Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Regulation of the Ni²⁺ Content in a Hierarchical Urchin-Like MOF for High-Performance Electrocatalytic Oxygen Evolution.

ABSTRACT: The exploitation of efficient non-precious electrocatalysts for the oxygen evolution reaction is extremely important but remains tremendously challenging. Here, we prepared a series of hierarchical urchin-like bimetallic Ni/Zn metal-organic framework nanomaterials that served as high-performance electrocatalysts, by regulating the Ni²⁺/Zn²⁺ ratio and using a facile one-step hydrothermal method for the application of the oxygen evolution reaction. The structure of the hierarchical urchin-like microspheres could improve the utilization efficiency of the active species by facilitating the diffusion of gas and reducing the transport resistance of ions, due to its features of a large interfacial area and convenient diffusion channels. In addition, we found that the higher the Ni ratio was, the better the electrocatalytic performance of these bimetallic metal-organic framework nanomaterials.

SUBMITTER: Tang Y

PROVIDER: S-EPMC6561350 | biostudies-literature | 2019

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Publications

Regulation of the Ni2+ Content in a Hierarchical Urchin-Like MOF for High-Performance Electrocatalytic Oxygen Evolution.

Tang Yijian Y Zheng Shasha S Xue Huaiguo H Pang Huan H

Frontiers in chemistry 20190605

The exploitation of efficient non-precious electrocatalysts for the oxygen evolution reaction is extremely important but remains tremendously challenging. Here, we prepared a series of hierarchical urchin-like bimetallic Ni/Zn metal-organic framework nanomaterials that served as high-performance electrocatalysts, by regulating the Ni2+/Zn2+ ratio and using a facile one-step hydrothermal method for the application of the oxygen evolution reaction. The structure of the hierar ...[more]

PMID: 31231637

Similar Datasets

Transition metal ions regulated oxygen evolution reaction performance of Ni-based hydroxides hierarchical nanoarrays.

Project description:Nickel-based hydroxide hierarchical nanoarrays (NiyM(OH)x HNAs M = Fe or Zn) are doped with non-noble transition metals to create nanostructures and regulate their activities for the oxygen evolution reaction. Catalytic performance in these materials depends on their chemical composition and the presence of nanostructures. These novel hierarchical nanostructures contain small secondary nanosheets that are grown on the primary nanowire arrays, providing a higher surface area and more efficient mass transport for electrochemical reactions. The activities of the NiyM(OH)x HNAs for the oxygen evolution reaction (OER) followed the order of Ni2.2Fe(OH)x > Ni(OH)2 > Ni2.1Zn(OH)x, and these trends are supported by density functional theory (DFT) calculations. The Fe-doped nickel hydroxide hierarchical nanoarrays (Ni2.2Fe(OH)x HNAs), which had an appropriate elemental composition and hierarchical nanostructures, achieve the lowest onset overpotential of 234 mV and the smallest Tafel slope of 64.3 mV dec-1. The specific activity, which is normalized to the Brunauer-Emmett-Teller (BET) surface area of the catalyst, of the Ni2.2Fe(OH)x HNAs is 1.15 mA cm-2BET at an overpotential of 350 mV. This is ~4-times higher than that of Ni(OH)2. These values are also superior to those of a commercial IrOx electrocatalyst.

| S-EPMC5382681 | biostudies-literature

Ni–Rh-based bimetallic conductive MOF as a high-performance electrocatalyst for the oxygen evolution reaction

Project description: Not available

| S-EPMC10570521 | biostudies-literature

LDH-assisted growth of FeCo bimetal-MOF nanorods for electrocatalytic oxygen evolution.

Project description:Metal-organic frameworks (MOFs) have emerged as alternative OER catalysts due to their easy regulation, such as in situ self-reconstruction from MOFs to metal hydroxides through alkaline hydrolysis. Herein, we demonstrate a facile strategy for the in situ transformation of FeCo layered double hydroxide (FeCo-LDH) nanosheets into 1D spindle-shaped FeCo-MOFs for efficient OER. An optimized electrode of FeCo-MOF on a nickel foam (NF) was achieved by adjusting the addition of organic ligands and the reaction time in the hydrothermal reaction. Based on the unique 1D nanostructure and the cation regulation, the obtained FeCo-MOF exhibits a good catalytic performance toward the OER with a low overpotential of 475 mV at 100 mA cm-2, a small Tafel slope of 121.8 mV dec-1, and high long-term durability. This study provides a facile strategy for preparing bimetal-MOFs as catalysts for efficient OER.

| S-EPMC9443477 | biostudies-literature

Boosting oxygen evolution reaction activity by tailoring MOF-derived hierarchical Co-Ni alloy nanoparticles encapsulated in nitrogen-doped carbon frameworks.

