@article{PerovicQinOschatz2020, author = {Perovic, Milena and Qin, Qing and Oschatz, Martin}, title = {From molecular precursors to nanoparticles}, series = {Advanced functional materials}, volume = {30}, journal = {Advanced functional materials}, number = {41}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {1616-301X}, doi = {10.1002/adfm.201908371}, pages = {21}, year = {2020}, abstract = {Nanoporous carbon materials (NCMs) provide the "function" of high specific surface area and thus have large interface area for interactions with surrounding species, which is of particular importance in applications related to adsorption processes. The strength and mechanism of adsorption depend on the pore architecture of the NCMs. In addition, chemical functionalization can be used to induce changes of electron density and/or electron density distribution in the pore walls, thus further modifying the interactions between carbons and guest species. Typical approaches for functionalization of nanoporous materials with regular atomic construction like porous silica, metal-organic frameworks, or zeolites, cannot be applied to NCMs due to their less defined local atomic construction and abundant defects. Therefore, synthetic strategies that offer a higher degree of control over the process of functionalization are needed. Synthetic approaches for covalent functionalization of NCMs, that is, for the incorporation of heteroatoms into the carbon backbone, are critically reviewed with a special focus on strategies following the concept "from molecules to materials." Approaches for coordinative functionalization with metallic species, and the functionalization by nanocomposite formation between pristine carbon materials and heteroatom-containing carbons, are introduced as well. Particular focus is given to the influences of these functionalizations in adsorption-related applications.}, language = {en} } @article{PochIstiqomahQuiricoetal.2020, author = {Poch, Olivier and Istiqomah, Istiqomah and Quirico, Eric and Beck, Pierre and Schmitt, Bernard and Theul{\´e}, Patrice and Faure, Alexandre and Hily-Blant, Pierre and Bonal, Lydie and Kappel, David}, title = {Ammonium salts are a reservoir of nitrogen on a cometary nucleus and possibly on some asteroids}, series = {Science}, volume = {367}, journal = {Science}, number = {6483}, publisher = {AAAS, American Association for the Advancement of Science}, address = {Washington, DC}, issn = {1095-9203}, doi = {10.1126/science.aaw7462}, pages = {1 -- 8}, year = {2020}, abstract = {The measured nitrogen-to-carbon ratio in comets is lower than for the Sun, a discrepancy which could be alleviated if there is an unknown reservoir of nitrogen in comets. The nucleus of comet 67P/Churyumov-Gerasimenko exhibits an unidentified broad spectral reflectance feature around 3.2 micrometers, which is ubiquitous across its surface. On the basis of laboratory experiments, we attribute this absorption band to ammonium salts mixed with dust on the surface. The depth of the band indicates that semivolatile ammonium salts are a substantial reservoir of nitrogen in the comet, potentially dominating over refractory organic matter and more volatile species. Similar absorption features appear in the spectra of some asteroids, implying a compositional link between asteroids, comets, and the parent interstellar cloud.}, language = {en} } @misc{PochIstiqomahQuiricoetal.2020, author = {Poch, Olivier and Istiqomah, Istiqomah and Quirico, Eric and Beck, Pierre and Schmitt, Bernard and Theul{\´e}, Patrice and Faure, Alexandre and Hily-Blant, Pierre and Bonal, Lydie and Kappel, David}, title = {Ammonium salts are a reservoir of nitrogen on a cometary nucleus and possibly on some asteroids}, series = {Zweitver{\"o}ffentlichungen der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe}, journal = {Zweitver{\"o}ffentlichungen der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe}, number = {6483}, issn = {1866-8372}, doi = {10.25932/publishup-51375}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-513751}, pages = {10}, year = {2020}, abstract = {The measured nitrogen-to-carbon ratio in comets is lower than for the Sun, a discrepancy which could be alleviated if there is an unknown reservoir of nitrogen in comets. The nucleus of comet 67P/Churyumov-Gerasimenko exhibits an unidentified broad spectral reflectance feature around 3.2 micrometers, which is ubiquitous across its surface. On the basis of laboratory experiments, we attribute this absorption band to ammonium salts mixed with dust on the surface. The depth of the band indicates that semivolatile ammonium salts are a substantial reservoir of nitrogen in the comet, potentially dominating over refractory organic matter and more volatile species. Similar absorption features appear in the spectra of some asteroids, implying a compositional link between asteroids, comets, and the parent interstellar cloud.