TY  - JOUR
A1  - Ellis, S. C.
A1  - Bland-Hawthorn, Joss
A1  - Lawrence, J.
A1  - Horton, A. J.
A1  - Trinh, C.
A1  - Leon-Saval, S. G.
A1  - Shortridge, K.
A1  - Bryant, J.
A1  - Case, S.
A1  - Colless, M.
A1  - Couch, W.
A1  - Freeman, K.
A1  - Gers, L.
A1  - Glazebrook, K.
A1  - Haynes, R.
A1  - Lee, S.
A1  - Löhmannsröben, Hans-Gerd
A1  - O'Byrne, J.
A1  - Miziarski, S.
A1  - Roth, M.
A1  - Schmidt, B.
A1  - Tinney, C. G.
A1  - Zheng, J.
T1  - Suppression of the near-infrared OH night-sky lines with fibre Bragg gratings - first results
JF  - Monthly notices of the Royal Astronomical Society
N2  - The background noise between 1 and 1.8 ?mu m in ground-based instruments is dominated by atmospheric emission from hydroxyl molecules. We have built and commissioned a new instrument, the Gemini Near-infrared OH Suppression Integral Field Unit (IFU) System (GNOSIS), which suppresses 103 OH doublets between 1.47 and 1.7?mu m by a factor of 1000 with a resolving power of 10?000. We present the first results from the commissioning of GNOSIS using the IRIS2 spectrograph at the Anglo-Australian Telescope. We present measurements of sensitivity, background and throughput. The combined throughput of the GNOSIS fore-optics, grating unit and relay optics is 36?per cent, but this could be improved to 46?per cent with a more optimal design. We measure strong suppression of the OH lines, confirming that OH suppression with fibre Bragg gratings will be a powerful technology for low-resolution spectroscopy. The integrated OH suppressed background between 1.5 and 1.7 mu m is reduced by a factor of 9 compared to a control spectrum using the same system without suppression. The potential of low-resolution OH-suppressed spectroscopy is illustrated with example observations of Seyfert galaxies and a low-mass star. The GNOSIS background is dominated by detector dark current below 1.67 mu m and by thermal emission above 1.67 mu m. After subtracting these, we detect an unidentified residual interline component of 860 +/- 210 photons s-1 m-2?arcsec-2?mu m-1, comparable to previous measurements. This component is equally bright in the suppressed and control spectra. We have investigated the possible source of the interline component, but were unable to discriminate between a possible instrumental artefact and intrinsic atmospheric emission. Resolving the source of this emission is crucial for the design of fully optimized OH suppression spectrographs. The next-generation OH suppression spectrograph will be focused on resolving the source of the interline component, taking advantage of better optimization for a fibre Bragg grating feed incorporating refinements of design based on our findings from GNOSIS. We quantify the necessary improvements for an optimal OH suppressing fibre spectrograph design.
KW  - atmospheric effects
KW  - instrumentation: miscellaneous
KW  - infrared: general
Y1  - 2012
U6  - https://doi.org/10.1111/j.1365-2966.2012.21602.x
SN  - 0035-8711
VL  - 425
IS  - 3
SP  - 1682
EP  - 1695
PB  - Wiley-Blackwell
CY  - Hoboken
ER  - 
TY  - GEN
A1  - Dosche, Carsten
A1  - Kumke, Michael Uwe
A1  - Ariese, F.
A1  - Bader, Arjen N.
A1  - Gooijer, C.
A1  - Dosa, P. I.
A1  - Han, S.
A1  - Miljanic, O. S.
A1  - Vollhardt, K. Peter C.
A1  - Puchta, R.
A1  - Eikema Hommes, N. J. R. van
T1  - Shpol’skii spectroscopy and vibrational analysis of [N]phenylenes
N2  - Vibrationally resolved fluorescence spectra of four angular [N]phenylenes were recorded with laser excited Shpol’skii spectroscopy (LESS) in an n-octane matrix at 10 K. In general, the same vibrational frequencies were observed in the fluorescence excitation and emission spectra, indicating that the geometries of ground and electronically excited state are very similar. Because of intensity borrowing from the S2 state, vibrations of two different symmetries were observed in the fluorescence excitation spectra of angular [3]phenylene and zig-zag[5]phenylene. This finding allowed the location of the S2 state for these compounds. DFT calculations(RB3LYP/6-31G*) of the ground state vibrational frequencies were made. The calculated vibrational modes were in reasonably good agreement with the experimental data. A new very low-frequency vibration of approximately 100 cm-1 was predicted and experimentally confirmed for all [N]phenylenes investigated. This vibration seems to be unique for [N]phenylenes and is attributed to an in-plane movement of the carbon backbone.
