同位素纯化167Er3+在多晶Y2O3中的超精细相互作用和相干自旋动力学

T. Rajh, Lei Sun, Shobhit Gupta, Jun Yang, Haitao Zhang, Tian Zhong
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引用次数: 2

摘要

由于铒的电信c波段光学跃迁和超长的超精细相干时间,167Er3+掺杂固体是一个很有前途的量子技术平台。利用电子顺磁共振(EPR)光谱实验研究了Y2O3中167Er3+自旋的哈密顿量和动力学。利用x波段(9.5 GHz) EPR光谱数据拟合各向异性电子塞曼矩阵、超精细矩阵和核四极矩阵。我们使用脉冲EPR光谱测量了各向异性g张量的3个主轴的自旋弛豫时间T1和相干时间T2。在4 K的最低g跃迁中,测量到长电子自旋相干时间高达24.4 μs,超过了先前报道的在更低温度下的值。退相干机制的测量表明T2受光谱扩散和瞬时扩散的限制。长自旋相干时间和强各向异性超精细相互作用使167Er3+:Y2O3成为一个丰富的体系,是基于自旋的量子技术的优秀候选者。
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Hyperfine Interactions and Coherent Spin Dynamics of Isotopically Purified 167Er3+ in Polycrystalline Y2O3
167Er3+ doped solids are a promising platform for quantum technology due to erbium’s telecom C-band optical transition and its long hyperfine coherence times. We experimentally study the spin Hamiltonian and dynamics of 167Er3+ spins in Y2O3 using electron paramagnetic resonance (EPR) spectroscopy. The anisotropic electron Zeeman, hyperfine and nuclear quadrupole matrices are fitted using data obtained by X-band (9.5 GHz) EPR spectroscopy. We perform pulsed EPR spectroscopy to measure spin relaxation time T1 and coherence time T2 for the 3 principal axes of an anisotropic g tensor. Long electronic spin coherence time up to 24.4 μs is measured for lowest g transition at 4 K, exceeding previously reported values at much lower temperatures. Measurements of decoherence mechanism indicates T2 limited by spectral diffusion and instantaneous diffusion. Long spin coherence times, along with a strong anisotropic hyperfine interaction makes 167Er3+:Y2O3 a rich system and an excellent candidate for spin-based quantum technologies.
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