?nm in thickness), with a tunable interspace, we achieve 10?C charge/discharge rate with reversible capacity exceeding 650?mAh?g(-1) after 500 cycles, with a 3?mg?cm(-2) loading. At 1 C, the capacity is approximately 1,200?mAh?g(-1) after 500 cycles. Our one-pot synthesis route is simple and industrially scalable. This result may reverse the lagging status of aluminium among high-theoretical-capacity anodes.

SUBMITTER: Li S

PROVIDER: S-EPMC4918313 | biostudies-literature | 2015 Aug

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

High-rate aluminium yolk-shell nanoparticle anode for Li-ion battery with long cycle life and ultrahigh capacity.

Li Sa S Niu Junjie J Zhao Yu Cheng YC So Kang Pyo KP Wang Chao C Wang Chang An CA Li Ju J

Nature communications 20150805

Alloy-type anodes such as silicon and tin are gaining popularity in rechargeable Li-ion batteries, but their rate/cycling capabilities should be improved. Here by making yolk-shell nanocomposite of aluminium core (30 nm in diameter) and TiO2 shell (∼3 nm in thickness), with a tunable interspace, we achieve 10 C charge/discharge rate with reversible capacity exceeding 650 mAh g(-1) after 500 cycles, with a 3 mg cm(-2) loading. At 1 C, the capacity is approximately 1,200 mAh g(-1) after 500 cycles ...[more]

PMID: 26243004

Similar Datasets

A Silicon Monoxide Lithium-Ion Battery Anode with Ultrahigh Areal Capacity.

Project description:Silicon monoxide (SiO) is an attractive anode material for next-generation lithium-ion batteries for its ultra-high theoretical capacity of 2680 mAh g-1. The studies to date have been limited to electrodes with a relatively low mass loading (< 3.5 mg cm-2), which has seriously restricted the areal capacity and its potential in practical devices. Maximizing areal capacity with such high-capacity materials is critical for capitalizing their potential in practical technologies. Herein, we report a monolithic three-dimensional (3D) large-sheet holey graphene framework/SiO (LHGF/SiO) composite for high-mass-loading electrode. By specifically using large-sheet holey graphene building blocks, we construct LHGF with super-elasticity and exceptional mechanical robustness, which is essential for accommodating the large volume change of SiO and ensuring the structure integrity even at ultrahigh mass loading. Additionally, the 3D porous graphene network structure in LHGF ensures excellent electron and ion transport. By systematically tailoring microstructure design, we show the LHGF/SiO anode with a mass loading of 44 mg cm-2 delivers a high areal capacity of 35.4 mAh cm-2 at a current of 8.8 mA cm-2 and retains a capacity of 10.6 mAh cm-2 at 17.6 mA cm-2, greatly exceeding those of the state-of-the-art commercial or research devices. Furthermore, we show an LHGF/SiO anode with an ultra-high mass loading of 94 mg cm-2 delivers an unprecedented areal capacity up to 140.8 mAh cm-2. The achievement of such high areal capacities marks a critical step toward realizing the full potential of high-capacity alloy-type electrode materials in practical lithium-ion batteries.

| S-EPMC8789978 | biostudies-literature

Ultrathin Si/CNTs Paper-Like Composite for Flexible Li-Ion Battery Anode With High Volumetric Capacity.

Project description:Thin and lightweight flexible lithium-ion batteries (LIBs) with high volumetric capacities are crucial for the development of flexible electronic devices. In the present work, we reported a paper-like ultrathin and flexible Si/carbon nanotube (CNT) composite anode for LIBs, which was realized by conformal electrodeposition of a thin layer of silicon on CNTs at ambient temperature. This method was quite simple and easy to scale up with low cost as compared to other deposition techniques, such as sputtering or CVD. The flexible Si/CNT composite exhibited high volumetric capacities in terms of the total volume of active material and current collector, surpassing the most previously reported Si-based flexible electrodes at various rates. In addition, the poor initial coulombic efficiency of the Si/CNT composites can be effectively improved by prelithiation treatment and a commercial red LED can be easily lighted by a full pouch cell using a Si/CNT composite as a flexible anode under flat or bent states. Therefore, the ultrathin and flexible Si/CNT composite is highly attractive as an anode material for flexible LIBs.

| S-EPMC6300474 | biostudies-literature

3D nitrogen-doped graphene foam with encapsulated germanium/nitrogen-doped graphene yolk-shell nanoarchitecture for high-performance flexible Li-ion battery.

