自旋电子学
自旋极化
自旋工程
自旋(空气动力学)
自旋等离子体光子学
铁磁性
材料科学
分子电子学
分子线
凝聚态物理
磁电阻
巨磁阻
隧道磁电阻
纳米技术
极化(电化学)
化学物理
分子开关
分子
Atom(片上系统)
断开连接
自旋霍尔效应
化学
隧道枢纽
光电子学
磁场
有机半导体
自旋晶体管
亚苯基
密度泛函理论
作者
L. Chen,J. Perrin,Imane Arbouch,Bruno Dlubak,P. Seneor,Richard Mattana,Florian Godel,Karen Sobnath,G. Wang,B. Janvier,P. Filloux,F. Mallet,Clément Barraud,J. Cornil,Colin Van Dyck,P. Martin
出处
期刊:Nano Letters
[American Chemical Society]
日期:2026-03-18
卷期号:26 (12): 4053-4060
标识
DOI:10.1021/acs.nanolett.5c05222
摘要
Molecular spintronics aims to control spin current transmission in magnetoresistive devices through molecular engineering. By tailoring the chemical structure of organic molecules atom by atom, chemistry offers a powerful route to designing media for spin transport. A key milestone of the field is to tune spin polarization at ferromagnetic metal-molecule interfaces according to their atomic-scale details. In parallel, research focuses on spin transport through functional molecules, such as conformational switches and chiral systems. In this study, we investigate active molecular layers made of anthraquinone (AQ) oligomers. Experimental and theoretical data are presented for Co/graphene/AQ/Co spin-valve junctions fabricated via an electrografting method on graphene-protected electrodes. Observation of bias-dependent spin filtering, including spin polarization reversal, demonstrates a novel LUMO hybridization mechanism that can enable quantum spin-selective effects in future molecular spintronic devices.
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