Browse
Submit Data
Databases
API
Help

Dataset Information

20 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Flocculant-Assisted Synthesis of Graphene-Like Carbon Nanosheets for Oxygen Reduction Reaction and Supercapacitor.

ABSTRACT: The rational treatment of hazardous textile sludge is critical and challenging for the environment and a sustainable future. Here, a water-soluble chitosan derivative was synthesized and used as an effective flocculant in removal of reactive dye from aqueous solution. Employing these chitosan-containing textile sludges as precursors, graphene-like carbon nanosheets were synthesized through simple one-step carbonization with the use of Fe (III) salt as graphitization catalyst. It was found that the resultant graphene-like carbon nanosheets material at thickness near 3.2 nm (NSC-Fe-2) showed a high graphitization degree, high specific surface area, and excellent bifunctional electrochemical performance. As-prepared NSC-Fe-2 catalyst exhibited excellent oxygen reduction reaction (ORR) activity (onset potential 1.05 V) and a much better methanol tolerance than that of commercial Pt/C (onset potential 0.98 V) in an alkaline medium. Additionally, as electrode materials for supercapacitors, NSC-Fe-2 also displayed an outstanding specific capacitance of 195 F g^-1 at 1 A g^-1 and superior cycling stability (loss of 3.4% after 2500 cycles). The good electrochemical properties of the as-prepared NSC-Fe materials could be attributed to the ultrathin graphene-like nanosheets structure and synergistic effects from codoping of iron and nitrogen. This work develops a simple but effective strategy for direct conversion of textile sewage sludge to value-added graphene-like carbon, which is considered as a promising alternative to fulfill the requirements of environment and energy.

SUBMITTER: Zhang Y

PROVIDER: S-EPMC6722949 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Nitrogen-Doped Carbon Nanosheets Decorated With Mn2O3 Nanoparticles for Excellent Oxygen Reduction Reaction.

Project description:The purpose of this study is to develop an active, low cost, non-precious, stable, and high-performance catalyst for oxygen reduction reaction (ORR). In this regard, Mn2O3-decorated nitrogen-doped carbon nanosheets (Mn2O3/NC) are fabricated by a two-step strategy involving a hydrothermal method and a solid-state method. In the resultant structures, very fine Mn2O3 nanoparticles with an average size of about 5 nm are strongly attached to nitrogen-doped carbon nanosheets. The role of the Mn2O3 nanoparticles is to provide active sites for ORR, while the presence of the nitrogen-doped carbon not only enhances the conductivity of the overall structure but is also helpful for overall stability. The Mn2O3/NC shows good onset potential (0.80 V@-1 mA/cm2), methanol crossover effect, and stability (90%).

| S-EPMC6856643 | biostudies-literature

Spinach-Derived Porous Carbon Nanosheets as High-Performance Catalysts for Oxygen Reduction Reaction.

Project description:Biomass-derived porous carbon materials are effective electrocatalysts for oxygen reduction reaction (ORR), with promising applications in low-temperature fuel cells and metal-air batteries. Herein, we developed a synthesis procedure that used spinach as a source of carbon, iron, and nitrogen for preparing porous carbon nanosheets and studied their ORR catalytic performance. These carbon sheets showed a very high ORR activity with a half-wave potential of +0.88 V in 0.1 M KOH, which is 20 mV more positive than that of commercial Pt/C catalysts. In addition, they showed a much better long-term stability than Pt/C and were insensitive to methanol. The remarkable ORR performance was attributed to the accessible high-density active sites that are primarily from Fe-N x moieties. This work paves the way toward the use of metal-enriching plants as a source for preparing porous carbon materials for electrochemical energy conversion and storage applications.

| S-EPMC7528166 | biostudies-literature

Biomass Juncus Derived Nitrogen-Doped Porous Carbon Materials for Supercapacitor and Oxygen Reduction Reaction.

