自旋电子学
对映体药物
自旋(空气动力学)
自旋极化
手性(物理)
材料科学
螺旋度
选择性
凝聚态物理
电子顺磁共振
镱
化学物理
化学
电子
铁磁性
物理
光电子学
核磁共振
对映选择合成
有机化学
量子力学
夸克
热力学
Nambu–Jona Lasinio模型
手征对称破缺
兴奋剂
催化作用
作者
Uxua Huizi-Rayo,Junkal Gutierrez,José M. Seco,Vladimiro Mújica,Ismael Díez‐Pérez,Jesús María Ugalde,Agnieszka Tercjak,Javier Cepeda,Eider San Sebastián
出处
期刊:Nano Letters
[American Chemical Society]
日期:2020-11-10
卷期号:20 (12): 8476-8482
被引量:115
标识
DOI:10.1021/acs.nanolett.0c02349
摘要
An enantiopure, conductive, and paramagnetic crystalline 3-D metal-organic framework (MOF), based on Dy(III) and the l-tartrate chiral ligand, is proved to behave as an almost ideal electron spin filtering material at room temperature, transmitting one spin component only, leading to a spin polarization (SP) power close to 100% in the ±2 V range, which is conserved over a long spatial range, larger than 1 μm in some cases. This impressive spin polarization capacity of this class of nanostructured materials is measured by means of magnetically polarized conductive atomic force microscopy and is attributed to the Chirality-Induced Spin Selectivity (CISS) effect of the material arising from a multidimensional helicity pattern, the inherited chirality of the organic motive, and the enhancing influence of Dy(III) ions on the CISS effect, with large spin-orbit coupling values. Our results represent the first example of a MOF-based and CISS-effect-mediated spin filtering material that shows a nearly perfect SP. These striking results obtained with our robust and easy-to-synthesize chiral MOFs constitute an important step forward in to improve the performance of spin filtering materials for spintronic device fabrication.
科研通智能强力驱动
Strongly Powered by AbleSci AI