Dipartimento di Chimica "Ugo Schiff" & INSTM RU, Università degli Studi di Firenze , Via della Lastruccia 3, I50019 Sesto Fiorentino (Firenze), Italy.
Dipartimento di Chimica & NIS Centre, Università di Torino , Via P. Giuria 7, I10125 Torino, Italy.
J Am Chem Soc. 2016 Feb 24;138(7):2154-7. doi: 10.1021/jacs.5b13408. Epub 2016 Feb 11.
Here we report the investigation of the magnetic relaxation and the quantum coherence of vanadyl phthalocyanine, VOPc, a multifunctional and easy-processable potential molecular spin qubit. VOPc in its pure form (1) and its crystalline dispersions in the isostructural diamagnetic host TiOPc in different stoichiometric ratios, namely VOPc:TiOPc 1:10 (2) and 1:1000 (3), were investigated via a multitechnique approach based on the combination of alternate current (AC) susceptometry, continuous wave, and pulsed electron paramagnetic resonance (EPR) spectroscopy. AC susceptibility measurements revealed a linear increase of the relaxation rate with temperature up to 20 K, as expected for a direct mechanism, but τ remains slow over a very wide range of applied static field values (up to ∼5 T). Pulsed EPR spectroscopy experiments on 3 revealed quantum coherence up to room temperature with T(m) ∼1 μs at 300 K, representing the highest value obtained to date for molecular electronic spin qubits. Rabi oscillations are observed in this nuclear spin-active environment ((1)H and (14)N nuclei) at room temperature also for 2, indicating an outstanding robustness of the quantum coherence in this molecular semiconductor exploitable in spintronic devices.
在这里,我们报告了对多功能且易于处理的潜在分子自旋量子位钒氧酞菁(VOPc)的磁弛豫和量子相干性的研究。通过基于交流(AC)磁化率、连续波和脉冲电子顺磁共振(EPR)光谱组合的多技术方法,研究了纯形式的 VOPc(1)及其在等结构反磁性主体 TiOPc 中的不同化学计量比的晶体分散体,即 VOPc:TiOPc 1:10(2)和 1:1000(3)。AC 磁化率测量表明,弛豫率随温度线性增加,直至 20 K,这与直接机制相符,但τ在非常宽的外加静态磁场值范围内(高达约 5 T)仍然很慢。在 3 上进行的脉冲 EPR 光谱实验表明,量子相干性直至室温,在 300 K 时 T(m) ∼1 μs,这是迄今为止在分子电子自旋量子位中获得的最高值。在这个核自旋活性环境((1)H 和 (14)N 核)中,在室温下也观察到 2 的拉比振荡,表明在可用于自旋电子器件的这种分子半导体中,量子相干性具有出色的鲁棒性。