}, language = {en} } @article{PhuongHosseiniSandbergetal.2020, author = {Phuong, Le Quang and Hosseini, Seyed Mehrdad and Sandberg, Oskar J. and Zou, Yingping and Woo, Han Young and Neher, Dieter and Shoaee, Safa}, title = {Quantifying quasi-fermi level splitting and open-circuit voltage losses in highly efficient nonfullerene organic solar cells}, series = {Solar RRL}, volume = {5}, journal = {Solar RRL}, number = {1}, publisher = {Wiley-VCH}, address = {Weinheim}, issn = {2367-198X}, doi = {10.1002/solr.202000649}, pages = {6}, year = {2020}, abstract = {The power conversion efficiency (PCE) of state-of-the-art organic solar cells is still limited by significant open-circuit voltage (V-OC) losses, partly due to the excitonic nature of organic materials and partly due to ill-designed architectures. Thus, quantifying different contributions of the V-OC losses is of importance to enable further improvements in the performance of organic solar cells. Herein, the spectroscopic and semiconductor device physics approaches are combined to identify and quantify losses from surface recombination and bulk recombination. Several state-of-the-art systems that demonstrate different V-OC losses in their performance are presented. By evaluating the quasi-Fermi level splitting (QFLS) and the V-OC as a function of the excitation fluence in nonfullerene-based PM6:Y6, PM6:Y11, and fullerene-based PPDT2FBT:PCBM devices with different architectures, the voltage losses due to different recombination processes occurring in the active layers, the transport layers, and at the interfaces are assessed. It is found that surface recombination at interfaces in the studied solar cells is negligible, and thus, suppressing the non-radiative recombination in the active layers is the key factor to enhance the PCE of these devices. This study provides a universal tool to explain and further improve the performance of recently demonstrated high-open-circuit-voltage organic solar cells.}, language = {en} } @misc{PhuongHosseiniSandbergetal.2020, author = {Phuong, Le Quang and Hosseini, Seyed Mehrdad and Sandberg, Oskar J. and Zou, Yingping and Woo, Han Young and Neher, Dieter and Shoaee, Safa}, title = {Quantifying quasi-fermi level splitting and open-circuit voltage losses in highly efficient nonfullerene organic solar cells}, series = {Zweitver{\"o}ffentlichungen der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe}, journal = {Zweitver{\"o}ffentlichungen der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe}, number = {1}, issn = {1866-8372}, doi = {10.25932/publishup-57001}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-570018}, pages = {8}, year = {2020}, abstract = {The power conversion efficiency (PCE) of state-of-the-art organic solar cells is still limited by significant open-circuit voltage (V-OC) losses, partly due to the excitonic nature of organic materials and partly due to ill-designed architectures. Thus, quantifying different contributions of the V-OC losses is of importance to enable further improvements in the performance of organic solar cells. Herein, the spectroscopic and semiconductor device physics approaches are combined to identify and quantify losses from surface recombination and bulk recombination. Several state-of-the-art systems that demonstrate different V-OC losses in their performance are presented. By evaluating the quasi-Fermi level splitting (QFLS) and the V-OC as a function of the excitation fluence in nonfullerene-based PM6:Y6, PM6:Y11, and fullerene-based PPDT2FBT:PCBM devices with different architectures, the voltage losses due to different recombination processes occurring in the active layers, the transport layers, and at the interfaces are assessed. It is found that surface recombination at interfaces in the studied solar cells is negligible, and thus, suppressing the non-radiative recombination in the active layers is the key factor to enhance the PCE of these devices. This study provides a universal tool to explain and further improve the performance of recently demonstrated high-open-circuit-voltage organic solar cells.