A new water stable zinc metal organic framework as an electrode material for hydrazine sensing

2018 ◽  
Vol 42 (15) ◽  
pp. 12486-12491 ◽  
Author(s):  
Manzar Sohail ◽  
Muhammad Altaf ◽  
Nadeem Baig ◽  
Rabia Jamil ◽  
Muhammad Sher ◽  
...  
Keyword(s):  
Single Molecule ◽  
Electrode Material ◽  
Electrode Materials ◽  
Metal Organic Framework ◽  
Metal Organic Frameworks ◽  
Redox Mediator ◽  
Electrochemical Sensing ◽  
Sensing Element ◽  
Zinc Metal ◽  
Metal Organic

Metal–organic frameworks (MOFs) as direct electrode materials for electrochemical sensing can offer inherent advantages such as containing sensing element and redox mediator in a single molecule.

Metal–organic framework derived petal-like Co3O4@CoNi2S4 hybrid on carbon cloth with enhanced performance for supercapacitors

2020 ◽  
Vol 7 (6) ◽  
pp. 1428-1436 ◽  
Author(s):  
Dandan Han ◽  
Jinhe Wei ◽  
Yuan Zhao ◽  
Ye Shen ◽  
Yifan Pan ◽  
...  
Keyword(s):  
Electrode Materials ◽  
Metal Organic Framework ◽  
Metal Organic Frameworks ◽  
Core Shell ◽  
Carbon Cloth ◽  
Step Method ◽  
Metal Organic ◽  
Organic Framework

Starting from 2D Co-based metal-organic frameworks, novel petal-like core-shell Co3O4@CoNi2S4 nanowall arrays are synthesized on carbon cloth using a facile two-step method and investigated as promising electrode materials for supercapacitors.

Metal–organic framework-derived porous carbon polyhedra for highly efficient capacitive deionization

2015 ◽  
Vol 51 (60) ◽  
pp. 12020-12023 ◽  
Author(s):  
Yong Liu ◽  
Xingtao Xu ◽  
Miao Wang ◽  
Ting Lu ◽  
Zhuo Sun ◽  
...  
Keyword(s):  
Electrode Material ◽  
Porous Carbon ◽  
Metal Organic Framework ◽  
Metal Organic Frameworks ◽  
Capacitive Deionization ◽  
Highly Efficient ◽  
Metal Organic ◽  
Organic Framework

Porous carbon polyhedra were synthesized through direct carbonization of metal–organic frameworks and used as an electrode material for capacitive deionization.

Mixed-metallic MOF based electrode materials for high performance hybrid supercapacitors

2017 ◽  
Vol 5 (3) ◽  
pp. 1094-1102 ◽  
Author(s):  
Yang Jiao ◽  
Jian Pei ◽  
Dahong Chen ◽  
Chunshuang Yan ◽  
Yongyuan Hu ◽  
...  
Keyword(s):  
Energy Storage ◽  
Electrode Material ◽  
High Performance ◽  
Electrode Materials ◽  
Metal Organic Frameworks ◽  
Energy Storage Devices ◽  
Storage Devices ◽  
Hybrid Supercapacitors ◽  
Metal Organic

Metal–organic frameworks (MOFs) have obtained increasing attention as a kind of novel electrode material for energy storage devices.

Rationally constructing hierarchical two-dimensional NiCo metal-organic framework/graphene hybrid for highly efficient Li+ ions storage

2021 ◽  
Author(s):  
Jun Jin ◽  
You-fang Zhang ◽  
Huanwen Wang ◽  
Yansheng Gong ◽  
Rui Wang ◽  
...  
Keyword(s):  
Metal Oxides ◽  
Porous Carbon ◽  
Electrode Materials ◽  
Metal Organic Framework ◽  
Metal Organic Frameworks ◽  
Metal Chalcogenides ◽  
Two Dimensional ◽  
Highly Efficient ◽  
Metal Organic ◽  
Organic Framework

Recently, metal–organic frameworks (MOFs) have been used to synthesize electrode materials such as porous carbon, metal oxides, and metal chalcogenides or directly utilized as electrodes. However, pristine MOF electrodes suffer...

scholarly journals Reversible Switching of Single-Molecule Magnetic Behaviour by Desorption/Adsorption of Solvent Ligand in a New Dy(III)-Based Metal Organic Framework

2021 ◽  
Vol 9 ◽  
Author(s):  
Xiao-Jiao Song ◽  
Zhao-Bo Hu ◽  
Miao-Miao Li ◽  
Xin Feng ◽  
Ming Kong ◽  
...  
Keyword(s):  
Single Molecule ◽  
Applied Field ◽  
Metal Organic Framework ◽  
Metal Organic Frameworks ◽  
Magnetic Behaviour ◽  
Zero Field ◽  
Single Molecule Magnet ◽  
Slow Magnetic Relaxation ◽  
Metal Organic ◽  
Solvent Molecules