Project description:Flexible electrochemical energy storage devices have attracted extensive attention as promising power sources for the ever-growing field of flexible and wearable electronic products. However, the rational design of a novel electrode structure with a good flexibility, high capacity, fast charge-discharge rate and long cycling lifetimes remains a long-standing challenge for developing next-generation flexible energy-storage materials. Herein, we develop a facile and general approach to three-dimensional (3D) interconnected porous nitrogen-doped graphene foam with encapsulated Ge quantum dot/nitrogen-doped graphene yolk-shell nano architecture for high specific reversible capacity (1,220?mAh?g-1), long cycling capability (over 96% reversible capacity retention from the second to 1,000 cycles) and ultra-high rate performance (over 800?mAh?g-1 at 40 C). This work paves a way to develop the 3D interconnected graphene-based high-capacity electrode material systems, particularly those that suffer from huge volume expansion, for the future development of high-performance flexible energy storage systems.

| S-EPMC5216101 | biostudies-literature

Electrochemical properties of yolk-shell structured ZnFe2O4 powders prepared by a simple spray drying process as anode material for lithium-ion battery.

Project description:ZnFe2O4 yolk-shell powders were prepared by applying a simple spray-drying process. Dextrin was used as a drying additive and carbon source material, and thus played a key role in the preparation of the powders. The combustion of precursor powders consisting of zinc and iron salts and dextrin obtained by a spray-drying process produced the yolk-shell-structured ZnFe2O4 powders even at a low post-treatment temperature of 350 °C. The ZnFe2O4 powders prepared from the spray solution without dextrin had a filled and pockmarked structure. The initial discharge capacities of the ZnFe2O4 yolk-shell and filled powders post-treated at 450 °C at a current density of 500 mA g(-1) were 1226 and 993 mA h g(-1), respectively, and the corresponding initial Coulombic efficiencies were 74 and 58%. The discharge capacities of the ZnFe2O4 powders with yolk-shell and filled structures post-treated at 450 °C after 200 cycles were 862 and 332 mA h g(-1), respectively. The ZnFe2O4 yolk-shell powders with high structural stability during cycling had superior electrochemical properties to those of the powders with filled structure.

| S-EPMC4148673 | biostudies-literature

An Ultrahigh Capacity Graphite/Li<sub>2</sub>S Battery with Holey-Li<sub>2</sub>S Nanoarchitectures.

Project description:The pairing of high-capacity Li2S cathode (1166 mAh g-1) and lithium-free anode (LFA) provides an unparalleled potential in developing safe and energy-dense next-generation secondary batteries. However, the low utilization of the Li2S cathode and the lack of electrolytes compatible to both electrodes are impeding the development. Here, a novel graphite/Li2S battery system, which features a self-assembled, holey-Li2S nanoarchitecture and a stable solid electrolyte interface (SEI) on the graphite electrode, is reported. The holey structure on Li2S is beneficial in decomposing Li2S at the first charging process due to the enhanced Li ion extraction and transfer from the Li2S to the electrolyte. In addition, the concentrated dioxolane (DOL)-rich electrolyte designed lowers the irreversible capacity loss for SEI formation. By using the combined strategies, the graphite/holey-Li2S battery delivers an ultrahigh discharge capacity of 810 mAh g-1 at 0.1 C (based on the mass of Li2S) and of 714 mAh g-1 at 0.2 C. Moreover, it exhibits a reversible capacity of 300 mAh g-1 after a record lifecycle of 600 cycles at 1 C. These results suggest the great potential of the designed LFA/holey-Li2S batteries for practical use.

| S-EPMC6051237 | biostudies-literature

Electrochemical properties of Sn-decorated SnO nanobranches as an anode of Li-ion battery.

Project description:Sn-based oxide materials as an anode of lithium ion batteries (LIBs) suffer from the unavoidable mechanical stress originated from huge volume changes during lithiation/delithiation reactions. We synthesized the hierarchical SnO nanobranches (NBs) decorated with Sn nanoparticles on Cu current collector using a vapor transport method. The Sn-decorated SnO NBs as an anode of LIB showed good electrochemical performance with high reversible capacity retention of as high as 502 mAh/g and rate capability of 455 mAh/g at a current density of 2.0 A/g after 50 cycles. Through the morphological and crystal structure analyses after the charge and discharge processes, it was found that the morphology of Sn-decorated SnO NBs was transformed to nanoporous layered-structure, composed of Sn and lithium oxide, during the repeated lithiation/delithiation reactions. The free-volume of Sn-decorated SnO NBs and nanoporous layered-structure effectively accommodate the huge volume changes and enhance the electrochemical cyclability by facilitating the diffusion of Li-ions.

| S-EPMC5271146 | biostudies-literature

Hierarchically Porous Carbon Derived from Biomass Reed Flowers as Highly Stable Li-Ion Battery Anode.

