Investigation of fill factor losses on 20.2% efficient n‐type mono‐like silicon solar cells with laser contact opening

Large area (243.36 cm²) back‐junction passivated emitter, rear totally diffused (PERT) solar cells with laser contact opening (LCO) on n‐type mono‐like crystalline Si with efficiencies of 20.2% are presented. Boron emitters with high electrical quality (implied open circuit voltage iV_OC up to 700 mV) are formed during a co‐diffusion step using SiO_x:B layers. Increasing the rear metal contact coverage, we observed a decrease in fill factor (FF) instead of the expected increase due to the decrease of the back side series resistance. We show that it can be attributed to recombination centers (RCs) in the space charge region underneath the contact spots inducing an increasing second diode contribution. The presented empirical model for the RCs implemented in Synopsys Sentaurus TCAD allows for a successful reproduction of the FF, pseudo FF and V_OC behaviour with contact coverage. According to this model, the RCs induced by laser ablation and subsequently evaporation of Al have a shallow exponential distribution with a characteristic length of L_T = 0.2 µm and an effective surface density of N *_T0 = 25 cm^–1. (© 2016 WILEY‐VCH Verlag GmbH &Co. KGaA, Weinheim)     

Model based prediction of the trap limited diffusion of hydrogen in post‐hydrogenated amorphous silicon

The diffusion of hydrogen within an hydrogenated amorphous silicon (a‐Si:H) layer is based on a trap limited process. Therefore, the diffusion becomes a self‐limiting process with a decreasing diffusion velocity for increasing hydrogen content. In consequence, there is a strong demand for accurate experimental determination of the hydrogen distribution. Nuclear resonant reaction analysis (NRRA) offers the possibility of a non‐destructive measurement of the hydrogen distribution in condensed matter like a‐Si:H thin films. However, the availability of a particle accelerator for NRR‐analysis is limited and the related costs are high. In comparison, Fourier transform infrared spectroscopy (FTIR) is also a common method to determine the total hydrogen content of an a‐Si:H layer. FTIR spectrometers are practical table‐top units but lack spatial resolution. In this study, an approach is discussed that greatly reduces the need for complex and expensive NRR‐analysis. A model based prediction of hydrogen depth profiles based on a single NRRA measurement and further FTIR measurements enables to investigate the trap limited hydrogen diffusion within a‐Si:H. The model is validated by hydrogen diffusion experiments during the post‐hydrogenation of hydrogen‐free sputtered a‐Si. The model based prediction of hydrogen depth profiles in a‐Si:H allows more precise design of experiments, prevents misinterpretations, avoids unnecessary NRRA measurements and thus saves time and expense. (© 2016 WILEY‐VCH Verlag GmbH &Co. KGaA, Weinheim)     

Physico-chemical properties and possible photocatalytic applications of titanate nanotubes synthesized via hydrothermal method

Titanate nanotubes (TNTs) were prepared from TiO₂ P25 via hydrothermal method. The reaction temperature was 130 or 140 °C and the reaction time was 24 or 48 h. The samples were characterized by transmission electron microscopy, X-ray diffraction, thermogravimetry and N₂ adsorption as well as Raman, FTIR-DRS and UV-vis/DR spectroscopy. The obtained samples exhibited similar properties, regardless of the preparation temperature and time. The most notable difference between properties of TNTs prepared under different conditions was observed in case of BET surface area, which was increasing from 386 to 478 m²/g along with increasing the reaction time and temperature. Based on TEM, XRD and TG measurements we have suggested that the structure of TNTs was H₂Ti₂O₄(OH)₂. The TEM and Raman spectroscopy measurements showed that the obtained products contained also low amount of anatase phase. The TNTs exhibited no photoactivity towards degradation of model azo dye Acid Red 18. However, TNTs were successfully applied for photocatalytic generation of CH₄ and H₂ in a solution of acetic acid. The amount of methane produced with application of TNTs synthesized at 140 °C was about 2.5 times higher than that generated with use of TiO₂ P25. To the best of our knowledge this is a first report on the photocatalytic generation of hydrocarbons using TNTs in the current state of the art.     

Connecting the quantum and classical worlds

By considering (non‐relativistic) quantum mechanics as it is done in practice in particular in condensed‐matter physics, it is argued that a deterministic, unitary time evolution within a chosen Hilbert space always has a limited scope, leaving a lot of room for embedding the quantum‐classical transition into our current theories without recurring to difficult‐to‐accept interpretations of quantum mechanics. Nonunitary projections to initial and final states, the breaking of time‐reversal symmetry, a change of Hilbert space, and the introduction of classical concepts such as external potentials or localized atomic nuclei are widespread in quantum mechanical calculations. Furthermore, quantum systems require classical environments that enable the symmetry breaking that is necessary for creating the atomic configurations of molecules and crystals. This paper argues that such classical environments are provided by finite‐temperature macroscopic systems in which the range of quantum correlations and entanglement is limited. This leads to classical behavior on larger scales, and to collapse‐like events in all dynamical processes that become coupled to the thermalized degrees of freedom.

