Browse
Submit Data
Databases
API
Help

Dataset Information

28 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Exceptional capacitive deionization rate and capacity by block copolymer-based porous carbon fibers.

ABSTRACT: Capacitive deionization (CDI) is energetically favorable for desalinating low-salinity water. The bottlenecks of current carbon-based CDI materials are their limited desalination capacities and time-consuming cycles, caused by insufficient ion-accessible surfaces and retarded electron/ion transport. Here, we demonstrate porous carbon fibers (PCFs) derived from microphase-separated poly(methyl methacrylate)-block-polyacrylonitrile (PMMA-b-PAN) as an effective CDI material. PCF has abundant and uniform mesopores that are interconnected with micropores. This hierarchical porous structure renders PCF a large ion-accessible surface area and a high desalination capacity. In addition, the continuous carbon fibers and interconnected porous network enable fast electron/ion transport, and hence a high desalination rate. PCF shows desalination capacity of 30 mgNaCl g-1 PCF and maximal time-average desalination rate of 38.0 mgNaCl g-1 PCF min-1, which are about 3 and 40 times, respectively, those of typical porous carbons. Our work underlines the promise of block copolymer-based PCF for mutually high-capacity and high-rate CDI.

SUBMITTER: Liu T

PROVIDER: S-EPMC7164930 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Block copolymer-based porous carbon fibers.

Project description:Carbon fibers have high surface areas and rich functionalities for interacting with ions, molecules, and particles. However, the control over their porosity remains challenging. Conventional syntheses rely on blending polyacrylonitrile with sacrificial additives, which macrophase-separate and result in poorly controlled pores after pyrolysis. Here, we use block copolymer microphase separation, a fundamentally disparate approach to synthesizing porous carbon fibers (PCFs) with well-controlled mesopores (~10 nm) and micropores (~0.5 nm). Without infiltrating any carbon precursors or dopants, poly(acrylonitrile-block-methyl methacrylate) is directly converted to nitrogen and oxygen dual-doped PCFs. Owing to the interconnected network and the highly optimal bimodal pores, PCFs exhibit substantially reduced ion transport resistance and an ultrahigh capacitance of 66 μF cm-2 (6.6 times that of activated carbon). The approach of using block copolymer precursors revolutionizes the synthesis of PCFs. The advanced electrochemical properties signify that PCFs represent a new platform material for electrochemical energy storage.

| S-EPMC6358319 | biostudies-literature

Graphene-carbon 2D heterostructures with hierarchically-porous P,N-doped layered architecture for capacitive deionization.

Project description:Exploring a new-family of carbon-based desalinators to optimize their performances beyond the current commercial benchmark is of significance for the development of practically useful capacitive deionization (CDI) materials. Here, we have fabricated a hierarchically porous N,P-doped carbon-graphene 2D heterostructure (denoted NPC/rGO) by using metal-organic framework (MOF)-nanoparticle-driven assembly on graphene oxide (GO) nanosheets followed by stepwise pyrolysis and phosphorization procedures. The resulting NPC/rGO-based CDI desalinator exhibits ultrahigh deionization performance with a salt adsorption capacity of 39.34 mg g-1 in a 1000 mg L-1 NaCl solution at 1.2 V over 30 min with good cycling stability over 50 cycles. The excellent performance is attributed to the high specific surface area, high conductivity, favorable meso-/microporous structure together with nitrogen and phosphorus heteroatom co-doping, all of which are beneficial for the accommodation of ions and charge transport during the CDI process. More importantly, NPC/rGO exhibits a state-of-the-art CDI performance compared to the commercial benchmark and most of the previously reported carbon materials, highlighting the significance of the MOF nanoparticle-driven assembly strategy and graphene-carbon 2D heterostructures for CDI applications.

| S-EPMC8336432 | biostudies-literature

Ultrahigh Content Boron and Nitrogen Codoped Hierarchically Porous Carbon Obtained from Biomass Byproduct Okara for Capacitive Deionization.

