@phdthesis{WindirschWoiwode2024, author = {Windirsch-Woiwode, Torben}, title = {Permafrost carbon stabilisation by recreating a herbivore-driven ecosystem}, doi = {10.25932/publishup-62424}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-624240}, school = {Universit{\"a}t Potsdam}, pages = {X, 104, A-57}, year = {2024}, abstract = {With Arctic ground as a huge and temperature-sensitive carbon reservoir, maintaining low ground temperatures and frozen conditions to prevent further carbon emissions that contrib-ute to global climate warming is a key element in humankind's fight to maintain habitable con-ditions on earth. Former studies showed that during the late Pleistocene, Arctic ground condi-tions were generally colder and more stable as the result of an ecosystem dominated by large herbivorous mammals and vast extents of graminoid vegetation - the mammoth steppe. Characterised by high plant productivity (grassland) and low ground insulation due to animal-caused compression and removal of snow, this ecosystem enabled deep permafrost aggrad-ation. Now, with tundra and shrub vegetation common in the terrestrial Arctic, these effects are not in place anymore. However, it appears to be possible to recreate this ecosystem local-ly by artificially increasing animal numbers, and hence keep Arctic ground cold to reduce or-ganic matter decomposition and carbon release into the atmosphere. By measuring thaw depth, total organic carbon and total nitrogen content, stable carbon iso-tope ratio, radiocarbon age, n-alkane and alcohol characteristics and assessing dominant vegetation types along grazing intensity transects in two contrasting Arctic areas, it was found that recreating conditions locally, similar to the mammoth steppe, seems to be possible. For permafrost-affected soil, it was shown that intensive grazing in direct comparison to non-grazed areas reduces active layer depth and leads to higher TOC contents in the active layer soil. For soil only frozen on top in winter, an increase of TOC with grazing intensity could not be found, most likely because of confounding factors such as vertical water and carbon movement, which is not possible with an impermeable layer in permafrost. In both areas, high animal activity led to a vegetation transformation towards species-poor graminoid-dominated landscapes with less shrubs. Lipid biomarker analysis revealed that, even though the available organic material is different between the study areas, in both permafrost-affected and sea-sonally frozen soils the organic material in sites affected by high animal activity was less de-composed than under less intensive grazing pressure. In conclusion, high animal activity af-fects decomposition processes in Arctic soils and the ground thermal regime, visible from reduced active layer depth in permafrost areas. Therefore, grazing management might be utilised to locally stabilise permafrost and reduce Arctic carbon emissions in the future, but is likely not scalable to the entire permafrost region.}, language = {en} } @phdthesis{SvirejevaHopkins2004, author = {Svirejeva-Hopkins, Anastasia}, title = {Urbanised territories as a specific component of the global carbon cycle}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-0001512}, school = {Universit{\"a}t Potsdam}, year = {2004}, abstract = {Wir betrachten folgende Teile: die zus{\"a}tzlichen Kohlenstoff(C)-emissionen, welche aus der Umwandlung von nat{\"u}rlichem Umland durch Stadtwachstum resultieren, und die {\"A}nderung des C-Flusses durch 'urbanisierte' {\"O}kosysteme, soweit atmosph{\"a}risches C durch diese in umliegende nat{\"u}rliche {\"O}kosysteme entlang der Kette \“Atmosph{\"a}re -> Vegetation -> abgestorbene organische Substanzen\” gepumpt wird: d.h. C-Export; f{\"u}r den Zeitraum von 1980 bis 2050. Als Szenario nutzen wir Prognosen der regionalen Stadtbev{\"o}lkerung, welche durch ein 'Hybridmodell' generiert werden f{\"u}r acht Regionen. Alle Sch{\"a}tzungen der C-Fl{\"u}sse basieren auf zwei Modellen: das Regression Modell und das sogenannte G-Modell. Die Siedlungsfl{\"a}che, welche mit dem Wachstum der Stadtbev{\"o}lkerung zunimmt, wird in 'Gr{\"u}nfl{\"a}chen' (Parks, usw.), Geb{\"a}udefl{\"a}chen und informell st{\"a}dtisch genutzte Fl{\"a}chen (Slums, illegale Lagerpl{\"a}tze, usw.) unterteilt. Es werden j{\"a}hrlich die regionale und globale Dynamik der C-Emissionen und des