Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Ultrathin sulfate-intercalated NiFe-layered double hydroxide nanosheets for efficient electrocatalytic oxygen evolution.

ABSTRACT: As an important two-dimensional material, layered double hydroxides (LDHs) show considerable potential in electrocatalytic reactions. However, the great thickness of the bulk LDH materials significantly limits their catalytic activity. In this work, we report ultrathin NiFe-LDH nanosheets with sulfate interlayer anions (Ni₆Fe₂(SO₄)(OH)₁₆·7H₂O) (U-LDH(SO₄ ^2-)), which can be synthesized in gram-scale by a simple solvothermal method. The U-LDH(SO₄ ^2-) shows excellent stability and great electrocatalytic performance in OER with a current density of 10 mA cm^-2 at a low overpotential of 212 mV and a small Tafel slope of 65.2 mV dec^-1, exhibiting its great potential for a highly efficient OER electrocatalyst.

SUBMITTER: Jiang XX

PROVIDER: S-EPMC9051218 | biostudies-literature | 2020 Mar

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Ultrathin sulfate-intercalated NiFe-layered double hydroxide nanosheets for efficient electrocatalytic oxygen evolution.

Jiang Xiao-Xiao XX Xue Jiang-Yan JY Zhao Zhong-Yin ZY Li Cong C Li Fei-Long FL Cao Chen C Niu Zheng Z Gu Hong-Wei HW Lang Jian-Ping JP

RSC advances 20200325 21

As an important two-dimensional material, layered double hydroxides (LDHs) show considerable potential in electrocatalytic reactions. However, the great thickness of the bulk LDH materials significantly limits their catalytic activity. In this work, we report ultrathin NiFe-LDH nanosheets with sulfate interlayer anions (Ni6Fe2(SO4)(OH)16·7H2O) (U-LDH(SO4 2-)), which can be synthesized in gram-scale by a simple solvother ...[more]

PMID: 35497616

Similar Datasets

Rapid large-scale synthesis of ultrathin NiFe-layered double hydroxide nanosheets with tunable structures as robust oxygen evolution electrocatalysts.

Project description:Transition metal layered double hydroxides (LDHs) with ultrathin two-dimensional (2D) structures, especially NiFe-based LDH nanosheets, have been extensively developed as advanced oxygen evolution reaction (OER) electrocatalysts for water splitting. Nevertheless, traditional synthetic approaches for these promising catalysts usually involve tedious pretreatment procedures and a subsequent time-consuming exfoliation process, and the obtained products possess a wide dispersion of thickness and limited production yield. Here, a sequence of ultrathin NiFe-LDH nanosheets with tunable components were prepared on a large scale via a rapid room-temperature method under ambient conditions, and were further used as a desired material model for studying the influence of Ni/Fe ratio modulation on the OER performance. Due to the synergetic effect of more exposed active sites, efficient electron transport and optimized OER kinetics, the resulting LDH samples manifest outstanding electrocatalytic performance toward water oxidation.

| S-EPMC9043841 | biostudies-literature

3D-printed NiFe-layered double hydroxide pyramid electrodes for enhanced electrocatalytic oxygen evolution reaction.

Project description:Electrochemical water splitting has been considered one of the most promising methods of hydrogen production, which does not cause environmental pollution or greenhouse gas emissions. Oxygen evolution reaction (OER) is a significant step for highly efficient water splitting because OER involves the four electron transfer, overcoming the associated energy barrier that demands a potential greater than that required by hydrogen evolution reaction. Therefore, an OER electrocatalyst with large surface area and high conductivity is needed to increase the OER activity. In this work, we demonstrated an effective strategy to produce a highly active three-dimensional (3D)-printed NiFe-layered double hydroxide (LDH) pyramid electrode for OER using a three-step method, which involves direct-ink-writing of a graphene pyramid array and electrodeposition of a copper conducive layer and NiFe-LDH electrocatalyst layer on printed pyramids. The 3D pyramid structures with NiFe-LDH electrocatalyst layers increased the surface area and the active sites of the electrode and improved the OER activity. The overpotential (η) and exchange current density (i0) of the NiFe-LDH pyramid electrode were further improved compared to that of the NiFe-LDH deposited Cu (NiFe-LDH/Cu) foil electrode with the same base area. The 3D-printed NiFe-LDH electrode also exhibited excellent durability without potential decay for 60 h. Our 3D printing strategy provides an effective approach for the fabrication of highly active, stable, and low-cost OER electrocatalyst electrodes.

| S-EPMC8748972 | biostudies-literature

Intracellular Delivery of Therapeutic Protein via Ultrathin Layered Double Hydroxide Nanosheets.

