Browse
Submit Data
Databases
API
Help

Dataset Information

35 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Synthesis of 3D Hexagram-Like Cobalt-Manganese Sulfides Nanosheets Grown on Nickel Foam: A Bifunctional Electrocatalyst for Overall Water Splitting.

ABSTRACT: The exploration of low-cost and efficient bifunctional electrocatalysts for oxygen evolution reaction and hydrogen evolution reaction through tuning the chemical composition is strongly required for sustainable resources. Herein, we developed a bimetallic cobalt-manganese sulfide supported on Ni foam (CMS/Ni) via a solvothermal method. It has discovered that after combining with the pure Co₉S₈ and MnS, the morphologies of CMS/Ni have modulated. The obtained three-dimensionally hexagram-like CMS/Ni nanosheets have a significant increase in electrochemical active surface area and charge transport ability. More than that, the synergetic effect of Co and Mn has also presented in this composite. Benefiting from these, the CMS/Ni electrode shows great performance toward hydrogen evolution reaction and oxygen evolution reaction in basic medium, comparing favorably to that of the pure Co₉S₈/Ni and MnS/Ni. More importantly, this versatile CMS/Ni can catalyze the water splitting in a two-electrode system at a potential of 1.47 V, and this electrolyzer can be efficiently driven by a 1.50 V commercial dry battery.

SUBMITTER: Li J

PROVIDER: S-EPMC6199054 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Molybdenum and Vanadium-Codoped Cobalt Carbonate Nanosheets Deposited on Nickel Foam as a High-Efficient Bifunctional Catalyst for Overall Alkaline Water Splitting.

Project description:To address issues of global energy sustainability, it is essential to develop highly efficient bifunctional transition metal-based electrocatalysts to accelerate the kinetics of both the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER). Herein, the heterogeneous molybdenum and vanadium codoped cobalt carbonate nanosheets loaded on nickel foam (VMoCoCOx@NF) are fabricated by facile hydrothermal deposition. Firstly, the mole ratio of V/Mo/Co in the composite is optimized by response surface methodology (RSM). When the optimized composite serves as a bifunctional catalyst, the water-splitting current density achieves 10 mA cm-2 and 100 mA cm-2 at cell voltages of 1.54 V and 1.61 V in a 1.0 M KOH electrolyte with robust stability. Furthermore, characterization is carried out using field emission scanning electron microscopy-energy dispersive spectroscopy (FESEM-EDS), high-resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS). Density functional theory (DFT) calculations reveal that the fabricated VMoCoCOx@NF catalyst synergistically decreases the Gibbs free energy of hydrogen and oxygen-containing intermediates, thus accelerating OER/HER catalytic kinetics. Benefiting from the concerted advantages of porous NF substrates and clustered VMoCoCOx nanosheets, the fabricated catalyst exhibits superior electrocatalytic performance. This work presents a novel approach to developing transition metal catalysts for overall water splitting.

| S-EPMC11314115 | biostudies-literature

Pseudocapacitive-battery-like behavior of cobalt manganese nickel sulfide (CoMnNiS) nanosheets grown on Ni-foam by electrodeposition for realizing high capacity.

Project description:Hierarchical interconnected nanosheets (HIN) of cobalt manganese nickel sulfide (CoMnNiS) were synthesized on Ni foam by a simple and economical electrodeposition technique for energy storage application. Sulfonated thin nanosheets of Co, Mn and Ni provide stability of chemical activity, surface functionalization and surface reactivity to the electrode. The fabricated electrode shows a specific capacity of 257.4 mA h g-1 (at 2.5 A g-1), measured by galvanostatic charging-discharging (GCD). Both diffusion and capacitive mechanisms in the sulfide layer contribute to the high electrical conductivity. Asymmetric devices CoMnNiS/NiCuO and CoMnNiS/CNT (CNT = carbon nanotubes) were fabricated, providing a maximum operating voltage of 1.7 V and 1 V, specific capacity of 20.8 and 50.8 mA h g-1, and energy density of 8.4 and 6.3 W h kg-1 corresponding to a power density of 985 and 211 W kg-1, respectively, at a current density of 0.5 and 0.63 A g-1. These results demonstrate a novel material for application in energy storage devices as an electrode.

| S-EPMC9091183 | biostudies-literature

Ni<sub>2</sub>P nanocrystals embedded Ni-MOF nanosheets supported on nickel foam as bifunctional electrocatalyst for urea electrolysis.

