{"title":"强垂直交换偏置调制0D核壳纳米粒子的自旋退相干。","authors":"Ao Chen, Guanhua Xu, Yuting Tang and Xiuyu Wang*, ","doi":"10.1021/acsnano.5c05624","DOIUrl":null,"url":null,"abstract":"<p >While recent advancements in spin manipulation have utilized topological insulators and non-collinear antiferromagnets confined to two-dimensional films, dimensional limitations have hindered the realization of truly freestanding spin-dependent quantum nanodevices (nm<sup>3</sup>). Here, we exploit a robust vertical exchange bias confined within core–shell FePt@MnO nanoparticles (<i>D</i> ∼ 9 nm) to control the spin decoherence time of Fe and Mn magnetic atoms. The magnitude (approximately 17% of interfacial spins are fully pinned) and robustness (the pinned spins remain stable even under a negative field of −5 T) of this anomalous exchange bias arise from a coherent interface where strain-induced lattice distortion displaces Mn cations by ångström-scale distances from their equilibrium positions, aligning them with Fe cations. This interfacial coherence enhances interfacial spin–spin exchange coupling─manifested as the anomalous exchange-bias effect─which directly modulates spin decoherence dynamics: τ<sub>2</sub> for Mn<sup>2+</sup> spins shortens by 9.8% (108.3 ps → 98.5 ps), while Fe spins exhibit a concomitant τ<sub>2</sub> enhancement. This work establishes a direct link between spin decoherence time and the exchange-bias effect, offering a pathway for the coherent engineering of quantum nanomaterials.</p>","PeriodicalId":21,"journal":{"name":"ACS Nano","volume":"19 27","pages":"25243–25252"},"PeriodicalIF":16.0000,"publicationDate":"2025-07-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Robust Vertical Exchange Bias Modulates Spin Decoherence in 0D Core–Shell Nanoparticles\",\"authors\":\"Ao Chen, Guanhua Xu, Yuting Tang and Xiuyu Wang*, \",\"doi\":\"10.1021/acsnano.5c05624\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >While recent advancements in spin manipulation have utilized topological insulators and non-collinear antiferromagnets confined to two-dimensional films, dimensional limitations have hindered the realization of truly freestanding spin-dependent quantum nanodevices (nm<sup>3</sup>). Here, we exploit a robust vertical exchange bias confined within core–shell FePt@MnO nanoparticles (<i>D</i> ∼ 9 nm) to control the spin decoherence time of Fe and Mn magnetic atoms. The magnitude (approximately 17% of interfacial spins are fully pinned) and robustness (the pinned spins remain stable even under a negative field of −5 T) of this anomalous exchange bias arise from a coherent interface where strain-induced lattice distortion displaces Mn cations by ångström-scale distances from their equilibrium positions, aligning them with Fe cations. This interfacial coherence enhances interfacial spin–spin exchange coupling─manifested as the anomalous exchange-bias effect─which directly modulates spin decoherence dynamics: τ<sub>2</sub> for Mn<sup>2+</sup> spins shortens by 9.8% (108.3 ps → 98.5 ps), while Fe spins exhibit a concomitant τ<sub>2</sub> enhancement. This work establishes a direct link between spin decoherence time and the exchange-bias effect, offering a pathway for the coherent engineering of quantum nanomaterials.</p>\",\"PeriodicalId\":21,\"journal\":{\"name\":\"ACS Nano\",\"volume\":\"19 27\",\"pages\":\"25243–25252\"},\"PeriodicalIF\":16.0000,\"publicationDate\":\"2025-07-07\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Nano\",\"FirstCategoryId\":\"88\",\"ListUrlMain\":\"https://pubs.acs.org/doi/10.1021/acsnano.5c05624\",\"RegionNum\":1,\"RegionCategory\":\"材料科学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Nano","FirstCategoryId":"88","ListUrlMain":"https://pubs.acs.org/doi/10.1021/acsnano.5c05624","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
While recent advancements in spin manipulation have utilized topological insulators and non-collinear antiferromagnets confined to two-dimensional films, dimensional limitations have hindered the realization of truly freestanding spin-dependent quantum nanodevices (nm3). Here, we exploit a robust vertical exchange bias confined within core–shell FePt@MnO nanoparticles (D ∼ 9 nm) to control the spin decoherence time of Fe and Mn magnetic atoms. The magnitude (approximately 17% of interfacial spins are fully pinned) and robustness (the pinned spins remain stable even under a negative field of −5 T) of this anomalous exchange bias arise from a coherent interface where strain-induced lattice distortion displaces Mn cations by ångström-scale distances from their equilibrium positions, aligning them with Fe cations. This interfacial coherence enhances interfacial spin–spin exchange coupling─manifested as the anomalous exchange-bias effect─which directly modulates spin decoherence dynamics: τ2 for Mn2+ spins shortens by 9.8% (108.3 ps → 98.5 ps), while Fe spins exhibit a concomitant τ2 enhancement. This work establishes a direct link between spin decoherence time and the exchange-bias effect, offering a pathway for the coherent engineering of quantum nanomaterials.
期刊介绍:
ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.