Multiexcitons confined within a sub-excitonic volume: Spectroscopic and dynamical signatures of neutral and charged biexcitons in ultrasmall semiconductor nanocrystals

The use of ultrafast gating techniques allows us to resolve both spectrally and temporally the emission from short-lived neutral and negatively charged biexcitons in ultrasmall (sub-10 nm) CdSe nanocrystals (nanocrystal quantum dots). Because of forced overlap of electronic wave functions and reduced dielectric screening, these states are characterized by giant interaction energies of tens (neutral biexcitons) to hundreds (charged biexcitons) of meV. Both types of biexcitons show extremely short lifetimes (from sub-100 picoseconds to sub-picosecond time scales) that rapidly shorten with decreasing nanocrystal size. These ultrafast relaxation dynamics are explained in terms of highly efficient nonradiative Auger recombination.Comment: 5 pages, 4 figures, to be published in Phys. Rev.

Dynamic shear suppression in quantum phase space

© 2019 American Physical Society. All rights reserved.Classical phase space flow is inviscid. Here we show that in quantum phase space Wigner's probability current J can be effectively viscous. This results in shear suppression in quantum phase space dynamics which enforces Zurek's limit for the minimum size scale of spotty structures that develop dynamically. Quantum shear suppression is given by gradients of the quantum terms of J's vorticity. Used as a new measure of quantum dynamics applied to several evolving closed conservative 1D bound state systems, we find that shear suppression explains the saturation at Zurek's scale limit and additionally singles out special quantum states.Peer reviewe

Infrared Behavior of High-Temperature QCD

The damping rate \gamma_t(p) of on-shell transverse gluons with ultrasoft momentum p is calculated in the context of next-to-leading-order hard-thermal-loop-summed perturbation of high-temperature QCD. It is obtained in an expansion to second order in p. The first coefficient is recovered but that of order p^2 is found divergent in the infrared. Divergences from light-like momenta do also occur but are circumvented. Our result and method are critically discussed, particularly regarding a Ward identity obtained in the literature. When enforcing the equality between \gamma_t(0) and \gamma_l(0), a rough estimate of the magnetic mass is obtained. Carrying a similar calculation in the context of scalar quantum electrodynamics shows that the early ultrasoft-momentum expansion we make has little to do with the infrared sensitivity of the result.Comment: REVTEX4, 55 page

Decay of a Yukawa fermion at finite temperature and applications to leptogenesis

We calculate the decay rate of a Yukawa fermion in a thermal bath using finite temperature cutting rules and effective Green's functions according to the hard thermal loop resummation technique. We apply this result to the decay of a heavy Majorana neutrino in leptogenesis. Compared to the usual approach where thermal masses are inserted into the kinematics of final states, we find that deviations arise through two different leptonic dispersion relations. The decay rate differs from the usual approach by more than one order of magnitude in the temperature range which is interesting for the weak washout regime. We discuss how to arrive at consistent finite temperature treatments of leptogenesis.Comment: 16 pages, 5 figure

Supergauge interactions and electroweak baryogenesis

We present a complete treatment of the diffusion processes for supersymmetric electroweak baryogenesis that characterizes transport dynamics ahead of the phase transition bubble wall within the symmetric phase. In particular, we generalize existing approaches to distinguish between chemical potentials of particles and their superpartners. This allows us to test the assumption of superequilibrium (equal chemical potentials for particles and sparticles) that has usually been made in earlier studies. We show that in the Minimal Supersymmetric Standard Model, superequilibrium is generically maintained -- even in the absence of fast supergauge interactions -- due to the presence of Yukawa interactions. We provide both analytic arguments as well as illustrative numerical examples. We also extend the latter to regions where analytical approximations are not available since down-type Yukawa couplings or supergauge interactions only incompletely equilibrate. We further comment on cases of broken superequilibrium wherein a heavy superpartner decouples from the electroweak plasma, causing a kinematic bottleneck in the chain of equilibrating reactions. Such situations may be relevant for baryogenesis within extensions of the MSSM. We also provide a compendium of inputs required to characterize the symmetric phase transport dynamics.Comment: 49 pages, 9 figure

observation of ultra high energy cosmic rays from space status and perspectives

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Unpolarized states and hidden polarization