     

Spatial unmasking of nearby pure-tone targets in a simulated anechoic environment

Detection thresholds were measured for different spatial configurations of 500- and 1000-Hz pure-tone targets and broadband maskers. Sources were simulated using individually measured head-related transfer functions (HRTFs) for source positions varying in both azimuth and distance. For the spatial configurations tested, thresholds ranged over 50 dB, primarily as a result of large changes in the target-to-masker ratio (TMR) with changes in target and masker locations. Intersubject differences in both HRTFs and in binaural sensitivity were large; however, the overall pattern of results was similar across subjects. As expected, detection thresholds were generally smaller when the target and masker were separated in azimuth than when they were at the same location. However, in some cases, azimuthal separation of target and masker yielded little change or even a small increase in detection threshold. Significant intersubject differences occurred as a result both of differences in monaural and binaural acoustic cues in the individualized HRTFs and of different binaural contributions to performance. Model predictions captured general trends in the pattern of spatial unmasking. However, subject-specific model predictions did not account for the observed individual differences in performance, even after taking into account individual differences in HRTF measurements and overall binaural sensitivity. These results suggest that individuals differ not only in their overall sensitivity to binaural cues, but also in how their binaural sensitivity varies with the spatial position of (and interaural differences in) the masker.     

Behaviour of LiF:Mg,Cu,P and LiF:Mg,Ti thermoluminescent detectors for electron doses up to 1 MGy

The behaviour of LiF:Mg,Cu,P and LiF:Mg,Ti detectors at ultra-high doses up to 1 MGy, has been investigated. The presence of the ultra-high-temperature peak (450 °C) of reproducible properties was observed in various batches of LiF:Mg,Cu,P, confirming earlier findings. The results indicate that this peak is not an effect of random impurities nor intrinsic effects of LiF, but it is rather connected with the doping.A parameter called ultra-high temperature ratio (UHTR) was defined in order to quantify the observed changes of LiF:Mg,Cu,P glow-curve shape at very high doses and very high temperatures. The use of this parameter allows to determine an absorbed dose in the range from 1 kGy to 1 MGy. This new method of high-dose dosimetry makes LiF:Mg,Cu,P a unique dosimeter, which is capable to cover at least 12 orders of magnitude of dose range: from a microgray to a megagray.     

Studies on Pyrazine Derivatives,XLII: Synthesis and Tuberculostatic Activity of 6-(1,4-Dioxa-8-azaspiro- [4, 5]-decano)- and 6-(1-Ethoxycarbonylpiperazino)- pyrazinocarboxylic Acid Derivatives

The 2-cyano-6-chloropyrazine's chlorine atom reactivity was substituted with amines 1,4-dioxo-8-azaspiro-[4, 5]-decane and 1-ethoxycarbonylpiperazine. The substrates thus obtained were used in the syntheses of the new derivatives, which were tested for their tuberculostatic activity. Minimum inhibitory concentration (MIC) value of the most active ones ( 5b , 12a , 14b , 16b , 21b ) was 25 μ g/mL.     

Preparation of partially functionalised resorcinarene derivatives

The conditions for synthesis of mono-, di- and trifunctionalised resorcinarenes by catalysed Mannich reaction are described. A series of these compounds are functionalised with different functional groups.     

Synthesis and Properties of Isobicyclo‐DNA

We present the synthesis of the isobicyclo‐DNA building blocks with the nucleobases A, C, G and T, as well as biophysical and biological properties of oligonucleotides derived thereof. The synthesis of the sugar part was achieved in 5 steps starting from a known intermediate of the tricyclo‐DNA synthesis. Dodecamers containing single isobicyclo‐thymidine incorporations, fully modified A‐ and T‐containing sequences, and fully modified oligonucleotides containing all four bases were synthesized and characterized. Isobicyclo‐DNA forms stable duplexes with natural nucleic acids with a pronounced preference for DNA over RNA as complements. The most stable duplexes, however, arise by self‐pairing. Isobicyclo‐DNA forms preferentially B‐DNA‐like duplexes with DNA and A‐like duplexes with complementary RNA as determined by circular dichroism (CD) spectroscopy. Self‐paired duplexes show a yet unknown structure, as judged from CD spectroscopy. Biochemical tests revealed that isobicyclo‐DNA is stable in fetal bovine serum and does not elicit RNaseH activity.