C-Exports sowie die C-Gesamtbilanz berechnet. Dabei liefern beide Modelle qualitativ {\"a}hnliche Ergebnisse, jedoch gibt es einige quantitative Unterschiede. Im ersten Modell erreicht die globale Jahresemission f{\"u}r die Dekade 2020-2030 resultierend aus der Landnutzungs{\"a}nderung ein Maximum von 205 Mt/a. Die maximalen Beitr{\"a}ge zur globalen Emission werden durch China, die asiatische und die pazifische Region erbracht. Im zweiten Modell erh{\"o}ht sich die j{\"a}hrliche globale Emission von 1.12 GtC/a f{\"u}r 1980 auf 1.25 GtC/a f{\"u}r 2005 (1Gt = 109 t). Danach beginnt eine Reduzierung. Vergleichen wir das Emissionmaximum mit der Emission durch Abholzung im Jahre 1980 (1.36 GtC/a), k{\"o}nnen wir konstatieren, daß die Urbanisierung damit in vergleichbarer Gr{\"o}sse zur Emission beitr{\"a}gt. Bezogen auf die globale Dynamik des j{\"a}hrlichen C-Exports durch Urbanisierung beobachten wir ein monotones Wachstum bis zum nahezu dreifachen Wert von 24 MtC/a f{\"u}r 1980 auf 66 MtC/a f{\"u}r 2050 im ersten Modell, bzw. im zweiten Modell von 249 MtC/a f{\"u}r 1980 auf 505 MtC/a f{\"u}r 2050. Damit ist im zweiten Fall die Transportleistung der Siedlungsgebiete mit dem C-Transport durch Fl{\"u}sse in die Ozeane (196 .. 537 MtC/a) vergleichbar. Bei der Absch{\"a}tzung der Gesamtbilanz finden wir, daß die Urbanisierung die Bilanz in Richtung zu einer 'Senke' verschiebt. Entsprechend dem zweiten Modell beginnt sich die C-Gesamtbilanz (nach ann{\"a}hernder Konstanz) ab dem Jahre 2000 mit einer fast konstanten Rate zu verringern. Wenn das Maximum im Jahre 2000 bei 905MtC/a liegt, f{\"a}llt dieser Wert anschliessend bis zum Jahre 2050 auf 118 MtC/a. Bei Extrapolation dieser Dynamik in die Zukunft k{\"o}nnen wir annehmen, daß am Ende des 21. Jahrhunderts die \“urbane\” C-Gesamtbilanz Null bzw. negative Werte erreicht.}, language = {en} } @phdthesis{Schutjajew2021, author = {Schutjajew, Konstantin}, title = {Electrochemical sodium storage in non-graphitizing carbons - insights into mechanisms and synthetic approaches towards high-energy density materials}, doi = {10.25932/publishup-54189}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-541894}, school = {Universit{\"a}t Potsdam}, pages = {v, 148}, year = {2021}, abstract = {To achieve a sustainable energy economy, it is necessary to turn back on the combustion of fossil fuels as a means of energy production and switch to renewable sources. However, their temporal availability does not match societal consumption needs, meaning that renewably generated energy must be stored in its main generation times and allocated during peak consumption periods. Electrochemical energy storage (EES) in general is well suited due to its infrastructural independence and scalability. The lithium ion battery (LIB) takes a special place, among EES systems due to its energy density and efficiency, but the scarcity and uneven geological occurrence of minerals and ores vital for many cell components, and hence the high and fluctuating costs will decelerate its further distribution. The sodium ion battery (SIB) is a promising successor to LIB technology, as the fundamental setup and cell chemistry is similar in the two systems. Yet, the most widespread negative electrode material in LIBs, graphite, cannot be used in SIBs, as it cannot store sufficient amounts of sodium at reasonable potentials. Hence, another carbon allotrope, non-graphitizing or hard carbon (HC) is used in SIBs. This material consists of turbostratically disordered, curved graphene layers, forming regions of graphitic stacking and zones of deviating layers, so-called internal or closed pores. The structural features of HC have a substantial impact of the charge-potential curve exhibited by the carbon when it is used as the negative electrode in an SIB. At defects and edges an adsorption-like mechanism of sodium storage is prevalent, causing a sloping voltage curve, ill-suited for the practical application in SIBs, whereas a constant voltage plateau of relatively high capacities is found immediately after the sloping region, which recent research attributed to the deposition of quasimetallic sodium into the closed pores of HC. Literature on the general mechanism of sodium storage in HCs and especially the role of the closed pore is abundant, but the influence of the pore geometry and chemical nature of the HC on the low-potential sodium deposition