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Now showing 1 - 8 of 8
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    Conversion of carbon dioxide into storable solar fuels using solar energy
    (London [u.a.] : Institute of Physics, 2019) Ennaceri, Houda; Abel, Bernd
    Nowadays, there are two main energy and environmental concerns, the first is the risk of running out of fossil fuels in the next few decades, and the second is the alarming increase in the carbon dioxide concentrations in the atmosphere, causing global warming and rise of see levels. Therefore, solar-driven technologies represent a substantial solution to fossil fuels dependence, global warming and climate change. Unlike most scientific research, which aim to use solar energy to generate electricity, solar energy can also be harnessed by recycling the carbon dioxide in the atmosphere through high-tech artificial photosynthesis with the objective of producing storable and liquid solar fuels from CO2 and water. There are two types of solar fuels, the first being hydrogen, which can be produced by mean of water splitting processes. The combustion of hydrogen generates water, which is a completely clean option for the environment. The second type of solar fuels consists of carbon-based fuels, such as methane (CH4), carbon monoxide (CO), or alcohols such as methanol (CH3OH) and ethanol (C2H5OH). The production to liquid solar fuels liquid fuels is of great interest, since they can be used in the current industrial infrastructures such as the automobiles' sector, without substantial changes in the vehicles' internal combustion engines. Therefore, guaranteeing a smooth transition from fossil fuel energy to renewable energy without radical economic consequences. Also, and most importantly, when these solar fuels are burned, they will only release the exact amount of CO2 which was initially used, which represents an optimal process for sustainable transport.
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    Developing a Laser Induced Liquid Beam Ion Desorption Spectral Database as Reference for Spaceborne Mass Spectrometers
    (Malden, Mass. : American Geophysical Union, 2022) Klenner, Fabian; Umair, Muhammad; Walter, Sebastian H. G.; Khawaja, Nozair; Hillier, Jon; Nölle, Lenz; Zou, Zenghui; Napoleoni, Maryse; Sanderink, Arnaud; Zuschneid, Wilhelm; Abel, Bernd; Postberg, Frank
    Spaceborne impact ionization mass spectrometers, such as the Cosmic Dust Analyzer on board the past Cassini spacecraft or the SUrface Dust Analyzer being built for NASA's upcoming Europa Clipper mission, are of crucial importance for the exploration of icy moons in the Solar System, such as Saturn's moon Enceladus or Jupiter's moon Europa. For the interpretation of data produced by these instruments, analogue experiments on Earth are essential. To date, thousands of laboratory mass spectra have been recorded with an analogue experiment for impact ionization mass spectrometers. Simulation of mass spectra of ice grains in space is achieved by a Laser Induced Liquid Beam Ion Desorption (LILBID) approach. The desorbed cations or anions are analyzed in a time-of-flight mass spectrometer. The amount of unstructured raw data is increasingly challenging to sort, process, interpret and compare with data from space. Thus far this has been achieved manually for individual mass spectra because no database containing the recorded reference spectra was available. Here we describe the development of a comprehensive, extendable database containing cation and anion mass spectra from the laboratory LILBID facility. The database is based on a Relational Database Management System with a web server interface and enables filtering of the laboratory data using a wide range of parameters. The mass spectra can be compared not only with data from past and future space missions but also mass spectral data generated by other, terrestrial, techniques. The validated and approved subset of the database is available for general public (https://lilbid-db.planet.fu-berlin.de).
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    Cryo-printed microfluidics enable rapid prototyping for optical-cell analysis
    (Heidelberg : Springer, 2022) Garmasukis, Rokas; Hackl, Claudia; Dusny, Christian; Elsner, Christian; Charvat, Ales; Schmid, Andreas; Abel, Bernd
    This paper highlights an innovative, low-cost rapid-prototyping method for generating microfluidic chips with extraordinary short fabrication times of only a few minutes. Microchannels and inlet/outlet ports are created by controlled deposition of aqueous microdroplets on a cooled surface resulting in printed ice microstructures, which are in turn coated with a UV-curable acrylic cover layer. Thawing leaves an inverse imprint as a microchannel structure. For an exemplary case, we applied this technology for creating a microfluidic chip for cell-customized optical-cell analysis. The chip design includes containers for cell cultivation and analysis. Container shape, length, position, and angle relative to the main channel were iteratively optimized to cultivate and analyze different cell types. With the chip, we performed physiological analyses of morphologically distinct prokaryotic Corynebacterium glutamicum DM1919, eukaryotic Hansenula polymorpha RB11 MOX-GFP, and phototrophic Synechocystis sp. PCC 6803 cells via quantitative time-lapse fluorescence microscopy. The technology is not limited to rapid prototyping of complex biocompatible microfluidics. Further exploration may include printing with different materials other than water, printing on other substrates in-situ biofunctionalization, the inclusion of electrodes and many other applications.
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    Investigation of room temperature multispin-assisted bulk diamond 13C hyperpolarization at low magnetic fields
    (Bristol : IOP Publ., 2018) Wunderlich, Ralf; Kohlrautz, Jonas; Abel, Bernd; Haase, Jürgen; Meijer, Jan
    In this work we investigated the time behavior of the polarization of bulk 13C nuclei in diamond above the thermal equilibrium. This nonthermal nuclear hyperpolarization is achieved by cross relaxation between two nitrogen related paramagnetic defect species in diamond in combination with optical pumping. The decay of the hyperpolarization at four different magnetic fields is measured. Furthermore, we use the comparison with conventional nuclear resonance measurements to identify the involved distances of the nuclear spin with respect to the defects and therefore the coupling strengths. Also, a careful look at the linewidth of the signal give valuable information to piece together the puzzle of the hyperpolarization mechanism.
