Magnification of label maps with a topology-preserving level-set method

Image segmentation aims at partitioning an image into multiple segments. The application of this procedure produces a label map (also referred to as segmentation map) that classifies the pixels of the original image. In contrast to "natural" images, label maps are nominal-scale images, typically represented as integer-valued images. Nominal-scaled label maps can also appear as a representation of the raw data in areas, such as in geostatistics. In some applications, the original resolution of a label map does not suffice and a larger size map has to be generated. In this paper, we present a magnification algorithm for label maps and nominal images. The main property of our method is that it preserves the topology during the magnification process, which means that no isolated pixel vanishes. To the best of our knowledge, apart from nearest-neighbor interpolation, the problem of label map magnification has not previously been addressed in the literature. The main idea of the proposed method is to accomplish a boundary refinement by smoothing the regions' boundaries on a finer grid. The method relies on well known methods, namely, the fundamental operations of morphological image processing-erosion and dilation-and the level-set method. The level-set method is well suited for our purposes since it does not depend on a parametrization and it is numerically stable. The topological flexibility of the level-set method-often found to be an advantage in applications-is a drawback here, since the topology of the original label map should be preserved. However, using the so-called simple point criterion from digital topology, one can adapt the conventional level-set method so that the topology will not be modified throughout the magnification procedure.     

Paradox of richness: a cognitive model of media choice

Researchers have long studied the effects of social presence and media richness on media choice and the effects of media use. This focus on social presence and social psychological theories has led to valuable research on communication. However, little research (either empirical or theoretical) has been done to understand the ways in which media choices influence the cognitive processes that underlie communication. In this paper, we present a cognitive-based view of media choice and media use, based on dual process theories of cognition, which argue that in order for individuals to systematically process messages, they must be motivated to process the message and have the ability to process it. We argue that the use of rich media high in social presence induces increased motivation but decreases the ability to process information, while the use of lean media low in social presence induces decreased motivation but increases the ability to process information. The paradox of richness lies in its duality of impact: from a cognitive perspective, rich media high in social presence simultaneously acts to both improve and impair performance.     

3G移动电话的系统级LSI

引言 无线移动电话仅具备语音功能的时代已经离我们远去了.目前的3G手机更多的是作为多媒体系统,提供彩显、游戏、音频、视频、相机、蓝牙、GPS、WLAN、高速广域数据服务以及其他高级特性.由于功能非常之多,因此处理新型3G电话比处理仅有语音功能的2G电话要复杂5倍至10倍,在应用处理方面则要求更高.     

Analysis of Current–Voltage Measurements on Long-Wavelength HgCdTe Photodiodes Fabricated on Si Composite Substrates

We have performed a detailed study of dark current versus voltage to understand existing limitations in dark current and address the nonuniformity of dark current in devices fabricated on HgCdTe grown on silicon substrates. One interesting observation is that trap-assisted tunneling, g-r currents, are not found close to zero bias in certain devices. Devices from the low end of the R ₀ A distribution show heavy shunting paths close to zero bias. We believe that these shunting paths may be the limiting cause of tail distributions in fabricated focal plane array tail distributions. Possible causes for these shunting paths are surface charges associated with dislocation cores and impurity gettering at dislocation cores. The measured non-anti-reflection (AR)-coated quantum efficiency (QE) was 0.576 at 78 K and displays the classical response versus wavelength. The measured QE on isolated single devices is consistent with the 256 × 256 focal-plane array mean QE. Obtained average dark currents are on the order of mid 10⁻⁵ A cm^–2, which is one order of magnitude higher than dark currents obtained from arrays on lattice-matched substrates. On average, arrays on lattice-mismatched substrates show performance characteristics inferior to those of arrays fabricated on lattice-matched substrates. This inferior performance is due to array pixel operability, as can be seen from the tail of the distribution and the average dark currents, which are one order of magnitude higher than those obtained on lattice-matched substrates.     

X‐Ray Spectroscopic Investigation of Chlorinated Graphene: Surface Structure and Electronic Effects

Chemical doping of graphene represents a powerful means of tailoring its electronic properties. Synchrotron‐based X‐ray spectroscopy offers an effective route to investigate the surface electronic and chemical states of functionalizing dopants. In this work, a suite of X‐ray techniques is used, including near edge X‐ray absorption fine structure spectroscopy, X‐ray photoemission spectroscopy, and photoemission threshold measurements, to systematically study plasma‐based chlorinated graphene on different substrates, with special focus on its dopant concentration, surface binding energy, bonding configuration, and work function shift. Detailed spectroscopic evidence of C–Cl bond formation at the surface of single layer graphene and correlation of the magnitude of p‐type doping with the surface coverage of adsorbed chlorine is demonstrated for the first time. It is shown that the chlorination process is a highly nonintrusive doping technology, which can effectively produce strongly p‐doped graphene with the 2D nature and long‐range periodicity of the electronic structure of graphene intact. The measurements also reveal that the interaction between graphene and chlorine atoms shows strong substrate effects in terms of both surface coverage and work function shift.     

