Nanostructured and Oriented Metal-Organic Framework Films enabling Extreme Surface Wetting Properties

2019 ◽  
Author(s):  
Andre Mähringer ◽  
Julian Rotter ◽  
Dana D. Medina

Herein, we report on the synthesis of highly oriented and nanostructured metal-organic framework (MOF) films featuring extreme surface wetting properties. The Ni- and Co- derivatives of the metal-catecholate series (M-CAT-1) were synthesized as highly crystalline bulk materials and thin films. Oriented pillar-like nanostructured M-CAT-1 films exhibiting pronounced needlelike morphology on gold substrates were established by incorporating a crystallization promoter into the film synthesis. These nanostructured M-CAT-1 MOF films feature extreme wetting phenomena, specifically superhydrophilic and underwater superoleophobic properties with water and underwater oil-contact angles of 0º and up to 174º, respectively. Self-cleaning capabilities for the nanostructured, needle-like M-CAT-1 films were illustrated by measuring time-dependent oil droplet rolling-off a tilted surface. The deposition of the nanostructured Ni-CAT-1 on large glass substrates allowed for the realization of an efficient transparent anti-fog coating enabling a clear view even at extreme temperature gaps up to ca. 120 ºC. This work illustrates the strong link between MOF film morphology and induced surface properties based on these framework materials.

2019 ◽  
Author(s):  
Andre Mähringer ◽  
Julian Rotter ◽  
Dana D. Medina

Herein, we report on the synthesis of highly oriented and nanostructured metal-organic framework (MOF) films featuring extreme surface wetting properties. The Ni- and Co- derivatives of the metal-catecholate series (M-CAT-1) were synthesized as highly crystalline bulk materials and thin films. Oriented pillar-like nanostructured M-CAT-1 films exhibiting pronounced needlelike morphology on gold substrates were established by incorporating a crystallization promoter into the film synthesis. These nanostructured M-CAT-1 MOF films feature extreme wetting phenomena, specifically superhydrophilic and underwater superoleophobic properties with water and underwater oil-contact angles of 0º and up to 174º, respectively. Self-cleaning capabilities for the nanostructured, needle-like M-CAT-1 films were illustrated by measuring time-dependent oil droplet rolling-off a tilted surface. The deposition of the nanostructured Ni-CAT-1 on large glass substrates allowed for the realization of an efficient transparent anti-fog coating enabling a clear view even at extreme temperature gaps up to ca. 120 ºC. This work illustrates the strong link between MOF film morphology and induced surface properties based on these framework materials.


2019 ◽  
Author(s):  
Andre Mähringer ◽  
Julian Rotter ◽  
Dana D. Medina

Herein, we report on the synthesis of highly oriented and nanostructured metal-organic framework (MOF) films featuring extreme surface wetting properties. The Ni- and Co- derivatives of the metal-catecholate series (M-CAT-1) were synthesized as highly crystalline bulk materials and thin films. Oriented pillar-like nanostructured M-CAT-1 films exhibiting pronounced needlelike morphology on gold substrates were established by incorporating a crystallization promoter into the film synthesis. These nanostructured M-CAT-1 MOF films feature extreme wetting phenomena, specifically superhydrophilic and underwater superoleophobic properties with water and underwater oil-contact angles of 0º and up to 174º, respectively. Self-cleaning capabilities for the nanostructured, needle-like M-CAT-1 films were illustrated by measuring time-dependent oil droplet rolling-off a tilted surface. The deposition of the nanostructured Ni-CAT-1 on large glass substrates allowed for the realization of an efficient transparent anti-fog coating enabling a clear view even at extreme temperature gaps up to ca. 120 ºC. This work illustrates the strong link between MOF film morphology and induced surface properties based on these framework materials.


