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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). Here, we exploit a robust vertical exchange bias confined within core-shell FePt@MnO nanoparticles ( ∼ 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 for Mn spins shortens by 9.8% (108.3 ps → 98.5 ps), while Fe spins exhibit a concomitant τ 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.
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http://dx.doi.org/10.1021/acsnano.5c05624 | DOI Listing |
Angew Chem Int Ed Engl
September 2025
Departament de Química Inorgànica i Orgànica, Universitat de Barcelona, Diagonal 645, Barcelona, 08028, Spain.
Spins within molecules benefit from the atomistic control of synthetic chemistry for the realization of qubits. One advantage is that the quantum superpositions of the spin states encoding the qubit can be coherently manipulated using electromagnetic radiation. The main challenge is the fragility of these superpositions when qubits are to partake of solid-state devices.
View Article and Find Full Text PDFJ Magn Reson
August 2025
ETH Zurich, Department of Chemistry and Applied Biosciences, Vladimir-Prelog-Weg 2, Zurich, 8093, Switzerland.
Methyl rotors have potential as local environment probes because their rotation barrier is sensitive to hindering interactions with the nearby surrounding. Quantum-rotor electron paramagnetic resonance (EPR) measurements allow access to this local environment information of the methyl rotor if it is coupled to an electron spin. This is the case for commonly used nitroxide-based spin-labels, where electron spin echo envelope modulation (ESEEM) signals exhibit two contributions on different time scales at low temperatures.
View Article and Find Full Text PDFEntropy (Basel)
July 2025
International Quantum Academy, Shenzhen 518048, China.
Dynamic decoupling (DD) can suppress decoherence caused by environmental noise, while in hybrid system it also hinders coherent manipulation between qubits. We realized the universal high-fidelity quantum gate set and the preparation of Bell states using dynamical decoupling gates (DD gates) in a silicon-based phosphorus-doped (Si:P) system, effectively resolving the contradiction between decoherence protection and manipulation of qubits. The simulation results show that the fidelity of the universal quantum gate set are all above 99%, and the fidelity of Bell state preparation is over 96%.
View Article and Find Full Text PDFInorg Chem
August 2025
Computational Inorganic Chemistry Group, Department of Chemistry Indian Institute of Technology Hyderabad, Kandi, Sangareddy, Telangana 502284, India.
Implementing magnetic bistability in single-molecule magnets (SMMs) for quantum technologies requires precise nanostructuring, spatial organization, and environmental stabilization of magnetic centers. Here, we report the first encapsulation of the lanthanide-based SMM in three mesoporous diamagnetic MOFs─NU-1000, PCN-222-Zn, and MOF-177─to design hybrid magnetic structures with long-range ordering. An integrated approach combining DFT and AIMD simulations was carried out to unravel the structure, dynamics, stability, and nature of host-guest interactions in hybrid assemblies.
View Article and Find Full Text PDFInorg Chem
August 2025
Institute of Physical Chemistry, University of Stuttgart, Pfaffenwaldring 55, Stuttgart D-70569, Germany.
The spin dynamics of a tris(dithiolate)vanadium complex dianion and perdeutero-tetraphenylarsonium cation, (AsPh4-)[V(mnt)], composed of spin-free and weakly magnetic nuclei are investigated in an analogously composed solvent system, CDCl/ClCCN (4:1). This gives the longest reported coherence times for a transition-metal-based spin in deuterated solvents with a of 164(4) ms, and a of 60(2) μs. Dynamic decoupling more than doubled , resulting in = 136(13) μs.
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