Project description:The growing demand for sustainable energy has led to in-depth research on hydrogen production from electrolyzed water, where the development of electrocatalysts is a top priority. We here report a controllable strategy for preparing the cobalt-nickel alloy nanoparticles encapsulated in nitrogen-doped porous carbon by annealing a bimetal-organic framework. The delicately tailored hierarchical Co2Ni@NC nanoparticles effectively realize abundant synergistic active sites and fast mass transfer for the oxygen evolution reaction (OER). Remarkably, the optimized Co2Ni@NC exhibits a small overpotential of 310 mV to achieve a current density of 10 mA cm-2 and an excellent long-term stability in alkaline electrolyte. Furthermore, the underlying synergistic effect mechanism of the Co-Ni model has been pioneeringly elucidated by density functional theory calculations.

| S-EPMC8695868 | biostudies-literature

Ni(ii)-based coordination polymers for efficient electrocatalytic oxygen evolution reaction.

Project description:The exploration of highly efficient, stable and cheap water oxidation electrocatalysts using earth-abundant elements is still a great challenge. Herein, alkaline-stable cationic Ni(ii) coordination polymers (Ni-CPs) were successfully obtained under hydrothermal conditions, which could stabilize the incorporation of Fe(iii) to form Fe-immobilized Fe@Ni-CPs. The newly developed Ni-based CPs were used for the first time as an effective electrocatalyst for the oxygen evolution reaction in strong alkaline media.

| S-EPMC9090564 | biostudies-literature

Hierarchical Co(OH)2 Dendrite Enriched with Oxygen Vacancies for Promoted Electrocatalytic Oxygen Evolution Reaction.

Project description:It is critical to develop efficient oxygen evolution reaction (OER) catalysts with high catalytic properties for overall water splitting. Electrocatalysts with enriched vacancies are crucial for enhancing the catalytic activity of OER through defect engineering. We demonstrated the dealloying method in a reducing alkaline solution using the Co5Al95 alloy foil as a precursor to produce a new oxygen-vacancy-rich cobalt hydroxide (OV-Co(OH)2) hierarchical dendrite. The as-synthesised OV-Co(OH)2 showed superior electrocatalytic activities toward OER when compared to pristine cobalt hydroxide (p-Co(OH)2), which had a low onset overpotential of only 242 mV and a small Tafel slope of 64.9 mV dec-1. Additionally, for the high surface area provided by the hierarchical dendrite, both p-Co(OH)2 and OV-Co(OH)2 showed a superior activity as compared to commercial catalysts. Furthermore, they retained good catalytic properties without remarkably decaying at an overpotential of 350 mV for 12 h. The as-made OV-Co(OH)2 has prospective applications as an anode electrocatalyst in electrochemical water-splitting technologies with the advantages of superior OER performances, large surface area and ease of preparation.

| S-EPMC9026458 | biostudies-literature

Atomically dispersed Ni activates adjacent Ce sites for enhanced electrocatalytic oxygen evolution activity.

Project description:Manipulating the intrinsic activity of heterogeneous catalysts at the atomic level is an effective strategy to improve the electrocatalytic performances but remains challenging. Here, atomically dispersed Ni anchored on CeO2 particles entrenched on peanut-shaped hollow nitrogen-doped carbon structures (a-Ni/CeO2@NC) is rationally designed and synthesized. The as-prepared a-Ni/CeO2@NC catalyst exhibits substantially boosted intrinsic activity and greatly reduced overpotential for the electrocatalytic oxygen evolution reaction. Experimental and theoretical results demonstrate that the decoration of isolated Ni species over the CeO2 induces electronic coupling and redistribution, thus resulting in the activation of the adjacent Ce sites around Ni atoms and greatly accelerated oxygen evolution kinetics. This work provides a promising strategy to explore the electronic regulation and intrinsic activity improvement at the atomic level, thereby improving the electrocatalytic activity.

| S-EPMC10306285 | biostudies-literature

Oxygen-Rich Carbon Nitrides from an Eutectic Template Strategy Stabilize Ni, Fe Nanosites for Electrocatalytic Oxygen Evolution.

