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Mapping Magnetic Properties and Relaxation in Vanadium(IV) Complexes with Lanthanides by Electron Paramagnetic Resonance

机译:电子顺磁共振分析钒与镧系元素配合物的磁性和弛豫

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摘要

Vanadium(IV) complexes are actively studied as potential candidates for molecular spin qubits operating at room temperatures. They have longer electron spin decoherence times than many other transition ions, being the key property for applications in quantum information processing. In most cases reported to date, the molecular complexes were optimized through the design for this purpose. In this work, we investigate the relaxation properties of vanadium(IV) ions incorporated in complexes with lanthanides using electron paramagnetic resonance (EPR). In all cases, the VO moieties with no nuclear spins in the first coordination sphere are addressed. We develop and implement the approaches for facile diagnostics of relaxation characteristics in individual VO moieties of such compounds. Remarkably, the estimated relaxation times are found to be close to those of other vanadium-based qubits obtained previously. In the future, a synergistic combination of qubit-friendly properties of vanadium ions with single-molecule magnetism and luminescence of lanthanides can be pursued to realize new functionalities of such materials.
机译:钒(IV)配合物已被积极研究作为在室温下运行的分子自旋量子位的潜在候选物。它们具有比许多其他过渡离子更长的电子自旋退相干时间,这是量子信息处理中应用的关键特性。在迄今为止报道的大多数情况下,为此目的通过设计优化了分子复合物。在这项工作中,我们使用电子顺磁共振(EPR)研究与镧系元素络合物中掺入的钒(IV)离子的弛豫特性。在所有情况下,都解决了第一个协调域中无核自旋的VO部分。我们开发并实现了此类化合物的各个VO部分中轻松诊断松弛特征的方法。值得注意的是,发现估计的弛豫时间接近于先前获得的其他基于钒的量子位的弛豫时间。将来,可以追求钒离子的量子位友好性质与单分子磁性和镧系元素的发光的协同组合,以实现这种材料的新功能。

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