}, language = {en} } @phdthesis{Feldmann2018, author = {Feldmann, David}, title = {Light-driven diffusioosmosis}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-417184}, school = {Universit{\"a}t Potsdam}, pages = {viii, 150}, year = {2018}, abstract = {The emergence of microfluidics created the need for precise and remote control of micron-sized objects. I demonstrate how light-sensitive motion can be induced at the micrometer scale by a simple addition of a photosensitive surfactant, which makes it possible to trigger hydrophobicity with light. With point-like laser irradiation, radial inward and outward hydrodynamic surface flows are remotely switched on and off. In this way, ensembles of microparticles can be moved toward or away from the irradiation center. Particle motion is analyzed according to varying parameters, such as surfactant and salt concentration, illumination condition, surface hydrophobicity, and surface structure. The physical origin of this process is the so-called light-driven diffusioosmosis (LDDO), a phenomenon that was discovered in the framework of this thesis and is described experimentally and theoretically in this work. To give a brief explanation, a focused light irradiation induces a local photoisomerization that creates a concentration gradient at the solid-liquid interface. To compensate for the change in osmotic pressure near the surface, a hydrodynamic flow along the surface is generated. Surface-surfactant interaction largely governs LDDO. It is shown that surfactant adsorption depends on the isomerization state of the surfactant. Photoisomerization, therefore, triggers a surfactant attachment or detachment from the surface. This change is considered to be one of the reasons for the formation of LDDO flow. These flows are introduced not only by a focused laser source but also by global irradiation. Porous particles show reversible repulsive and attractive interactions when dispersed in the solution of photosensitive surfactant. Repulsion and attraction is controlled by the irradiation wavelength. Illumination with red light leads to formation of aggregates, while illumination with blue light leads to the formation of a well-separated grid with equal interparticle distances, between 2µm and 80µm, depending on the particle surface density. These long-range interactions are considered to be a result of an increase or decrease of surfactant concentration around each particle, depending on the irradiation wavelength. Surfactant molecules adsorb inside the pores of the particles. A light-induced photoisomerization changes adsorption to the pores and drives surfactant molecules to the outside. The concentration gradients generate symmetric flows around each single particle resulting in local LDDO. With a break of the symmetry (i.e., by closing one side of the particle with a metal cap), one can achieve active self-propelled particle motion.}, language = {en} } @misc{GuentnerReichMikolajetal.2017, author = {G{\"u}ntner, Andreas and Reich, Marvin and Mikolaj, Michal and Creutzfeldt, Benjamin and Schroeder, Stephan and Wziontek, Hartmut}, title = {Landscape-scale water balance monitoring with an iGrav superconducting gravimeter in a field enclosure}, series = {Postprints der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe}, journal = {Postprints der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe}, number = {663}, issn = {1866-8372}, doi = {10.25932/publishup-41910}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-419105}, pages = {16}, year = {2017}, abstract = {In spite of the fundamental role of the landscape water balance for the Earth's water and energy cycles, monitoring the water balance and its components beyond the point scale is notoriously difficult due to the multitude of flow and storage processes and their spatial heterogeneity. Here, we present the first field deployment of an iGrav superconducting gravimeter (SG) in a minimized enclosure for long-term integrative monitoring of water storage changes. Results of the field SG on a grassland site under wet-temperate climate conditions were compared to data provided by a nearby SG located in the controlled environment of an observatory building. The field system proves to provide gravity time series that are similarly precise as those of the observatory SG. At the same time, the field SG is more sensitive to hydrological variations than the observatory SG. We demonstrate that the gravity variations observed by the field setup are almost independent of the depth below the terrain surface where water storage changes occur (contrary to SGs in buildings), and thus the field SG system directly observes the total water storage change, i.e., the water balance, in its surroundings in an integrative way. We provide a framework to single out the water balance components actual evapotranspiration and lateral subsurface discharge from the gravity time series on annual to daily timescales. With about 99 and 85\% of the gravity signal due to local water storage changes originating within a radius of 4000 and 200m around the instrument, respectively, this setup paves the road towards gravimetry as a continuous hydrological field-monitoring technique at the landscape scale.