T3  - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - paper 024 
Y1  - 2003
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus-13075
ER  - 
TY  - GEN
A1  - Dosche, Carsten
A1  - Kumke, Michael Uwe
A1  - Löhmannsröben, Hans-Gerd
A1  - Ariese, F.
A1  - Bader, Arjen N.
A1  - Gooijer, C.
A1  - Miljanic, O. S.
A1  - Iwamoto, M.
A1  - Vollhardt, K. Peter C.
A1  - Puchta, R. ; van Eikema Hommes, N. J. R.
T1  - Deuteration effects on the vibronic structure of the fluorescence spectra and the internal conversion rates of triangular [4]Phenylene
N2  - Deuteration effects on the vibronic structure of the emission and excitation spectra of triangular [4]phenylene (D3h[4]phenylene) were studied using laser-excited Shpolskii spectroscopy (LESS) in an octane matrix at 4.2 K. For correct assignment of the vibrational modes, the experimental results were compared with calculated frequencies (B3LYP/6-31G*). CH vibrations were identified by their characteristic isotopic shifts in the spectra of deuterated triangular [4]phenylenes. Two CC stretching modes, at 100 cm–1 and 1176 cm–1, suitable as probes for bond strength changes in the excited state, were identified. The isotope effect on the internal conversion rates of triangular [4]phenylene was evaluated from measurements of temperature dependent lifetime. Isotope dependency and the magnitude of the internal conversion rates indicate that internal conversion in triangular [4]phenylene is most likely induced by CH vibrations. The results obtained by LESS and lifetime measurements were compared with PM3 PECI calculations of the excited state structure. The theoretical results and the relation between ground and excited state vibration energies of the 1176 cm–1 probe vibration indicate a reduction of bond alternation of the central cyclohexatriene ring in the excited state.
T3  - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - paper 002 
Y1  - 2004
U6  - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus-11881
ER  - 
TY  - GEN
A1  - Ellis, S. C.
A1  - Bauer, S.
A1  - Bacigalupo, C.
A1  - Bland-Hawthorn, J.
A1  - Bryant, J. J.
A1  - Case, S.
A1  - Content, R.
A1  - Fechner, T.
A1  - Giannone, D.
A1  - Haynes, R.
A1  - Hernandez, E.
A1  - Horton, A. J.
A1  - Klauser, U.
A1  - Lawrence, J. S.
A1  - Leon-Saval, S. G.
A1  - Lindley, E.
A1  - Löhmannsröben, Hans-Gerd
A1  - Min, S. -S.
A1  - Pai, N.
A1  - Roth, M.
A1  - Shortridge, K.
A1  - Waller, L.
A1  - Xavier, Pascal
A1  - Zhelem, Ross
T1  - PRAXIS: an OH suppression optimised near infrared spectrograph
T2  - Ground-based and Airborne Instrumentation for Astronomy VII
N2  - The problem of atmospheric emission from OH molecules is a long standing problem for near-infrared astronomy. PRAXIS is a unique spectrograph which is fed by fibres that remove the OH background and is optimised specifically to benefit from OH-Suppression. The OH suppression is achieved with fibre Bragg gratings, which were tested successfully on the GNOSIS instrument. PRAXIS uses the same fibre Bragg gratings as GNOSIS in its first implementation, and will exploit new, cheaper and more efficient, multicore fibre Bragg gratings in the second implementation. The OH lines are suppressed by a factor of similar to 1000, and the expected increase in the signal-to-noise in the interline regions compared to GNOSIS is a factor of similar to 9 with the GNOSIS gratings and a factor of similar to 17 with the new gratings. PRAXIS will enable the full exploitation of OH suppression for the first time, which was not achieved by GNOSIS (a retrofit to an existing instrument that was not OH-Suppression optimised) due to high thermal emission, low spectrograph transmission and detector noise. PRAXIS has extremely low thermal emission, through the cooling of all significantly emitting parts, including the fore-optics, the fibre Bragg gratings, a long length of fibre, and the fibre slit, and an optical design that minimises leaks of thermal emission from outside the spectrograph. PRAXIS has low detector noise through the use of a Hawaii-2RG detector, and a high throughput through a efficient VPH based spectrograph. PRAXIS will determine the absolute level of the interline continuum and enable observations of individual objects via an IFU. In this paper we give a status update and report on acceptance tests.
