Browse
Submit Data
Databases
API
Help

Dataset Information

23 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Fabrication of Pd NPs-supported porous carbon by integrating the reducing reactivity and carbon-rich network of lignin.

ABSTRACT: The renewable resource as a major feedstock to prepare porous carbon has showed many advantages compared to fossil-based materials. This study proposes a new strategy to synthesize palladium nanoparticles (Pd NPs)-supported porous carbon, utilizing both the chemical reactivity and the carbon-rich 3D network of lignin. The Pd NPs-supported porous carbons were prepared in one-pot synthesis, with Pd(NH3)2Cl2 as precursor, lignin as reducing and stabilizing agents of Pd NPs, nano SiO2 as hard-template, followed by carbonization and removal of the template. The results reveal a positive effect of Pd precursor dosage on the development and excellent texture of the Pd NPs-supported porous carbon. Accordingly, the synthesized porous carbon was proved to have large micropore volume and good micro-mesopore porous structure, revealing it a promising hydrogen adsorbent.

SUBMITTER: Han G

PROVIDER: S-EPMC6514013 | biostudies-literature | 2019 May

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Fabrication of Pd NPs-supported porous carbon by integrating the reducing reactivity and carbon-rich network of lignin.

Han Guocheng G Jiang Qimeng Q Ye Weijie W Liu Chuanfu C Wang Xiaoying X

Scientific reports 20190513 1

The renewable resource as a major feedstock to prepare porous carbon has showed many advantages compared to fossil-based materials. This study proposes a new strategy to synthesize palladium nanoparticles (Pd NPs)-supported porous carbon, utilizing both the chemical reactivity and the carbon-rich 3D network of lignin. The Pd NPs-supported porous carbons were prepared in one-pot synthesis, with Pd(NH3)2Cl2 as precursor, lignin as reducing and stabilizing agents of ...[more]

PMID: 31086221

Similar Datasets

Lignin-Based Porous Supraparticles for Carbon Capture.

Project description:Multiscale carbon supraparticles (SPs) are synthesized by soft-templating lignin nano- and microbeads bound with cellulose nanofibrils (CNFs). The interparticle connectivity and nanoscale network in the SPs are studied after oxidative thermostabilization of the lignin/CNF constructs. The carbon SPs are formed by controlled sintering during carbonization and develop high mechanical strength (58 N·mm-3) and surface area (1152 m2·g-1). Given their features, the carbon SPs offer hierarchical access to adsorption sites that are well suited for CO2 capture (77 mg CO2·g-1), while presenting a relatively low pressure drop (∼33 kPa·m-1 calculated for a packed fixed-bed column). The introduced lignin-derived SPs address the limitations associated with mass transport (diffusion of adsorbates within channels) and kinetics of systems that are otherwise based on nanoparticles. Moreover, the carbon SPs do not require doping with heteroatoms (as tested for N) for effective CO2 uptake (at 1 bar CO2 and 40 °C) and are suitable for regeneration, following multiple adsorption/desorption cycles. Overall, we demonstrate porous SP carbon systems of low cost (precursor, fabrication, and processing) and superior activity (gas sorption and capture).

| S-EPMC8155330 | biostudies-literature

Lignin-derived 3D porous graphene on carbon cloth for flexible supercapacitors.

Project description:In this work, we reported a new method to fabricate flexible carbon-based supercapacitor electrodes derived from a commercialized and low-cost lignin. The fabrication process skips traditional stabilization/carbonization/activation for lignin-based carbon production. Also, the process reported here was green and facile, with minimum solvent use and no pretreatment required. Characterization of the lignin showed that it has common properties among all types of lignin. The lignin was impregnated on carbon cloth and then subjected to direct laser writing to form the desired electrodes (LLC). The results showed that lignin was successfully bonded to carbon cloth. The LLC has a good porous carbon structure with a high I G/I D ratio of 1.39, and a small interlayer spacing d 002 of 0.3436 nm, which are superior to most of the reported lignin-based carbons. Although not optimized, the fabricated LLC showed good supercapacitance behavior with an areal capacitance of 157.3 mF cm-2 at 0.1 mA cm-2. In addition, the superior flexibility of LLC makes it a promising electrode that can be used more widely in portable devices. Conceptually, this method can be generalized to all types of lignin and can define intriguing new research interests towards lignin applications.

| S-EPMC9033565 | biostudies-literature

Defect Rich Hierarchical Porous Carbon for High Power Supercapacitors.

