scholarly journals Magnetic ordering in TCNQ-based metal–organic frameworks with host–guest interactions

2015 ◽  
Vol 2 (10) ◽  
pp. 904-911 ◽  
Author(s):  
Xuan Zhang ◽  
Mohamed R. Saber ◽  
Andrey P. Prosvirin ◽  
Joseph H. Reibenspies ◽  
Lei Sun ◽  
...  

Host–guest interactions between the TCNQ-based MOF and aromatic molecules have been found to modulate spontaneous magnetization behavior at low temperatures.

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>


Author(s):  
Javier López-Cabrelles ◽  
Samuel Mañas-Valero ◽  
Iñigo J. Vitórica-Yrezábal ◽  
Makars Šiškins ◽  
Martin Lee ◽  
...  

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>


2013 ◽  
Vol 25 (42) ◽  
pp. 6106-6111 ◽  
Author(s):  
Ziguang Chen ◽  
Gonghua Wang ◽  
Zhanping Xu ◽  
Hui Li ◽  
Alexandre Dhôtel ◽  
...  

2011 ◽  
Vol 50 (17) ◽  
pp. 8144-8152 ◽  
Author(s):  
Qian Sun ◽  
Ai-ling Cheng ◽  
Yan-Qin Wang ◽  
Yu Ma ◽  
En-Qing Gao

Author(s):  
Zhu Zhuo ◽  
Guoling Li ◽  
Chenglin Shu ◽  
Wei Wang ◽  
Caiping Liu ◽  
...  

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>


Nanoscale ◽  
2020 ◽  
Vol 12 (46) ◽  
pp. 23620-23625
Author(s):  
Jie Li ◽  
Ruqian Wu

New functional two-dimensional metal–organic framework materials with room-temperature magnetic ordering, large out-of-plane magnetic anisotropic energy, huge topological band gap, and excellent spin-filtering performance were theoretically predicted.


RSC Advances ◽  
2015 ◽  
Vol 5 (94) ◽  
pp. 76752-76758 ◽  
Author(s):  
Xiu-Mei Zhang ◽  
Peng Li ◽  
Wei Gao ◽  
Jie-Ping Liu

Three 3D frameworks built from strip-shaped Δ-chains were prepared and magnetically characterized. The Cu(ii) compound shows spin canting, magnetic ordering and metamagnetism, while the Co(ii) and Ni(ii) compounds show canted antiferromagnetism.


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