2,155 research outputs found

    Organizational learning and emotion: constructing collective meaning in support of strategic themes

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    Missing in the organizational learning literature is an integrative framework that reflects the emotional as well as the cognitive dynamics involved. Here, we take a step in this direction by focusing in depth over time (five years) on a selected organization which manufactures electronic equipment for the office industry. Drawing on personal construct theory, we define organizational learning as the collective re-construal of meaning in the direction of strategically significant themes. We suggest that emotions arise as members reflect on progress or lack of progress in achieving organizational learning. Our evidence suggests that invalidation – where organizational learning fails to correspond with expectations – gives rise to anxiety and frustration, while validation – where organizational learning is aligned with or exceeds expectations – evokes comfort or excitement. Our work aims to capture the key emotions involved as organizational learning proceeds

    Muonium Decay

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    Modifications of the mu+ lifetime in matter due to muonium (M = mu+ e-) formation and other medium effects are examined. Muonium and free mu+ decay spectra are found to differ at O(alpha m_e/m_mu) from Doppler broadening and O(alpha^2 m_e/m_mu) from the Coulomb bound state potential. However, both types of corrections are shown to cancel in the total decay rate due to Lorentz and gauge invariance respectively, leaving a very small time dilation lifetime difference, (tau_M - tau_mu+)/tau_mu+ = alpha^2 m_e^2/ 2m_mu^2 \simeq 6\times 10^-10, as the dominant bound state effect. It is argued that other medium effects on the stopped mu+ lifetime are similarly suppressed.Comment: 14 pages, revte

    Characterizing Mode Anharmonicity and Huang–Rhys Factors Using Models of Femtosecond Coherence Spectra

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    Femtosecond laser pulses readily produce coherent quantum beats in transient–absorption spectra. These oscillatory signals often arise from molecular vibrations and therefore may contain information about the excited-state potential energy surface near the Franck–Condon region. Here, by fitting the measured spectra of two laser dyes to microscopic models of femtosecond coherence spectra (FCS) arising from molecular vibrations, we classify coherent quantum-beat signals as fundamentals or overtones and quantify their Huang–Rhys factors and anharmonicity values. We discuss the extracted Huang–Rhys factors in the context of quantum-chemical computations. This work solidifies the use of FCS for analysis of coherent quantum beats arising from molecular vibrations, which will aid studies of molecular aggregates and photosynthetic proteins

    High-Sensitivity Electronic Stark Spectrometer Featuring a Laser-Driven Light Source

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    We report developmental details of a high-sensitivity Stark absorption spectrometer featuring a laser-driven light source. The light source exhibits intensity fluctuations of ∼0.3% over timescales ranging from 1 min to 12 h, minimal drift (≤ 0.1%/h), and very little 1/f noise at frequencies greater than 200 Hz, which are comparable to or better than an arc-driven light source. Additional features of the spectrometer include balanced detection with multiplex sampling, which yielded lower noise in A, and constant wavelength or wavenumber (energy) spectral bandpass modes. We achieve noise amplitudes of ∼7 × 10−4 and ∼6 × 10−6 in measurements of single A and ΔA spectra (with 92 data points) taking ∼7 and ∼19 min, respectively

    Calibrating the relation of low-frequency radio continuum to star formation rate at 1 kpc scale with LOFAR