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    Weak electron irradiation suppresses the anomalous magnetization of N-doped diamond crystals
    (Weinheim : Wiley-VCH, 2021) Setzer, Annette; Esquinazi, Pablo D.; Daikos, Olesya; Scherzer, Tom; Pöppl, Andreas; Staacke, Robert; Lühmann, Tobias; Pezzagna, Sebastien; Knolle, Wolfgang; Buga, Sergei; Abel, Bernd; Meijer, Jan
    Several diamond bulk crystals with a concentration of electrically neutral single substitutional nitrogen atoms of ≲80 ppm, the so-called C or P1 centers, are irradiated with electrons at 10 MeV energy and low fluence. The results show a complete suppression of the irreversible behavior in field and temperature of the magnetization below 30 K, after a decrease in ≲40 ppm in the concentration of C centers produced by the electron irradiation. This result indicates that magnetic C centers are at the origin of the large hysteretic behavior found recently in nitrogen-doped diamond crystals. This is remarkable because of the relatively low density of C centers, stressing the extraordinary role of the C centers in triggering those phenomena in diamond at relatively high temperatures. After annealing the samples at high temperatures in vacuum, the hysteretic behavior is partially recovered.
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    Magnetic field and angle-dependent photoluminescence of a fiber-coupled nitrogen vacancy rich diamond
    (Melville, NY : American Inst. of Physics, 2021) Wunderlich, Ralf; Staacke, Robert; Knolle, Wolfgang; Abel, Bernd; Meijer, Jan
    Here, we investigate the magnetic field dependent photoluminescence (PL) of a fiber-coupled diamond single crystal with a high density of nitrogen vacancy (NV) centers. Angle-dependent magnetic field sweep measurements between 0 and 111 mT were performed using an oscillating illumination combined with lock-in techniques. Besides the expected superposed PL of differently oriented NV centers, a zoo of features in the PL are found. These features can be associated with level anti-crossings and cross relaxations. In particular, PL measurements allowed us to detect auto-cross relaxation between coupled NV centers. Moreover, the PL measurements at low magnetic fields show dips suggesting an interaction of NV centers with additional spin defects. The results presented here are not only a study for NV-based fiber-coupled sensors made of diamond, but also show a way to investigate with manageable effort and purely an optical multispin interaction with at least one NV center as a constituent.
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    Robust nuclear hyperpolarization driven by strongly coupled nitrogen vacancy centers
    (Melville, NY : American Inst. of Physics, 2021) Wunderlich, Ralf; Staacke, Robert; Knolle, Wolfgang; Abel, Bernd; Haase, Jürgen; Meijer, Jan
    Nuclear magnetic resonance techniques are widely used in the natural sciences but they lack sensitivity. Therefore, large sample volumes or long measurement times are necessary. In this work, we investigate the polarization of bulk 13C nuclei in a diamond above the thermal equilibrium at room temperature. Previously studied mechanisms utilize direct coupling to nitrogen vacancy centers or the additional assistance of substitutional nitrogen impurities for this purpose. We exploit strongly coupled nitrogen vacancy centers as polarization sources. We study two approaches to transfer the optically induced polarization of the electron spins of the nitrogen vacancy centers to nearby nuclear spins. First, the electron-nuclear polarization transfer is achieved by energy matching conditions or, second, by magnetic field sweeps inducing Landau–Zener-like transitions. Simulations according to a quantum mechanical system consisting of two coupled nitrogen vacancy centers and a weakly coupled 13C spin show an excellent agreement with the experimental data. Both approaches allow a reduction of the measurement time by roughly three orders of magnitude.
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    Efficient synthesis of triarylamine-based dyes for p-type dye-sensitized solar cells
    (London : Nature Publishing Group, 2016) Wild, Martin; Griebel, Jan; Hajduk, Anna; Friedrich, Dirk; Stark, Annegret; Abel, Bernd; Siefermann, Katrin R.
    The class of triarylamine-based dyes has proven great potential as efficient light absorbers in inverse (p-type) dye sensitized solar cells (DSSCs). However, detailed investigation and further improvement of p-type DSSCs is strongly hindered by the fact that available synthesis routes of triarylamine-based dyes are inefficient and particularly demanding with regard to time and costs. Here, we report on an efficient synthesis strategy for triarylamine-based dyes for p-type DSSCs. A protocol for the synthesis of the dye-precursor (4-(bis(4-bromophenyl)amino)benzoic acid) is presented along with its X-ray crystal structure. The dye precursor is obtained from the commercially available 4(diphenylamino)benzaldehyde in a yield of 87% and serves as a starting point for the synthesis of various triarylamine-based dyes. Starting from the precursor we further describe a synthesis protocol for the dye 4-{bis[4′-(2,2-dicyanovinyl)-[1,1′-biphenyl]-4-yl]amino}benzoic acid (also known as dye P4) in a yield of 74%. All synthesis steps are characterized by high yields and high purities without the need for laborious purification steps and thus fulfill essential requirements for scale-up.