Single-molecule magnetostrictor: an {Fe8Gd8} cubic crystal exhibits temperature-dependent magnetostriction
Year: 2026
Type: article
Abstract: ABSTRACT Molecular magnets, as an important category of nanosized magnetic materials have attracted considerable interest for their wide applications such as contrasting agents for magnetic resonance imaging, low-temperature magnetic refrigerants, and spintronic devices. Up to date, though magnet-type behaviour has been enhanced to 100 K for single-molecule magnets, the investigation of molecule-originated magnetostriction (MS) is still in its infancy. Here, we report the observation of a large MS effect (50 ppm at 2 K under a field of 7 T) in a crystal solid of the wheel-like {Fe8Gd8} coordination molecules. The {Fe8Gd8} molecules crystallized in a highly symmetric cubic space group of $Pn\bar{3}n$ and have no long-range magnetic ordering down to 0.2 K. Therefore, we are convinced that such a giant magnetostrictive effect for {Fe8Gd8} is a single-molecule origin. We further used quantum Monte Carlo simulation to fit the temperature-dependent magnetostriction data and gave an excellent overlap with JFe–Gd = 4.81(5) K. Such a strong ferromagnetic interaction between Fe3+ and Gd3+ ensures a large magnetic momentum for {Fe8Gd8}, which is the key source of magnetoelastic response to the external field at low temperatures. Therefore, this work explicitly demonstrates that predominantly intramolecular exchange-coupling can cause magnetostriction, inspiring the design of new magnetostrictive materials.
Source: National Science Review
DOI: 10.1093/nsr/nwag300
Language: English
Field: Materials Science
Domain: Physical Sciences
Open Access status: gold
Estimated APC paid: $2,000
Funders: National Natural Science Foundation of China, Xi’an Jiaotong University, State Key Laboratory of Electrical Insulation and Power Equipment, Project 211, Fundamental Research Funds for the Central Universities, Institute for Materials Research, Tohoku University, Division of Materials Research
OpenAlex ID: W7161999466
