Donglin Li
;
Nan Cao
;
Marvin Metzelaars
;
Orlando J. Silveira
;
Joakim Jestilä
;
Adolfo Fumega
;
Tomohiko Nishiuchi
;
Jose Lado
;
Adam S. Foster
;
Takashi Kubo
;
Shigeki Kawai
Description:
(abstract)Frustrated spin systems, where competing interactions prevent conventional magnetic ordering, provide a platform for uncovering emergent quantum phases and exotic many-body phenomena. Particularly, low-dimensional and symmetric geometries without boundary conditions allow us to study the unconventional spin states. Here, we present S = 1/2 anti-ferromagnetic Heisenberg cyclic pentamer and hexamer via homocoupling of air-stable phenalenyl derivatives on Au(111). With a combination of scanning tunnelling microscopy/scanning tunnelling spectroscopy at 4.3 K and compre-hensive theoretical simulations, we found that while large magnetic exchange interactions exist in both rings, the pen-tamer features an increased geometric frustration of the system. This frustration induces rotational symmetry in the spin wavefunction, leading to a four-fold degenerate ground states of the pentamer. The interplay between molecular geometry and magnetic interactions creates the unique quantum spin environment. Our findings offer a powerful approach for constructing spin-frustrated molecular architectures, allowing precise control over quantum magnetic interactions.
Rights:
Keyword: scanning tunneling microscopy, quantum spin, spin-frustrated molecular, quantum magnetic interactions, scanning tunneling spectroscopy
Date published: 2025-07-30
Publisher: American Chemical Society (ACS)
Journal:
Funding:
Manuscript type: Publisher's version (Version of record)
MDR DOI:
First published URL: https://doi.org/10.1021/jacs.5c03112
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Updated at: 2025-08-20 08:30:20 +0900
Published on MDR: 2025-08-20 08:24:23 +0900
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20250819 Donglin-Kawai 2025A00441A SI.pdf
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