论文标题
在超导纳米收缩处增强的分子自旋光子耦合
Enhanced molecular spin-photon coupling at superconducting nanoconstrictions
论文作者
论文摘要
我们将自上而下和自下而上的纳米光刻结合起来,以优化小分子旋转合奏的耦合到$ 1.4 $ GHz的芯片上超导谐振器。在中央传输线上用聚焦的离子束制造的纳米收缩,局部将微波磁场浓缩。自由基分子的滴剂已从溶液沉积到电路上。对于最小的,分子是通过原子力显微镜在相关电路区域传递的。有效耦合到每个设备的旋转$ n _ {\ rm eff} $由扫描电子和原子力显微镜进行了准确确定。对于$ n _ {\ rm eff} $的样品的集体自旋耦合常数已确定,范围在$ 2 \ times 10^{6} $和$ 10^{12} $旋转之间,温度降低到$ 44 $ MK。结果表明,与$ n _ {\ rm eff} $的平方根成正比的耦合的众所周知的集体增强。当传输线宽度从400美元的$ 42 $ nm减少到42美元的$ NM时,单个旋转的平均耦合的平均耦合将增加了四个以上的数量级(从$ 4 $ MHz到高于$ 180 $ Hz),并达到接近$ 1 $ kHz的分子的最大值。这一结果为实现纳米级的磁光谱实验以及基于分子自旋矩形的杂交量子计算体系结构的开发提供了有希望的途径。
We combine top-down and bottom-up nanolithography to optimize the coupling of small molecular spin ensembles to $1.4$ GHz on-chip superconducting resonators. Nanoscopic constrictions, fabricated with a focused ion beam at the central transmission line, locally concentrate the microwave magnetic field. Drops of free-radical molecules have been deposited from solution onto the circuits. For the smallest ones, the molecules were delivered at the relevant circuit areas by means of an atomic force microscope. The number of spins $N_{\rm eff}$ effectively coupled to each device was accurately determined combining Scanning Electron and Atomic Force Microscopies. The collective spin-photon coupling constant has been determined for samples with $N_{\rm eff}$ ranging between $2 \times 10^{6}$ and $10^{12}$ spins, and for temperatures down to $44$ mK. The results show the well-known collective enhancement of the coupling proportional to the square root of $N_{\rm eff}$. The average coupling of individual spins is enhanced by more than four orders of magnitude (from $4$ mHz up to above $180$ Hz) when the transmission line width is reduced from $400$ microns down to $42$ nm, and reaches maximum values near $1$ kHz for molecules located on the smallest nanoconstrictions. This result opens promising avenues for the realization of magnetic spectroscopy experiments at the nanoscale and for the development of hybrid quantum computation architectures based on molecular spin qubits.