Many-body contributions to spin relaxation in semiconductors

Spintronics has the potential to play a significant role in future electronic devices. The success of the field hinges on our ability to maintain and propagate spin signals over various length scales and periods of time. Common to all devices designed to carry spin signals is a need to hold the spin orientation of constituent particles, individually or in bulk. Spin relaxation is a measure of how long particle spins remain polarized while subjected to both spin-dependent and spin-independent interactions. An effect typically driven by the spin-orbit interaction in semiconductors, spin relaxation describes the rate at which spin polarized particles return to an equilibrium spin distribution. This is generally in competition with the goals of spintronic devices which generate out-of-equilibrium spin populations to represent signals. By studying the various mechanisms of spin relaxation in different systems, we learn which materials are appropriate for specific applications and get hints about how to minimize signal loss. This report focuses largely on Dyakonov-Perel spin relaxation of carriers in III-V semiconductors. Of the spin relaxation mechanisms in III-V semiconductors, Dyakonov-Perel often dominates or is at least a primary contributor. We study the mechanism in detail for both non-magnetic and dilute magnetic semiconductors, deriving analytic expressions that include contributions from many-body interactions. The results shed light on the validity of commonly made approximations in calculating spin relaxation for various systems. More importantly, we show how spin relaxation can affect other physical observables, such as spin diffusion. By investigating this spin relaxation mechanism in a dilute magnetic semiconductor, we include the effects of spin-dependent interactions. These interactions result in some peculiarities of spin relaxation for carriers undergoing a ferromagnetic transition.Includes bibliographical references (pages 103-112)

D'yakonov-Perel' spin relaxation for degenerate electrons in the electron-hole liquid

http://arxiv.org/PS_cache/arxiv/pdf/1010/1010.5544v1.pdfWe present an analytical study of the D'yakonov-Perel' spin relaxation time for degenerate electrons in a photo-excited electron-hole liquid in intrinsic semiconductors exhibiting a spin-split band structure. The D'yakonov-Perel' spin relaxation of electrons in these materials is controlled by electron-hole scattering, with small corrections from electron-electron scattering and virtually none from electron-impurity scattering. We derive simple expressions (one-dimensional and two- dimensional integrals respectively) for the effective electron-hole and electron-electron scattering rates which enter the spin relaxation time calculation. The electron-hole scattering rate is found to be comparable to the scattering rates from impurities in the electron liquid - a common model for n-type doped semiconductors. As the density of electron-hole pairs decreases (within the degenerate regime), a strong enhancement of the scattering rates and a corresponding slowing down of spin relaxation is predicted due to exchange and correlation effects in the electron-hole liquid. In the opposite limit of high density, the original D'yakonov-Perel' model fails due to decreasing scattering rates and is eventually superseded by free precession of individual quasiparticle spins.This work was supported by the National Science Foundation under grant number DMR-0705460 and the Department of Energy under grant number DE-FG02-05ER46203. The work of IVT was supported by Spanish MEC (FIS2007-65702-C02-01), \Grupos Consolidados UPV/EHU del Gobierno Vasco" (IT-319-07), and the European Union through e-I3 ETSF project (Contract No. 211956)

D'yakonov-Perel' spin relaxation for degenerate electrons in the electron-hole liquid

We present an analytical study of the D'yakonov-Perel' spin relaxation time for degenerate electrons in a photo-excited electron-hole liquid in intrinsic semiconductors exhibiting a spin-split band structure. The D'yakonov-Perel' spin relaxation of electrons in these materials is controlled by electron-hole scattering, with small corrections from electron-electron scattering and virtually none from electron-impurity scattering. We derive simple expressions (one-dimensional and two-dimensional integrals respectively) for the effective electron-hole and electron-electron scattering rates which enter the spin relaxation time calculation. The electron-hole scattering rate is found to be comparable to the scattering rates from impurities in the electron liquid - a common model for n-type doped semiconductors. As the density of electron-hole pairs decreases (within the degenerate regime), a strong enhancement of the scattering rates and a corresponding slowing down of spin relaxation is predicted due to exchange and correlation effects in the electron-hole liquid. In the opposite limit of high density, the original D'yakonov-Perel' model fails due to decreasing scattering rates and is eventually superseded by free precession of individual quasiparticle spins.Comment: 16 pages, 5 figure

Entanglement-based quantum communication secured by nonlocal dispersion cancellation

Quantum key distribution (QKD) enables participants to exchange secret information over long distances with unconditional security. However, the performance of today's QKD systems is subject to hardware limitations, such as those of available nonclassical-light sources and single-photon detectors. By encoding photons in high-dimensional states, the rate of generating secure information under these technical constraints can be maximized. Here, we demonstrate a complete time-energy entanglement-based QKD system with proven security against the broad class of arbitrary collective attacks. The security of the system is based on nonlocal dispersion cancellation between two time-energy entangled photons. This resource-efficient QKD system is implemented at telecommunications wavelength, is suitable for optical fiber and free-space links, and is compatible with wavelength-division multiplexing.United States. Army Research Office (Defense Advanced Research Projects Agency. Information in a Photon (InPho) Program (Grant W911NF-10-1-0416))National Science Foundation (U.S.). Integrative Graduate Education and Research Traineeship (Grant DGE-1069420

