Browse
Submit Data
Databases
API
Help

Dataset Information

32 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Cyanogel-Derived Synthesis of Porous PdFe Nanohydrangeas as Electrocatalysts for Oxygen Reduction Reaction.

ABSTRACT: It is important to develop cost-efficient electrocatalysts used in the oxygen reduction reaction (ORR) for widespread applications in fuel cells. Palladium (Pd) is a promising catalyst, due to its more abundant reserves and lower price than platinum (Pt), and doping an earth-abundant 3d-transition metal M into Pd to form Pd-M bimetallic alloys may not only further reduce the use of expensive Pd but also promote the electrocatalytic performance of ORR, owing to the synergistic effect between Pd and M. Here we report a cyanogel-derived synthesis of PdFe alloys with porous nanostructure via a simple coinstantaneous reduction reaction by using K₂Pd^IICl₄/K₄Fe^II(CN)₆ cyanogel as precursor. The synthesized PdFe alloys possess hydrangea-like morphology and porous nanostructure, which are beneficial to the electrochemical performance in ORR. The onset potential of the porous PdFe nanohydrangeas is determined to be 0.988 V, which is much more positive than that of commercial Pt/C catalyst (0.976 V) and Pd black catalyst (0.964 V). Resulting from the unique structural advantages and synergetic effect between bimetals, the synthesized PdFe nanohydrangeas with porous structure have outstanding electrocatalytic activity and stability for ORR, compared with the commercial Pd black and Pt/C.

SUBMITTER: Wan J

PROVIDER: S-EPMC8708350 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Heteroatoms ternary-doped porous carbons derived from MOFs as metal-free electrocatalysts for oxygen reduction reaction.

Project description:The nitrogen (N), phosphorus (P) and sulphur (S) ternary-doped metal-free porous carbon materials have been successfully synthesized using MOFs as templates (denoted as NPS-C-MOF-5) for oxygen reduction reaction (ORR) for the first time. The influences of porous carbons from carbonizing different MOFs and carbonization temperature on ORR have been systematically investigated. Due to the synergistic effect of N, P and S ternary-doping, the NPS-C-MOF-5 catalyst shows a higher onset potential as a metal-free electrocatalyst for ORR among the currently reported metal-free electrocatalysts, very close to the commercial Pt-C catalyst. In particular, the kinetic limiting current density of NPS-C-MOF-5 catalyst at -0.6 V is up to approximate -11.6 mA cm(-2), which is 1.2 times higher than that of the commercial Pt-C catalyst. Furthermore, the outstanding methanol tolerance and excellent long-term stability of NPS-C-MOF-5 are superior to those of the commercial Pt-C catalyst for ORR in alkaline media.

| S-EPMC4038808 | biostudies-literature

Carbon-Based Electrocatalysts Derived From Biomass for Oxygen Reduction Reaction: A Minireview.

Project description:Oxygen reduction reaction (ORR) electrocatalysts derived from biomass have become one of the research focuses in hetero-catalysis due to their low cost, high performance, and reproducibility properties. Related researches are of great significance for the development of next-generation fuel cells and metal-air batteries. Herein, the preparation methods of various biomass-derived catalysts and their performance in alkaline, neutral, and acidic media are summarized. This review clarifies the research progress of biomass carbon-based electrocatalysts for ORR in acidic, alkaline and neutral media, and discusses the future development trends. This minireview can give us an important enlightenment to practical application in the future.

| S-EPMC7059099 | biostudies-literature

Zinc-Mediated Template Synthesis of Hierarchical Porous N-Doped Carbon Electrocatalysts for Efficient Oxygen Reduction.

Project description:The development of highly active and low-cost catalysts for use in oxygen reduction reaction (ORR) is crucial to many advanced and eco-friendly energy techniques. N-doped carbons are promising ORR catalysts. However, their performance is still limited. In this work, a zinc-mediated template synthesis strategy for the development of a highly active ORR catalyst with hierarchical porous structures was presented. The optimal catalyst exhibited high ORR performance in a 0.1 M KOH solution, with a half-wave potential of 0.89 V vs. RHE. Additionally, the catalyst exhibited excellent methanol tolerance and stability. After a 20,000 s continuous operation, no obvious performance decay was observed. When used as the air-electrode catalyst in a zinc-air battery (ZAB), it delivered an outstanding discharging performance, with peak power density and specific capacity as high as 196.3 mW cm-2 and 811.5 mAh gZn-1, respectively. Its high performance and stability endow it with potential in practical and commercial applications as a highly active ORR catalyst. Additionally, it is believed that the presented strategy can be applied to the rational design and fabrication of highly active and stable ORR catalysts for use in eco-friendly and future-oriented energy techniques.

| S-EPMC10254328 | biostudies-literature

Glucose-derived carbon materials with tailored properties as electrocatalysts for the oxygen reduction reaction.