}, language = {en} } @misc{RubeyBruneHeineetal.2017, author = {Rubey, Michael and Brune, Sascha and Heine, Christian and Davies, D. Rhodri and Williams, Simon E. and M{\"u}ller, R. Dietmar}, title = {Global patterns in Earth's dynamic topography since the Jurassic}, series = {Postprints der Universit{\"a}t Potsdam : Mathematisch Naturwissenschaftliche Reihe}, journal = {Postprints der Universit{\"a}t Potsdam : Mathematisch Naturwissenschaftliche Reihe}, number = {623}, issn = {1866-8372}, doi = {10.25932/publishup-41824}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-418241}, pages = {899 -- 919}, year = {2017}, abstract = {We evaluate the spatial and temporal evolution of Earth's long-wavelength surface dynamic topography since the Jurassic using a series of high-resolution global mantle convection models. These models are Earth-like in terms of convective vigour, thermal structure, surface heat-flux and the geographic distribution of heterogeneity. The models generate a degree-2-dominated spectrum of dynamic topography with negative amplitudes above subducted slabs (i.e. circum-Pacific regions and southern Eurasia) and positive amplitudes elsewhere (i.e. Africa, north-western Eurasia and the central Pacific). Model predictions are compared with published observations and subsidence patterns from well data, both globally and for the Australian and southern African regions. We find that our models reproduce the long-wavelength component of these observations, although observed smaller-scale variations are not reproduced. We subsequently define "geodynamic rules" for how different surface tectonic settings are affected by mantle processes: (i) locations in the vicinity of a subduction zone show large negative dynamic topography amplitudes; (ii) regions far away from convergent margins feature long-term positive dynamic topography; and (iii) rapid variations in dynamic support occur along the margins of overriding plates (e.g. the western US) and at points located on a plate that rapidly approaches a subduction zone (e.g. India and the Arabia Peninsula). Our models provide a predictive quantitative framework linking mantle convection with plate tectonics and sedimentary basin evolution, thus improving our understanding of how subduction and mantle convection affect the spatio-temporal evolution of basin architecture.}, language = {en} } @misc{PuppeHoehnKaczoreketal.2017, author = {Puppe, Daniel and H{\"o}hn, Axel and Kaczorek, Danuta and Wanner, Manfred and Wehrhan, Marc and Sommer, Michael}, title = {How big is the influence of biogenic silicon pools on short-term changes in water-soluble silicon in soils?}, series = {Postprints der Universit{\"a}t Potsdam : Mathematisch Naturwissenschaftliche Reihe}, journal = {Postprints der Universit{\"a}t Potsdam : Mathematisch Naturwissenschaftliche Reihe}, number = {633}, doi = {10.25932/publishup-41714}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-417141}, pages = {5239 -- 5252}, year = {2017}, abstract = {The significance of biogenic silicon (BSi) pools as a key factor for the control of Si fluxes from terrestrial to aquatic ecosystems has been recognized for decades. However, while most research has been focused on phytogenic Si pools, knowledge of other BSi pools is still limited. We hypothesized that different BSi pools influence short-term changes in the water-soluble Si fraction in soils to different extents. To test our hypothesis we took plant (Calamagrostis epigejos, Phragmites australis) and soil samples in an artificial catchment in a post-mining landscape in the state of Brandenburg, Germany. We quantified phytogenic (phytoliths), protistic (diatom frustules and testate amoeba shells) and zoogenic (sponge spicules) Si pools as well as Tironextractable and water-soluble Si fractions in soils at the beginning (t(0)) and after 10 years (t(10)) of ecosystem development. As expected the results of Tiron extraction showed that there are no consistent changes in the amorphous Si pool at Chicken Creek (Huhnerwasser) as early as after 10 years. In contrast to t(0) we found