Unconventional bipartite entanglement in the quantum dimer magnet Yb2Be2SiO7

A A. Brassington Q Q. Ma G G. Duan S S. Calder A A. I. Kolesnikov K K. M. Taddei G G. Sala E E. S. Choi H H. Wang W W. Xie B B. A. Frandsen N N. Li X X. F. Sun C C. Liu R R. Yu H H. D. Zhou A A. A. Aczel

Abstract

Abstract The quantum dimer magnet, with antiferromagnetic intradimer and interdimer Heisenberg exchange between spin-1/2 moments, is known to host an $$(\left|\uparrow \downarrow \right\rangle -\left|\downarrow \uparrow \right\rangle )/\sqrt{2}$$ ( ↑ ↓ − ↓ ↑ ) / 2 singlet ground state when the intradimer exchange is dominant. Rare-earth-based quantum dimer systems with strong spin-orbit coupling offer the opportunity for tuning their magnetic properties by using magnetic anisotropy as a control knob. Here, we present bulk characterization and neutron scattering measurements of the quantum dimer magnet Yb 2 Be 2 SiO 7 . We find that the Yb 3+ ions can be described by an effective spin-1/2 model at low temperatures and the system does not show signs of magnetic order down to 50 mK. The magnetization, heat capacity, and neutron spectroscopy data can be well-described by an isolated dimer model with highly anisotropic exchange that stabilizes a singlet ground state with a wavefunction $$(\left|\uparrow \uparrow \right\rangle -\left|\downarrow \downarrow \right\rangle )/\sqrt{2}$$ ( ↑ ↑ − ↓ ↓ ) / 2 or $$(\left|\uparrow \uparrow \right\rangle+\left|\downarrow \downarrow \right\rangle )/\sqrt{2}$$ ( ↑ ↑ + ↓ ↓ ) / 2 . Our results show that strong spin-orbit coupling can induce unusual entangled states of matter in quantum dimer magnets.

Article Details

Volume / Issue Vol. 17, Issue 1
Published March 25, 2026
ISSN 2041-1723
Publisher Nature Portfolio

Journal Info

Nature Communications

Nature Portfolio

ISSN: 2041-1723 Open Access Life Sciences

Authors (17)

A

A. Brassington

Q

Q. Ma

G

G. Duan

S

S. Calder

A

A. I. Kolesnikov

K

K. M. Taddei

G

G. Sala

E

E. S. Choi

H

H. Wang

W

W. Xie

B

B. A. Frandsen

N

N. Li

X

X. F. Sun

C

C. Liu

R

R. Yu

H

H. D. Zhou

A

A. A. Aczel