Project description:It's highly desired but challenging to synthesize self-supporting nanohybrid made of conductive nanoparticles with metal organic framework (MOF) materials for the application in the electrochemical field. In this work, we report the preparation of Ni2P embedded Ni-MOF nanosheets supported on nickel foam through partial phosphidation (Ni2P@Ni-MOF/NF). The self-supporting Ni2P@Ni-MOF/NF was directly tested as electrode for urea electrolysis. When served as anode for urea oxidation reaction (UOR), it only demands 1.41 V (vs RHE) to deliver a current of 100 mA cm-2. And the overpotential of Ni2P@Ni-MOF/NF to reach 10 mA cm-2 for hydrogen evolution reaction HER was only 66 mV, remarkably lower than Ni2P/NF (133 mV). The exceptional electrochemical performance was attributed to the unique structure of Ni2P@Ni-MOF and the well exposed surface of Ni2P. Furthermore, the Ni2P@Ni-MOF/NF demonstrated outstanding longevity for both HER and UOR. The electrolyzer constructed with Ni2P@Ni-MOF/NF as bifunctional electrode can attain a current density of 100 mA cm-2 at a cell voltage as low as 1.65 V. Our work provides new insights for prepare MOF based nanohydrid for electrochemical application.

| S-EPMC8560839 | biostudies-literature

Ni2P/rGO/NF Nanosheets As a Bifunctional High-Performance Electrocatalyst for Water Splitting.

Project description:The hydrogen generated via the water splitting method is restricted by the high level of theoretical potential exhibited by the anode. The work focuses on synthesizing a bifunctional catalyst with a high efficiency, that is, a nickel phosphide doped with the reduced graphene oxide nanosheets supported on the Ni foam (Ni2P/rGO/NF), via the hydrothermal approach together with the calcination approach specific to the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER). The Raman, X-Ray Diffraction (XRD), X-ray Photoelectron Spectroscopy (XPS), Transmission Electron Microscope (TEM), Scanning Electron Microscopy (SEM), High-Resolution Transmission Electron Microscopy (HRTEM), as well as elemental mapping, are adopted to study the composition and morphology possessed by Ni2P/rGO/NF. The electrochemical testing is performed by constructing a parallel two-electrode electrolyzer (Ni2P/rGO/NF||Ni2P/rGO/NF). Ni2P/rGO/NF||Ni2P/rGO/NF needs a voltage of only 1.676 V for driving 10 mA/cm2, which is extremely close to Pt/C/NF||IrO2/NF (1.502 V). It is possible to maintain the current density for no less than 30 hours. It can be demonstrated that Ni2P/rGO/NF||Ni2P/rGO/NF has commercial feasibility, relying on the strong activity and high stability.

| S-EPMC7041371 | biostudies-literature

Bimetallic Nickel Cobalt Sulfide as Efficient Electrocatalyst for Zn-Air Battery and Water Splitting.

Project description:The development of efficient earth-abundant electrocatalysts for oxygen reduction, oxygen evolution, and hydrogen evolution reactions (ORR, OER, and HER) is important for future energy conversion and energy storage devices, for which both rechargeable Zn-air batteries and water splitting have raised great expectations. Herein, we report a single-phase bimetallic nickel cobalt sulfide ((Ni,Co)S2) as an efficient electrocatalyst for both OER and ORR. Owing to the synergistic combination of Ni and Co, the (Ni,Co)S2 exhibits superior electrocatalytic performance for ORR, OER, and HER in an alkaline electrolyte, and the first principle calculation results indicate that the reaction of an adsorbed O atom with a H2O molecule to form a *OOH is the potential limiting step in the OER. Importantly, it could be utilized as an advanced air electrode material in Zn-air batteries, which shows an enhanced charge-discharge performance (charging voltage of 1.71 V and discharge voltage of 1.26 V at 2 mA cm-2), large specific capacity (842 mAh gZn -1 at 5 mA cm-2), and excellent cycling stability (480 h). Interestingly, the (Ni,Co)S2-based Zn-air battery can efficiently power an electrochemical water-splitting unit with (Ni,Co)S2 serving as both the electrodes. This reveals that the prepared (Ni,Co)S2 has promising applications in future energy conversion and energy storage devices.

| S-EPMC6325096 | biostudies-literature

Salt-Templated Nanoarchitectonics of CoSe2-NC Nanosheets as an Efficient Bifunctional Oxygen Electrocatalyst for Water Splitting

Project description:Recently, the extensive research of efficient bifunctional electrocatalysts (oxygen evolution reaction (OER) and hydrogen evolution reaction (HER)) on water splitting has drawn increasing attention. Herein, a salt-template strategy is prepared to synthesize nitrogen-doped carbon nanosheets encapsulated with dispersed CoSe2 nanoparticles (CoSe2-NC NSs), while the thickness of CoSe2-NC NSs is only about 3.6 nm. Profiting from the ultrathin morphology, large surface area, and promising electrical conductivity, the CoSe2-NC NSs exhibited excellent electrocatalytic of 10 mA·cm−2 current density at small overpotentials of 247 mV for OER and 75 mV for HER. Not only does the nitrogen-doped carbon matrix effectively avoid self-aggregation of CoSe2 nanoparticles, but it also prevents the corrosion of CoSe2 from electrolytes and shows favorable durability after long-term stability tests. Furthermore, an overall water-splitting system delivers a current density of 10 mA·cm−2 at a voltage of 1.54 V with resultants being both the cathode and anode catalyst in alkaline solutions. This work provides a new way to synthesize efficient and nonprecious bifunctional electrocatalysts for water splitting.

| S-EPMC9099664 | biostudies-literature

Carved nanoframes of cobalt-iron bimetal phosphide as a bifunctional electrocatalyst for efficient overall water splitting.