KW  - Near infrared
KW  - spectroscopy
KW  - OH suppression
KW  - astrophotonics
KW  - fibre Bragg gratings
Y1  - 2018
SN  - 978-1-5106-1958-6
U6  - https://doi.org/10.1117/12.2311898
SN  - 0277-786X
SN  - 1996-756X
VL  - 10702
PB  - SPIE-INT Soc Optical Engineering
CY  - Bellingham
ER  - 
TY  - JOUR
A1  - Sangoro, Joshia R.
A1  - Iacob, C.
A1  - Agapov, A. L.
A1  - Wang, Yangyang
A1  - Berdzinski, Stefan
A1  - Rexhausen, Hans
A1  - Strehmel, Veronika
A1  - Friedrich, C.
A1  - Sokolov, A. P.
A1  - Kremer, F.
T1  - Decoupling of ionic conductivity from structural dynamics in polymerized ionic liquids
JF  - Soft matter
N2  - Charge transport and structural dynamics in low molecular weight and polymerized 1-vinyl-3-pentylimidazolium bis(trifluoromethylsulfonyl) imide ionic liquids (ILs) are investigated by a combination of broadband dielectric spectroscopy, dynamic mechanical spectroscopy and differential scanning calorimetry. While the dc conductivity and fluidity exhibit practically identical temperature dependence for the non-polymerized IL, a significant decoupling of ionic conduction from structural dynamics is observed for the polymerized IL. In addition, the dc conductivity of the polymerized IL exceeds that of its molecular counterpart by four orders of magnitude at their respective calorimetric glass transition temperatures. This is attributed to the unusually high mobility of the anions especially at lower temperatures when the structural dynamics is significantly slowed down. A simple physical explanation of the possible origin of the remarkable decoupling of ionic conductivity from structural dynamics is proposed.
Y1  - 2014
U6  - https://doi.org/10.1039/c3sm53202j
SN  - 1744-683X
SN  - 1744-6848
VL  - 10
IS  - 20
SP  - 3536
EP  - 3540
PB  - Royal Society of Chemistry
CY  - Cambridge
ER  - 
TY  - JOUR
A1  - Bland-Hawthorn, Joss
A1  - Ellis, S. C.
A1  - Leon-Saval, S. G.
A1  - Haynes, R.
A1  - Roth, Martin M.
A1  - Löhmannsröben, Hans-Gerd
A1  - Horton, A. J.
A1  - Cuby, J. -G.
A1  - Birks, T. A.
A1  - Lawrence, J. S.
A1  - Gillingham, P.
A1  - Ryder, S. D.
A1  - Trinh, C.
T1  - A complex multi-notch astronomical filter to suppress the bright infrared sky
JF  - Nature Communications
N2  - A long-standing and profound problem in astronomy is the difficulty in obtaining deep near-infrared observations due to the extreme brightness and variability of the night sky at these wavelengths. A solution to this problem is crucial if we are to obtain the deepest possible observations of the early Universe, as redshifted starlight from distant galaxies appears at these wavelengths. The atmospheric emission between 1,000 and 1,800 nm arises almost entirely from a forest of extremely bright, very narrow hydroxyl emission lines that varies on timescales of minutes. The astronomical community has long envisaged the prospect of selectively removing these lines, while retaining high throughput between them. Here we demonstrate such a filter for the first time, presenting results from the first on-sky tests. Its use on current 8 m telescopes and future 30 m telescopes will open up many new research avenues in the years to come.
Y1  - 2011
U6  - https://doi.org/10.1038/ncomms1584
SN  - 2041-1723
VL  - 2
IS  - 50
PB  - Nature Publ. Group
CY  - London
ER  - 
TY  - JOUR
A1  - Bartlett, Nate C. -M.
A1  - Jankunas, Justin
A1  - Goswami, Tapas
A1  - Zare, Richard N.
