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Engineering intramolecular exchange interactions between magnetic metal atoms is a ubiquitous strategy for designing molecular magnets. For lanthanides, the localized nature of 4 f electrons usually results in weak exchange coupling. Mediating magnetic interactions between lanthanide ions via radical bridges is a fruitful strategy towards stronger coupling. In this work we explore the limiting case when the role of a radical bridge is played by a single unpaired electron. We synthesize an array of air-stable Ln 2 @C 80 (CH 2 Ph) dimetallofullerenes (Ln 2 = Y 2 , Gd 2 , Tb 2 , Dy 2 , Ho 2 , Er 2 , TbY, TbGd) featuring a covalent lanthanide-lanthanide bond. The lanthanide spins are glued together by very strong exchange interactions between 4 f moments and a single electron residing on the metal–metal bonding orbital. Tb 2 @C 80 (CH 2 Ph) shows a gigantic coercivity of 8.2 Tesla at 5 K and a high 100-s blocking temperature of magnetization of 25.2 K. The Ln-Ln bonding orbital in Ln 2 @C 80 (CH 2 Ph) is redox active, enabling electrochemical tuning of the magnetism.

Highly dense nanocrystalline MgB 2 bulk superconductors with distinctly improved pinning were prepared by mechanical alloying of Mg and B powders and hot compaction at ambient temperatures. The nanocrystalline samples reveal high j c = 10 5 A/cm 2 at 20 K and 1 T together with a strongly shifted irreversibility line towards higher fields resulting in H irr (T) ∼ 0.8 H c2 (T), whereas typically H irr (T) ∼ 0.5 H c2 (T) is observed for bulk untextured samples. These values exceed that of all other so far reported bulk samples and are in the range of the values of thin films. The improved pinning of this material which mainly consists of spherical grains of about 40-100 nm in size is attributed to the large number of grain boundaries.

The effect of hydrostatic pressure on thermally and field-induced first-order magnetic phase transitions is studied in the La(Fe,Si)_(13)-type compounds. A peculiar series of consecutive field-induced transitions is realized using a distinct combination of hydrostatic pressure and negative pressure created by the interstitial insertion of hydrogen. The pressure-induced discontinuous magnetization jumps result in an enhanced cooling power, thus opening up the possibility to exploit in full the magnetocaloric potential of this compound class.

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