Browse
Submit Data
Databases
API
Help

Dataset Information

31 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

A Quinone-Based Cathode Material for High-Performance Organic Lithium and Sodium Batteries.

ABSTRACT: With the increased application of batteries in powering electric vehicles as well as potential contributions to utility-scale storage, there remains a need to identify and develop efficient and sustainable active materials for use in lithium (Li)- and sodium (Na)-ion batteries. Organic cathode materials provide a desirable alternative to inorganic counterparts, which often come with harmful environmental impact and supply chain uncertainties. Organic materials afford a sustainable route to active electrodes that also enable fine-tuning of electrochemical potentials through structural design. Here, we report a bis-anthraquinone-functionalized s-indacene-1,3,5,7(2H,6H)-tetraone (BAQIT) synthesized using a facile and inexpensive route as a high-capacity cathode material for use in Li- and Na-ion batteries. BAQIT provides multiple binding sites for Li- and Na-ions, while maintaining low solubility in commercial organic electrolytes. Electrochemical Li-ion cells demonstrate excellent stability with discharge capacities above 190 mAh g^-1 after 300 cycles at a 0.1C rate. The material also displayed excellent high-rate performance with a reversible capacity of 142 mAh g^-1 achieved at a 10C rate. This material affords high power capabilities superior to current state-of-the-art organic cathode materials, with values reaching 5.09 kW kg^-1. The Na-ion performance was also evaluated, exhibiting reversible capacities of 130 mAh g^-1 after 90 cycles at a 0.1C rate. This work offers a structural design to encourage versatile, high-power, and long cycle-life electrochemical energy-storage materials.

SUBMITTER: Wilkinson D

PROVIDER: S-EPMC8611644 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

High-Performance Organic Lithium Batteries with an Ether-Based Electrolyte and 9,10-Anthraquinone (AQ)/CMK-3 Cathode.

Project description:Organic carbonyl electrode materials of lithium batteries have shown multifunctional molecule design and high capacity, but have the problems of poor cycling and low rate performance due to their high solubility in traditional carbonate-based electrolytes and low conductivity. High-performance organic lithium batteries with modified ether-based electrolyte (2 m LiN(CF3SO2)2 in 1,3-dioxolane/dimethoxyethane solvent with 1% LiNO3 additive (2m-DD-1%L)) and 9,10-anthraquinone (AQ)/CMK-3 (AQC) nanocomposite cathode are reported here. The electrochemical results manifest that 2m-DD-1%L electrolyte promotes the cycling performance due to the restraint of AQ dissolution in ether-based electrolyte with high Li salt concentration and formation of a protection film on the surface of the anode. Additionally, the AQC nanocomposite improves the rate performance because of the nanoconfinement effect of CMK-3 and the decrease of charge transfer impedance. In 2m-DD-1%L electrolyte, AQC nanocomposite delivers an initial discharge capacity of 205 mA h g-1 and a capacity of 174 mA h g-1 after 100 cycles at 0.2 C. Even at a high rate of 2 C, its capacity is 146 mA h g-1. This strategy is also used for other organic carbonyl compounds with quinone substructures and they maintain high stable capacities. This sheds light on the development of advanced organic lithium batteries with carbonyl electrode materials and ether-based electrolytes.

| S-EPMC5115363 | biostudies-literature

Effect of Nb and F Co-doping on Li1.2Mn0.54Ni0.13Co0.13O2 Cathode Material for High-Performance Lithium-Ion Batteries.