Project description:Tuning hierarchical pore structure of carbon materials is an effective way to achieve high energy density under high power density of carbon-based supercapacitors. However, at present, most of methods for regulating pores of carbon materials are too complicated to be achieved. In this work, a durian shell derived porous carbon (DSPC) with abundant porous is prepared through chemical activation as a defect strategy. Hierarchical porous structure can largely enhance the transfer rate of electron/ion. Furthermore, DSPC with multiple porous structure exhibits excellent properties when utilized as electrode materials for electric double layer capacitors (EDLCs), delivering a specific capacitance of 321 F g-1 at 0.5 A g-1 in aqueous electrolyte. Remarkably, a high energy density of 27.7 Wh kg-1 is obtained at 675 W kg-1 in an organic two-electrode device. And large capacity can be remained even at high charge/discharge rate. Significantly, hierarchical porous structure allows efficient ion diffusion and charge transfer, resulting in a prominent cycling stability. This work is looking forward to providing a promising strategy to prepare hierarchical porous carbon-based materials for supercapacitors with ultrafast electron/ion transport.

| S-EPMC7011847 | biostudies-literature

Design and fabrication of hierarchically porous carbon with a template-free method.

Project description:Fabrication of hierarchically porous carbon materials (HPCs) with high surface area and pore volume has always been pursued. However, the currently effective template methods and acid/base activation strategies suffer from the drawbacks of either high costs or tedious steps. Herein, HPCs with 3D macro-mesopores and short-range meso-micropores were fabricated via an easy and sustainable two-step method from biomass. Macro-mesopores were constructed by slightly accumulation/aggregation of carbon spheres ranging from 60?nm to 80?nm, providing efficient mass diffusion pathways. Short-range mesopores and micropores with high electrolyte accessibility were developed in these spheres by air activation. The obtained HPCs showed surface area values up to 1306?m(2)/g and high mesopore volume proportion (63.9%). They demonstrated excellent capacitance and low equivalent series resistance (ESR) as supercapacitor electrode materials, suggesting the efficient diffusion and adsorption of electrolyte ions in the designed hierarchically porous structure.

| S-EPMC4162313 | biostudies-literature

Fabrication of Lignin-Based Nano Carbon Film-Copper Foil Composite with Enhanced Thermal Conductivity.

Project description:Technical lignin from pulping, an aromatic polymer with ~59% carbon content, was employed to develop novel lignin-based nano carbon thin film (LCF)-copper foil composite films for thermal management applications. A highly graphitized, nanoscale LCF (~80-100 nm in thickness) was successfully deposited on both sides of copper foil by spin coating followed by annealing treatment at 1000 °C in an argon atmosphere. The conditions of annealing significantly impacted the morphology and graphitization of LCF and the thermal conductivity of LCF-copper foil composite films. The LCF-modified copper foil exhibited an enhanced thermal conductivity of 478 W m-1 K-1 at 333 K, which was 43% higher than the copper foil counterpart. The enhanced thermal conductivity of the composite films compared with that of the copper foil was characterized by thermal infrared imaging. The thermal properties of the copper foil enhanced by LCF reveals its potential applications in the thermal management of advanced electronic products and highlights the potential high-value utility of lignin, the waste of pulping.

| S-EPMC6956031 | biostudies-literature

Fabrication of Hierarchical Lignin-Based Carbon through Direct High-Temperature Pyrolysis and Its Electrochemical Application.

Project description:Green synthesis of lignin-based carbon materials can accelerate the development of energy storage and conversion in supercapacitors. In this work, hierarchical graphenelike carbon was prepared by alkali lignin (AL) pyrolysis at a high temperature of 1700 °C. Accompanied by metal salt catalysis and a nitrogen hybridization reaction, a unique nanostructure of graphitized ALC was obtained with both a well-ordered 2D sheet lamellar structure and a uniform bowl-like porous structure. ALC exhibited a graphenelike lattice structure, a BET specific surface area of 1190 m2·g-1, and excellent electrochemical performance (104 F·g-1/0.5 A·g-1). The study offers a prospective way to the high-value application of industrial lignin in supercapacitor electrode materials.

| S-EPMC8675156 | biostudies-literature

Fabrication of Carbon-Like, π-Conjugated Organic Layer on a Nano-Porous Silica Surface.

