Spin noise of localized electrons in CdTe/CdMgTe quantum well
A. L. Zibinskiy, S. Cronenberger, B. Gribakin, R. Baye, D. Scalbert, R. André, D. S. Smirnov, M. Vladimirova
TL;DR
This work uses spin noise spectroscopy to disentangle spin dephasing and relaxation of donor-bound electrons in a CdTe/CdMgTe quantum well. By analyzing a clearly resolved satellite peak at $\bar{\delta}_e/2\pi\approx27$ MHz and a Larmor peak, the authors separate hyperfine-induced dephasing from temperature-activated spin relaxation, attributing the latter to donor-to-conduction-band hopping and spin exchange among donors. The study extracts quantitative values for the average nuclear-field fluctuation $\bar{\delta}_e$, its dispersion $\alpha$, spin-relaxation rate $\gamma$, and donor density $N_d\approx 10^{10}$ cm$^{-2}$, and explains the absence of motional narrowing in this QW due to strong impurity-band broadening. The results connect SN spectral features to microscopic processes and provide a framework to estimate donor density from SN measurements in quantum wells.
Abstract
The spin dynamics of localized electrons in bulk semiconductors is governed by the interplay of effective nuclear field fluctuations, spin exchange between electrons, and spin transitions into the conduction band. Using spin noise spectroscopy, we reveal this interplay for donor-bound electrons in a CdTe/CdMgTe quantum well and spectrally separate electron spin relaxation and dephasing in zero magnetic field. We identify a specific regime of the electron spin dynamics, where temperature-induced activation of spin-independent hopping leads to a monotonic acceleration of electron spin relaxation. This behavior contrasts with bulk CdTe crystals, where the motional narrowing effect is observed. We attribute this difference to the significantly larger inhomogeneous broadening of the donor-related trion resonance in our quantum well compared to bulk samples. The theoretical analysis of the spin noise power and the strength of the spin exchange interaction provides the estimation of the donor concentration in our unintentionally doped structure.
