Browse
Submit Data
Databases
API
Help

Dataset Information

22 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Electrochemical performance of composite electrodes based on rGO, Mn/Cu metal-organic frameworks, and PANI.

ABSTRACT: Benzendicarboxylic acid (BDC)-based metal-organic frameworks (MOFs) have been widely utilized in various applications, including supercapacitor electrode materials. Manganese and copper have solid diamond frames formed with BDC linkers among transition metals chosen for MOF formation. They have shown the possibility to enlarge capacitance at different combinations of MOFs and polyaniline (PANI). Herein, reduced graphene oxide (rGO) was used as the matrix to fabricate electrochemical double-layer SCs. PANI and Mn/Cu-MOF's effect on the properties of electrode materials was investigated through electrochemical analysis. As a result, the highest specific capacitance of about 276 F/g at a current density of 0.5 A/g was obtained for rGO/Cu-MOF@PANI composite.

SUBMITTER: Le QB

PROVIDER: S-EPMC8758744 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Smart Nanocomposites of Cu-Hemin Metal-Organic Frameworks for Electrochemical Glucose Biosensing.

Project description:Herein, a smart porous material, Cu-hemin metal-organic-frameworks (Cu-hemin MOFs), was synthesized via assembling of Cu2+ with hemin to load glucose oxidase (GOD) for electrochemical glucose biosensing for the first time. The formation of the Cu-hemin MOFs was verified by scanning electron microscopy, X-ray powder diffraction, Fourier transform infrared spectroscopy, N2 adsorption/desorption isotherms, UV-vis absorption spectroscopy, fluorescence spectroscopy, thermal analysis and electrochemical techniques. The results indicated that the Cu-hemin MOFs showed a ball-flower-like hollow cage structure with a large specific surface area and a large number of mesopores. A large number of GOD molecules could be successfully loaded in the pores of Cu-hemin MOFs to keep their bioactivity just like in a solution. The GOD/Cu-hemin MOFs exhibited both good performance toward oxygen reduction reaction via Cu-hemin MOFs and catalytic oxidation of glucose via GOD, superior to other GOD/MOFs and GOD/nanomaterials. Accordingly, the performance of GOD/Cu-hemin MOFs-based electrochemical glucose sensor was enhanced greatly, showing a wide linear range from 9.10 μM to 36.0 mM and a low detection limit of 2.73 μM. Moreover, the sensor showed satisfactory results in detection of glucose in human serum. This work provides a practical design of new electrochemical sensing platform based on MOFs and biomolecules.

| S-EPMC5095656 | biostudies-literature

General synthesis of hierarchical sheet/plate-like M-BDC (M = Cu, Mn, Ni, and Zr) metal-organic frameworks for electrochemical non-enzymatic glucose sensing.

Project description:Two-dimensional metal-organic frameworks (2D MOFs) are an attractive platform to develop new kinds of catalysts because of their structural tunability and large specific surface area that exposes numerous active sites. In this work, we report a general method to synthesize benzene dicarboxylic acid (BDC)-based MOFs with hierarchical 3D morphologies composed of 2D nanosheets or nanoplates. In our proposed strategy, acetonitrile helps solvate the metal ions in solution and affects the morphology, while polyvinylpyrrolidone (PVP) serves as a shape-control agent to assist in the nucleation and growth of MOF nanosheets. PVP also acts as a depletion agent to drive the assembly of the hierarchical sheet/plate-like M-BDC under solvothermal conditions. Further, we also demonstrate the flexibility of the proposed method using numerous coordinating metal ions (M = Cu, Mn, Ni, and Zr). The potential of these MOFs for electrochemical glucose sensing is examined using the hierarchical sheet-like Ni-BDC MOF as the optimum sample. It drives the electrocatalytic oxidation of glucose over a wide range (0.01 mM to 0.8 mM) with high sensitivity (635.9 μA mM-1 cm-2) in the absence of modification with carbon or the use of conductive substrates. It also demonstrates good selectivity with low limit of detection (LoD = 6.68 μM; signal/noise = 3), and fast response time (<5 s).

| S-EPMC8152586 | biostudies-literature

Enhanced electrochemical properties of cerium metal-organic framework based composite electrodes for high-performance supercapacitor application.