increased water-soluble Si and BSi pools at t(10); thus we concluded that BSi pools are the main driver of short-term changes in water-soluble Si. However, because total BSi represents only small proportions of water-soluble Si at t(0) (< 2 \%) and t(10) (2.8-4.3 \%) we further concluded that smaller (< 5 mu m) and/or fragile phytogenic Si structures have the biggest impact on short-term changes in water-soluble Si. In this context, extracted phytoliths (> 5 mu m) only amounted to about 16\% of total Si con-tents of plant materials of C. epigejos and P. australis at t(10); thus about 84\% of small-scale and/or fragile phytogenic Si is not quantified by the used phytolith extraction method. Analyses of small-scale and fragile phytogenic Si structures are urgently needed in future work as they seem to represent the biggest and most reactive Si pool in soils. Thus they are the most important drivers of Si cycling in terrestrial biogeosystems.}, language = {en} } @misc{EhlertHolzweberLippitzetal.2016, author = {Ehlert, Christopher and Holzweber, Markus and Lippitz, Andreas and Unger, Wolfgang E. S. and Saalfrank, Peter}, title = {A detailed assignment of NEXAFS resonances of imidazolium based ionic liquids}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-394417}, pages = {8654 -- 8661}, year = {2016}, abstract = {In Near Edge X-Ray Absorption Fine Structure (NEXAFS) spectroscopy X-Ray photons are used to excite tightly bound core electrons to low-lying unoccupied orbitals of the system. This technique offers insight into the electronic structure of the system as well as useful structural information. In this work, we apply NEXAFS to two kinds of imidazolium based ionic liquids ([CnC1im]+[NTf2]- and [C4C1im]+[I]-). A combination of measurements and quantum chemical calculations of C K and N K NEXAFS resonances is presented. The simulations, based on the transition potential density functional theory method (TP-DFT), reproduce all characteristic features observed by the experiment. Furthermore, a detailed assignment of resonance features to excitation centers (carbon or nitrogen atoms) leads to a consistent interpretation of the spectra.}, language = {en} } @misc{FrielerMengelLevermann2016, author = {Frieler, Katja and Mengel, Matthias and Levermann, Anders}, title = {Delaying future sea-level rise by storing water in Antarctica}, series = {Postprints der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe}, journal = {Postprints der Universit{\"a}t Potsdam : Mathematisch-Naturwissenschaftliche Reihe}, number = {533}, issn = {1866-8372}, doi = {10.25932/publishup-41023}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-410234}, pages = {8}, year = {2016}, abstract = {Even if greenhouse gas emissions were stopped today, sea level would continue to rise for centuries, with the long-term sea-level commitment of a 2 degrees C warmer world significantly exceeding 2 m. In view of the potential implications for coastal populations and ecosystems worldwide, we investigate, from an ice-dynamic perspective, the possibility of delaying sea-level rise by pumping ocean water onto the surface of the Antarctic ice sheet. We find that due to wave propagation ice is discharged much faster back into the ocean than would be expected from a pure advection with surface velocities. The delay time depends strongly on the distance from the coastline at which the additional mass is placed and less strongly on the rate of sea-level rise that is mitigated. A millennium-scale storage of at least 80\% of the additional ice requires placing it at a distance of at least 700 km from the coastline. The pumping energy required to elevate the potential energy of ocean water to mitigate the currently observed 3 mmyr(-1) will exceed 7\% of the current global primary energy supply. At the same time, the approach offers a comprehensive protection for entire coastlines particularly including regions that cannot be protected by dikes.