Institute of Physical Chemistry and Center for Integrated Quantum Science and Technology, University of Stuttgart, Pfaffenwaldring 55, 70569 Stuttgart, Germany.
Phys Chem Chem Phys. 2019 Mar 27;21(13):6976-6983. doi: 10.1039/c9cp00745h.
Molecular quantum bits based on copper(ii) or vanadium(iv) have been shown to possess long coherence times on multiple occasions. In contrast, studies in which non-spin-½ ions are employed are relatively scarce. High-spin ions provide additional states that can be used to encode further quantum bits. Furthermore, an optical rather than a microwave readout of molecular quantum bits is highly desirable, because in principle it could allow addressing at the single quantum bit level. The chromium(iii) complex [Cr(ddpd)2]3+ (ddpd = N,N'-dimethyl-N,N'-dipyridine-2-yl-pyridine-2,6-diamine) combines both the large spin (S = 3/2) and optical activity (strong, long lived luminescence). Here we demonstrate that the compound possesses coherence times of up to 8.4(1) μs, which are much longer (at least three times) than those for other chromium(iii)-based compounds. On the other hand, it is proved to be impossible to read out or influence the quantum state by optical means, underlining that further work is needed in this direction.
基于铜(II)或钒(IV)的分子量子位多次显示出具有长相干时间。相比之下,使用非自旋-½离子的研究相对较少。高自旋离子提供了可以用来进一步编码量子位的附加状态。此外,分子量子位的光学而不是微波读出是非常理想的,因为它原则上可以允许在单个量子位水平上寻址。铬(III)配合物[Cr(ddpd)2]3+(ddpd = N,N'-二甲基-N,N'-二吡啶-2-基-吡啶-2,6-二胺)结合了大自旋(S = 3/2)和光学活性(强,长寿命发光)。在这里,我们证明该化合物具有长达 8.4(1)μs 的相干时间,比其他基于铬(III)的化合物的相干时间长得多(至少三倍)。另一方面,证明不可能通过光学手段读出或影响量子态,这突出表明需要在这方面进一步研究。