Project description:This paper presents a new type of black organic material-porous silica composite providing an extremely highly selective adsorption surface. This black composite was prepared by lamination on nano-sized pores with a carbon-like, π-extended structure, which can be converted via the on-site polymerization of 1,5-dihydroxynaphthalene with a triazinane derivative and a thermally induced condensation reaction with denitrification. This bottom-up fabrication method on porous materials had the great advantage of maintaining the pore characteristics of a raw porous material, but also the resultant black surface exhibited an extremely high molecular-shape selectivity; for example, that for trans- and cis-stilbenes reached 14.0 with the black layer-laminated porous silica, whereas it was below 1.2 with simple hydrophobized silica.

| S-EPMC7558701 | biostudies-literature

Stepwise Fabrication of Co-Embedded Porous Multichannel Carbon Nanofibers for High-Efficiency Oxygen Reduction.

Project description:A novel nonprecious metal material consisting of Co-embedded porous interconnected multichannel carbon nanofibers (Co/IMCCNFs) was rationally designed for oxygen reduction reaction (ORR) electrocatalysis. In the synthesis, ZnCo2O4 was employed to form interconnected mesoporous channels and provide highly active Co3O4/Co core-shell nanoparticle-based sites for the ORR. The IMC structure with a large synergistic effect of the N and Co active sites provided fast ORR electrocatalysis kinetics. The Co/IMCCNFs exhibited a high half-wave potential of 0.82 V (vs. reversible hydrogen electrode) and excellent stability with a current retention up to 88% after 12,000 cycles in a current-time test, which is only 55% for 30 wt% Pt/C.

| S-EPMC7770944 | biostudies-literature

Tragacanth Gum Hydrogel-Derived Trimetallic Nanoparticles Supported on Porous Carbon Catalyst for Urea Electrooxidation.

Project description:The fabrication of electrocatalysts with high catalytic activity, high durability and low cost towards urea oxidation by a facile method is a great challenge. In this study, non-precious NiCoFe trimetallic supported on porous carbon (NiCoFe@PC) was prepared via gelation and pyrolysis method, presenting a remarkable electrocatalytic activity with low onset potential for urea oxidation in an alkaline medium. Field-emission scanning electron microscopy (FESEM) and transmission electron microscopy (TEM) were used to clarify the morphology of the NiCoFe@PC nanostructure and its nanoparticle size of 17.77 nm. The prepared catalyst with the composition ratio of 24.67, 5.92 and 5.11% for Ni, Fe and Co, respectively, with highly crystalline nanoparticles, fixed on porous carbon, according to energy-dispersive X-ray (EDX) and X-ray diffraction (XRD) analysis. The FeCoNi@PC catalyst showed a catalytic activity of 44.65 mA/cm2 at 0.57 V vs. Ag/AgCl and a low onset potential of 218 mV, which is superior to many other transition bi/trimetallic-based catalysts previously reported.

| S-EPMC9141339 | biostudies-literature

Nitrogen-Rich Porous Organic Polymers with Supported Ag Nanoparticles for Efficient CO2 Conversion.

Project description:As CO2 emissions increase and the global climate deteriorates, converting CO2 into valuable chemicals has become a topic of wide concern. The development of multifunctional catalysts for efficient CO2 conversion remains a major challenge. Herein, two porous organic polymers (NPOPs) functionalized with covalent triazine and triazole N-heterocycles are synthesized through the copper(I)-catalyzed azide-alkyne cycloaddition (CuAAC) reaction. The NPOPs have an abundant microporous content and high specific surface area, which confer them excellent CO2 affinities with a CO2 adsorption capacity of 84.0 mg g-1 and 63.7 mg g-1, respectively, at 273 K and 0.1 MPa. After wet impregnation and in situ reductions, Ag nanoparticles were supported in the NPOPs to obtain Ag@NPOPs with high dispersion and small particle size. The Ag@NPOPs were applied to high-value conversion reactions of CO2 with propargylic amines and terminal alkynes under mild reaction conditions. The carboxylative cyclization transformation of propargylic amine into 2-oxazolidinone and the carboxylation transformation of terminal alkynes into phenylpropiolic acid had the highest TOF values of 1125.1 and 90.9 h-1, respectively. The Ag@NPOP-1 was recycled and used five times without any significant decrease in catalytic activity, showing excellent catalytic stability and durability.

| S-EPMC9501012 | 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