is yet in an early stage. Therefore, the scope of this thesis is to investigate these relationships using suitable synthetic and characterization methods. Materials of precisely known morphology, porosity, and chemical structure are prepared in clear distinction to commonly obtained ones and their impact on the sodium storage characteristics is observed. Electrochemical impedance spectroscopy in combination with distribution of relaxation times analysis is further established as a technique to study the sodium storage process, in addition to classical direct current techniques, and an equivalent circuit model is proposed to qualitatively describe the HC sodiation mechanism, based on the recorded data. The obtained knowledge is used to develop a method for the preparation of closed porous and non-porous materials from open porous ones, proving not only the necessity of closed pores for efficient sodium storage, but also providing a method for effective pore closure and hence the increase of the sodium storage capacity and efficiency of carbon materials. The insights obtained and methods developed within this work hence not only contribute to the better understanding of the sodium storage mechanism in carbon materials of SIBs, but can also serve as guidance for the design of efficient electrode materials.}, language = {en} } @phdthesis{Schipper2014, author = {Schipper, Florian}, title = {Biomass derived carbon for new energy storage technologies}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-72045}, school = {Universit{\"a}t Potsdam}, year = {2014}, abstract = {The thesis deals with the production and evaluation of porous carbon materials for energy storage technologies, namely super capacitors and lithium sulfur batteries.}, language = {de} } @phdthesis{Herbrich2017, author = {Herbrich, Marcus}, title = {Einfluss der erosionsbedingten Pedogenese auf den Wasserund Stoffhaushalt ackerbaulich genutzter B{\"o}den der Grundmor{\"a}nenbodenlandschaft NO-Deutschlands - hydropedologische Untersuchungen mittels w{\"a}gbarer Pr{\"a}zisionslysimeter}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-408561}, school = {Universit{\"a}t Potsdam}, pages = {186}, year = {2017}, abstract = {In the arable soil landscape of hummocky ground moraines, an erosion-affected spatial differentiation of soils can be observed. Man-made erosion leads to soil profile modifications along slopes with changed solum thickness and modified properties of soil horizons due to water erosion in combination with tillage operations. Soil erosion creates, thereby, spatial patterns of soil properties (e.g., texture and organic matter content) and differences in crop development. However, little is known about the manner in which water fluxes are affected by soil-crop interactions depending on contrasting properties of differently-developed soil horizons and how water fluxes influence the carbon transport in an eroded landscape. To identify such feedbacks between erosion-induced soil profile modifications and the 1D-water and solute balance, high-precision weighing lysimeters equipped with a wide range of sensor technique were filled with undisturbed soil monoliths that differed in the degree of past soil erosion. Furthermore, lysimeter effluent concentrations were analyzed for dissolved carbon fractions in bi-weekly intervals. The water balance components measured by high precision lysimeters varied from the most eroded to the less eroded monolith up to 83 \% (deep drainage) primarily caused due to varying amounts of precipitation and evapotranspiration for a 3-years period. Here, interactions between crop development and contrasting rainfall interception by above ground biomass could explain differences in water balance components. Concentrations of dissolved carbon in soil water samples were relatively constant in time, suggesting carbon leaching was mainly affected by water fluxes in this observation period. For the lysimeter-based water balance analysis, a filtering scheme was developed considering temporal autocorrelation. The minute-based autocorrelation analysis of mass changes from lysimeter time series revealed characteristic autocorrelation lengths ranging from 23 to 76 minutes. Thereby, temporal autocorrelation provided an optimal approximation of precipitation quantities. However, the high temporal resolution in lysimeter time series is restricted by