Project description:Juncus is a perennial herb aquatic plant found worldwide, with high reproductive ability in warm regions. It has three-dimensional hierarchical porous triangular networks structures composited of tubular fibers. Here, juncus derived nitrogen-doped porous carbon (NDPC) was prepared by mixing juncus and ZnCl2 through one-step pyrolysis and activation which is a low-cost, simple, and environmentally friendly method. The NDPC had hierarchical porous structures and a high specific surface area and was applied for supercapacitor and oxygen reduction reaction (ORR). The resulted NDPC-3-800 was prepared by mixing juncus with ZnCl2 at a mass ratio of 1:3 and then carbonized at 800°C, it was used as electrode material of a supercapacitor. The supercapacitor exhibited excellent specific capacitance of 290.5 F g-1 and 175.0 F g-1 in alkaline electrolyte at the current densities of 0.5 A g-1 and 50 A g-1, respectively. The supercapacitor showed good cycle stability, and the capacitance was maintained at 94.5% after 10,000 cycles. The NDPC-5-800 was prepared by mixing juncus with ZnCl2 at a mass ratio of 1:5 and then carbonized at 800°C. It exhibited outstanding ORR catalytic activity and stability attributing to their high specific surface area and abundant actives sites. The juncus can derive various materials for application in different fields.

| S-EPMC7174754 | biostudies-literature

Superstructured Macroporous Carbon Rods Composed of Defective Graphitic Nanosheets for Efficient Oxygen Reduction Reaction.

Project description:Rationally designed carbon materials with superstructures are promising candidates in applications such as electrocatalysis. However, the synthesis of highly porous carbon superstructures with macropores and carbon defects from a simple crystalline solid remains challenging. In this work, superstructured macroporous carbon rods composed of defective graphitic nanosheets are synthesized by direct carbonization of crystalline poly tannic acid (PTA) rods as precursors. During carbonization, PTA rods with a highly ordered lamellar structure induce a spatially confined two-step localized contraction that takes place in different dimensions and directions in each step. The unexpected contraction behavior results in the sponge-like macroporous carbon superstructure with large surface area, high porosity, and abundant defects, thus showing a superior electrocatalytic performance with high activity and selectivity for oxygen reduction reaction. The study provides new understandings in the design of functional carbon materials with distinctive structures and applications.

| S-EPMC8456237 | biostudies-literature

In-situ formation of cobalt-phosphate oxygen-evolving complex-anchored reduced graphene oxide nanosheets for oxygen reduction reaction.

Project description:Oxygen conversion process between O? and H?O by means of electrochemistry or photochemistry has lately received a great deal of attention. Cobalt-phosphate (Co-Pi) catalyst is a new type of cost-effective artificial oxygen-evolving complex (OEC) with amorphous features during photosynthesis. However, can such Co-Pi OEC also act as oxygen reduction reaction (ORR) catalyst in electrochemical processes? The question remains unanswered. Here for the first time we demonstrate that Co-Pi OEC does be rather active for the ORR. Particularly, Co-Pi OEC anchoring on reduced graphite oxide (rGO) nanosheet is shown to possess dramatically improved electrocatalytic activities. Differing from the generally accepted role of rGO as an "electron reservoir", we suggest that rGO serves as "peroxide cleaner" in enhancing the electrocatalytic behaviors. The present study may bridge the gap between photochemistry and electrochemistry towards oxygen conversion.

| S-EPMC3719074 | biostudies-literature

Ionic-Liquid-Assisted One-Step Synthesis of CoO Nanosheets as Electrocatalysts for Oxygen Evolution Reaction.

Project description:The sluggish oxygen evolution reaction (OER) hinders the development of electrocatalytic water splitting for energy conversion and storage. Therefore, it is imperative to explore the cost-effective and highly efficient noble-metal-free electrocatalysts for OER. Herein, we are introducing such OER electrocatalyst based on Co, fabricated through an ionic-liquid-assisted one-step synthesis, where ionic liquid played a dual role as solvent cum structure-directing agent. Besides possessing large-accessible surface area and numerous active sites, the as-prepared stable CoO nanosheets exhibited excellent electrochemical activity through establishing an extensive contact with the electrolyte. Under alkaline conditions, the overpotential to achieve a current density of 10 mA cm-2 is only 320 mV, and the Tafel slope is as small as 70 mV dec-1. Thus, our work provides a new pathway for designing and engineering the highly efficient non-noble metal OER electrocatalysts by using ionic liquids.

| S-EPMC6645614 | biostudies-literature

Coral-like Co3O4 Decorated N-doped Carbon Particles as active Materials for Oxygen Reduction Reaction and Supercapacitor.