Two metal-organic frameworks (MOFs), [Dy(BDC)(NO3)(DMF)2]n (1, H2BDC = terephthalic acid) and [Dy(BDC)(NO3)]n (1a), were synthesized. The structures of MOFs 1 and 1a are easy to be reversibly transformed into each other by the desorption or adsorption of coordination solvent molecules. Accordingly, their magnetic properties can also be changed reversibly, which realizes our goals of manipulating on/off single-molecule magnet behaviour. MOF 1 behaves as a single-molecule magnet either with or without DC field. Contrarily, no slow magnetic relaxation was observed in 1a both under zero field and applied field.

scholarly journals Highly Sensitive Detection of Trace Tetracycline in Water Using a Metal-Organic Framework-Enabled Sensor

2021 ◽  
Vol 2021 ◽  
pp. 1-11
Author(s):  
Jiezeng Chen ◽  
Hongying Shu ◽  
Pingping Niu ◽  
Pinghua Chen ◽  
Hualin Jiang
Keyword(s):  
Electrochemical Sensor ◽  
Electrode Materials ◽  
Limit Of Detection ◽  
Metal Organic Framework ◽  
Electrochemical Sensing ◽  
Sensitive Detection ◽  
Active Electrode ◽  
Sensing Platform ◽  
Metal Organic ◽  
Organic Framework

Due to the abuse application of antibiotics in the recent decades, a high level of antibiotics has been let out and remains in our environment. Electrochemical sensing is a useful method to sensitively detect antibiotics, and the key factor for a successful electrochemical sensor is the active electrode materials. In this study, a sensitive electrochemical sensing platform based on a metal-organic framework (MOF) of MIL-53 (Fe) was facilely fabricated. It shows highly selective and sensitive detection performance for trace tetracycline. Differential pulse voltammetry (DPV) was applied to analyze the detection of tetracycline. The linear range of tetracycline detection was 0.0643 μmol/L-1.53 μmol/L, and the limit of detection (LOD) is 0.0260 μmol/L. Furthermore, the MOF-enabled sensor can be effectively used in actual water bodies. The results indicate that the electrochemical sensor is a high potential sensing platform for tetracycline.

Facile synthesis and characterization of the Mn-MOF electrode material for flexible supercapacitors

2021 ◽  
pp. 1-19
Author(s):  
Yanhong Liu ◽  
Jiahong Liu ◽  
Yijun Cao ◽  
Wei Shang ◽  
Ning Peng ◽  
...  
Keyword(s):  
Current Density ◽  
Electrode Material ◽  
High Performance ◽  
Electrode Materials ◽  
Metal Organic Frameworks ◽  
Charge Transfer Resistance ◽  
Carbon Cloth ◽  
Flexible Electrode ◽  
Transfer Resistance ◽  
Metal Organic

Abstract Metal-organic frameworks (MOFs) due to their porosity and well-defined structures are considered to be very promising electrode materials for the construction of high-performance supercapacitor. In this paper, manganese-based metal organic frameworks (Mn-MOF) were prepared on the surface of carbon cloth (CC) by hydrothermal method. The morphology and structure of the electrode material were characterized by SEM, XRD, FT-IR, and XPS. Its electrochemical studies show that the Mn-MOF electrode materials exhibit low charge transfer resistance, the excellent specific capacitance of 433.5 mF·cm−2 in 1.0 M Na2SO4 aqueous solution at the current density of 0.8 mA·cm−2. It is noteworthy that the flexible electrode has excellent cycle stability and 105% capacitance retention even after 5000 cycles at a current density of 5 mA·cm−2. The high electrochemical performance of Mn-MOF/CC flexible electrode materials can be attributed to its three-dimensional porous structure.

