Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Polymer of intrinsic microporosity-based macroporous membrane with high thermal stability as a Li-ion battery separator.

ABSTRACT: Polymers of intrinsic microporosity (PIMs) have numerous advantages such as good thermal stability (T _g > 300 °C) and mechanical stability (tensile strength at break > 60 MPa) as well as excellent electrical insulation performance and chemical/electrochemical stability. Herein, a macroporous membrane made up of a polymer of intrinsic microporosity (PIM-1) was fabricated and used as a separator of a rechargeable Li-ion battery for the first time. The PIM-1-based separator showed good thermal resistance with T _g > 300 °C, high electrolyte uptake, and excellent Li-ion conductivity.

SUBMITTER: Tian Y

PROVIDER: S-EPMC9066188 | biostudies-literature | 2019 Jul

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Polymer of intrinsic microporosity-based macroporous membrane with high thermal stability as a Li-ion battery separator.

Tian Yangyang Y Lin Chong C Wang Zhenggong Z Jin Jian J

RSC advances 20190710 37

Polymers of intrinsic microporosity (PIMs) have numerous advantages such as good thermal stability (T g > 300 °C) and mechanical stability (tensile strength at break > 60 MPa) as well as excellent electrical insulation performance and chemical/electrochemical stability. Herein, a macroporous membrane made up of a polymer of intrinsic microporosity (PIM-1) was fabricated and used as a separator of a rechargeable Li-ion battery for the first time. The PIM-1-based separator showed ...[more]

PMID: 35521324

Similar Datasets

Multicore-shell nanofiber architecture of polyimide/polyvinylidene fluoride blend for thermal and long-term stability of lithium ion battery separator.

Project description:Li-ion battery, separator, multicoreshell structure, thermal stability, long-term stability. A nanofibrous membrane with multiple cores of polyimide (PI) in the shell of polyvinylidene fluoride (PVdF) was prepared using a facile one-pot electrospinning technique with a single nozzle. Unique multicore-shell (MCS) structure of the electrospun composite fibers was obtained, which resulted from electrospinning a phase-separated polymer composite solution. Multiple PI core fibrils with high molecular orientation were well-embedded across the cross-section and contributed remarkable thermal stabilities to the MCS membrane. Thus, no outbreaks were found in its dimension and ionic resistance up to 200 and 250 °C, respectively. Moreover, the MCS membrane (at ~200 °C), as a lithium ion battery (LIB) separator, showed superior thermal and electrochemical stabilities compared with a widely used commercial separator (~120 °C). The average capacity decay rate of LIB for 500 cycles was calculated to be approximately 0.030 mAh/g/cycle. This value demonstrated exceptional long-term stability compared with commercial LIBs and with two other types (single core-shell and co-electrospun separators incorporating with functionalized TiO2) of PI/PVdF composite separators. The proper architecture and synergy effects of multiple PI nanofibrils as a thermally stable polymer in the PVdF shell as electrolyte compatible polymers are responsible for the superior thermal performance and long-term stability of the LIB.

| S-EPMC5105080 | biostudies-literature

A Modified Ceramic-Coating Separator with High-Temperature Stability for Lithium-Ion Battery.

Project description:In this work, the ceramic coating separator (CCS-CS) prepared with polyethylene (PE) separator, Al₂O₃ inorganic particles, carboxymethyl cellulose sodium (CMC) and styrene-butadiene rubber (SBR) mix binders is further modified by coating with a thin polydopamine (PDA) layer through a simple chemical deposition method. Compared with the bare ceramic coating separator, the PDA-modified CCS-CS (CCS-CS-PDA) exhibits excellent thermal stability, which shows no thermal shrinkage after storing at 200 °C for 30 min. Compared with the PE separator, both the uptake and wettability with the electrolyte and water of CCS-CS-PDA are improved significantly. Meanwhile, when saturated with liquid electrolyte, the CCS-CS-PDA also shows enabled high ionic conductance. Furthermore, the test of the electrochemical impedances changing with the temperatures suggests that only the PE separator exhibits no thermal shutdown behaviors, and the CCS-CS separator only has a shutdown temperature range from 138 to 160 °C, while the CCS-CS-PDA shows a shutdown temperature range from 138 to more than 200 °C. The cells prepared with the CCS-CS-PDA also show stable repeated cycling performance and good rate capacity at room temperature.

| S-EPMC6432417 | biostudies-literature

Electrospun MXene/polyimide nanofiber composite separator for enhancing thermal stability and ion transport of lithium-ion batteries.

