有機分子で世界初!1次元スピン1/2ハイゼンベルグ分子鎖を実現 ~鎖の長さによって特性が変化 量子コンピュータへの新たな可能性~

2025-03-03 物質・材料研究機構

物質・材料研究機構(NIMS)を中心とする国際共同研究チームは、特定の電子状態を持つ有機分子を1次元に連結した「分子鎖」の合成に世界で初めて成功しました。この分子鎖は「スピン1/2ハイゼンベルグ反強磁性鎖」と呼ばれ、分子の数によって特性が変化することが明らかになりました。本成果は、有機分子の量子コンピュータ素子への展開につながることが期待されています。

<関連情報>

ハイゼンベルグスピン1/2反強磁性分子鎖の表面合成 On-surface synthesis of Heisenberg spin-1/2 antiferromagnetic molecular chains

Kewei Sun, Nan Cao, Orlando J. Silveira, Adolfo O. Fumega, […], and Shigeki Kawai
Science Advances  Published:28 Feb 2025
DOI:https://doi.org/10.1126/sciadv.ads1641

有機分子で世界初!1次元スピン1/2ハイゼンベルグ分子鎖を実現 ~鎖の長さによって特性が変化 量子コンピュータへの新たな可能性~

Abstract

Magnetic exchange interactions between localized spins in π-electron magnetism of carbon-based nanostructures have attracted tremendous interest due to their great potential for nano spintronics. Unique many-body quantum characteristics, such as gaped excitations, strong spin entanglement, and fractionalized excitations, have been demonstrated, but the spin-1/2 Heisenberg model with a single antiferromagnetic coupling J value remained unexplored. Here, we realized the entangled antiferromagnetic quantum spin-1/2 Heisenberg model with diazahexabenzocoronene oligomers (up to 7 units) on Au(111). Extensive low-temperature scanning tunneling microscopy/spectroscopy measurements and density functional theory and many-body calculations show that even-numbered spin chains host a collective state with gapped excitations, while odd-numbered chains feature a Kondo excitation. We found that a given antiferromagnetic coupling J value between first neighbors in the entangled quantum states is responsible for the quantum phenomena, strongly relating to their parities of the chain. The tunable molecular building blocks act as an ideal platform for the experimental realization of topological spin lattices.

1700応用理学一般
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