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Register a new userProbing quantum-mechanical level repulsion in disordered systems by means of time-resolved selectively-excited resonance fluorescence
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We argue that the time-resolved spectrum of selectively-excited resonance fluorescence at low temperature provides a tool for probing the quantum-mechanical level repulsion in the Lifshits tail of the electronic density of states in a wide variety of disordered materials. The technique, based on detecting the fast growth of a fluorescence peak that is red-shifted relative to the excitation frequency, is demonstrated explicitly by simulations on linear Frenkel exciton chains.
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We temporally resolve the resonance fluorescence from an electron spin confined to a single self-assembled quantum dot to measure directly the spins optical initialization and natural relaxation timescales. Our measurements demonstrate that spin initialization occurs on the order of microseconds in the Faraday configuration when a laser resonantly drives the quantum dot transition. We show that the mechanism mediating the optically induced spin-flip changes from electron-nuclei interaction to hole-mixing interaction at 0.6 Tesla external magnetic field. Spin relaxation measurements result in times on the order of milliseconds and suggest that a $B^{-5}$ magnetic field dependence, due to spin-orbit coupling, is sustained all the way down to 2.2 Tesla.
Two-level systems (TLS) in amorphous materials limit coherence times of a number of solid-state quantum devices. Interactions between TLS become prominent below 100 mK, but the coupling mechanism and statistical properties are still unclear. Here we determine the homogeneous linewidth of ytterbium ions (Yb$ ^{3+} $) in silica glass at 10-80 mK by using photon echo techniques as a probe of TLS. First, the homogeneous linewidth can be reduced by applying a magnetic field of 0.3 T. This effect is due to reduced magnetic interactions between adjacent Yb$ ^{3+} $. Secondly, we observe saturation of the linewidth below 50 mK to a level of approximately 30 kHz, which is much larger than the lifetime-limited value of 0.2 kHz. This saturation behavior is in conflict with the coupling to independent TLS. We show that this effect can be explained by coherently coupled TLS.
The local distribution of exciton levels in disordered cyanine-dye-based molecular nano-aggregates has been elucidated using fluorescence line narrowing spectroscopy. The observation of a Wigner-Dyson-type level spacing distribution provides direct evidence of the existence of level repulsion of strongly overlapping states in the molecular wires, which is important for the understanding of the level statistics, and therefore the `functional properties, of a large variety of nano-confined systems.
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The Anderson delocalization-localization transition is studied in multilayered systems with randomly placed interlayer bonds of density $p$ and strength $t$. In the absence of diagonal disorder (W=0), following an appropriate perturbation expansion, we estimate the mean free paths in the main directions and verify by scaling of the conductance that the states remain extended for any finite $p$, despite the interlayer disorder. In the presence of additional diagonal disorder ($W > 0$) we obtain an Anderson transition with critical disorder $W_c$ and localization length exponent $ u$ independently of the direction. The critical conductance distribution $P_{c}(g)$ varies, however, for the parallel and the perpendicular directions. The results are discussed in connection to disordered anisotropic materials.
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