Project description:Nitrogen-doped biomass-derived carbon materials were prepared by hydrothermal carbonization of glucose, and their textural and chemical properties were subsequently tailored to achieve materials with enhanced electrochemical performance towards the oxygen reduction reaction. Carbonization and physical activation were applied to modify the textural properties, while nitrogen functionalities were incorporated via different N-doping methodologies (ball milling and conventional methods) using melamine. A direct relationship between the microporosity of the activated carbons and the limiting current density was found, with the increase of microporosity leading to interesting improvements of the limiting current density. Regardless of the doping method used, similar amounts of nitrogen were incorporated into the carbon structures. However, significant differences were observed in the nitrogen functionalities according to the doping method applied: ball milling appeared to originate preferentially quaternary and oxidized nitrogen groups, while the formation of pyridinic and pyrrolic groups was favoured by conventional doping. The onset potential was improved and the two-electron mechanism of the original activated sample was shifted closer to a four-electron pathway due to the presence of nitrogen. Interestingly, the high pyridinic content related to a high ratio of pyridinic/quaternary nitrogen results in an increase of the onset potential, while a decrease in the quaternary/pyrrolic nitrogen ratio favors an increase in the number of electrons. Accordingly, the electrocatalyst with the highest performance was obtained from the activated sample doped with nitrogen by the conventional method, which combined the most appropriate textural and chemical properties: high microporosity and adequate proportion of the nitrogen functionalities.

| S-EPMC6541360 | biostudies-literature

Development of Porous Pt Electrocatalysts for Oxygen Reduction and Evolution Reactions.

Project description:Porous Pt electrocatalysts have been developed as an example of carbon-free porous metal catalysts in anticipation of polymer electrolyte membrane (PEM) fuel cells and PEM water electrolyzers through the assembly of the metal precursor and surfactant. In this study, porous Pt was structurally evaluated and found to have a porous structure composed of connected Pt particles. The resulting specific electrochemical surface area (ECSA) of porous Pt was 12.4 m2 g-1, which was higher than that of commercially available Pt black. Accordingly, porous Pt showed higher oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) activity than Pt black. When the activity was compared to that of a common carbon-supported electrocatalyst, Pt/ketjen black (KB), porous Pt showed a comparable ORR current density (2.5 mA cm-2 at 0.9 V for Pt/KB and 2.1 mA cm-2 at 0.9 V for porous Pt), and OER current density (6.8 mA cm-2 at 1.8 V for Pt/KB and 7.0 mA cm-1 at 1.8 V), even though the ECSA of porous Pt was only one-sixth that of Pt/KB. Moreover, it exhibited a higher durability against 1.8 V. In addition, when catalyst layers were spray-printed on the Nafion® membrane, porous Pt displayed more uniform layers in comparison to Pt black, showing an advantage in its usage as a thin layer.

| S-EPMC7287804 | biostudies-literature

Synthesis of Ti4O7/Ti3O5 Dual-Phase Nanofibers with Coherent Interface for Oxygen Reduction Reaction Electrocatalysts.

Project description:Electrocatalysts play an important role in oxygen reduction reaction (ORR) in promoting the reaction process. Although commercial Pt/C exhibits excellent performance in ORR, the low duration, high cost, and poor methanol tolerance seriously restrict its sustainable development and application. TinO2n-1 (3 ≤ n ≤ 10) is a series of titanium sub-oxide materials with excellent electrical conductivity, electrochemical activity, and stability, which have been widely applied in the field of energy storage and catalysis. Herein, we design and synthesize Ti4O7/Ti3O5 (T4/T3) dual-phase nanofibers with excellent ORR catalytic performance through hydrothermal growth, which is followed by a precisely controlled calcination process. The H2Ti3O7 precursor with uniform size can be first obtained by optimizing the hydrothermal growth parameters. By precisely controlling the amount of reducing agent, calcination temperature, and holding time, the T4/T3 dual-phase nanofibers with uniform morphology and coherent interfaces can be obtained. The orientation relationships between T4 and T3 are confirmed to be [ 001 ] T 3 / / [ 031 ] T 4 , ( 100 ) T 3 / / ( 92 6 ¯ ) T 4 , and ( 010 ) T 3 / / ( 1 2 ¯ 6 ) T 4 , respectively, based on comprehensive transmission electron microscopy (TEM) investigations. Furthermore, such dual-phase nanofibers exhibit the onset potential and half-wave potential of 0.90 V and 0.75 V as the ORR electrocatalysts in alkaline media, respectively, which illustrates the excellent ORR catalytic performance. The rotating ring-disk electrode (RRDE) experiment confirmed the electron transfer number of 3.0 for such catalysts, which indicates a mixture of two electron and four electron transfer reaction pathways. Moreover, the methanol tolerance and cycling stability of the catalysts are also investigated accordingly.

