Superhydrophobic Metal–Organic Framework Nanocoating Induced by Metal-Phenolic Networks for Oily Water Treatment

2020 ◽  
Vol 8 (4) ◽  
pp. 1831-1839 ◽  
Author(s):  
Weiran Li ◽  
Jiafu Shi ◽  
Yang Zhao ◽  
Qian Huo ◽  
Yiying Sun ◽  
...  
2017 ◽  
Vol 9 (43) ◽  
pp. 37848-37855 ◽  
Author(s):  
Xuerui Wang ◽  
Linzhi Zhai ◽  
Yuxiang Wang ◽  
Ruitong Li ◽  
Xuehong Gu ◽  
...  

2017 ◽  
Vol 4 (11) ◽  
pp. 2205-2214 ◽  
Author(s):  
Hsiang Ting ◽  
Heng-Yu Chi ◽  
Chon Hei Lam ◽  
Kuan-Ying Chan ◽  
Dun-Yen Kang

This paper reports on a novel membrane adsorber comprising metal–organic frameworks (MOFs) for water treatment.


2018 ◽  
Vol 6 (2) ◽  
pp. 334-341 ◽  
Author(s):  
Huixin Liang ◽  
Xiuling Jiao ◽  
Cheng Li ◽  
Dairong Chen

A wide range of flexible MOF-only mats are prepared and exhibit enhanced performances in water treatment, air purification and catalysis.


Author(s):  
Shujun Yu ◽  
Hongwei Pang ◽  
Shuyi Huang ◽  
Hao Tang ◽  
Shuqin Wang ◽  
...  

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>


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