the lengths of autocorrelation. Erosion-induced but also gradual changes in soil properties were reflected by dynamics of soil water retention properties in the lysimeter soils. Short-term and long-term hysteretic water retention data suggested seasonal wettability problems of soils increasingly limited rewetting of previously dried pore regions. Differences in water retention were assigned to soil tillage operations and the erosion history at different slope positions. The threedimensional spatial pattern of soil types that result from erosional soil profile modifications were also reflected in differences of crop root development at different landscape positions. Contrasting root densities revealed positive relations of root and aboveground plant characteristics. Differences in the spatially-distributed root growth between different eroded soil types provided indications that root development was affected by the erosion-induced soil evolution processes. Overall, the current thesis corroborated the hypothesis that erosion-induced soil profile modifications affect the soil water balance, carbon leaching and soil hydraulic properties, but also the crop root system is influenced by erosion-induced spatial patterns of soil properties in the arable hummocky post glacial soil landscape. The results will help to improve model predictions of water and solute movement in arable soils and to understand interactions between soil erosion and carbon pathways regarding sink-or-source terms in landscapes.}, language = {en} } @phdthesis{FrankFahle2013, author = {Frank-Fahle, B{\´e}atrice A.}, title = {Methane-cycling microbial communities in permafrost affected soils on Herschel Island and the Yukon Coast, Western Canadian Arctic}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-65345}, school = {Universit{\"a}t Potsdam}, year = {2013}, abstract = {Permafrost-affected ecosystems including peat wetlands are among the most obvious regions in which current microbial controls on organic matter decomposition are likely to change as a result of global warming. Wet tundra ecosystems in particular are ideal sites for increased methane production because of the waterlogged, anoxic conditions that prevail in seasonally increasing thawed layers. The following doctoral research project focused on investigating the abundance and distribution of the methane-cycling microbial communities in four different polygons on Herschel Island and the Yukon Coast. Despite the relevance of the Canadian Western Arctic in the global methane budget, the permafrost microbial communities there have thus far remained insufficiently characterized. Through the study of methanogenic and methanotrophic microbial communities involved in the decomposition of permafrost organic matter and their potential reaction to rising environmental temperatures, the overarching goal of the ensuing thesis is to fill the current gap in understanding the fate of the organic carbon currently stored in Artic environments and its implications regarding the methane cycle in permafrost environments. To attain this goal, a multiproxy approach including community fingerprinting analysis, cloning, quantitative PCR and next generation sequencing was used to describe the bacterial and archaeal community present in the active layer of four polygons and to scrutinize the diversity and distribution of methane-cycling microorganisms at different depths. These methods were combined with soil properties analyses in order to identify the main physico-chemical variables shaping these communities. In addition a climate warming simulation experiment was carried-out on intact active layer cores retrieved from Herschel Island in order to investigate the changes in the methane-cycling communities associated with an increase in soil temperature and to help better predict future methane-fluxes from polygonal wet tundra environments in the context of climate change. Results showed that the microbial community found in the water-saturated and carbon-rich polygons on Herschel Island and the Yukon Coast was diverse and showed a similar distribution with depth in all four polygons sampled. Specifically, the methanogenic community identified resembled the communities found in other similar Arctic study sites and showed comparable potential methane production rates, whereas the methane oxidizing bacterial community differed from