Project description:Safety of lithium-ion batteries (LIBs) has garnered significant attention. As an essential component of batteries, the separator plays a crucial role in separating the positive and negative electrodes, preventing short circuits, and allowing ion transport. Therefore, it is necessary to develop a high-performance separator that is both thermally stable and capable of rapid Li+ transport. Polyimide (PI) is a material with high thermal stability, but low electrolyte wettability and high interfacial resistance of PI restrict its application in high-performance LIBs batteries. MXene possesses excellent mechanical properties and good electrolyte affinity. PI/MXene nanofiber composite separator. Combines the high thermal stability of PI with the superior electrolyte wettability of MXene. It exhibits a high tensile strength of 19.6 MPa, low bulk resistance (2.5 Ω), and low interfacial resistance (174 Ω), as well as a low electrolyte contact angle of 29°, while retaining the high-temperature resistance and flame retardancy of PI. Batteries assembled with this composite separator demonstrated a specific capacity of 111.0 mAh g-1 and a capacity retention rate of 66% at 2C. In long-term cycling tests of LiFePO₄ half-cells at 1C, after 200 charge-discharge cycles, the PI/MXene battery showed a discharge specific capacity of 126.7 mAh g-1 and a capacity retention rate of 91%. Additionally, the battery operated normally at 120°C. The composite separator, by integrating the high thermal stability of PI with the excellent electrolyte wettability and conductivity of MXene, demonstrates significant advantages in enhancing battery safety and cycling performance. Through this composite structure can provide a more reliable and safe solution for high-performance LIBs.

| S-EPMC11885268 | biostudies-literature

Novel polymer coating for chemically absorbing CO2 for safe Li-ion battery.

Project description:Gas evolution in Li-ion batteries remains a barrier for the implementation of high voltage materials in a pouch cell format; the inflation of the pouch cell is a safety issue that can cause battery failure. In particular, for manganese-based materials employed for fabricating cathodes, the dissolution of Mn2+ in the electrolyte can accelerate cell degradation, and subsequently gas evolution, of which carbon dioxide (CO2) is a major component. We report on the utilization of a mixture of polymers that can chemically absorb the CO2, including the coating of aluminum foils, which serve as trapping sheets, introduced into two Ah pouch cells-based on a LiMnFePO4 (cathode) and a Li4Ti5O12 (anode). The pouch cells with trapping sheets experienced only an 8.0 vol% inflation (2.7 mmol CO2 per gram of polymers) as opposed to the 40 vol% inflation for the reference sample. Moreover, the cells were cycled for 570 cycles at 1 C and 45 °C before reaching 80% of their retention capacity.

| S-EPMC7316716 | biostudies-literature

Fast Blood Oxygenation through Hemocompatible Asymmetric Polymer of Intrinsic Microporosity Membranes.

Project description:Membrane technology has attracted considerable attention for chemical and medical applications, among others. Artificial organs play important roles in medical science. A membrane oxygenator, also known as artificial lung, can replenish O2 and remove CO2 of blood to maintain the metabolism of patients with cardiopulmonary failure. However, the membrane, a key component, is subjected to inferior gas transport property, leakage propensity, and insufficient hemocompatibility. In this study, we report efficient blood oxygenation by using an asymmetric nanoporous membrane that is fabricated using the classic nonsolvent-induced phase separation method for polymer of intrinsic microporosity-1. The intrinsic superhydrophobic nanopores and asymmetric configuration endow the membrane with water impermeability and gas ultrapermeability, up to 3,500 and 1,100 gas permeation units for CO2 and O2, respectively. Moreover, the rational hydrophobic-hydrophilic nature, electronegativity, and smoothness of the surface enable the substantially restricted protein adsorption, platelet adhesion and activation, hemolysis, and thrombosis for the membrane. Importantly, during blood oxygenation, the asymmetric nanoporous membrane shows no thrombus formation and plasma leakage and exhibits fast O2 and CO2 transport processes with exchange rates of 20 to 60 and 100 to 350 ml m-2 min-1, respectively, which are 2 to 6 times higher than those of conventional membranes. The concepts reported here offer an alternative route to fabricate high-performance membranes and expand the possibilities of nanoporous materials for membrane-based artificial organs.

