5 research outputs found
Demagnetization of Quantum Dot Nuclear Spins: Breakdown of the Nuclear Spin Temperature Approach
The physics of interacting nuclear spins arranged in a crystalline lattice is
typically described using a thermodynamic framework: a variety of experimental
studies in bulk solid-state systems have proven the concept of a spin
temperature to be not only correct but also vital for the understanding of
experimental observations. Using demagnetization experiments we demonstrate
that the mesoscopic nuclear spin ensemble of a quantum dot (QD) can in general
not be described by a spin temperature. We associate the observed deviations
from a thermal spin state with the presence of strong quadrupolar interactions
within the QD that cause significant anharmonicity in the spectrum of the
nuclear spins. Strain-induced, inhomogeneous quadrupolar shifts also lead to a
complete suppression of angular momentum exchange between the nuclear spin
ensemble and its environment, resulting in nuclear spin relaxation times
exceeding an hour. Remarkably, the position dependent axes of quadrupolar
interactions render magnetic field sweeps inherently non-adiabatic, thereby
causing an irreversible loss of nuclear spin polarization.Comment: 15 pages, 3 figure
High resolution nuclear magnetic resonance spectroscopy of highly-strained quantum dot nanostructures
Much new solid state technology for single-photon sources, detectors,
photovoltaics and quantum computation relies on the fabrication of strained
semiconductor nanostructures. Successful development of these devices depends
strongly on techniques allowing structural analysis on the nanometer scale.
However, commonly used microscopy methods are destructive, leading to the loss
of the important link between the obtained structural information and the
electronic and optical properties of the device. Alternative non-invasive
techniques such as optically detected nuclear magnetic resonance (ODNMR) so far
proved difficult in semiconductor nano-structures due to significant
strain-induced quadrupole broadening of the NMR spectra. Here, we develop new
high sensitivity techniques that move ODNMR to a new regime, allowing high
resolution spectroscopy of as few as 100000 quadrupole nuclear spins. By
applying these techniques to individual strained self-assembled quantum dots,
we measure strain distribution and chemical composition in the volume occupied
by the confined electron. Furthermore, strain-induced spectral broadening is
found to lead to suppression of nuclear spin magnetization fluctuations thus
extending spin coherence times. The new ODNMR methods have potential to be
applied for non-invasive investigations of a wide range of materials beyond
single nano-structures, as well as address the task of understanding and
control of nuclear spins on the nanoscale, one of the central problems in
quantum information processing