Magnetic Ordering via Itinerant Ferromagnetism in a Metal-Organic Framework

2020 ◽  
Author(s):  
Jesse Park ◽  
Brianna Collins ◽  
Lucy Darago ◽  
Tomce Runcevski ◽  
Michael Aubrey ◽  
...  
Keyword(s):  
Charge Transport ◽  
Magnetic Order ◽  
Metal Organic Framework ◽  
Metal Organic Frameworks ◽  
Magnetic Ordering ◽  
Double Exchange ◽  
Itinerant Ferromagnetism ◽  
Organic Solids ◽  
Metal Organic ◽  
Organic Framework

<b>Materials that combine magnetic order with other desirable physical attributes offer to revolutionize our energy landscape. Indeed, such materials could find transformative applications in spintronics, quantum sensing, low-density magnets, and gas separations. As a result, efforts to design multifunctional magnetic materials have recently moved beyond traditional solid-state materials to metal–organic solids. Among these, metal–organic frameworks in particular bear structures that offer intrinsic porosity, vast chemical and structural programmability, and tunability of electronic properties. Nevertheless, magnetic order within metal–organic frameworks has generally been limited to low temperatures, owing largely to challenges in creating strong magnetic exchange in extended metal–organic solids. Here, we employ the phenomenon of itinerant ferromagnetism to realize magnetic ordering at <i>T</i><sub>C</sub> = 225 K in a mixed-valence chromium(II/III) triazolate compound, representing the highest ferromagnetic ordering temperature yet observed in a metal–organic framework. The itinerant ferromagnetism is shown to proceed via a double-exchange mechanism, the first such observation in any metal–organic material. Critically, this mechanism results in variable-temperature conductivity with barrierless charge transport below <i>T</i><sub>C</sub> and a large negative magnetoresistance of 23% at 5 K. These observations suggest applications for double-exchange-based coordination solids in the emergent fields of magnetoelectrics and spintronics. Taken together, the insights gleaned from these results are expected to provide a blueprint for the design and synthesis of porous materials with synergistic high-temperature magnetic and charge transport properties. </b>

Engineering Porosity Through Defects in a Giant Pore Metal–Organic Framework

2020 ◽  
Author(s):  
Adam Sapnik ◽  
Duncan Johnstone ◽  
Sean M. Collins ◽  
Giorgio Divitini ◽  
Alice Bumstead ◽  
...  
Keyword(s):  
Distribution Function ◽  
Ball Milling ◽  
Local Structure ◽  
Pair Distribution Function ◽  
Function Analysis ◽  
Metal Organic Framework ◽  
Metal Organic Frameworks ◽  
Defect Engineering ◽  
Metal Organic ◽  
Unsaturated Metal Sites

<p>Defect engineering is a powerful tool that can be used to tailor the properties of metal–organic frameworks (MOFs). Here, we incorporate defects through ball milling to systematically vary the porosity of the giant pore MOF, MIL-100 (Fe). We show that milling leads to the breaking of metal–linker bonds, generating more coordinatively unsaturated metal sites, and ultimately causes amorphisation. Pair distribution function analysis shows the hierarchical local structure is partially</p><p>retained, even in the amorphised material. We find that the solvent toluene stabilises the MIL-100 (Fe) framework against collapse and leads to a substantial rentention of porosity over the non-stabilised material.</p>

Metal-Organic Frameworks vs. Buffers: Case Study of UiO-66 Stability

2020 ◽  
Author(s):  
Daniel Bůžek ◽  
Slavomír Adamec ◽  
Kamil Lang ◽  
Jan Demel
Keyword(s):  
Inductively Coupled Plasma ◽  
Buffer Capacity ◽  
Metal Organic Framework ◽  
Metal Organic Frameworks ◽  
Analytical Techniques ◽  
Aqueous Dispersions ◽  
Inductively Coupled ◽  
Plasma Mass Spectrometry ◽  
Metal Organic

<div><p>UiO-66 is a zirconium-based metal-organic framework (MOF) that has numerous applications. Our group recently determined that UiO-66 is not as inert in aqueous dispersions as previously reported in the literature. The present work therefore assessed the behaviour of UiO-66 in buffers: 2-amino-2-(hydroxymethyl)-1,3-propanediol (TRIS), 4-(2-hydroxyethyl)piperazine-1-ethane sulfonic acid (HEPES), N-ethylmorpholine (NEM) and phosphate buffer (PB), all of which are commonly used in many UiO-66 applications. High pressure liquid chromatography and inductively coupled plasma mass spectrometry were used to monitor degradation of the MOF. In each buffer, the terephthalate linker was released to some extent, with a more pronounced leaching effect in the saline forms of these buffers. The HEPES buffer was found to be the most benign, whereas NEM and PB should be avoided at any concentration as they were shown to rapidly degrade the UiO-66 framework. Low concentration TRIS buffers are also recommended, although these offer minimal buffer capacity to adjust pH. Regardless of the buffer used, rapid terephthalate release was observed, indicating that the UiO-66 was attacked immediately after mixing with the buffer. In addition, the dissolution of zirconium, observed in some cases, intensified the UiO-66 decomposition process. These results demonstrate that sensitive analytical techniques have to be used to monitor the release of MOF components so as to quantify the stabilities of these materials in liquid environments.</p></div>

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