Project description:As lithium-ion battery (LIB) anode materials, porous carbons with high specific surface area are highly required because they can well accommodate huge volume expansion/contraction during cycling. In this work, hierarchically porous carbon (HPC) with high specific surface area (~1714.83 m2 g-1) is synthesized from biomass reed flowers. The material presents good cycling stability as an LIB anode, delivering an excellent reversible capacity of 581.2 mAh g-1 after cycling for 100 cycles at a current density of 100 mA g-1, and still remains a reversible capacity of 298.5 mAh g-1 after cycling for 1000 cycles even at 1000 mA g-1. The good electrochemical performance can be ascribed to the high specific surface area of the HPC network, which provides rich and fast paths for electron and ion transfer and provides large contact area and mutual interactions between the electrolyte and active materials. The work proposes a new route for the preparation of low cost carbon-based anodes and may promote the development of other porous carbon materials derived from various biomass carbon sources.

| S-EPMC7075112 | biostudies-literature

Conjugation with carbon nanotubes improves the performance of mesoporous silicon as Li-ion battery anode.

Project description:Carbon nanotubes can be utilized in several ways to enhance the performance of silicon-based anodes. In the present work, thermally carbonized mesoporous silicon (TCPSi) microparticles and single-walled carbon nanotubes (CNTs) are conjugated to create a hybrid material that performs as the Li-ion battery anode better than the physical mixture of TCPSi and CNTs. It is found out that the way the conjugation is done has an essential role in the performance of the anode. The conjugation should be made between negatively charged TCPSi and positively charged CNTs. Based on the electrochemical experiments it is concluded that the positive charges, i.e., excess amine groups of the hybrid material interfere with the diffusion of the lithium cations and thus they should be removed from the anode. Through the saturation of the excess positive amine groups on the CNTs with succinic anhydride, the performance of the hybrid material is even further enhanced.

| S-EPMC7101375 | biostudies-literature

High Capacity and Superior Rate Performances Coexisting in Carbon-Based Sodium-Ion Battery Anode.

Project description:Amorphous carbon is considered as a prospective and serviceable anode for the storage of sodium. In this contribution, we illuminate the transformation rule of defect/void ratio and the restrictive relation between specific capacity and rate capability. Inspired by this mechanism, ratio of plateau/slope capacity is regulated via temperature-control pyrolysis. Moreover, pore-forming reaction is induced to create defects, open up the isolated voids, and build fast ion channels to further enhance the capacity and rate ability. Numerous fast ion channels, high ion-electron conductivity, and abundant defects lead the designed porous hard carbon/Co3O4 anode to realize a high specific capacity, prolonged circulation ability, and enhanced capacity at high rates. This research deepens the comprehension of sodium storage behavior and proposes a fabrication approach to achieve high performance carbonaceous anodes for sodium-ion batteries.

| S-EPMC6753608 | biostudies-literature

Preparations of NiFe2O4 Yolk-Shell@C Nanospheres and Their Performances as Anode Materials for Lithium-Ion Batteries.

Project description:At present, lithium-ion batteries (LIBs) have received widespread attention as substantial energy storage devices; thus, their electrochemical performances must be continuously researched and improved. In this paper, we demonstrate a simple self-template solvothermal method combined with annealing for the synthesis of NiFe2O4 yolk-shell (NFO-YS) and NiFe2O4 solid (NFO-S) nanospheres by controlling the heating rate and coating them with a carbon layer on the surface via high-temperature carbonization of resorcinol and formaldehyde resin. Among them, NFO-YS@C has an obvious yolk-shell structure, with a core-shell spacing of about 60 nm, and the thicknesses of the NiFe2O4 shell and carbon shell are approximately 15 and 30 nm, respectively. The yolk-shell structure can alleviate volume changes and shorten the ion/electron diffusion path, while the carbon shell can improve conductivity. Therefore, NFO-YS@C nanospheres as the anode materials of LIBs show a high initial capacity of 1087.1 mA h g-1 at 100 mA g-1, and the capacity of NFO-YS@C nanospheres impressively remains at 1023.5 mA h g-1 after 200 cycles at 200 mA g-1. The electrochemical performance of NFO-YS@C is significantly beyond NFO-S@C, which proves that the carbon coating and yolk-shell structure have good stability and excellent electron transport ability.

| S-EPMC7600623 | 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