2019 ◽  
Vol 10 ◽  
pp. 1994-2003 ◽  
Author(s):  
Andre Mähringer ◽  
Julian M Rotter ◽  
Dana D Medina

We report on the synthesis of highly oriented and nanostructured metal–organic framework (MOF) films featuring extreme surface wetting properties. The Ni- and Co- derivatives of the metal–catecholate series (M-CAT-1) were synthesized as highly crystalline bulk materials and thin films. Oriented pillar-like nanostructured M-CAT-1 films exhibiting pronounced needle-like morphology on gold substrates were established by incorporating a crystallization promoter into the film synthesis. These nanostructured M-CAT-1 MOF films feature extreme wetting phenomena, specifically superhydrophilic and underwater superoleophobic properties with water and underwater oil-contact angles of 0° and up to 174°, respectively. The self-cleaning capability of the nanostructured, needle-like M-CAT-1 films was illustrated by measuring time-dependent oil droplet rolling-off a tilted surface. The deposition of the nanostructured Ni-CAT-1 film on a large glass substrate allowed for the realization of an efficient, transparent, antifog coating, enabling a clear view even at extreme temperature gaps up to ≈120 °C. This work illustrates the strong link between MOF film morphology and surface properties based on these framework materials.


Polymers ◽  
2019 ◽  
Vol 11 (8) ◽  
pp. 1298 ◽  
Author(s):  
Long ◽  
Park ◽  
Chae ◽  
Lee ◽  
Bae ◽  
...  

For the fabrication of a peelable coating material that decomposes methyl paraoxone (MPO), a nerve agent simulant, self-crosslinkable waterborne polyurethanes (PUs) containing silane groups at the ends and a metal organic framework (UiO-66) were synthesized. UiO-66 dispersed PU solutions for spray coating were prepared by controlling the amount of silane in PU and the content of UiO-66. PUs with a large amount of silane (more than 7.2 wt.%) were easily gelated by adding UiO-66 because the solution was changed from neutral (pH = 7.3) to strongly acidic (pH = 2.5). Therefore, the silane content in PUs should be carefully controlled for the fabrication of composite films. When UiO-66 was added to the PU with a silane content of 2.7 wt.%, the reinforcing effect by UiO-66 was observed up to 15.3 wt.%, but a further increase in UiO-66 content decreased both the tensile strength and the elongation. The peel strength of the PU composite films on polyethylene (PET) and glass substrates decreased with increasing UiO-66 content, but their MPO conversion increased with increasing UiO-66 content. The PU composite film with 49.5 wt.% of added UiO-66 showed the MPO conversion of 63.2% and was easily peeled off from PET and glass substrates.


2017 ◽  
Vol 46 (9) ◽  
pp. 2751-2755 ◽  
Author(s):  
Huimin Yang ◽  
Honghan Fei

We present a facile and compelling method for the fabrication of metal–organic framework (MOF) thin films on TiO2-coated conductive glass substrates. The functionalized MOF films serve as a robust and efficient catalyst for photo-oxidation of thioanisole, overcoming the defragmentation problem of MOF powders.


2021 ◽  
Author(s):  
Jintong Liu ◽  
Jing Huang ◽  
Lei Zhang ◽  
Jianping Lei

We review the general principle of the design and functional modulation of nanoscaled MOF heterostructures, and biomedical applications in enhanced therapy.


2020 ◽  
Author(s):  
Jesse Park ◽  
Brianna Collins ◽  
Lucy Darago ◽  
Tomce Runcevski ◽  
Michael Aubrey ◽  
...  

<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>


2019 ◽  
Author(s):  
Timothée Stassin ◽  
Ivo Stassen ◽  
Joao Marreiros ◽  
Alexander John Cruz ◽  
Rhea Verbeke ◽  
...  

A simple solvent- and catalyst-free method is presented for the synthesis of the mesoporous metal-organic framework (MOF) MAF-6 (RHO-Zn(eIm)2) based on the reaction of ZnO with 2-ethylimidazole vapor at temperatures ≤ 100 °C. By translating this method to a chemical vapor deposition (CVD) protocol, mesoporous crystalline films could be deposited for the first time entirely from the vapor phase. A combination of PALS and Kr physisorption measurements confirmed the porosity of these MOF-CVD films and the size of the MAF-6 supercages (diam. ~2 nm), in close agreement with powder data and calculations. MAF-6 powders and films were further characterized by XRD, TGA, SEM, FTIR, PDF and EXAFS. The exceptional uptake capacity of the mesoporous MAF-6 in comparison to the microporous ZIF-8 is demonstrated by vapor-phase loading of a molecule larger than the ZIF-8 windows.


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