We investigate the properties of CuVOF4(H2O)6⋅H2O, in which two different spin species, Cu(II) and V(IV), form antiferromagnetic spin-1/2 dimers with weak interdimer coupling provided via hydrogen bonding. Using radio-frequency susceptometry and electron-spin resonance (ESR), we show how the temperature-magnetic field spin-dimer phase diagram evolves as a function of applied hydrostatic pressure and correlate this with pressure-induced changes to the crystal structure. These results, coupled with pressure-tuned DFT calculations, confirm the prior prediction that the primary exchange interaction is mediated via an unusual mechanism in which the V(IV) ions provide considerable spin density to the oxygen that joins the two spins in each dimer and which lies along the Jahn-Teller axis of the Cu(II) ion. In addition, the dissimilarity in the spins that make up each dimer unit leads to a non-linear field dependence of the electronic energy levels as detected in the ESR measurements.
@article{arxiv.2512.01994,
title = {Heterometallic spin-1/2 quantum magnet under hydrostatic pressure},
author = {M. J. Coak and D. Kamenskyi and S. P. M. Curley and B. M. Huddart and J. P. Tidey and A. Chmeruk and T. Sakurai and S. Okubo and H. Ohta and S. Kimura and H. Nojiri and D. Graf and S. J. Clark and Z. E. Manson and J. L. Manson and T. Lancaster and P. A. Goddard},
journal= {arXiv preprint arXiv:2512.01994},
year = {2026}
}