A1  - Bouakline, Foudhil
A1  - Althorpe, Stuart C.
T1  - Differential cross sections for H + D-2 -> HD(v '=2, j '=0,3,6,9) + D at center-of-mass collision energies of 1.25, 1.61, and 1.97 eV
JF  - Physical chemistry, chemical physics : a journal of European Chemical Societies
N2  - We have measured differential cross sections (DCSs) for the reaction H + D-2 -> HD- (v' = 2, j' = 0,3,6,9) + D at center-of-mass collision energies E-coll of 1.25, 1.61, and 1.97 eV using the photoloc technique. The DCSs show a strong dependence on the product rotational quantum number. For the HD(v' = 2, j' = 0) product, the DCS is bimodal but becomes oscillatory as the collision energy is increased. For the other product states, they are dominated by a single peak, which shifts from back to sideward scattering as j' increases, and they are in general less sensitive to changes in the collision energy. The experimental results are compared to quantum mechanical calculations and show good, but not fully quantitative agreement.
Y1  - 2011
U6  - https://doi.org/10.1039/c0cp02460k
SN  - 1463-9076
VL  - 13
IS  - 18
SP  - 8175
EP  - 8179
PB  - Royal Society of Chemistry
CY  - Cambridge
ER  - 
TY  - JOUR
A1  - Soliveres, Santiago
A1  - Manning, Peter
A1  - Prati, Daniel
A1  - Gossner, Martin M.
A1  - Alt, Fabian
A1  - Arndt, Hartmut
A1  - Baumgartner, Vanessa
A1  - Binkenstein, Julia
A1  - Birkhofer, Klaus
A1  - Blaser, Stefan
A1  - Bluethgen, Nico
A1  - Boch, Steffen
A1  - Boehm, Stefan
A1  - Boerschig, Carmen
A1  - Buscot, Francois
A1  - Diekoetter, Tim
A1  - Heinze, Johannes
A1  - Hoelzel, Norbert
A1  - Jung, Kirsten
A1  - Klaus, Valentin H.
A1  - Klein, Alexandra-Maria
A1  - Kleinebecker, Till
A1  - Klemmer, Sandra
A1  - Krauss, Jochen
A1  - Lange, Markus
A1  - Morris, E. Kathryn
A1  - Mueller, Joerg
A1  - Oelmann, Yvonne
A1  - Overmann, Jörg
A1  - Pasalic, Esther
A1  - Renner, Swen C.
A1  - Rillig, Matthias C.
A1  - Schaefer, H. Martin
A1  - Schloter, Michael
A1  - Schmitt, Barbara
A1  - Schoening, Ingo
A1  - Schrumpf, Marion
A1  - Sikorski, Johannes
A1  - Socher, Stephanie A.
A1  - Solly, Emily F.
A1  - Sonnemann, Ilja
A1  - Sorkau, Elisabeth
A1  - Steckel, Juliane
A1  - Steffan-Dewenter, Ingolf
A1  - Stempfhuber, Barbara
A1  - Tschapka, Marco
A1  - Tuerke, Manfred
A1  - Venter, Paul
A1  - Weiner, Christiane N.
A1  - Weisser, Wolfgang W.
A1  - Werner, Michael
A1  - Westphal, Catrin
A1  - Wilcke, Wolfgang
A1  - Wolters, Volkmar
A1  - Wubet, Tesfaye
A1  - Wurst, Susanne
A1  - Fischer, Markus
A1  - Allan, Eric
T1  - Locally rare species influence grassland ecosystem multifunctionality
JF  - Philosophical transactions of the Royal Society of London : B, Biological sciences
N2  - Species diversity promotes the delivery of multiple ecosystem functions (multifunctionality). However, the relative functional importance of rare and common species in driving the biodiversity multifunctionality relationship remains unknown. We studied the relationship between the diversity of rare and common species (according to their local abundances and across nine different trophic groups), and multifunctionality indices derived from 14 ecosystem functions on 150 grasslands across a land use intensity (LUI) gradient. The diversity of above- and below-ground rare species had opposite effects, with rare above-ground species being associated with high levels of multifunctionality, probably because their effects on different functions did not trade off against each other. Conversely, common species were only related to average, not high, levels of multifunctionality, and their functional effects declined with LUI. Apart from the community level effects of diversity, we found significant positive associations between the abundance of individual species and multifunctionality in 6% of the species tested. Species specific functional effects were best predicted by their response to LUI: species that declined in abundance with land use intensification were those associated with higher levels of multifunctionality. Our results highlight the importance of rare species for ecosystem multifunctionality and help guiding future conservation priorities.
