Organic Photodiodes: The Future of Full Color Detection and Image Sensing

Major growth in the image sensor market is largely as a result of the expansion of digital imaging into cameras, whether stand‐alone or integrated within smart cellular phones or automotive vehicles. Applications in biomedicine, education, environmental monitoring, optical communications, pharmaceutics and machine vision are also driving the development of imaging technologies. Organic photodiodes (OPDs) are now being investigated for existing imaging technologies, as their properties make them interesting candidates for these applications. OPDs offer cheaper processing methods, devices that are light, flexible and compatible with large (or small) areas, and the ability to tune the photophysical and optoelectronic properties ? both at a material and device level. Although the concept of OPDs has been around for some time, it is only relatively recently that significant progress has been made, with their performance now reaching the point that they are beginning to rival their inorganic counterparts in a number of performance criteria including the linear dynamic range, detectivity, and color selectivity. This review covers the progress made in the OPD field, describing their development as well as the challenges and opportunities.     

Development of a proton-transfer reaction-linear ion trap mass spectrometer for quantitative determination of volatile organic compounds

Currently, proton-transfer reaction mass spectrometry (PTR-MS) allows for quantitative determination of volatile organic compounds in real time at concentrations in the low ppt range, but cannot differentiate isomers or isobaric molecules, using the conventional quadrupole mass filter. Here we pursue the application of linear quadrupole ion trap (LIT) mass spectrometry in combination with proton-transfer reaction chemical ionization to provide the advantages of specificity from MS/MS. A commercial PTR-MS platform composed of a quadrupole mass filter with the addition of end cap electrodes enabled the mass filter to operate as a linear ion trap. The rf drive electronics were adapted to enable the application of dipolar excitation to opposing rods, for collision-induced dissociation (CID) of trapped ions. This adaptation enabled ion isolation, ion activation, and mass analysis. The utility of the PTR-LIT was demonstrated by distinguishing between the isomeric isoprene oxidation pair, methyl vinyl ketone (MVK) and methacrolein (MACR). The CID voltage was adjusted to maximize the m/ z 41 to 43 fragment ratio of MACR while still maintaining adequate sensitivity. Linear calibration curves for MVK and MACR fragments at m/ z 41 and 43 were obtained with limits of detection of approximately 100 ppt, which should enable ambient measurements. Finally, the PTR-LIT method was compared to an established GC/MS method by quantifying MVK and MACR production during a smog chamber isoprene-NO x irradiation experiment.     

Die Hauptstrommessung als Innovation in der industriellen Helium‐Dichtheitsprüfung

Main flow measurement as an innovation in industrial helium leak testing So‐called main flow measurement with its special vacuum pump stations brings numerous technological advantages to helium leak testing, making it possible to significantly enhance the cost profile and efficiency of industrial inline test systems. The suppression of ambient influences and the achievability of the shortest clock rates are the key factors for the successful automation of test processes. The reduction in helium consumption and the achievable energy savings improve the cost benefits of investing in a test system working on the main flow principle still further. PINK leak test systems are equipped with numerous diagnostic features ranging from continuous self‐monitoring and fully automatic leak rate control to the independent calculation of new test parameters.     

Tuning the Structural and Optoelectronic Properties of Cs2AgBiBr6 Double-Perovskite Single Crystals through Alkali-Metal Substitution

Lead-free double perovskites have great potential as stable and nontoxic optoelectronic materials. Recently, Cs₂AgBiBr₆ has emerged as a promising material, with suboptimal photon-to-charge carrier conversion efficiency, yet well suited for high-energy photon-detection applications. Here, the optoelectronic and structural properties of pure Cs₂AgBiBr₆ and alkali-metal-substituted (Cs_1−xY_x)₂AgBiBr₆ (Y: Rb⁺, K⁺, Na⁺; x = 0.02) single crystals are investigated. Strikingly, alkali-substitution entails a tunability to the material system in its response to X-rays and structural properties that is most strongly revealed in Rb-substituted compounds whose X-ray sensitivity outperforms other double-perovskite-based devices reported. While the fundamental nature and magnitude of the bandgap remains unchanged, the alkali-substituted materials exhibit a threefold boost in their fundamental carrier recombination lifetime at room temperature. Moreover, an enhanced electron–acoustic phonon scattering is found compared to Cs₂AgBiBr₆. The study thus paves the way for employing cation substitution to tune the properties of double perovskites toward a new material platform for optoelectronics.     

Beyond Activated Carbon: Graphite‐Cathode‐Derived Li‐Ion Pseudocapacitors with High Energy and High Power Densities

Supercapacitors have aroused considerable attention due to their high power capability, which enables charge storage/output in minutes or even seconds. However, to achieve a high energy density in a supercapacitor has been a long‐standing challenge. Here, graphite is reported as a high‐energy alternative to the frequently used activated carbon (AC) cathode for supercapacitor application due to its unique Faradaic pseudocapacitive anion intercalation behavior. The graphite cathode manifests both higher gravimetric and volumetric energy density (498 Wh kg^?1 and 431.2 Wh l^?1) than an AC cathode (234 Wh kg^?1 and 83.5 Wh l^?1) with peak power densities of 43.6 kW kg^?1 and 37.75 kW l^?1. A new type of Li‐ion pseudocapacitor (LIpC) is thus proposed and demonstrated with graphite as cathode and prelithiated graphite or Li₄Ti₅O₁₂ (LTO) as anode. The resultant graphite–graphite LIpCs deliver high energy densities of 167–233 Wh kg^?1 at power densities of 0.22–21.0 kW kg^?1 (based on active mass in both electrodes), much higher than 20–146 Wh kg^?1 of AC‐derived Li‐ion capacitors and 23–67 Wh kg^?1 of state‐of‐the‐art metal oxide pseudocapacitors. Excellent rate capability and cycling stability are further demonstrated for LTO‐graphite LIpCs.     

Correction to Fortier et al. (2008).

Reports an error in "Delay discrimination and reversal eyeblink classical conditioning in abstinent chronic alcoholics" by Catherine Brawn Fortier, Elizabeth M. Steffen, Ginette LaFleche, Jonathan R. Venne, John F. Disterhoft and Regina E. McGlinchey (Neuropsychology, 2008[Mar], Vol 22[2], 196-208). The lifetime drinking data listed in Table 1 on p. 198 was not correctly calculated and underestimated lifetime exposure to alcohol. The corrected lifetime variables from that table are included. (The following abstract of the original article appeared in record 2008-02526-007.) Evidence has shown that alcoholism leads to volume reductions in brain regions critical for associative learning using the eyeblink classical conditioning paradigm (EBCC). Evidence indicates that cerebellar shrinkage causes impairment in simple forms of EBCC, whereas changes in forebrain structures result in impairment in more complex tasks. In this study, the ability of abstinent alcoholics and matched control participants to acquire learned responses during delay discrimination and discrimination reversal was examined and related to severity of drinking history and neuropsychological performance. During discrimination learning, one tone (CS+) predicted the occurrence of an airpuff (unconditioned stimulus), and another tone (CS-) served as a neutral stimulus; then the significance of the tones was reversed. Alcoholics who learned the initial discrimination were impaired in acquiring the new CS+ after the tones reversed; this is a function that has previously been linked to forebrain structures. It is suggested that a factor important to alcoholic addiction may be the presence of alcoholic-related associative responses that interfere with the ability to learn new more adaptive associations. (PsycINFO Database Record (c) 2010 APA, all rights reserved)