}, language = {en} } @phdthesis{Schroeder2015, author = {Schr{\"o}der, Sarah}, title = {Modelling surface evolution coupled with tectonics}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-90385}, school = {Universit{\"a}t Potsdam}, pages = {viii, 129}, year = {2015}, abstract = {This study presents the development of 1D and 2D Surface Evolution Codes (SECs) and their coupling to any lithospheric-scale (thermo-)mechanical code with a quadrilateral structured surface mesh. Both SECs involve diffusion as approach for hillslope processes and the stream power law to reflect riverbed incision. The 1D SEC settles sediment that was produced by fluvial incision in the appropriate minimum, while the supply-limited 2D SEC DANSER uses a fast filling algorithm to model sedimantation. It is based on a cellular automaton. A slope-dependent factor in the sediment flux extends the diffusion equation to nonlinear diffusion. The discharge accumulation is achieved with the D8-algorithm and an improved drainage accumulation routine. Lateral incision enhances the incision's modelling. Following empirical laws, it incises channels of several cells width. The coupling method enables different temporal and spatial resolutions of the SEC and the thermo-mechanical code. It transfers vertical as well as horizontal displacements to the surface model. A weighted smoothing of the 3D surface displacements is implemented. The smoothed displacement vectors transmit the deformation by bilinear interpolation to the surface model. These interpolation methods ensure mass conservation in both directions and prevent the two surfaces from drifting apart. The presented applications refer to the evolution of the Pamir orogen. A calibration of DANSER's parameters with geomorphological data and a DEM as initial topography highlights the advantage of lateral incision. Preserving the channel width and reflecting incision peaks in narrow channels, this closes the huge gap between current orogen-scale incision models and observed topographies. River capturing models in a system of fault-bounded block rotations reaffirm the importance of the lateral incision routine for capturing events with channel initiation. The models show a low probability of river capturings with large deflection angles. While the probability of river capturing is directly depending on the uplift rate, the erodibility inside of a dip-slip fault speeds up headward erosion along the fault: The model's capturing speed increases within a fault. Coupling DANSER with the thermo-mechanical code SLIM 3D emphasizes the versatility of the SEC. While DANSER has minor influence on the lithospheric evolution of an indenter model, the brittle surface deformation is strongly affected by its sedimentation, widening a basin in between two forming orogens and also the southern part of the southern orogen to south, east and west.}, language = {en} } @article{ZamponiPenfoldNachtegaaletal.2014, author = {Zamponi, Flavio and Penfold, Thomas J. and Nachtegaal, Maarten and L{\"u}bcke, Andrea and Rittmann, Jochen and Milne, Chris J. and Chergui, Majed and van Bokhoven, Jeroen A.}, title = {Probing the dynamics of plasmon-excited hexanethiol-capped gold nanoparticles by picosecond X-ray absorption spectroscopy}, series = {physical chemistry, chemical physics : PCCP}, volume = {2014}, journal = {physical chemistry, chemical physics : PCCP}, number = {16}, issn = {1463-9076}, doi = {10.1039/c4cp03301a}, pages = {23157 -- 23163}, year = {2014}, abstract = {Picosecond X-ray absorption spectroscopy (XAS) is used to investigate the electronic and structural dynamics initiated by plasmon excitation of 1.8 nm diameter Au nanoparticles (NPs) functionalised with 1-hexanethiol. We show that 100 ps after photoexcitation the transient XAS spectrum is consistent with an 8\% expansion of the Au-Au bond length and a large increase in disorder associated with melting of the NPs. Recovery of the ground state occurs with a time constant of ∼1.8 ns, arising from thermalisation with the environment. Simulations reveal that the transient spectrum exhibits no signature of charge separation at 100 ps and allows us to estimate an upper limit for the quantum yield (QY) of this process to be <0.1.}, language = {en} } @misc{ZamponiPenfoldNachtegaaletal.2014, author = {Zamponi, Flavio and Penfold, Thomas J. and Nachtegaal, Maarten and L{\"u}bcke, Andrea and Rittmann, Jochen and Milne, Chris J. and Chergui, Majed and van Bokhoven, Jeroen A.}, title = {Probing the dynamics of plasmon-excited hexanethiol-capped gold nanoparticles by picosecond X-ray absorption spectroscopy}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-74492}, pages = {23157 -- 23163}, year = {2014}, abstract = {Picosecond X-ray absorption spectroscopy (XAS) is used to investigate the electronic and structural dynamics initiated by plasmon excitation of 1.8 nm diameter Au nanoparticles (NPs) functionalised with 1-hexanethiol. We show that 100 ps after photoexcitation the transient XAS spectrum is consistent with an 8\% expansion of the Au-Au bond length and a large increase in disorder associated with melting of the NPs. Recovery of the ground state occurs with a time constant of ∼1.8 ns, arising from thermalisation with the environment. Simulations reveal that the transient spectrum exhibits no signature of charge separation at 100 ps and allows us to estimate an upper limit for the quantum yield (QY) of this process to be <0.1.