We capitalize on a multipolar expansion of the polarisation density matrix, in which multipoles appear as successive moments of the Stokes variables. When all the multipoles up to a given order $K$ vanish, we can properly say that the state is $K$th-order unpolarized, as it lacks of polarization information to that order. First-order unpolarized states coincide with the corresponding classical ones, whereas unpolarized to any order tally with the quantum notion of fully invariant states. In between these two extreme cases, there is a rich variety of situations that are explored here. The existence of \textit{hidden} polarisation emerges in a natural way in this context.Comment: 7 pages, 3 eps-color figures. Submitted to PRA. Comments welcome

Origin and higher-level diversification of acariform mites – evidence from nuclear ribosomal genes, extensive taxon sampling, and secondary structure alignment

Abstract Background Acariformes is the most species-rich and morphologically diverse radiation of chelicerate arthropods, known from the oldest terrestrial ecosystems. It is also a key lineage in understanding the evolution of this group, with the most vexing question whether mites, or Acari (Parasitiformes and Acariformes) is monophyletic. Previous molecular studies recovered Acari either as monophyletic or non-monophyletic, albeit with a limited taxon sampling. Similarly, relationships between basal acariform groups (include little-known, deep-soil 'endeostigmatan' mites) and major lineages of Acariformes (Sarcoptiformes, Prostigmata) are virtually unknown. We infer phylogeny of chelicerate arthropods, using a large and representative dataset, comprising all main in- and outgroups (228 taxa). Basal diversity of Acariformes is particularly well sampled. With this dataset, we conduct a series of phylogenetically explicit tests of chelicerate and acariform relationships and present a phylogenetic framework for internal relationships of acariform mites. Results Our molecular data strongly support a diphyletic Acari, with Acariformes as the sister group to Solifugae (PP =1.0; BP = 100), the so called Poecilophysidea. Among Acariformes, some representatives of the basal group Endeostigmata (mainly deep-soil mites) were recovered as sister-groups to the remaining Acariformes (i. e., Trombidiformes + and most of Sarcoptiformes). Desmonomatan oribatid mites (soil and litter mites) were recovered as the monophyletic sister group of Astigmata (e. g., stored product mites, house dust mites, mange mites, feather and fur mites). Trombidiformes (Sphaerolichida + Prostigmata) is strongly supported (PP =1.0; BP = 98–100). Labidostommatina was inferred as the basal lineage of Prostigmata. Eleutherengona (e. g., spider mites) and Parasitengona (e. g., chiggers, fresh water mites) were recovered as monophyletic. By contrast, Eupodina (e. g., snout mites and relatives) was not. Marine mites (Halacaridae) were traditionally regarded as the sister-group to Bdelloidea (Eupodina), but our analyses show their close relationships to Parasitengona. Conclusions Non-trivial relationships recovered by our analyses with high support (i.e., basal arrangement of endeostigmatid lineages, the position of marine mites, polyphyly of Eupodina) had been  proposed by previous underappreciated morphological studies. Thus, we update currently the accepted taxonomic classification to reflect these results: the superfamily Halacaroidea Murray, 1877 is moved from the infraorder Eupodina Krantz, 1978 to Anystina van der Hammen, 1972; and the subfamily Erythracarinae Oudemans, 1936 (formerly in Anystidae Oudemans, 1902) is elevated to family rank, Erythracaridae stat. ressur., leaving Anystidae only with the nominal subfamily. Our study also shows that a clade comprising early derivative Endeostigmata (Alycidae, Nanorchestidae, Nematalycidae, and maybe Alicorhagiidae) should be treated as a taxon with the same rank as Sarcoptiformes and Trombidiformes, and the scope of the superfamily Bdelloidea should  be changed. Before turning those findings into nomenclatural changes, however, we consider that our study calls for (i) finding shared apomorphies of the early derivative Endeostigmata clade and the clade including the remaining Acariformes; (ii) a well-supported hypothesis  for Alicorhagiidae placement; (iii) sampling the families Proterorhagiidae, Proteonematalycidae and Grandjeanicidae not yet included in molecular analyses; (iv) undertake a denser sampling of clades traditionally placed in Eupodina, Anystina (Trombidiformes) and Palaeosomata (Sarcoptiformes), since consensus networks and Internode certainty (IC) and IC All (ICA) indices indicate high levels of conflict in these tree regions. Our study shows that regions of ambiguous alignment may provide useful phylogenetic signal when secondary structure information is used to guide the alignment procedure and provides an R implementation to the Bayesian Relative Rates test.http://deepblue.lib.umich.edu/bitstream/2027.42/113097/1/12862_2015_Article_458.pd