| S-EPMC10195972 | biostudies-literature

An Alternative Polymer Material to PVDF Binder and Carbon Additive in Li-Ion Battery Positive Electrode.

Project description:Li-ion battery performance relies fundamentally on modulation at the microstructure and interface levels of the composite electrodes. Correspondingly, the binder is a crucial component for mechanical integrity of the electrode, serving to interconnect the active material and conductive additive and to firmly attach this composite to the current collector. However, the commonly used poly(vinylidenefluoride) (PVDF) binder presents several limitations, including the use of toxic solvent during processing, a low electrical conductivity which for compensation requires the addition of carbon black, and weak interactions with active materials and collectors. This study investigates Poly(3,4-ethylenedioxythiophene):poly[(4-styrenesulfonyl) (trifluoromethylsulfonyl) imide] (PEDOT:PSSTFSI) as an alternative binder and conductive additive, in replacement of both PVDF and carbon black, in Li-ion batteries with LiFe0.4Mn0.6PO4 at the positive electrode. Complex PEDOT:PSSTFSI significantly improves the electronic conductivity and lithium diffusion coefficient within the electrode, in comparison to standard PVDF binder and carbon black. This enhances significantly the electrochemical performance at high C-rates and for high active mass loading electrodes. Furthermore, an excellent long-range cyclability is achieved.

| S-EPMC11633511 | biostudies-literature

Superior Low-Temperature Power and Cycle Performances of Na-Ion Battery over Li-Ion Battery.

Project description:The most simple and clear advantage of Na-ion batteries (NIBs) over Li-ion batteries (LIBs) is the natural abundance of Na, which allows inexpensive production of NIBs for large-scale applications. However, although strenuous research efforts have been devoted to NIBs particularly since 2010, certain other advantages of NIBs have been largely overlooked, for example, their low-temperature power and cycle performances. Herein, we present a comparative study of spirally wound full-cells consisting of Li0.1Na0.7Co0.5Mn0.5O2 (or Li0.8Co0.5Mn0.5O2) and hard carbon and report that the power of NIB at -30 °C is ∼21% higher than that of LIB. Moreover, the capacity retention in cycle testing at 0 °C is ∼53% for NIB but only ∼29% for LIB. Raman spectroscopy and density functional theory calculations revealed that the superior performance of NIB is due to the relatively weak interaction between Na+ ions and aprotic polar solvents.

| S-EPMC6640915 | biostudies-literature

Solvent Sorption-Induced Actuation of Composites Based on a Polymer of Intrinsic Microporosity.

Project description:Materials that are capable of actuation in response to a variety of external stimuli are of significant interest for applications in sensors, soft robotics, and biomedical devices. Here, we present a class of actuators using composites based on a polymer of intrinsic microporosity (PIM). By adding an activated carbon (AX21) filler to a PIM, the composite exhibits repeatable actuation upon solvent evaporation and wetting and it is possible to achieve highly controlled three-dimensional actuation. Curled composite actuators are shown to open upon exposure to a solvent and close as a result of solvent evaporation. The degree of curling and actuation is controlled by adjusting the amount of filler and evaporation rate of the solvent casting process, while the actuation speed is controlled by adjusting the type of solvent. The range of forces and actuation speed produced by the composite is demonstrated using acetone, ethanol, and dimethyl sulfoxide as the solvent. The maximum contractile stress produced upon solvent desorption in the pure PIM polymer reached 12 MPa, with an ultimate force over 20 000 times the weight of a sample. This form of the composite actuator is insensitive to humidity and water, which makes it applicable in an aqueous environment, and can survive a wide range of temperatures. These characteristics make it a promising actuator for the diverse range of operating conditions in robotic and medical applications. The mechanism of actuation is discussed, which is based on the asymmetric distribution of the carbon filler particles that leads to a bilayer structure and the individual layers expand and contract differently in response to solvent wetting and evaporation, respectively. Finally, we demonstrate the application of the actuator as a potential drug delivery vehicle, with capacity for encapsulating two kinds of drugs and reduced drug leakage in comparison to existing technologies.