Project description:Cerium metal-organic framework based composites (Ce-MOF/GO and Ce-MOF/CNT) were synthesized by a wet chemical route and characterized with different techniques to characterize their crystal nature, morphology, functional groups, and porosity. The obtained Ce-MOF in the composites exhibit a nanorod structure with a size of ∼150 nm. The electrochemical performance of the composites was investigated in 3 M KOH and 3 M KOH + 0.2 M K3Fe(CN)6 electrolytes. Enhanced electrochemical behavior was obtained for the Ce-MOF/GO composite in both electrolytes and exhibited a maximum specific capacitance of 2221.2 F g-1 with an energy density of 111.05 W h kg-1 at a current density of 1 A g-1. The large mesoporous structure and the presence of oxygen functional groups in Ce-MOF/GO could facilitate ion transport in the electrode/electrolyte interface, and the results suggested that the Ce-MOF/GO composite could be used as a high-performance supercapacitor electrode material.

| S-EPMC9077682 | biostudies-literature

A Polymeric Composite Material (rGO/PANI) for Acid Blue 129 Adsorption.

Project description:Over the years, polyaniline (PANI) has received enormous attention due to its unique properties. Herein, it was chosen to develop a new polymeric composite material: reduced graphene oxide/polyaniline (rGO/PANI). The composite was prepared by a simple and cost-effective fabrication method of formation by mixing and sonication in various conditions. The obtained materials were characterized and identified using various techniques such as scanning electron microscopy (SEM), Raman and ATR-FTIR spectroscopy, and X-ray diffraction (XRD). The objective of the paper was to confirm its applicability for the removal of contaminants from water. Water could be contaminated by various types of pollutants, e.g., inorganics, heavy metals, and many other industrial compounds, including dyes. We confirmed that the Acid Blue 129 dyes can be substantially removed through adsorption on prepared rGO/PANI. The adsorption kinetic data were modeled using the pseudo-first-order and pseudo-second-order models and the adsorption isotherm model was identified.

| S-EPMC7285098 | biostudies-literature

Effect of Crystal Morphology on Electrochemical Performances of IRH-2 and IRH-2/PANI Composite for Supercapacitor Electrodes.

Project description:In the context of recent progress in designing metal-organic framework (MOF)-based supercapacitor electrodes, we report herein the successful growth of two different crystal morphologies of a cerium-based MOF, octahedral crystals named IRH-2-O and elongated square-bipyramidal crystals named IRH-2-ESBP (IRH = Institute de Recherche sur l'Hydrogène). The identical crystal structure of both materials was confirmed by powder X-ray diffraction (PXRD). Furthermore, scanning electron microscopy and energy-dispersive X-ray mapping analysis corroborated this fact and showed the crystal shape variation versus the surface composition of synthesized materials. Fourier transform infrared spectroscopy, UV-vis spectroscopy, and PXRD were used to confirm the purity of pristine MOFs as well as desired MOF//PANI composites. Cyclic voltammetry and electrochemical impedance spectroscopy highlighted the effect of crystal shape on the electrochemical performance of IRH-2 MOFs; the specific capacitance tripled from 43.1 F·g-1 for IRH-2-O to 125.57 F·g-1 for IRH-2-ESBP at 5 mV·s-1. The cycling stability was notably ameliorated from 7 K for IRH-2-O to 20 K for IRH-2-ESBP. Regarding the composites, the cell voltage was notably ameliorated from 1.8 to 1.95 V. However, the electrochemical performance of IRH-2/PANI composites was drastically decreased due to instability in the acidic media. To the best of our knowledge, our work is the first work that related the MOF crystal shape and the electrochemical performance.

| S-EPMC10666263 | biostudies-literature

Cu(I/II) Metal-Organic Frameworks Incorporated Nanofiltration Membranes for Organic Solvent Separation.

Project description:Copper-based metal-organic frameworks (MOFs) with different oxidation states and near-uniform particle sizes have been successfully synthesized. Mixed-matrix polyimide membranes incorporating 0.1-7 wt% of Cu(II) benzene-1,2,5-tricarboxylic acid (Cu(II)BTC), Cu(I/II)BTC and Cu(I) 1,2-ethanedisulfonic acid (EDS) (Cu(I)EDS) MOFs were fabricated via non-solvent-induced phase inversion process. These membranes are found to be solvent resistant and mechanically stable. Liquid phase nanofiltration experiments were performed to separate toluene from n-heptane at room temperature. These membranes demonstrate preferential adsorption and permeation of the aromatic toluene over aliphatic n-heptane. The amount of MOF particles incorporated, the oxidation state of the Cu ion and membrane, and barrier layer thickness have a significant impact on the separation factor. Toluene/heptane separation factor at 1.47, 1.67 and 1.79 can be obtained for membranes incorporating 7 wt% Cu(II)BTC, Cu(I/II)BTC and Cu(I)EDS respectively at room temperature.

| S-EPMC7692870 | biostudies-literature

An experimental and computational study of CO2 adsorption in the sodalite-type M-BTT (M = Cr, Mn, Fe, Cu) metal-organic frameworks featuring open metal sites.