Project description:Functionalized porous carbons are central to various important applications such as energy storage and conversion. Here, a simple synthetic route to prepare oxygen-rich carbon nitrides (CNOs) decorated with stable Ni and Fe-nanosites is demonstrated. The CNOs are prepared via a salt templating method using ribose and adenine as precursors and CaCl2 ·2H2 O as a template. The formation of supramolecular eutectic complexes between CaCl2 ·2H2 O and ribose at relatively low temperatures facilitates the formation of a homogeneous starting mixture, promotes the condensation of ribose through the dehydrating effect of CaCl2 ·2H2 O to covalent frameworks, and finally generates homogeneous CNOs. As a specific of the recipe, the condensation of the precursors at higher temperatures and the removal of water promotes the recrystallization of CaCl2 (T < Tm = 772 °C), which then acts as a hard porogen. Due to salt catalysis, CNOs with oxygen and nitrogen contents as high as 12 and 20 wt%, respectively, can be obtained, while heteroatom content stayed about unchanged even at higher temperatures of synthesis, pointing to the extraordinarily high stability of the materials. After decorating Ni and Fe-nanosites onto the CNOs, the materials exhibit high activity and stability for electrochemical oxygen evolution reaction with an overpotential of 351 mV.

| S-EPMC10401138 | biostudies-literature

In-Situ Construction of Fe-Doped NiOOH on the 3D Ni(OH)2 Hierarchical Nanosheet Array for Efficient Electrocatalytic Oxygen Evolution Reaction.

Project description:Accessible and superior electrocatalysts to overcome the sluggish oxygen evolution reaction (OER) are pivotal for sustainable and low-cost hydrogen production through electrocatalytic water splitting. The iron and nickel oxohydroxide complexes are regarded as the most promising OER electrocatalyst attributed to their inexpensive costs, easy preparation, and robust stability. In particular, the Fe-doped NiOOH is widely deemed to be superior constituents for OER in an alkaline environment. However, the facile construction of robust Fe-doped NiOOH electrocatalysts is still a great challenge. Herein, we report the facile construction of Fe-doped NiOOH on Ni(OH)2 hierarchical nanosheet arrays grown on nickel foam (FeNi@NiA) as efficient OER electrocatalysts through a facile in-situ electrochemical activation of FeNi-based Prussian blue analogues (PBA) derived from Ni(OH)2. The resultant FeNi@NiA heterostructure shows high intrinsic activity for OER due to the modulation of the overall electronic energy state and the electrical conductivity. Importantly, the electrochemical measurement revealed that FeNi@NiA exhibits a low overpotential of 240 mV at 10 mA/cm2 with a small Tafel slope of 62 mV dec-1 in 1.0 M KOH, outperforming the commercial RuO2 electrocatalysts for OER.

| S-EPMC11434255 | biostudies-literature

Investigating metal (M = Mn, Fe, and Ni)-doped Co(OH)2 nanofibers for electrocatalytic oxygen evolution and electrochemical biosensing performance.

Project description:To achieve efficient and cost-effective electrochemical water splitting, highly active and affordable nanostructured catalysts are the key requirement. The current study presents the investigations of the efficacy of metal (Mn, Fe and Ni)-doped Co(OH)2 nanofibers towards oxygen evolution via water splitting. Notably, Ni-doped Co(OH)2 demonstrates superior OER performance in KOH electrolyte, surpassing standard IrO2 with a modest potential of 1.62 V at 10 mA cm-2. The remarkable activity is attributed to the nanofiber structure, facilitating faster conduction and offering readily available active sites. Ni-doped Co(OH)2 nanofibers displayed enduring stability even after 1000 cycles. This work underscores the importance of transition-metal based catalysts as effective electrocatalysts, providing the groundwork for the development of cutting-edge catalysts. Additionally, the electrochemical sensing capability towards ascorbic acid is evaluated, with Ni-doped Co(OH)2 showing the most promising response, characterized by the lowest LOD and LOQ values. These findings highlight the potential of Ni-doped Co(OH)2 nanofibers for upcoming diagnostic detection devices.

| S-EPMC11339775 | biostudies-literature