KW  - biodiversity
KW  - common species
KW  - ecosystem function
KW  - identity hypothesis
KW  - land use
KW  - multitrophic
Y1  - 2016
U6  - https://doi.org/10.1098/rstb.2015.0269
SN  - 0962-8436
SN  - 1471-2970
VL  - 371
SP  - 3175
EP  - 3185
PB  - Royal Society
CY  - London
ER  - 
TY  - JOUR
A1  - Lendlein, Andreas
A1  - Balk, Maria
A1  - Tarazona, Natalia A.
A1  - Gould, Oliver E. C.
T1  - Bioperspectives for Shape-Memory Polymers as Shape Programmable, Active Materials
JF  - Biomacromolecules : an interdisciplinary journal focused at the interface of polymer science and the biological sciences
N2  - Within the natural world, organisms use information stored in their material structure to generate a physical response to a wide variety of environmental changes. The ability to program synthetic materials to intrinsically respond to environmental changes in a similar manner has the potential to revolutionize material science. By designing polymeric devices capable of responsively changing shape or behavior based on information encoded into their structure, we can create functional physical behavior, including a shape memory and an actuation capability. Here we highlight the stimuli-responsiveness and shape-changing ability of biological materials and biopolymer-based materials, plus their potential biomedical application, providing a bioperspective on shape-memory materials. We address strategies to incorporate a shape memory (actuation) function in polymeric materials, conceptualized in terms of its relationship with inputs (environmental stimuli) and outputs (shape change). Challenges and opportunities associated with the integration of several functions in a single material body to achieve multifunctionality are discussed. Finally, we describe how elements that sense, convert, and transmit stimuli have been used to create multisensitive materials.
Y1  - 2019
U6  - https://doi.org/10.1021/acs.biomac.9b01074
SN  - 1525-7797
SN  - 1526-4602
VL  - 20
IS  - 10
SP  - 3627
EP  - 3640
PB  - American Chemical Society
CY  - Washington
ER  - 
TY  - JOUR
A1  - Guha, S.
A1  - Warsinke, A.
A1  - Tientcheu, Ch. M.
A1  - Schmalz, K.
A1  - Meliani, C.
A1  - Wenger, Ch.
T1  - Label free sensing of creatinine using a 6 GHz CMOS near-field dielectric immunosensor
JF  - The analyst : the analytical journal of the Royal Society of Chemistry
N2  - In this work we present a CMOS high frequency direct immunosensor operating at 6 GHz (C-band) for label free determination of creatinine. The sensor is fabricated in standard 0.13 μm SiGe:C BiCMOS process. The report also demonstrates the ability to immobilize creatinine molecules on a Si3N4 passivation layer of the standard BiCMOS/CMOS process, therefore, evading any further need of cumbersome post processing of the fabricated sensor chip. The sensor is based on capacitive detection of the amount of non-creatinine bound antibodies binding to an immobilized creatinine layer on the passivated sensor. The chip bound antibody amount in turn corresponds indirectly to the creatinine concentration used in the incubation phase. The determination of creatinine in the concentration range of 0.88–880 μM is successfully demonstrated in this work. A sensitivity of 35 MHz/10 fold increase in creatinine concentration (during incubation) at the centre frequency of 6 GHz is gained by the immunosensor. The results are compared with a standard optical measurement technique and the dynamic range and sensitivity is of the order of the established optical indication technique. The C-band immunosensor chip comprising an area of 0.3 mm2 reduces the sensing area considerably, therefore, requiring a sample volume as low as 2 μl. The small analyte sample volume and label free approach also reduce the experimental costs in addition to the low fabrication costs offered by the batch fabrication technique of CMOS/BiCMOS process.
Y1  - 2015
U6  - https://doi.org/10.1039/c4an02194k
SN  - 0003-2654
SN  - 1364-5528
VL  - 9
IS  - 140
SP  - 3019
EP  - 3027
PB  - Royal Society of Chemistry
CY  - Cambridge
ER  -