Localized Heating Driven Selective Growth of Metal-Organic Frameworks (MOFs) in Wood: A Novel Synthetic Strategy for Significantly Enhancing MOF Loadings in Wood

2021 ◽  
pp. 150325
Author(s):  
Guoshun Huang ◽  
Cheng Huang ◽  
Yingle Tao ◽  
Haiqing Li
2014 ◽  
Vol 53 (7) ◽  
pp. 3434-3440 ◽  
Author(s):  
Huan Dong ◽  
Hailiang Hu ◽  
Yang Liu ◽  
Jun Zhong ◽  
Guangju Zhang ◽  
...  

2017 ◽  
Vol 890 ◽  
pp. 68-73 ◽  
Author(s):  
Zhou Ran Zhang ◽  
Yi Zhong Huang ◽  
Shu Xin Bai

A facile strategy of uniform flower-shaped binary-metal-based metal-organic frameworks (MOFs) has been successfully synthesized via a simple hydrothermal method as the precursor of porous Mn2NiO4 nanostructures. After heat treatment at different temperatures, the as-prepared Mn2NiO4 inherits the morphologies of MOFs and can hold until 450°C. This porous Mn2NiO4, used as supercapacitor electrodes, exhibits a high specific capacitance (531.5 F g-1 at a current density of 1.0 A g-1), with a relatively high specific surface area (114.2 m2 g-1). The high capacitance is mainly attributed to the porous and hierarchical structure, which facilitates fast diffusion of active ions, improves structural stability and large contact area between Mn2NiO4 and the electrolyte. The developed synthetic strategy may provide design guidelines for constructing advanced ternary nanostructured supercapacitors electrode.


RSC Advances ◽  
2016 ◽  
Vol 6 (81) ◽  
pp. 77297-77300 ◽  
Author(s):  
Takaaki Tsuruoka ◽  
Tetsuhiro Matsuyama ◽  
Ayumi Miyanaga ◽  
Takashi Ohhashi ◽  
Yohei Takashima ◽  
...  

A novel approach combined with interfacial growth and photolithography has been developed for the site-selective growth of MOF crystals.


2013 ◽  
Vol 4 ◽  
pp. 638-648 ◽  
Author(s):  
Tatjana Ladnorg ◽  
Alexander Welle ◽  
Stefan Heißler ◽  
Christof Wöll ◽  
Hartmut Gliemann

Surface anchored metal-organic frameworks, SURMOFs, are highly porous materials, which can be grown on modified substrates as highly oriented, crystalline coatings by a quasi-epitaxial layer-by-layer method (liquid-phase epitaxy, or LPE). The chemical termination of the supporting substrate is crucial, because the most convenient method for substrate modification is the formation of a suitable self-assembled monolayer. The choice of a particular SAM also allows for control over the orientation of the SURMOF. Here, we demonstrate for the first time the site-selective growth of the SURMOF HKUST-1 on thiol-based self-assembled monolayers patterned by the nanografting technique, with an atomic force microscope as a structuring tool. Two different approaches were applied: The first one is based on 3-mercaptopropionic acid molecules which are grafted in a 1-decanethiolate SAM, which serves as a matrix for this nanolithography. The second approach uses 16-mercaptohexadecanoic acid, which is grafted in a matrix of an 1-octadecanethiolate SAM. In both cases a site-selective growth of the SURMOF is observed. In the latter case the roughness of the HKUST-1 is found to be significantly higher than for the 1-mercaptopropionic acid. The successful grafting process was verified by time-of-flight secondary ion mass spectrometry and atomic force microscopy. The SURMOF structures grown via LPE were investigated and characterized by atomic force microscopy and Fourier-transform infrared microscopy.


2016 ◽  
Vol 7 (2) ◽  
pp. 1063-1069 ◽  
Author(s):  
Lanfang Zou ◽  
Dawei Feng ◽  
Tian-Fu Liu ◽  
Ying-Pin Chen ◽  
Shuai Yuan ◽  
...  

Through a versatile synthetic strategy, High Valence Metathesis and Oxidation (HVMO), a series of Ti-MOFs with predesigned topologies and structures were synthesized.


2018 ◽  
Vol 9 ◽  
pp. 2775-2787 ◽  
Author(s):  
Pierre Farger ◽  
Cédric Leuvrey ◽  
Mathieu Gallart ◽  
Pierre Gilliot ◽  
Guillaume Rogez ◽  
...  

The synthesis and characterization of six new lanthanide networks [Ln(L)(ox)(H2O)] with Ln = Eu3+, Gd3+, Tb3+, Dy3+, Ho3+ and Yb3+ is reported. They were synthesized by solvo-ionothermal reaction of lanthanide nitrate Ln(NO3)3·xH2O with the 1,3-bis(carboxymethyl)imidazolium [HL] ligand and oxalic acid (H2ox) in a water/ethanol solution. The crystal structure of these compounds has been solved on single crystals and the magnetic and luminescent properties have been investigated relying on intrinsic properties of the lanthanide ions. The synthetic strategy has been extended to mixed lanthanide networks leading to four isostructural networks of formula [Tb1− x Eu x (L)(ox)(H2O)] with x = 0.01, 0.03, 0.05 and 0.10. These materials were assessed as luminescent ratiometric thermometers based on the emission intensities of ligand, Tb3+ and Eu3+. The best sensitivities were obtained using the ratio between the emission intensities of Eu3+ (5D0→7F2 transition) and of the ligand as the thermometric parameter. [Tb0.97Eu0.03(L)(ox)(H2O)] was found to be one of the best thermometers among lanthanide-bearing coordination polymers and metal-organic frameworks, operative in the physiological range with a maximum sensitivity of 1.38%·K−1 at 340 K.


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