Pritzker School of Molecular Engineering, University of Chicago, Chicago, IL 60637, USA.
Department of Chemistry, Northwestern University, Evanston, IL 60208, USA.
Science. 2020 Dec 11;370(6522):1309-1312. doi: 10.1126/science.abb9352. Epub 2020 Nov 12.
Spin-bearing molecules are promising building blocks for quantum technologies as they can be chemically tuned, assembled into scalable arrays, and readily incorporated into diverse device architectures. In molecular systems, optically addressing ground-state spins would enable a wide range of applications in quantum information science, as has been demonstrated for solid-state defects. However, this important functionality has remained elusive for molecules. Here, we demonstrate such optical addressability in a series of synthesized organometallic, chromium(IV) molecules. These compounds display a ground-state spin that can be initialized and read out using light and coherently manipulated with microwaves. In addition, through atomistic modification of the molecular structure, we vary the spin and optical properties of these compounds, indicating promise for designer quantum systems synthesized from the bottom-up.
含自旋的分子是量子技术中很有前途的构建模块,因为它们可以进行化学调控、组装成可扩展的阵列,并且很容易纳入到各种器件结构中。在分子体系中,对基态自旋的光学寻址将使量子信息科学中的一系列应用成为可能,就像在固态缺陷中已经证明的那样。然而,对于分子来说,这种重要的功能一直难以实现。在这里,我们在一系列合成的有机金属、铬(IV)分子中证明了这种光学可寻址性。这些化合物显示出一个基态自旋,可以使用光来初始化和读出,并使用微波进行相干操纵。此外,通过对分子结构的原子级修饰,我们改变了这些化合物的自旋和光学性质,这表明有可能从底层合成设计的量子系统。