Microglial Interactions with Synapses Are Modulated by Visual Experience

Microglia, the brain's immune cells, show unique interactions with nearby synaptic elements under non-pathological conditions that are sensitive to changes in sensory experience

SARS-CoV-2 Omicron is an immune escape variant with an altered cell entry pathway

Vaccines based on the spike protein of SARS-CoV-2 are a cornerstone of the public health response to COVID-19. The emergence of hypermutated, increasingly transmissible variants of concern (VOCs) threaten this strategy. Omicron (B.1.1.529), the fifth VOC to be described, harbours multiple amino acid mutations in spike, half of which lie within the receptor-binding domain. Here we demonstrate substantial evasion of neutralization by Omicron BA.1 and BA.2 variants in vitro using sera from individuals vaccinated with ChAdOx1, BNT162b2 and mRNA-1273. These data were mirrored by a substantial reduction in real-world vaccine effectiveness that was partially restored by booster vaccination. The Omicron variants BA.1 and BA.2 did not induce cell syncytia in vitro and favoured a TMPRSS2-independent endosomal entry pathway, these phenotypes mapping to distinct regions of the spike protein. Impaired cell fusion was determined by the receptor-binding domain, while endosomal entry mapped to the S2 domain. Such marked changes in antigenicity and replicative biology may underlie the rapid global spread and altered pathogenicity of the Omicron variant

Investigation of hospital discharge cases and SARS-CoV-2 introduction into Lothian care homes

Background The first epidemic wave of severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2) in Scotland resulted in high case numbers and mortality in care homes. In Lothian, over one-third of care homes reported an outbreak, while there was limited testing of hospital patients discharged to care homes. Aim To investigate patients discharged from hospitals as a source of SARS-CoV-2 introduction into care homes during the first epidemic wave. Methods A clinical review was performed for all patients discharges from hospitals to care homes from 1st March 2020 to 31st May 2020. Episodes were ruled out based on coronavirus disease 2019 (COVID-19) test history, clinical assessment at discharge, whole-genome sequencing (WGS) data and an infectious period of 14 days. Clinical samples were processed for WGS, and consensus genomes generated were used for analysis using Cluster Investigation and Virus Epidemiological Tool software. Patient timelines were obtained using electronic hospital records. Findings In total, 787 patients discharged from hospitals to care homes were identified. Of these, 776 (99%) were ruled out for subsequent introduction of SARS-CoV-2 into care homes. However, for 10 episodes, the results were inconclusive as there was low genomic diversity in consensus genomes or no sequencing data were available. Only one discharge episode had a genomic, time and location link to positive cases during hospital admission, leading to 10 positive cases in their care home. Conclusion The majority of patients discharged from hospitals were ruled out for introduction of SARS-CoV-2 into care homes, highlighting the importance of screening all new admissions when faced with a novel emerging virus and no available vaccine

The complete chloroplast genome sequence of Pelargonium x hortorum: Organization and evolution of the largest and most highly rearranged chloroplast genome of land plants

The chloroplast genome of Pelargonium x hortorum has been completely sequenced. It maps as a circular molecule of 217,942 bp and is both the largest and most rearranged land plant chloroplast genome yet sequenced. It features 2 copies of a greatly expanded inverted repeat (IR) of 75,741 bp each and, consequently, diminished single-copy regions of 59,710 and 6,750 bp. Despite the increase in size and complexity of the genome, the gene content is similar to that of other angiosperms, with the exceptions of a large number of pseudogenes, the recognition of 2 open reading frames (ORF56 and ORF42) in the trnA intron with similarities to previously identified mitochondrial products (ACRS and pvs-trnA), the losses of accD and trnT-ggu and, in particular, the presence of a highly divergent set of rpoA-like ORFs rather than a single, easily recognized gene for rpoA. The 3-fold expansion of the IR (relative to most angiosperms) accounts for most of the size increase of the genome, but an additional 10% of the size increase is related to the large number of repeats found. The Pelargonium genome contains 35 times as many 31 bp or larger repeats than the unrearranged genome of Spinacia. Most of these repeats occur near the rearrangement hotspots, and 2 different associations of repeats are localized in these regions. These associations are characterized by full or partial duplications of several genes, most of which appear to be nonfunctional copies or pseudogenes. These duplications may also be linked to the disruption of at least 1 but possibly 2 or 3 operons. We propose simple models that account for the major rearrangements with a minimum of 8 IR boundary changes and 12 inversions in addition to several insertions of duplicated sequence