Project description:Water electrolysis for hydrogen production has long been regarded as an ideal tactic for renewable energy conversion and storage, but is impeded by the sluggish kinetics of both the hydrogen and oxygen evolution reactions, which are therefore in urgent need for high-performance but low-cost electrocatalysts. Herein, nanoframes of transition metal phosphides (TMPs) with the 3D framework carved open have been demonstrated as highly potent bifunctional catalysts for overall water splitting, reaching the benchmark performance of the Pt/C‖RuO2 couple, and are much superior to their nanocubic counterparts. This excellent water splitting behavior can be attributed to the enlarged active surface area, less obstructed electrolyte infiltration, promoted charge transfer, and facilitated gas release. Further through in-depth activity analysis and post-electrocatalysis characterization, special attention has been paid to the fate and role of phosphorus in the electrocatalytic process, suggesting that despite the chemical instability of the TMPs (especially under OER conditions), excellent electrocatalytic stability can still be achieved through the amorphous bimetallic hydroxides/oxides formed in situ.

| S-EPMC6334264 | biostudies-literature

A Self-Reconstructed Bifunctional Electrocatalyst of Pseudo-Amorphous Nickel Carbide @ Iron Oxide Network for Seawater Splitting.

Project description:Here, a sol-gel method is used to prepare a Prussian blue analogue (NiFe-PBA) precursor with a 2D network, which is further annealed to an Fe3 O4 /NiCx composite (NiFe-PBA-gel-cal), inheriting the ultrahigh specific surface area of the parent structure. When the composite is used as both anode and cathode catalyst for overall water splitting, it requires low voltages of 1.57 and 1.66 V to provide a current density of 100 mA cm-2 in alkaline freshwater and simulated seawater, respectively, exhibiting no obvious attenuation over a 50 h test. Operando Raman spectroscopy and X-ray photoelectron spectroscopy indicate that NiOOH2-x active species containing high-valence Ni3+ /Ni4+ are in situ generated from NiCx during the water oxidation. Density functional theory calculations combined with ligand field theory reveal that the role of high valence states of Ni is to trigger the production of localized O 2p electron holes, acting as electrophilic centers for the activation of redox reactions for oxygen evolution reaction. After hydrogen evolution reaction, a series of ex situ and in situ investigations indicate the reduction from Fe3+ to Fe2+ and the evolution of Ni(OH)2 are the origin of the high activity.

| S-EPMC9131433 | biostudies-literature

Extraction of nickel from NiFe-LDH into Ni2P@NiFe hydroxide as a bifunctional electrocatalyst for efficient overall water splitting.

Project description:The development of highly efficient, low-cost and stable electrocatalysts for overall water splitting is highly desirable for the storage of intermittent solar energy and wind energy sources. Herein, we show for the first time that nickel can be extracted from NiFe-layered double hydroxide (NiFe-LDH) to generate an Ni2P@FePO x heterostructure. The Ni2P@FePO x heterostructure was converted to an Ni2P@NiFe hydroxide heterostructure (P-NiFe) during water splitting, which displays high electrocatalytic performance for both the hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) in 1.0 M KOH solution, with an overpotential of 75 mV at 10 mA cm-2 for HER, and overpotentials of 205, 230 and 430 mV at 10, 100 and 1000 mA cm-2 for OER, respectively. Moreover, it could afford a stable current density of 10 mA cm-2 for overall water splitting at 1.51 V in 1.0 M KOH with long-term durability (100 h). This cell voltage is among the best reported values for bifunctional electrocatalysts. The results of theoretical calculations demonstrate that P-NiFe displays optimized adsorption energies for both HER and OER intermediates at the nickel active sites, thus dramatically enhancing its electrocatalytic activity.

| S-EPMC5885978 | biostudies-literature

Two-Dimensional Core-Shell Structure of Cobalt-Doped@MnO<sub>2</sub> Nanosheets Grown on Nickel Foam as a Binder-Free Battery-Type Electrode for Supercapacitor Application.

Project description:Herein, we present an interfacial engineering strategy to construct an efficient hydrothermal approach by in situ growing cobalt-doped@MnO2 nanocomposite on highly conductive nickel foam (Ni foam) for supercapacitors (SCs). The remarkably high specific surface area of Co dopant provides a larger contacting area for MnO2. In the meantime, the excellent retentions of the hierarchical phase-based pore architecture of the cobalt-doped surface could beneficially condense the electron transportation pathways. In addition, the nickel foam (Ni foam) nanosheets provide charge-transport channels that lead to the outstanding improved electrochemical activities of cobalt-doped@MnO2. The unique cobalt-doped@MnO2 nanocomposite electrode facilitates stable electrochemical architecture, multi-active electrochemical sites, and rapid electro-transports channels; which act as a key factor in enhancing the specific capacitances, stability, and rate capacities. As a result, the cobalt-doped@MnO2 nanocomposite electrode delivered superior electrochemical activities with a specific capacitance of 337.8 F g-1 at 0.5 A g-1; this is greater than pristine MnO2 (277.9 F g-1). The results demonstrate a worthy approach for the designing of high-performance SCs by the grouping of the nanostructured dopant material and metal oxides.

| S-EPMC9505914 | 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