Project description:We present a comprehensive investigation of the CO2 adsorption properties of an isostructural series of metal-organic frameworks, M-BTT (M = Cr, Mn, Fe, Cu; BTT3- = 1,3,5-benzenetristetrazolate), which exhibit a high density of open metal sites capable of polarizing and binding guest molecules. Coupling gas adsorption measurements with in situ neutron and X-ray diffraction experiments provides molecular-level insight into the adsorption process and enables rationalization of the observed adsorption isotherms. In particular, structural data confirms that the high initial isosteric heats of CO2 adsorption for the series are directly correlated with the presence of open metal sites and further reveals the positions and orientations of as many as three additional adsorption sites. Density functional theory calculations that include van der Waals dispersion corrections quantitatively support the observed structural features associated with the primary and secondary CO2 binding sites, including CO2 positions and orientations, as well as the experimentally determined isosteric heats of CO2 adsorption.

| S-EPMC5969499 | biostudies-literature

2D/3D Copper-Based Metal-Organic Frameworks for Electrochemical Detection of Hydrogen Peroxide.

Project description:Metal-organic frameworks (MOFs) have been extensively used as modified materials of electrochemical sensors in the food industry and agricultural system. In this work, two kinds of copper-based MOFs (Cu-MOFs) with a two dimensional (2D) sheet-like structure and three dimensional (3D) octahedral structure for H2O2 detection were synthesized and compared. The synthesized 2D and 3D Cu-MOFs were modified on the glassy carbon electrode to fabricate electrochemical sensors, respectively. The sensor with 3D Cu-MOF modification (HKUST-1/GCE) presented better electrocatalytic performance than the 2D Cu-MOF modified sensor in H2O2 reduction. Under optimal conditions, the prepared sensor displayed two wide linear ranges of 2 μM-3 mM and 3-25 mM and a low detection limit of 0.68 μM. In addition, the 3D Cu-MOF sensor exhibited good selectivity and stability. Furthermore, the prepared HKUST-1/GCE was used for the detection of H2O2 in milk samples with a high recovery rate, indicating great potential and applicability for the detection of substances in food samples. This work provides a convenient, practical, and low-cost route for analysis and extends the application range of MOFs in the food industry, agricultural and environmental systems, and even in the medical field.

| S-EPMC8530376 | biostudies-literature

Characterisation of redox states of metal-organic frameworks by growth on modified thin-film electrodes.

Project description:The application of metal-organic framework (MOF) materials in electrochemical and electrochromic devices remains rare. One of the main reasons for this is the inability to readily access their detailed electrochemistry. The inherent insolubility of these materials does not allow interrogation by traditional solution-based electrochemical or spectroscopic methods. In this study, we report a straightforward alternative approach to the spectroelectrochemical study of MOFs. We have used two systems as exemplars in this study, MFM-186 and MFM-180. The method involves chemical modification of a working electrode to attach MOF materials without using corrosive reagents such as inorganic acids or bases which otherwise could limit their application in device development. MFM-186 demonstrates the formation of a stable radical species [MFM-186]?+ on electrochemical oxidation, and this has been characterised by electrochemical, spectroelectrochemical and EPR spectroscopic techniques coupled to DFT analysis.

| S-EPMC6115678 | biostudies-other

Retrofitting metal-organic frameworks.

Project description:The post-synthetic installation of linker molecules between open-metal sites (OMSs) and undercoordinated metal-nodes in a metal-organic framework (MOF) - retrofitting - has recently been discovered as a powerful tool to manipulate macroscopic properties such as the mechanical robustness and the thermal expansion behavior. So far, the choice of cross linkers (CLs) that are used in retrofitting experiments is based on qualitative considerations. Here, we present a low-cost computational framework that provides experimentalists with a tool for evaluating various CLs for retrofitting a given MOF system with OMSs. After applying our approach to the prototypical system CL@Cu3BTC2 (BTC?=?1,3,5-benzentricarboxylate) the methodology was expanded to NOTT-100 and NOTT-101 MOFs, identifying several promising CLs for future CL@NOTT-100 and CL@NOTT-101 retrofitting experiments. The developed model is easily adaptable to other MOFs with OMSs and is set-up to be used by experimentalists, providing a guideline for the synthesis of new retrofitted MOFs with modified physicochemical properties.

| S-EPMC6820732 | 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