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    9 figures, 6 tables and 17 pages. This paper is part of the LOFAR surveys data release 1 and has been accepted for publication in a special edition of A&A that will appear in Feb 2019, volume 622. The catalogues and images from the data release will be publicly available on lofar-surveys.org upon publication of the journal. Reproduced with permission from Astronomy & Astrophysics. © 2018 ESO.Radio continuum (RC) emission in galaxies allows us to measure star formation rates (SFRs) unaffected by extinction due to dust, of which the low-frequency part is uncontaminated from thermal (free-free) emission. We calibrate the conversion from the spatially resolved 140 MHz RC emission to the SFR surface density (ΣSFR\Sigma_{\rm SFR}) at 1 kpc scale. We used recent observations of three galaxies (NGC 3184, 4736, and 5055) from the LOFAR Two-metre Sky Survey (LoTSS), and archival LOw-Frequency ARray (LOFAR) data of NGC 5194. Maps were created with the facet calibration technique and converted to radio ΣSFR\Sigma_{\rm SFR} maps using the Condon relation. We compared these maps with hybrid ΣSFR\Sigma_{\rm SFR} maps from a combination of GALEX far-ultraviolet and Spitzer 24 μm\mu\rm m data using plots tracing the relation at 1.2×1.21.2\times 1.2-kpc2^2 resolution. The RC emission is smoothed with respect to the hybrid ΣSFR\Sigma_{\rm SFR} owing to the transport of cosmic-ray electrons (CREs). This results in a sublinear relation (ΣSFR)RC[(ΣSFR)hyb]a(\Sigma_{\rm SFR})_{\rm RC} \propto [(\Sigma_{\rm SFR})_{\rm hyb}]^{a}, where a=0.59±0.13a=0.59\pm 0.13 (140 MHz) and a=0.75±0.10a=0.75\pm 0.10 (1365 MHz). Both relations have a scatter of σ=0.3 dex\sigma = 0.3~\rm dex. If we restrict ourselves to areas of young CREs (α>0.65\alpha > -0.65; IνναI_\nu \propto \nu^\alpha), the relation becomes almost linear at both frequencies with a0.9a\approx 0.9 and a reduced scatter of σ=0.2 dex\sigma = 0.2~\rm dex. We then simulate the effect of CRE transport by convolving the hybrid ΣSFR\Sigma_{\rm SFR} maps with a Gaussian kernel until the RC-SFR relation is linearised; CRE transport lengths are l=1l=1-5 kpc. Solving the CRE diffusion equation, we find diffusion coefficients of D=(0.13D=(0.13-1.5)×1028cm2s11.5) \times 10^{28} \rm cm^2\,s^{-1} at 1 GeV. A RC-SFR relation at 1.41.4 GHz can be exploited to measure SFRs at redshift z10z \approx 10 using 140140 MHz observations.Peer reviewe

    Symmetry Breaking Charge Transfer in DNA-Templated Perylene Dimer Aggregates

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    Molecular aggregates are of interest to a broad range of fields including light harvesting, organic optoelectronics, and nanoscale computing. In molecular aggregates, nonradiative decay pathways may emerge that were not present in the constituent molecules. Such nonradiative decay pathways may include singlet fission, excimer relaxation, and symmetry-breaking charge transfer. Singlet fission, sometimes referred to as excitation multiplication, is of great interest to the fields of energy conversion and quantum information. For example, endothermic singlet fission, which avoids energy loss, has been observed in covalently bound, linear perylene trimers and tetramers. In this work, the electronic structure and excited-state dynamics of dimers of a perylene derivative templated using DNA were investigated. Specifically, DNA Holliday junctions were used to template the aggregation of two perylene molecules covalently linked to a modified uracil nucleobase through an ethynyl group. The perylenes were templated in the form of monomer, transverse dimer, and adjacent dimer configurations. The electronic structure of the perylene monomers and dimers were characterized via steady-state absorption and fluorescence spectroscopy. Initial insights into their excited-state dynamics were gleaned from relative fluorescence intensity measurements, which indicated that a new nonradiative decay pathway emerges in the dimers. Femtosecond visible transient absorption spectroscopy was subsequently used to elucidate the excited-state dynamics. A new excited-state absorption feature grows in on the tens of picosecond timescale in the dimers, which is attributed to the formation of perylene anions and cations resulting from symmetry-breaking charge transfer. Given the close proximity required for symmetry-breaking charge transfer, the results shed promising light on the prospect of singlet fission in DNA-templated molecular aggregates

    Probing DNA Structural Heterogeneity by Identifying Conformational Subensembles of a Bicovalently Bound Cyanine Dye

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    DNA is a re-configurable, biological information-storage unit, and much remains to be learned about its heterogeneous structural dynamics. For example, while it is known that molecular dyes templated onto DNA exhibit increased photostability, the mechanism by which the structural dynamics of DNA affect the dye photophysics remains unknown. Here, we use femtosecond, two-dimensional electronic spectroscopy measurements of a cyanine dye, Cy5, to probe local conformations in samples of single-stranded DNA (ssDNA–Cy5), double-stranded DNA (dsDNA–Cy5), and Holliday junction DNA (HJ–DNA–Cy5). A line shape analysis of the 2D spectra reveals a strong excitation–emission correlation present in only the dsDNA–Cy5 complex, which is a signature of inhomogeneous broadening. Molecular dynamics simulations support the conclusion that this inhomogeneous broadening arises from a nearly degenerate conformer found only in the dsDNA–Cy5 complex. These insights will support future studies on DNA’s structural heterogeneity
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