}, language = {en} } @misc{MondalBhuniaDemeshkoetal.2013, author = {Mondal, Suvendu Sekhar and Bhunia, Asamanjoy and Demeshko, Serhiy and Kelling, Alexandra and Schilde, Uwe and Janiak, Christoph and Holdt, Hans-J{\"u}rgen}, title = {Synthesis of a Co(II)-imidazolate framework from an anionic linker precursor}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-94424}, pages = {39 -- 42}, year = {2013}, abstract = {A Co(II)-imidazolate-4-amide-5-imidate based MOF, IFP-5, is synthesized by using an imidazolate anion-based novel ionic liquid as a linker precursor under solvothermal conditions. IFP-5 shows significant amounts of gas (N2, CO2, CH4 and H2) uptake capacities. IFP-5 exhibits an independent high spin Co(II) centre and antiferromagnetic coupling.}, language = {en} } @phdthesis{Rader2005, author = {Rader, Oliver}, title = {Electron quantization and localization in metal films and nanostructures}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-0001912}, school = {Universit{\"a}t Potsdam}, year = {2005}, abstract = {Es ist seit einigen Jahren bekannt, dass Elektronen unter bestimmten Bedingungen in d{\"u}nne Filme eingeschlossen werden k{\"o}nnen, selbst wenn diese Filme aus Metall bestehen und auf Metall-Substrat aufgebracht werden. In Photoelektronenspektren zeigen diese Filme charakteristische diskrete Energieniveaus, und es hat sich herausgestellt, dass sie zu großen, technisch nutzbaren Effekten f{\"u}hren k{\"o}nnen, wie der oszillatorischen magnetischen Kopplung in modernen Festplatten-Lesek{\"o}pfen. In dieser Arbeit wird untersucht, inwieweit die der Quantisierung in zweidimensionalen Filmen zu Grunde liegenden Konzepte auf niedrigere Dimensionalit{\"a}t {\"u}bertragbar sind. Das bedeutet, dass schrittweise von zweidimensionalen Filmen auf eindimensionale Nanostrukturen {\"u}bergegangen wird. Diese Nanostrukturen sind zum einen die Terrassen auf atomar gestuften Oberfl{\"a}chen, aber auch Atomketten, die auf diese Terrassen aufgebracht werden, bis hin zu einer vollst{\"a}ndigen Bedeckung mit atomar d{\"u}nnen Nanostreifen. Daneben werden Selbstorganisationseffekte ausgenutzt, um zu perfekt eindimensionalen Atomanordnungen auf Oberfl{\"a}chen zu gelangen. Die winkelaufgel{\"o}ste Photoemission ist als Untersuchungsmethode deshalb so geeignet, weil sie das Verhalten der Elektronen in diesen Nanostrukturen in Abh{\"a}ngigkeit von der Raumrichtung zeigt, und unterscheidet sich darin beispielsweise von der Rastertunnelmikroskopie. Damit ist es m{\"o}glich, deutliche und manchmal {\"u}berraschend große Effekte der eindimensionalen Quantisierung bei verschiedenen exemplarischen Systemen zum Teil erstmals nachzuweisen. Die f{\"u}r zweidimensionale Filme wesentliche Rolle von Bandl{\"u}cken im Substrat wird f{\"u}r Nanostrukturen best{\"a}tigt. Hinzu kommt jedoch eine bei zweidimensionalen Filmen nicht vorhandene Ambivalenz zwischen r{\"a}umlicher Einschr{\"a}nkung der Elektronen in den Nanostrukturen und dem Effekt eines {\"U}bergitters aus Nanostrukturen sowie zwischen Effekten des Elektronenverhaltens in der Probe und solchen des Messprozesses. Letztere sind sehr groß und k{\"o}nnen die Photoemissionsspektren dominieren. Abschließend wird der Effekt der verminderten Dimensionalit{\"a}t speziell f{\"u}r die d-Elektronen von Mangan untersucht, die zus{\"a}tzlich starken Wechselwirkungseffekten unterliegen. Auch hierbei treten {\"u}berraschende Ergebnisse zu Tage.}, language = {en} } @phdthesis{Henkel2004, author = {Henkel, Carsten}, title = {Coherence theory of atomic de Broglie waves and electromagnetic near fields}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-0001272}, school = {Universit{\"a}t Potsdam}, year = {2004}, abstract = {Die Arbeit untersucht theoretisch die Wechselwirkung neutraler Teilchen (Atome, Molek{\"u}le) mit Oberfl{\"a}chen, soweit sie durch das elektromagnetische Feld vermittelt wird. Spektrale Energiedichten und Koh{\"a}renzfunktionen werden hergeleitet und liefern eine umfassende Charakterisierung des Felds auf der sub-Wellenl{\"a}ngen-Skala. Die Ergebnisse finden auf zwei Teilgebieten Anwendung: in der integrierten Atomoptik, wo ultrakalte Atome an thermische Oberfl{\"a}chen koppeln, und in der Nahfeldoptik, wo eine Aufl{\"o}sung unterhalb der Beugungsbegrenzung mit einzelnen Molek{\"u}len als Sonden und Detektoren erzielt werden kann.}, language = {en} }