Project description:Coral reef has a unique dendritic structure with large specific surface area, rich pore structure, so that it can be attached to a large number of zooxanthellae for gas exchange. Coral reef ecosystems are also known as underwater rainforests. Inspired by this biological structure, we designed and fabricated coral-like Co3O4 decorated N-doped carbon particles (Co3O4/N-CP). The obtained Co3O4/N-CP-900 catalyst shows efficient ORR electrocatalytic performances in an alkaline medium with a positive onset and half-wave potentials of 0.97 and 0.90?V (vs. RHE), as well as a high diffusion-limited current density (5.50?mA?cm-2) comparable to that of a Pt/C catalyst (5.15?mA?cm-2). It also displays better stability and methanol tolerance than commercial Pt/C. In addition, the Co3O4/N-CP-900 electrode has a high specific capacitance of 316.2?F?g-1 in 6?M KOH, as well as good rate capabilities and excellent cycle performance. These results are due to large surface area, narrow pore size distribution, high density electrochemical energy conversion and storage activity centers. This method presented here offers an effective path for the development of high performance multi-functional carbon-based materials for ORR and supercapacitor applications.

| S-EPMC5789056 | biostudies-literature

Fe@N-Graphene Nanoplatelet-Embedded Carbon Nanofibers as Efficient Electrocatalysts for Oxygen Reduction Reaction.

Project description:An activated carbon nanofiber (CNF) is prepared with incorporated Fe-N-doped graphene nanoplatelets (Fe@NGnPs), via a novel and simple synthesis approach. The activated CNF-Fe@NGnP catalysts exhibit substantially improved activity for the oxygen reduction reaction compared to those of commercial carbon blacks and Pt/carbon catalysts.

| S-EPMC5049621 | biostudies-literature

Synthesis of 2D Nitrogen-Doped Mesoporous Carbon Catalyst for Oxygen Reduction Reaction.

Project description:2D nitrogen-doped mesoporous carbon (NMC) is synthesized by using a mesoporous silica film as hard template, which is then investigated as a non-precious metal catalyst for the oxygen reduction reaction (ORR). The effect of the synthesis conditions on the silica template and carbon is extensively investigated. In this work, we employ dual templates-viz. graphene oxide and triblock copolymer F127-to control the textural features of a 2D silica film. The silica is then used as a template to direct the synthesis of a 2D nitrogen-doped mesoporous carbon. The resultant nitrogen-doped mesoporous carbon is characterized by transmission electron microscopy (TEM), nitrogen ad/desorption isotherms, X-ray photoelectron spectroscopy (XPS), cyclic voltammetry (CV), and rotating disk electrode measurements (RDE). The electrochemical test reveals that the obtained 2D-film carbon catalyst yields a highly electrochemically active surface area and superior electrocatalytic activity for the ORR compared to the 3D-particle. The superior activity can be firstly attributed to the difference in the specific surface area of the two catalysts. More importantly, the 2D-film morphology makes more active sites accessible to the reactive species, resulting in a much higher utilization efficiency and consequently better activity. Finally, it is noted that all the carbon catalysts exhibit a higher ORR activity than a commercial Pt catalyst, and are promising for use in fuel cells.

| S-EPMC5459128 | biostudies-literature

Ultrasonic-assisted hydrothermal synthesis of cobalt oxide/nitrogen-doped graphene oxide hybrid as oxygen reduction reaction catalyst for Al-air battery.

Project description:A persistent ultrasound-assisted hydrothermal method has been developed to prepare cobalt oxide incorporated nitrogen-doped graphene (Co3O4/N-GO) hybrids. The electrochemical behaviors and catalytic activity of the prepared hybrids have been systematically investigated as cathode materials for Al-air battery. The results show that ultrasonication can promote the yield ratio of Co3O4 from 63.1% to 70.6%. The prepared Co3O4/N-GO hybrid with ultrasonication exhibits better ORR activity over that without ultrasonication. The assembled Al-air battery using the ultrasonicated Co3O4/N-GO hybrid exhibited an average working voltage of 1.02 V in 4 M KOH electrolyte at 60 mA∙cm-2, approximately 60 mV higher than that using hybrid without ultrasonication. This should be attributed to large number density of fine Co3O4 particles growing on the dispersed GO sheets under the persistent ultrasonication. The related ultrasonic mechanism has been discussed in details.

| S-EPMC7808954 | 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