Synthesis and Characterization of CdSe/ZnS Core/Shell Quantum Dot Sensitized PCPDTBT-P3HT:PCBM Organic Photovoltaics

Durable, cheap, and lightweight polymer based solar cells are needed, if simply to meet the demand for decentralized electrical power production in traditionally “off-grid” areas. Using a blend of Poly(3-hexylthiophene-2,5-diyl) (P3HT), Phenyl-C61-butyric acid methyl ester (PCBM), and the low band-gap polymer Poly[2,6-(4,4-bis-(2- ethylhexyl)-4H-cyclopenta [2,1-b;3,4-b′]dithiophene)-alt-4,7(2,1,3-benzothiadiazole)] (PCPDTBT), we have fabricated devices with a wide spectral response and 3% power conversion efficiency in AM 1.5 conditions; however, this thin film system exhibits only 0.43 optical density at 500 nm. To improve the performance of this polymer blend photovoltaic, we aim to increase absorption by adding CdSe(ZnS) core (shell) quantum dots. Four groups of devices are fabricated: a control group with an active polymer layer of 16 mg/mL P3HT, 16 mg/mL PCBM, and 4 mg/mL PCPDTBT; and three groups with dispersed quantum dots at 4 mg/ml, 1 mg/mL, and 0.25 mg/mL. The (CdSe)ZnS quantum dots are coated with octadecylamine ligands and have a peak absorbance at 560 nm and peak emission at 577 nm. The active layer was dissolved in chlorobenzene solvent and spun on glass substrates, patterned with indium tin oxide. The devices were then annealed for fifteen minutes at 110° C, 140° C, and 170° C. Current-voltage characteristic curves v and optical density data were taken before and after the anneal step. Finally, surface characterization was conducted with atomic force microscopy and electrostatic force microscopy. When compared to the control, the sensitized devices exhibited increased absorption and depressed electrical performance with increasing quantum dot loading. The surface morphology, both electrical and physical, showed deviation from the typical values and patterns shown by the control that increased with quantum dot loading. When the degrading electrical characteristics, increasing optical absorbance, and surface changes, are considered together, it becomes likely that the quantum dots interact in a significant manner with the morphology of the P3HT phase, which leads to an overall decrease in performance

Factorial Schur functions and the Yang-Baxter equation

Factorial Schur functions are generalizations of Schur functions that have, in addition to the usual variables, a second family of "shift" parameters. We show that a factorial Schur function times a deformation of the Weyl denominator may be expressed as the partition function of a particular statistical-mechanical system (six vertex model). The proof is based on the Yang-Baxter equation. There is a deformation parameter $t$ which may be specialized in different ways. If $t=-1$, then we recover the expression of the factorial Schur function as a ratio of alternating polynomials. If $t=0$, we recover the description as a sum over tableaux. If $t=\infty$ we recover a description of Lascoux that was previously considered by McNamara. We also are able to prove using the Yang-Baxter equation the asymptotic symmetry of the factorial Schur functions in the shift parameters. Finally, we give a proof using our methods of the dual Cauchy identity for factorial Schur functions. Thus using our methods we are able to give thematic proofs of many of the properties of factorial Schur functions

Who Takes the Bait? Non-target Species Use of Bear Hunter Bait Sites

Hunting bears (Ursus spp.) over baits is legal in many countries, states, and provinces, but the practice remains a controversial topic among wildlife managers, hunting groups, and the general public. The baits used to attract bears may also provide a pulsed resource on the landscape that can be used by other wildlife species, particularly carnivores. To determine what other species might use bear bait sites, we constructed and monitored 21 bear bait sites with camera traps from August to October 2016 in the western Upper Peninsula of Michigan, USA. The sites mimicked typical American black bear (U. americanus) hunter bait sites. We tested recorded changes in carnivore visitation before and during hunting season using paired t-test and analyzed carnivore temporal shifts between the 2 periods using a nonparametric kernel density estimation procedure. We analyzed 7,915 images, of which 81.9% were nontarget species. Bear daily visitation at the bait sites was reduced by 49.3% during hunting season while nontarget carnivore visitation increased by 33.0%. Bears also increased their nocturnal activity by 22.4% during the legal hunting season while other carnivore species maintained their diel patterns. Because of the high rates of nontarget species use of the bear hunter bait sites, there is a potential for disease spread and conflict with hunters. Managers should evaluate the potential impacts on target and nontarget species when establishing hunter bait regulations

Haar expectations of ratios of random characteristic polynomials

We compute Haar ensemble averages of ratios of random characteristic polynomials for the classical Lie groups K = O(N), SO(N), and USp(N). To that end, we start from the Clifford-Weyl algebera in its canonical realization on the complex of holomorphic differential forms for a C-vector space V. From it we construct the Fock representation of an orthosymplectic Lie superalgebra osp associated to V. Particular attention is paid to defining Howe's oscillator semigroup and the representation that partially exponentiates the Lie algebra representation of sp in osp. In the process, by pushing the semigroup representation to its boundary and arguing by continuity, we provide a construction of the Shale-Weil-Segal representation of the metaplectic group. To deal with a product of n ratios of characteristic polynomials, we let V = C^n \otimes C^N where C^N is equipped with its standard K-representation, and focus on the subspace of K-equivariant forms. By Howe duality, this is a highest-weight irreducible representation of the centralizer g of Lie(K) in osp. We identify the K-Haar expectation of n ratios with the character of this g-representation, which we show to be uniquely determined by analyticity, Weyl group invariance, certain weight constraints and a system of differential equations coming from the Laplace-Casimir invariants of g. We find an explicit solution to the problem posed by all these conditions. In this way we prove that the said Haar expectations are expressed by a Weyl-type character formula for all integers N \ge 1. This completes earlier work by Conrey, Farmer, and Zirnbauer for the case of U(N).Comment: LaTeX, 70 pages, Complex Analysis and its Synergies (2016) 2:

Hall viscosity, orbital spin, and geometry: paired superfluids and quantum Hall systems

The Hall viscosity, a non-dissipative transport coefficient analogous to Hall conductivity, is considered for quantum fluids in gapped or topological phases. The relation to mean orbital spin per particle discovered in previous work by one of us is elucidated with the help of examples, using the geometry of shear transformations and rotations. For non-interacting particles in a magnetic field, there are several ways to derive the result (even at non-zero temperature), including standard linear response theory. Arguments for the quantization, and the robustness of Hall viscosity to small changes in the Hamiltonian that preserve rotational invariance, are given. Numerical calculations of adiabatic transport are performed to check the predictions for quantum Hall systems, with excellent agreement for trial states. The coefficient of k^4 in the static structure factor is also considered, and shown to be exactly related to the orbital spin and robust to perturbations in rotation invariant systems also.Comment: v2: Now 30 pages, 10 figures; new calculation using disk geometry; some other improvements; no change in result

Does persistent snowpack inhibit degradation of fecal stress indicators?

Physiological stress in wildlife can be a useful indicator of a population’s response to environmental factors. By using non-invasive endocrinological techniques, such as fecal sampling, potential confounding factors associated with the stress of capture can be avoided. A potential drawback of fecal sampling, however, is degradation of samples which may produce aberrant measurements of fecal glucocorticoid metabolites. In vertebrates, glucocorticoids, such as corticosterone, become elevated in response to stress. We sought to gauge the reliability of measurement of fecal glucocorticoid metabolites from white-tailed deer (Odocoileus virginianus) fecal samples exposed to a temperate winter with substantial snow cover and cold temperatures for up to 90 days, by repeatedly subsampling fecal samples every 10 days and performing a corticosterone enzyme-linked immunosorbent assay (ELISA). Measurements of fecal glucocorticoid metabolites at 10 days were consistent with initial measurements, after which (20 days) they became aberrant following a period of thawing. Consequently, glucocorticoid metabolite levels in feces appear to remain stable under ambient conditions if temperatures remain below freezing at least for 10 days. While it’s possible that samples may remain useful beyond this time frame based on previous laboratory studies of samples stored in a freezer, further work is needed to determine how samples weather in situ under extreme cold (e.g. Arctic) or periods of partial thawing

Crystal constructions in Number Theory

Weyl group multiple Dirichlet series and metaplectic Whittaker functions can be described in terms of crystal graphs. We present crystals as parameterized by Littelmann patterns and we give a survey of purely combinatorial constructions of prime power coefficients of Weyl group multiple Dirichlet series and metaplectic Whittaker functions using the language of crystal graphs. We explore how the branching structure of crystals manifests in these constructions, and how it allows access to some intricate objects in number theory and related open questions using tools of algebraic combinatorics

Central limit theorem for multiplicative class functions on the symmetric group

Hambly, Keevash, O'Connell and Stark have proven a central limit theorem for the characteristic polynomial of a permutation matrix with respect to the uniform measure on the symmetric group. We generalize this result in several ways. We prove here a central limit theorem for multiplicative class functions on symmetric group with respect to the Ewens measure and compute the covariance of the real and the imaginary part in the limit. We also estimate the rate of convergence with the Wasserstein distance.Comment: 23 pages; the mathematics is the same as in the previous version, but there are several improvments in the presentation, including a more intuitve name for the considered function

Molecular evidence for a single origin of ultrafiltration-based excretory organs

Under embargo until: 2021-06-23Excretion is an essential physiological process, carried out by all living organisms, regardless of their size or complexity.1, 2, 3 Both protostomes (e.g., flies and flatworms) and deuterostomes (e.g., humans and sea urchins) possess specialized excretory organs serving that purpose. Those organs exhibit an astonishing diversity, ranging from units composed of just few distinct cells (e.g., protonephridia) to complex structures, built by millions of cells of multiple types with divergent morphology and function (e.g., vertebrate kidneys).4,5 Although some molecular similarities between the development of kidneys of vertebrates and the regeneration of the protonephridia of flatworms have been reported,6,7 the molecular underpinnings of the development of excretory organs have never been systematically studied in a comparative context.4 Here, we show that a set of transcription factors (eya, six1/2, pou3, sall, lhx1/5, and osr) and structural proteins (nephrin, kirre, and zo1) is expressed in the excretory organs of a phoronid, brachiopod, annelid, onychophoran, priapulid, and hemichordate that represent major protostome lineages and non-vertebrate deuterostomes. We demonstrate that the molecular similarity observed in the vertebrate kidney and flatworm protonephridia6,7 is also seen in the developing excretory organs of those animals. Our results show that all types of ultrafiltration-based excretory organs are patterned by a conserved set of developmental genes, an observation that supports their homology. We propose that the last common ancestor of protostomes and deuterostomes already possessed an ultrafiltration-based organ that later gave rise to the vast diversity of extant excretory organs, including both proto- and metanephridia.acceptedVersio