| S-EPMC8383273 | biostudies-literature

Greener Synthesis of the Polymer of Intrinsic Microporosity PIM-1 for Gas Separation.

Project description:Polymers of intrinsic microporosity (PIMs) are studied as membranes for energy-efficient and environmentally friendly separation technologies, but greener polymerization methods are desirable for further scale up. This work aimed to synthesize the prototypical PIM (PIM-1) via a greener synthetic route by changing the solvent system to methyl-5-(dimethylamino)-2,2-dimethyl-5-oxopentanoate (MDDOP), a structural analogue of the green solvent Rhodiasolv PolarClean. Mass-based green metrics analysis was performed on MDDOP, determining atom economy, complete environmental factor, and total carbon intensity, comparing each to synthetic routes to PolarClean. Green metrics analysis found MDDOP synthesis produced less waste than PolarClean. MDDOP solvent capabilities were exemplified via PIM-1 polymerizations using 5,5',6,6'-tetrahydroxy-3,3,3',3'-tetramethyl-1,1'-spirobisindane (TTSBI) with either tetrafluoroterephthalonitrile (TFTPN) or tetrachloroterephthalonitrile (TCTPN), varying the temperature (120-160 °C) and reaction duration (50 min-6 h). Recovery of methanol and MDDOP post PIM-1 synthesis reduced solvent waste by 22%. Reactions using TCTPN produced polymers with higher molar masses than those produced using TFTPN. All samples showed varied topology, with evidence of branching and colloidal network. The polymer from the most successful reaction conditions (TCTPN, T = 140 °C, 6 h) was fabricated into thick film membranes and tested with pure gases for CO2/CH4 and CO2/N2 gas pairs, performing comparably with PIM-1 synthesized using conventional solvent systems.

| S-EPMC11863552 | biostudies-literature

Modulating Ion Behavior by Functional Nanodiamond Modified Separator for High-Rate Durable Aqueous Zinc-Ion Battery.

Project description:Aqueous zinc-ion batteries (AZIBs) have garnered widespread attention due to their promising development and application prospects. However, progress of AZIBs has been hindered by zinc (Zn) dendrites and side reactions at the electrode-electrolyte interface (EEI). In particular, the large and uneven pores of commercial glass fiber (GF) separators lead to nonuniform Zn2+ transport, which causes side reactions. In this study, we employed nanodiamonds (NDs) to regulate the separator pore structure and utilized its surface oxygen-containing functional groups to control the Zn2+ transport properties. Due to their excellent chemical inertness, superhardness, ultrahigh thermal conductivity, and abundant surface functional groups, NDs modified GF separators for dendrite-free and high-performance AZIBs. Experimental outcomes demonstrate that Zn||Zn symmetric cells using NDs-GF separators exhibit regular charge-discharge profiles, minimal fluctuations, and an ultralong cycling lifespan of nearly 1800 h under a current density of 5 mA cm-2 with a capacity density of 1 mAh cm-2 and 240 h under a high current density of 10 mA cm-2 with a capacity density of 10 mAh cm-2. The Zn||MnO2 full cells using NDs-GF separators showcase a high retention after 1000 cycles at 1 A g-1. This research proposes a modification method for developing advanced separators in AZIBs technology.

| S-EPMC11660037 | 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