Experimental study reveals ferrimagnetic ordering above 400 K in a vanadium-hexacyanomolybdate Prussian blue analog, highlighting a route to room-temperature molecule-based magnets.
Molecule-based magnets hold promise for a variety of applications in information technologies owing to their chemical tunability. This feature can facilitate the integration of desired magnetic properties alongside additional functionalities within a single material. Although numerous cyanido-bridged assemblies are identified as multifunctional materials at cryogenic temperatures, achieving analogous behavior at room temperature remains a challenge. This study reports a cyanido-bridged compound, which shows ferrimagnetic ordering with a critical temperature exceeding 400 K. This breakthrough is achieved through the mechanochemical synthesis of vanadium(II)-hexacyanomolybdate(III) Prussian Blue Analog (PBA) under anhydrous conditions. The ferrimagnetic order is evidenced by SQUID (SQUID = superconducting quantum interference device) magnetometry and X-ray Magnetic Circular Dichroism (XMCD) spectroscopy. Both techniques unambiguously confirm the antiparallel alignment of vanadium and molybdenum magnetic moments. As a result, hexacyanomolybdate(III) is experimentally established as a viable precursor for the preparation of a new generation of high-temperature molecule-based magnets and multifunctional materials.
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Magott et al. (2025) studied this question.
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