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Room temperature coherent control of spin defects in hexagonal boron nitride

机译:六边形氮化物中旋转缺陷的室温相干控制

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Optically active spin defects are promising candidates for solid-state quantum information and sensing applications. To use these defects in quantum applications coherent manipulation of their spin state is required. Here, we realize coherent control of ensembles of boron vacancy centers in hexagonal boron nitride (hBN). Specifically, by applying pulsed spin resonance protocols, we measure a spin-lattice relaxation time of 18 microseconds and a spin coherence time of 2 microseconds at room temperature. The spin-lattice relaxation time increases by three orders of magnitude at cryogenic temperature. By applying a method to decouple the spin state from its inhomogeneous nuclear environment the optically detected magnetic resonance linewidth is substantially reduced to several tens of kilohertz. Our results are important for the employment of van der Waals materials for quantum technologies, specifically in the context of high resolution quantum sensing of two-dimensional heterostructures, nanoscale devices, and emerging atomically thin magnets.
机译:光学主动旋转缺陷是用于固态量子信息和传感应用的候选候选者。为了在量子应用中使用这些缺陷,需要对其自旋状态的相干操作。在这里,我们实现了在六边形氮化物(HBN)中的硼空位中心集合的相干控制。具体地,通过施加脉冲自旋共振方案,我们测量18微秒的旋转晶格弛豫时间,在室温下测量18微秒的旋转相干时间2微秒。旋转晶格松弛时间在低温温度下增加了三个数量级。通过将方法从其不均匀的核环境中施加到旋转状态,光学检测的磁共振线宽显着降低到几十千赫兹。我们的结果对于van der WALS材料对量子技术的使用非常重要,特别是在高分辨率量子传感的二维异质结构,纳米级装置和新出现的原子薄磁体的上下文中。

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