Multifunctional Prussian blue analogue magnets: Emerging opportunities

被引:41
|
作者
Huang, Yulong [1 ]
Ren, Shenqiang [1 ,2 ,3 ]
机构
[1] Univ Buffalo State Univ New York, Dept Mech & Aerosp Engn, Buffalo, NY 14260 USA
[2] Univ Buffalo State Univ New York, Dept Chem, Buffalo, NY 14260 USA
[3] Univ Buffalo State Univ New York, Res & Educ Energy Environm & Water Inst, Buffalo, NY 14260 USA
关键词
Molecular magnets; Prussian blue analogues; Structure; Magnetic properties; NEGATIVE THERMAL-EXPANSION; PHOTOINDUCED FERRIMAGNETIC SYSTEMS; INDUCED ELECTRON-TRANSFER; ROOM-TEMPERATURE; SINGLE-CRYSTAL; X-RAY; ORDERING TEMPERATURE; NEUTRON-DIFFRACTION; HYDROGEN STORAGE; POLE INVERSION;
D O I
10.1016/j.apmt.2020.100886
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
There is a surge of interest to expand the search for entirely new classes of molecular magnets as the emergence of information storage and quantum computing devices. Prussian blue analogues as a family of molecular magnets are especially attracting wide attention due to their large number of derivatives with a range of magnetic ordering temperature from cryogenic to room temperature. This review presents Prussian blue analogues as multifunctional molecular magnets, which involves the development of molecular magnet syntheses and crystal structures, and magnetic properties under external stimuli. In addition, the porous network structures and vacancy order of Prussian blue analogues present a wide capability to interact with water molecules and gas adsorption. External stimuli, such as thermal, pressure, electric and magnetic field and photoexcitation, play an important role in controlling the hidden states and cooperative phenomena of high temperature molecular magnets based on Prussian blue analogues. (c) 2020 Elsevier Ltd. All rights reserved.
引用
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页数:11
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