Project description:The therapeutic application of biofunctional proteins relies on their intracellular delivery, which is hindered by poor cellular uptake and transport from endosomes to cytoplasm. Herein, we constructed a two-dimensional (2D) ultrathin layered double hydroxide (LDH) nanosheet for the intracellular delivery of a cell-impermeable protein, gelonin, towards efficient and specific cancer treatment. The LDH nanosheet was synthesized via a facile method without using exfoliation agents and showed a high loading capacity of proteins (up to 182%). Using 2D and 3D 4T1 breast cancer cell models, LDH-gelonin demonstrated significantly higher cellular uptake efficiency, favorable endosome escape ability, and deep tumor penetration performance, leading to a higher anticancer efficiency, in comparison to free gelonin. This work provides a promising strategy and a generalized nanoplatform to efficiently deliver biofunctional proteins to unlock their therapeutic potential for cancer treatment.

| S-EPMC10974414 | biostudies-literature

Enhancing Electrocatalytic Activity through Liquid-Phase Exfoliation of NiFe Layered Double Hydroxide Intercalated with Metal Phthalocyanines in the Presence of Graphene.

Project description:Earth-abundant transition-metal-based catalysts are attractive for alkaline water electrolysis. However, their catalytic properties are often limited by their poor electrical conductivity. Here, we present a strategy for enhancing the electrical conductivity of NiFe layered double hydroxide (LDH) in order to further improve its properties as an electrocatalyst for the oxygen evolution reaction (OER) in alkaline media. We show that NiFe LDH containing metal tetrasulfonate phthalocyanine in the interlayers between the NiFe oxide galleries can be coupled with graphene during liquid-phase exfoliation by taking advantage of their π-π stacking capabilities. A substantial enhancement in the electrocatalytic activity of NiFe LDH with respect to the OER was observed. Moreover, the activity and selectivity of the catalyst materials towards the oxygen reduction reaction were investigated, demonstrating that both the metal hydroxide layer and the interlayer species contribute to the electrocatalytic performance of the composite material.

| S-EPMC6899937 | biostudies-literature

Ultrathin layered double hydroxide nanosheets with Ni(III) active species obtained by exfoliation for highly efficient ethanol electrooxidation.

Project description:The development of non-precious metal electrocatalysts for renewable energy conversion and storage is compelling but greatly challenging due to low activity of the existing catalysts. Herein, the ultrathin NiAl-layered double hydroxide nanosheets (NiAl-LDH-NSs) are prepared by simple liquid-exfoliation of bulk NiAl-LDHs and first used as ethanol electrooxidation catalysts. The ultrathin two-dimensional (2D) structure ensures that the LDH nanosheets expose a greater number of active sites. More importantly, much Ni(III) active species (NiOOH) in the ultrathin nanosheets are formed by the exfoliation process, which play an authentic catalytic role in the ethanol oxidation reaction (EOR). The presence of NiOOH remarkably improves the reactivity and electrical conductivity of LDH nanosheets. These synergistic effects lead to strikingly more than 30 times enhanced EOR activity of NiAl-LDH-NSs compared to bulk NiAl-LDHs. The obtained electrocatalytic activity is also much better than those of most Ni- and LDH-based EOR catalysts reported to date. In addition, the ultrathin NiAl-LDH-NS electrocatalyst also exhibits good long-term stability (maintain 81.8% of the original value after 10000 s). This study not only provides a highly competitive EOR catalyst, but also opens new avenues toward the design of highly efficient electrode materials that have various potential applications in supercapacitor, Ni-MH battery and other electrocatalytic systems.

| S-EPMC5881604 | biostudies-literature

Ultrathin 2D Cobalt Zeolite-Imidazole Framework Nanosheets for Electrocatalytic Oxygen Evolution.

Project description:2D layered materials, including metal-di-chalcogenides and transition metal layered double hydroxides, among others, are intensively studied because of new properties that emerge from their 2D confinement, which are attractive for advanced applications. Herein, 2D cobalt ion (Co2+) and benzimidazole (bIm) based zeolite-imidazole framework nanosheets, ZIF-9(III), are reported as exceptionally efficient electrocatalysts for the oxygen evolution reaction (OER). Specifically, liquid-phase ultrasonication is applied to exfoliate a [Co4(bIm)16] zeolite-imidazole framework (ZIF), named as ZIF-9(III) phase, into nanoscale sheets. ZIF-9(III) is selectively prepared through simple mechanical grinding of cobalt nitrate and benzimidazole in the presence of a small amount of ethanol. The resultant exfoliated nanosheets exhibit significantly higher OER activity in alkaline conditions than the corresponding bulk phases ZIF-9 and ZIF-9(III). The electrochemical and physicochemical characterization data support the assignment of the OER activity of the exfoliated nanosheet derived material to nitrogen coordinated cobalt oxyhydroxide N4CoOOH sites, following a mechanism known for Co-porphyrin and related systems. Thus, exfoliated 2D nanosheets hold promise as potential alternatives to commercial noble metal electrocatalysts for the OER.

| S-EPMC6247023 | biostudies-literature

Structure and release properties of pyrethroid/sulfobutyl ether β-cyclodextrin intercalated into layered double hydroxide and layered hydroxide salt.