Tuning the optical absorption of potential blue emitters

The quest for more efficient blue emitters to be applied in organic light-emitting diodes is one of the challenging tasks of contemporary nanotechnologies. An approach to enhance substantially the intrinsic efficiency of luminescent organic molecules is the so-called thermally activated delayed fluorescence. A prerequisite for its occurrence is a vanishing energy separation between the first singlet and triplet excited states. A series of donor–acceptor molecules is investigated theoretically within this study in order to validate a molecular model for design of efficient organic blue emitters with closely spaced singlet and triplet excited states. The model is based on meta-linkage of the donor and acceptor residues to a spacer ensuring frontier molecular orbitals partitioning. The optimal geometries of the molecules are obtained with density functional theory (B3LYP/6-31G^*) and the singlet and triplet absorption spectra are simulated within the time-dependent density functional framework. The excited singlet-triplet energy gap is estimated and correlated to structural and energetic characteristics of the donors and acceptors. Several requirements for achieving high-energy triplet states at the molecular level in such donor–acceptor systems are outlined, the main being disjoint character of the molecular orbitals on the spacer and sufficient energy separation of the two topmost occupied orbitals. It is shown that by variation of the acceptor moiety the optical absorption transitions of the compounds can be fine-tuned in a systematic fashion. Molecules with degenerate singlet and triplet first excited states are proposed, combining bisdimethylaminotriphenylamine or phenoxazine as donors with diphenyloxadiazole or diphenyl-2,2′-bipyridine as acceptors. Bipolar molecules derived from this model could be used as prospective building blocks for efficient emissive materials in blue organic light-emitting diodes.     

Atomic Insights into the Enhanced Surface Stability in High Voltage Cathode Materials by Ultrathin Coating

Surface properties of electrode materials play a critical role in the function of batteries. Therefore, surface modifications, such as coatings, have been widely used to improve battery performance. Understanding how these coatings function to improve battery performance is crucial for both scientific research and applications. In this study the electrochemical performance of coated and uncoated LiNi_0.5Mn_1.5O₄ (LNMO) electrodes is correlated with ensemble‐averaged soft X‐ray absorption spectroscopy (XAS) and spatially resolved scanning transmission electron microscopy‐electron energy loss spectroscopy (STEM‐EELS) to illustrate the mechanism of how ultrathin layer Al₂O₃ coatings improve the cycle life of LiNi_0.5Mn_1.5O₄. Mn²⁺ evolution on the surface is clearly observed in the uncoated sample, which results from the reaction between the electrolytic solution and the surfaces of LiNi_0.5Mn_1.5O₄ particles, and also possibly atomic structure reconstructions and oxygen loss from the surface region in LiNi_0.5Mn_1.5O₄. The coating effectively suppresses Mn²⁺ evolution and improves the battery performance by decelerating the impedance buildup from the surface passivation. This study demonstrates the importance of combining ensemble‐averaged techniques (e.g., XAS) with localized techniques (e.g., STEM‐EELS), as the latter may yield unrepresentative information due to the limited number of studied particles, and sheds light on the design of future coating processes and materials.     

Ultrathin Polydopamine Films with Phospholipid Nanodiscs Containing a Glycophorin A Domain

Cellular membranes have long served as an inspiration for nanomaterial research. The preparation of ultrathin polydopamine (PDA) films with integrated protein pores containing phospholipids and an embedded domain of a membrane protein glycophorin A as simplified cell membrane mimics is reported. Large area, ultrathin PDA films are obtained by electropolymerization on gold surfaces with 10–18 nm thickness and dimensions of up to 2.5 cm². The films are transferred from gold to various other substrates such as nylon mesh, silicon, or substrates containing holes in the micrometer range, and they remain intact even after transfer. The novel transfer technique gives access to freestanding PDA films that remain stable even at the air interfaces with elastic moduli of ≈6–12 GPa, which are higher than any other PDA films reported before. As the PDA film thickness is within the range of cellular membranes, monodisperse protein nanopores, so‐called “nanodiscs,” are integrated as functional entities. These nanodisc‐containing PDA films can serve as semi‐permeable films, in which the embedded pores control material transport. In the future, these simplified cell membrane mimics may offer structural investigations of the embedded membrane proteins to receive an improved understanding of protein‐mediated transport processes in cellular membranes.