Project description:The Li1.2Mn0.54-xNbxCo0.13Ni0.13O2-6xF6x (x = 0, 0.01, 0.03, 0.05) is prepared by traditional solid-phase method, and the Nb and F ions are successfully doped into Mn and O sites of layered materials Li1.2Mn0.54Co0.13Ni0.13O2, respectively. The incorporating Nb ion in Mn site can effectively restrain the migration of transition metal ions during long-term cycling, and keep the stability of the crystal structure. The Li1.2Mn0.54-xNbxCo0.13Ni0.13O2-6xF6x shows suppressed voltage fade and higher capacity retention of 98.1% after 200 cycles at rate of 1 C. The replacement of O2- by the strongly electronegative F- is beneficial for suppressed the structure change of Li2MnO3 from the eliminating of oxygen in initial charge process. Therefore, the initial coulombic efficiency of doped Li1.2Mn0.54-xNbxCo0.13Ni0.13O2-6xF6x gets improved, which is higher than that of pure Li1.2Mn0.54Co0.13Ni0.13O2. In addition, the Nb and F co-doping can effectively enhance the transfer of lithium-ion and electrons, and thus improving rate performance.

| S-EPMC5896303 | biostudies-literature

Heteroaromatic organic compound with conjugated multi-carbonyl as cathode material for rechargeable lithium batteries.

Project description:The heteroaromatic organic compound, N,N'-diphenyl-1,4,5,8-naphthalenetetra- carboxylic diimide (DP-NTCDI-250) as the cathode material of lithium batteries is prepared through a simple one-pot N-acylation reaction of 1,4,5,8-naphthalenetetra-carboxylic dianhydride (NTCDA) with phenylamine (PA) in DMF solution followed by heat treatment in 250?°C. The as prepared sample is characterized by the combination of elemental analysis, NMR, FT-IR, TGA, XRD, SEM and TEM. The electrochemical measurements show that DP-NTCDI-250 can deliver an initial discharge capacity of 170?mAh g(-1) at the current density of 25?mA g(-1). The capacity of 119?mAh g(-1) can be retained after 100 cycles. Even at the high current density of 500?mA g(-1), its capacity still reaches 105?mAh g(-1), indicating its high rate capability. Therefore, the as-prepared DP-NTCDI-250 could be a promising candidate as low cost cathode materials for lithium batteries.

| S-EPMC4827395 | biostudies-literature

A high capacity small molecule quinone cathode for rechargeable aqueous zinc-organic batteries.

Project description:Rechargeable aqueous zinc-organic batteries are promising energy storage systems with low-cost aqueous electrolyte and zinc metal anode. The electrochemical properties can be systematically adjusted with molecular design on organic cathode materials. Herein, we use a symmetric small molecule quinone cathode, tetraamino-p-benzoquinone (TABQ), with desirable functional groups to protonate and accomplish dominated proton insertion from weakly acidic zinc electrolyte. The hydrogen bonding network formed with carbonyl and amino groups on the TABQ molecules allows facile proton conduction through the Grotthuss-type mechanism. It guarantees activation energies below 300 meV for charge transfer and proton diffusion. The TABQ cathode delivers a high capacity of 303 mAh g-1 at 0.1 A g-1 in a zinc-organic battery. With the increase of current density to 5 A g-1, 213 mAh g-1 capacity is still preserved with stable cycling for 1000 times. Our work proposes an effective approach towards high performance organic electrode materials.

| S-EPMC8292436 | biostudies-literature

High Rate and Long Lifespan Sodium-Organic Batteries Using Pseudocapacitive Porphyrin Complexes-Based Cathode.

Project description: Not available

| S-EPMC8187698 | biostudies-literature

In situ wrapping of the cathode material in lithium-sulfur batteries.