| S-EPMC7412102 | 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

Porous Carbon Networks Derived From Graphitic Carbon Nitride for Efficient Oxygen Reduction Reaction.

Project description:Great efforts have been dedicated to finding economic and efficient oxygen reduction reaction (ORR) for fuel cell technology. Among various catalysts, N-doped carbon-based nanomaterials have attracted much attention due to low-cost, noble metal free, and good durability. Herein, we developed a facile and economic strategy to prepare nitrogen-doped carbon networks for efficient ORR application. The g-C3N4 is used as the template and N source, and dopamine is used as the carbon source. By simple hydrothermal treatment and sintering, N-doped carbon network structures with high specific surface area, effective ORR activity, and superior durability could be acquired. The present strategy is free of involving generally multistep, poisonous reagents, and complication of removing template for fabrication of 3D carbon structures.

| S-EPMC6656852 | biostudies-literature

Recent Advances in Single-Atom Electrocatalysts for Oxygen Reduction Reaction.

Project description:Oxygen reduction reaction (ORR) plays significant roles in electrochemical energy storage and conversion systems as well as clean synthesis of fine chemicals. However, the ORR process shows sluggish kinetics and requires platinum-group noble metal catalysts to accelerate the reaction. The high cost, rare reservation, and unsatisfied durability significantly impede large-scale commercialization of platinum-based catalysts. Single-atom electrocatalysts (SAECs) featuring with well-defined structure, high intrinsic activity, and maximum atom efficiency have emerged as a novel field in electrocatalytic science since it is promising to substitute expensive platinum-group noble metal catalysts. However, finely fabricating SAECs with uniform and highly dense active sites, fully maximizing the utilization efficiency of active sites, and maintaining the atomically isolated sites as single-atom centers under harsh electrocatalytic conditions remain urgent challenges. In this review, we summarized recent advances of SAECs in synthesis, characterization, oxygen reduction reaction (ORR) performance, and applications in ORR-related H2O2 production, metal-air batteries, and low-temperature fuel cells. Relevant progress on tailoring the coordination structure of isolated metal centers by doping other metals or ligands, enriching the concentration of single-atom sites by increasing metal loadings, and engineering the porosity and electronic structure of the support by optimizing the mass and electron transport are also reviewed. Moreover, general strategies to synthesize SAECs with high metal loadings on practical scale are highlighted, the deep learning algorithm for rational design of SAECs is introduced, and theoretical understanding of active-site structures of SAECs is discussed as well. Perspectives on future directions and remaining challenges of SAECs are presented.

| S-EPMC7443255 | biostudies-literature

Hydrogel-derived non-precious electrocatalysts for efficient oxygen reduction.

Project description:The development of highly active, cheap and robust oxygen reduction reaction (ORR) electrocatalysts to replace precious metal platinum is extremely urgent and challenging for renewable energy devices. Herein we report a novel, green and especially facile hydrogel strategy to construct N and B co-doped nanocarbon embedded with Co-based nanoparticles as an efficient non-precious ORR catalyst. The agarose hydrogel provides a general host matrix to achieve a homogeneous distribution of key precursory components including cobalt (II) acetate and buffer salts, which, upon freeze-drying and carbonization, produces the highly active ORR catalyst. The gel buffer containing Tris base, boric acid and ethylenediaminetetraacetic acid, commonly adopted for pH and ionic strength control, plays distinctively different roles here. These include a green precursor for N- and B-doping, a salt porogen and a Co(2+) chelating agent, all contributing to the excellent ORR activity. This hydrogel-based process is potentially generalizable for many other catalytic materials.

| S-EPMC4486930 | 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