Spin-crossover complex encapsulation within a magnetic metal–organic framework

2016 ◽  
Vol 52 (46) ◽  
pp. 7360-7363 ◽  
Author(s):  
Alexandre Abhervé ◽  
Thais Grancha ◽  
Jesús Ferrando-Soria ◽  
Miguel Clemente-León ◽  
Eugenio Coronado ◽  
...  

We report the solid-state incorporation of a mononuclear iron(iii) spin-crossover (SCO) complex within the pores of a magnetic metal–organic framework (MOF).

2015 ◽  
Vol 22 (2) ◽  
pp. 441-441 ◽  
Author(s):  
Marta Mon ◽  
Alejandro Pascual-Álvarez ◽  
Thais Grancha ◽  
Joan Cano ◽  
Jesús Ferrando-Soria ◽  
...  

2015 ◽  
Vol 22 (2) ◽  
pp. 437-437
Author(s):  
Marta Mon ◽  
Alejandro Pascual-Álvarez ◽  
Thais Grancha ◽  
Joan Cano ◽  
Jesús Ferrando-Soria ◽  
...  

2015 ◽  
Vol 22 (2) ◽  
pp. 539-545 ◽  
Author(s):  
Marta Mon ◽  
Alejandro Pascual-Álvarez ◽  
Thais Grancha ◽  
Joan Cano ◽  
Jesús Ferrando-Soria ◽  
...  

2021 ◽  
Author(s):  
Faezeh Taghavi ◽  
Amir Khojastehnezhad ◽  
Reza Khalifeh ◽  
Maryam Rajabzadeh ◽  
Fahimeh Rezaei ◽  
...  

The first report of the use of an acidic magnetic metal organic framework for the chemical fixation of CO2 as an environmentally friendly reaction.


Nanomaterials ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 1759
Author(s):  
Neda Motamedi ◽  
Mahmood Barani ◽  
Azadeh Lohrasbi-Nejad ◽  
Mojtaba Mortazavi ◽  
Ali Riahi-Medvar ◽  
...  

The improvement in the enzyme activity of Aspergillus flavus urate oxidase (Uox) was attained by immobilizing it on the surface of a Ni-based magnetic metal–organic framework (NimMOF) nanomaterial; physicochemical properties of NimMOF and its application as an enzyme stabilizing support were evaluated, which revealed a significant improvement in its stability upon immobilization on NimMOF (Uox@NimMOF). It was affirmed that while the free Uox enzyme lost almost all of its activity at ~40–45 °C, the immobilized Uox@NimMOF retained around 60% of its original activity, even retaining significant activity at 70 °C. The activation energy (Ea) of the enzyme was calculated to be ~58.81 kJ mol−1 after stabilization, which is approximately half of the naked Uox enzyme. Furthermore, the external spectroscopy showed that the MOF nanomaterials can be coated by hydrophobic areas of the Uox enzyme, and the immobilized enzyme was active over a broad range of pH and temperatures, which bodes well for the thermal and long-term stability of the immobilized Uox on NimMOF.


Nanomaterials ◽  
2021 ◽  
Vol 11 (3) ◽  
pp. 736
Author(s):  
Man Li ◽  
Tao Chen ◽  
Seunghyun Song ◽  
Yang Li ◽  
Joonho Bae

The challenge of safety problems in lithium batteries caused by conventional electrolytes at high temperatures is addressed in this study. A novel solid electrolyte (HKUST-1@IL-Li) was fabricated by immobilizing ionic liquid ([EMIM][TFSI]) in the nanopores of a HKUST-1 metal–organic framework. 3D angstrom-level ionic channels of the metal–organic framework (MOF) host were used to restrict electrolyte anions and acted as “highways” for fast Li+ transport. In addition, lower interfacial resistance between HKUST-1@IL-Li and electrodes was achieved by a wetted contact through open tunnels at the atomic scale. Excellent high thermal stability up to 300 °C and electrochemical properties are observed, including ionic conductivities and Li+ transference numbers of 0.68 × 10-4 S·cm-1 and 0.46, respectively, at 25 °C, and 6.85 × 10-4 S·cm-1 and 0.68, respectively, at 100 °C. A stable Li metal plating/stripping process was observed at 100 °C, suggesting an effectively suppressed growth of Li dendrites. The as-fabricated LiFePO4/HKUST-1@IL-Li/Li solid-state battery exhibits remarkable performance at high temperature with an initial discharge capacity of 144 mAh g-1 at 0.5 C and a high capacity retention of 92% after 100 cycles. Thus, the solid electrolyte in this study demonstrates promising applicability in lithium metal batteries with high performance under extreme thermal environmental conditions.


2021 ◽  
pp. 1-30
Author(s):  
Homeira Nasiri ◽  
Farshad Yazdani ◽  
Jalal Zeinali ◽  
Hamid Reza Mortaheb

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