Project description:The aim of this study was to realize the intercalation of the pyrethroid pesticides beta-cypermethrin (BCT) and lambda-cyhalothrin (LCT) into ZnAl-layered double hydroxides (LDH) and NiZn-layered hydroxide salt (LHS). BCT (LCT)/SBECD-LDH and BCT (LCT)/SBECD-LHS hybrids were obtained with the aid of sulfobutyl ether β-cyclodextrin (SBECD) through one step method. The hybrids were characterized by powder X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), and thermogravimetry and differential thermal analysis (TGA/DTA). The hybrids based on LHS had larger basal spacing than those on LDH. The LDH-hybrids prepared in N-methylpyrrolidone (NMP) had larger basal spacing than those in ethanol. These results were discussed in terms of the matrix structure and solvent properties. The supramolecular structure of the hybrid was reasonably proposed. Furthermore, the release properties of BCT (LCT) from the hybrids were investigated and discussed in two media. The release rate in pH = 5.0 was slower than that in pH = 6.8. The accumulated release amount of pesticide in pH = 5.0 was lower than that in pH = 6.8. LHS-hybrids synthesized in ethanol exhibit a sustainable release property. These depend on the inclusion complexes' arrangement and release medium. The release kinetic processes could be described by pseudo-second order and parabolic diffusion models. The release behavior can be controlled by adjusting the synthesis conditions and the releasing media. This provides the guidance for the application of SBECD and LDH (LHS) in pesticide formulation.

| S-EPMC9388771 | biostudies-literature

Role of Co in the Electrocatalytic Activity of Monolayer Ternary NiFeCo-Double Hydroxide Nanosheets for Oxygen Evolution Reaction.

Project description:Monolayer nanosheets have gained significant attention as functional materials and also in photo/electrocatalysis due to their unique physical/chemical properties, abundance of highly exposed coordination sites, edges, and corner sites, motivating the pursuit of highly active monolayer nanosheets. NiFe-based layered double hydroxide (NiFe-LDH) nanosheets have been regarded as the most efficient electrocatalysis for oxygen evolution. However, the limited catalytic active site and the stacking layer limited the performance. Therefore, by introducing highly electroactive Co ions into monolayer NiFe-LDH, the obtained ternary NiFeCo-LDH monolayer structure possessed an increased concentration of defect (oxygen and metal vacancies), providing enough unsaturated coordination sites, benefitting the electrocatalytic water oxidation, as also explained by the density functional theory (DFT). This work reported an efficient strategy for the synthesis of ternary monolayer LDH in the application of energy conversion and storage.

| S-EPMC7795402 | biostudies-literature

One-Step Synthesis of NiFe Layered Double Hydroxide Nanosheet Array/N-Doped Graphite Foam Electrodes for Oxygen Evolution Reactions.

Project description:Developing cost-effective and highly efficient oxygen evolution reaction (OER) electrocatalysts is vital for the production of clean hydrogen by electrocatalytic water splitting. Here, three dimensional nickel-iron layered double hydroxide (NiFe LDH) nanosheet arrays are in-situ fabricated on self-supporting nitrogen doped graphited foam (NGF) via a one-step hydrothermal process under an optimized amount of urea. The as prepared NiFe LDH/NGF electrode exhibits a remarkable activity toward OER with a low onset overpotential of 233 mV and a Tafel slope of 59.4 mV dec-1 as well as a long-term durability. Such good performance is attributed to the synergy among the doping effect, the binder-free characteristic, and the architecture of the nanosheet array.

| S-EPMC6652109 | biostudies-literature

Anti-Inflammatory and Analgesic Evaluation of a Phytochemical Intercalated into Layered Double Hydroxide.

Project description:Coumaric acid (CouH), an antioxidant molecule assimilated by food consumption, was intercalated into layered double hydroxide (LDH) nanocarrier, having zinc and aluminium ions in the layers (LDH-Cou), to evaluate its pharmacological activity through in vitro and in vivo assays in mice. Therefore, the following tests were performed: coumarate delivery in saline solution, fibroblasts’ cell viability using neutral red, peritonitis induced by carrageenan, formalin test, acetic-acid-induced writhing, and tail-flick assay, for the non-intercalated CouH and the intercalated LDH-Cou system. Furthermore, different pharmacological pathways were also investigated to evaluate their possible anti-inflammatory and antinociceptive mechanisms of action, in comparison to traditionally used agents (morphine, naloxone, caffeine, and indomethacin). The LDH-Cou drug delivery system showed more pronounced anti-inflammatory effect than CouH but not more than that evoked by the classic non-steroidal anti-inflammatory drug (NSAID) indomethacin. For the analgesic effect, according to the tail-flick test, the treatment with LDH-Cou expressively increased the analgesia duration (p < 0.001) by approximately 1.7−1.8 times compared to CouH or indomethacin. Thus, the results pointed out that the LDH-Cou system induced in vivo analgesic and anti-inflammatory activities and possibly uses similar mechanisms to that observed for classic NSAIDs, such as indomethacin.

| S-EPMC9144641 | 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