Project description:Capacitive deionization (CDI) is an environmentally friendly, energy efficient, and low cost water purification technique in comparison with other conventional techniques, and it has attracted considerable attention in recent years. Here, we use biomass byproduct okara as the starting material to fabricate a boron and nitrogen codoped hierarchically porous carbon (BNC) with ultrahigh heteroatom contents and abundant in-plane nanoholes for CDI application. With the interconnected hierarchical porous structure, the BNC not only exhibits a large surface area (647.0 m3 g-1) for the adsorption of ions but also offers abundant ion transport channels to access the entire internal surface. Meanwhile, the ultrahigh dopants' content of B (11.9 at%) and N (14.8 at%) further gives rise to the increased surface polarity and enhanced capacitance for BNC. Owing to these favorable properties, BNC exhibits top-level salt adsorption capacity (21.5 mg g-1) and charge efficiency (59.5%) at the initial NaCl concentration of ∼500 mg L-1. Moreover, we performed first-principle simulations to explore the different effects between N-doping and N,B-codoping on the capacitive property, which indicate that the boron and nitrogen codoping of carbon can largely increase the quantum capacitance over the double layer capacitance. The results of this work suggest a promising prospect for the BNC material in practical CDI application.

| S-EPMC9798738 | biostudies-literature

Ion-selective asymmetric carbon electrodes for enhanced capacitive deionization.

Project description:With the development of capacitive deionization technology, charge efficiency and electrosorption capacity have become some of the biggest technical bottlenecks. Asymmetric activated carbon electrodes with ion-selective functional groups inspired by membrane capacitive deionization were developed to conquer these issues. The deionization capacity increased from 11.0 mg g-1 to 23.2 mg g-1, and the charge efficiency increased from 0.54 to 0.84, due to ion-selective functional groups minimizing the co-ion effect. The charge efficiency and electrosorption capacity resulting from better wettability of these electrodes are effectively enhanced by grafting ion-selective functional groups, which are propitious to ion movement. In addition, asymmetric deionization capacitors show better cycling stability and higher desalination rates. These experimental results have demonstrated that the modification of the ion-selective (oxygen-containing) functional groups on the surfaces of activated carbon could greatly minimize the co-ion effects and increase the salt removal from the solution. These results have indicated that the ion-selective asymmetric carbon electrodes can promote well the development of deionization capacitors for practical desalination.

| S-EPMC9077380 | biostudies-literature

Freestanding Activated Carbon Nanocomposite Electrodes for Capacitive Deionization of Water.

Project description:Freshwater reserves are being polluted every day due to the industrial revolution. Man-made activities have adverse effects upon the ecosystem. It is thus the hour of need to explore newer technologies to save and purify water for the growing human population. Capacitive deionization (CDI) is being considered as an emerging technique for removal of excess ions to produce potable water including desalination. Herein, cost-effective activated carbon incorporated with carbon nanotubes (CNT) was used as a freestanding electrode. Further, the desalination efficiency of the designed electrodes was tuned by varying binder concentration, i.e., polyvinylidene difluoride (PVDF) in the activated carbon powder and CNT mixture. PVDF concentration of 5, 7.5, 10, and 12.5 wt% was selected to optimize the freestanding electrode formation and further applied for desalination of water. PVDF content affected the surface morphology, specific surface area, and functional groups of the freestanding electrodes. Moreover, the electrical conductivity and specific surface area changed with PVDF concentration, which ultimately affected the desalination capacity using the freestanding electrodes. This study paves the way to produce cost effective carbon-based freestanding electrodes for capacitive deionization and other applications including battery electrodes.

| S-EPMC9319057 | biostudies-literature

Particulate-free porous silicon networks for efficient capacitive deionization water desalination.

Project description:Energy efficient water desalination processes employing low-cost and earth-abundant materials is a critical step to sustainably manage future human needs for clean water resources. Here we demonstrate that porous silicon - a material harnessing earth abundance, cost, and environmental/biological compatibility is a candidate material for water desalination. With appropriate surface passivation of the porous silicon material to prevent surface corrosion in aqueous environments, we show that porous silicon templates can enable salt removal in capacitive deionization (CDI) ranging from 0.36% by mass at the onset from fresh to brackish water (10 mM, or 0.06% salinity) to 0.52% in ocean water salt concentrations (500 mM, or ~0.3% salinity). This is on par with reports of most carbon nanomaterial based CDI systems based on particulate electrodes and covers the full salinity range required of a CDI system with a total ocean-to-fresh water required energy input of ~1.45 Wh/L. The use of porous silicon for CDI enables new routes to directly couple water desalination technology with microfluidic systems and photovoltaics that natively use silicon materials, while mitigating adverse effects of water contamination occurring from nanoparticulate-based CDI electrodes.

| S-EPMC4840374 | biostudies-other

Polyacrylonitrile-b-Polystyrene Block Copolymer-Derived Hierarchical Porous Carbon Materials for Supercapacitor.