Project description:While lithium-sulfur batteries are poised to be the next-generation high-density energy storage devices, the intrinsic polysulfide shuttle has limited their practical applications. Many recent investigations have focused on the development of methods to wrap the sulfur material with a diffusion barrier layer. However, there is a trade-off between a perfect preassembled wrapping layer and electrolyte infiltration into the wrapped sulfur cathode. Here, we demonstrate an in situ wrapping approach to construct a compact layer on carbon/sulfur composite particles with an imperfect wrapping layer. This special configuration suppresses the shuttle effect while allowing polysulfide diffusion within the interior of the wrapped composite particles. As a result, the wrapped cathode for lithium-sulfur batteries greatly improves the Coulombic efficiency and cycle life. Importantly, the capacity decay of the cell at 1000 cycles is as small as 0.03% per cycle at 1672 mA g-1.To suppress the polysulfide shuttling effect in Li-S batteries, here the authors report a carbon/sulfur composite cathode with a wrapping layer that overcomes the trade-off between limiting polysulfide diffusion and allowing electrolyte infiltration, and affords extraordinary cycling stability.

| S-EPMC5589852 | biostudies-literature

Defect-free potassium manganese hexacyanoferrate cathode material for high-performance potassium-ion batteries.

Project description:Potassium-ion batteries (KIBs) are promising electrochemical energy storage systems because of their low cost and high energy density. However, practical exploitation of KIBs is hampered by the lack of high-performance cathode materials. Here we report a potassium manganese hexacyanoferrate (K2Mn[Fe(CN)6]) material, with a negligible content of defects and water, for efficient high-voltage K-ion storage. When tested in combination with a K metal anode, the K2Mn[Fe(CN)6]-based electrode enables a cell specific energy of 609.7 Wh kg-1 and 80% capacity retention after 7800 cycles. Moreover, a K-ion full-cell consisting of graphite and K2Mn[Fe(CN)6] as anode and cathode active materials, respectively, demonstrates a specific energy of 331.5 Wh kg-1, remarkable rate capability, and negligible capacity decay for 300 cycles. The remarkable electrochemical energy storage performances of the K2Mn[Fe(CN)6] material are attributed to its stable frameworks that benefit from the defect-free structure.

| S-EPMC8041879 | biostudies-literature

A novel graphene-polysulfide anode material for high-performance lithium-ion batteries.

Project description:We report a simple and efficient approach for fabrication of novel graphene-polysulfide (GPS) anode materials, which consists of conducting graphene network and homogeneously distributed polysulfide in between and chemically bonded with graphene sheets. Such unique architecture not only possesses fast electron transport channels, shortens the Li-ion diffusion length but also provides very efficient Li-ion reservoirs. As a consequence, the GPS materials exhibit an ultrahigh reversible capacity, excellent rate capability and superior long-term cycling performance in terms of 1600, 550, 380 mAh g(-1) after 500, 1300, 1900 cycles with a rate of 1, 5 and 10 A g(-1) respectively. This novel and simple strategy is believed to work broadly for other carbon-based materials. Additionally, the competitive cost and low environment impact may promise such materials and technique a promising future for the development of high-performance energy storage devices for diverse applications.

| S-EPMC3730167 | biostudies-literature

Multifunctional semi-interpenetrating polymer network-nanoencapsulated cathode materials for high-performance lithium-ion batteries.

Project description:As a promising power source to boost up advent of next-generation ubiquitous era, high-energy density lithium-ion batteries with reliable electrochemical properties are urgently requested. Development of the advanced lithium ion-batteries, however, is staggering with thorny problems of performance deterioration and safety failures. This formidable challenge is highly concerned with electrochemical/thermal instability at electrode material-liquid electrolyte interface, in addition to structural/chemical deficiency of major cell components. Herein, as a new concept of surface engineering to address the abovementioned interfacial issue, multifunctional conformal nanoencapsulating layer based on semi-interpenetrating polymer network (semi-IPN) is presented. This unusual semi-IPN nanoencapsulating layer is composed of thermally-cured polyimide (PI) and polyvinyl pyrrolidone (PVP) bearing Lewis basic site. Owing to the combined effects of morphological uniqueness and chemical functionality (scavenging hydrofluoric acid that poses as a critical threat to trigger unwanted side reactions), the PI/PVP semi-IPN nanoencapsulated-cathode materials enable significant improvement in electrochemical performance and thermal stability of lithium-ion batteries.

| S-EPMC3978500 | 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

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