Project description:The use of block copolymers as a sacrificial template has been demonstrated to be a powerful method for obtaining porous carbons as electrode materials in energy storage devices. In this work, a block copolymer of polystyrene and polyacrylonitrile (PS-b-PAN) has been used as a precursor to produce fibers by electrospinning and powdered carbons, showing high carbon yield (~50%) due to a low sacrificial block content (fPS ≈ 0.16). Both materials have been compared structurally (in addition to comparing their electrochemical behavior). The porous carbon fibers showed superior pore formation capability and exhibited a hierarchical porous structure, with small and large mesopores and a relatively high surface area (~492 m2/g) with a considerable quantity of O/N surface content, which translates into outstanding electrochemical performance with excellent cycle stability (close to 100% capacitance retention after 10,000 cycles) and high capacitance value (254 F/g measured at 1 A/g).

| S-EPMC9739205 | biostudies-literature

Three-dimensional honeycomb-like porous carbon derived from corncob for the removal of heavy metals from water by capacitive deionization.

Project description:In this study, porous carbon (3DHPC) with a 3D honeycomb-like structure was synthesized from waste biomass corncob via hydrothermal carbonization coupled with KOH activation and investigated as a capacitive deionization (CDI) electrode material. The obtained 3DHPC possesses a hierarchal macroporous and mesoporous structure, and a large accessible specific surface area (952 m2 g-1). Electrochemical tests showed that the 3DHPC electrode exhibited a specific capacitance of 452 F g-1 and good electric conductivity. Moreover, the feasibility of electrosorptive removal of chromium(vi) from an aqueous solution using the 3DHPC electrode was demonstrated. When 1.0 V was applied to a solution containing 30 mg L-1 chromium(vi), the 3DHPC electrode exhibited a higher removal efficiency of 91.58% compared with that in the open circuit condition. This enhanced adsorption results from the improved affinity between chromium(vi) and the electrode under electrochemical assistance involving a non-faradic process. Consequently, the 3DHPC electrode with typical double-layer capacitor behavior is demonstrated to be a favorable electrode material for capacitive deionization.

| S-EPMC9076976 | biostudies-literature

Activated Carbon Blended with Reduced Graphene Oxide Nanoflakes for Capacitive Deionization.

Project description:Capacitive deionization is a second-generation water desalination technology in which porous electrodes (activated carbon materials) are used to temporarily store ions. In this technology, porous carbon used as electrodes have inherent limitations, such as low electrical conductivity, low capacitance, etc., and, as such, optimization of electrode materials by rational design to obtain hybrid electrodes is key towards improvement in desalination performance. In this work, different compositions of mixture of reduced graphene oxide (RGO) and activated carbon (from 5 to 20 wt% RGO) have been prepared and tested as electrodes for brackish water desalination. The physico-chemical and electrochemical properties of the activated carbon (AC), reduced graphene oxide (RGO), and as-prepared electrodes (AC/RGO-x) were characterized by low-temperature nitrogen adsorption measurement, scanning electron microscope (SEM), X-ray diffraction (XRD), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), Fourier transform infra-red (FT-IR), cyclic voltammetry (CV), and electrochemical impedance spectroscopy (EIS). Among all the composite electrodes, AC/RGO-5 (RGO at 5 wt%) possessed the highest specific capacitance (74 F g-1) and the highest maximum salt adsorption capacity (mSAC) of 8.10 mg g-1 at an operating voltage ∆E = 1.4 V. This shows that this simple approach could offer a potential way of fabricating electrodes of accentuated carbon network of an improved electronic conductivity that's much coveted in CDI technology.

| S-EPMC8144981 | biostudies-literature

Single-Walled Carbon Nanotube (SWCNT) Loaded Porous Reticulated Vitreous Carbon (RVC) Electrodes Used in a Capacitive Deionization (CDI) Cell for Effective Desalination.

Project description:Acid-functionalized single-walled carbon nanotube (a-SWCNT)-coated reticulated vitreous carbon (RVC) composite electrodes have been prepared and the use of these electrodes in capacitive deionization (CDI) cells for water desalination has been the focus of this study. The performance of these electrodes was tested based on the applied voltage, flow rate, bias potential and a-SWCNT loadings, and then evaluated by electrosorption dynamics. The effect of the feed stream directly through the electrodes, between the electrodes, and the distance between the electrodes in the CDI system on the performance of the electrodes has been investigated. The interaction of ions with the electrodes was tested through Langmuir and Freundlich isotherm models. A new CDI cell was developed, which shows an increase of 23.96% in electrosorption capacity compared to the basic CDI cells. Moreover, a comparison of our results with the published results reveals that RVC/a-SWCNT electrodes produce 16 times more pure water compared to the ones produced using only CNT-based electrodes. Finally, it can be inferred that RVC/a-SWCNT composite electrodes in newly-developed CDI cells can be effectively used in desalination technology for water purification.

| S-EPMC6071079 | biostudies-other

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