what has been found so far, being dominated by type-II rather than type-I methanotrophs. After being subjected to strong increases in soil temperature, the active-layer microbial community demonstrated the ability to quickly adapt and as a result shifts in community composition could be observed. These results contribute to the understanding of carbon dynamics in Arctic permafrost regions and allow an assessment of the potential impact of climate change on methane-cycling microbial communities. This thesis constitutes the first in-depth study of methane-cycling communities in the Canadian Western Arctic, striving to advance our understanding of these communities in degrading permafrost environments by establishing an important new observatory in the Circum-Arctic.}, language = {en} } @phdthesis{Eren2024, author = {Eren, Enis Oğuzhan}, title = {Covalent anode materials for high-energy sodium-ion batteries}, doi = {10.25932/publishup-62258}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus4-622585}, school = {Universit{\"a}t Potsdam}, pages = {xi, 153}, year = {2024}, abstract = {The reliance on fossil fuels has resulted in an abnormal increase in the concentration of greenhouse gases, contributing to the global climate crisis. In response, a rapid transition to renewable energy sources has begun, particularly lithium-ion batteries, playing a crucial role in the green energy transformation. However, concerns regarding the availability and geopolitical implications of lithium have prompted the exploration of alternative rechargeable battery systems, such as sodium-ion batteries. Sodium is significantly abundant and more homogeneously distributed in the crust and seawater, making it easier and less expensive to extract than lithium. However, because of the mysterious nature of its components, sodium-ion batteries are not yet sufficiently advanced to take the place of lithium-ion batteries. Specifically, sodium exhibits a more metallic character and a larger ionic radius, resulting in a different ion storage mechanism utilized in lithium-ion batteries. Innovations in synthetic methods, post-treatments, and interface engineering clearly demonstrate the significance of developing high-performance carbonaceous anode materials for sodium-ion batteries. The objective of this dissertation is to present a systematic approach for fabricating efficient, high-performance, and sustainable carbonaceous anode materials for sodium-ion batteries. This will involve a comprehensive investigation of different chemical environments and post-modification techniques as well. This dissertation focuses on three main objectives. Firstly, it explores the significance of post-synthetic methods in designing interfaces. A conformal carbon nitride coating is deposited through chemical vapor deposition on a carbon electrode as an artificial solid-electrolyte interface layer, resulting in improved electrochemical performance. The interaction between the carbon nitride artificial interface and the carbon electrode enhances initial Coulombic efficiency, rate performance, and total capacity. Secondly, a novel process for preparing sulfur-rich carbon as a high-performing anode material for sodium-ion batteries is presented. The method involves using an oligo-3,4-ethylenedioxythiophene precursor for high sulfur content hard carbon anode to investigate the sulfur heteroatom effect on the electrochemical sodium storage mechanism. By optimizing the condensation temperature, a significant transformation in the materials' nanostructure is achieved, leading to improved electrochemical performance. The use of in-operando small-angle X-ray scattering provides valuable insights into the interaction between micropores and sodium ions during the electrochemical processes. Lastly, the development of high-capacity hard carbon, derived from 5-hydroxymethyl furfural, is examined. This carbon material exhibits exceptional performance at both low and high current densities. Extensive electrochemical and physicochemical characterizations shed light on the sodium storage mechanism concerning the chemical environment, establishing the material's stability and potential applications in sodium-ion batteries.}, language = {en} } @phdthesis{Chung2013, author = {Chung, Kang Ko}, title = {Heteroatom-containing carbons for high energy density supercapacitor}, url = {http://nbn-resolving.de/urn:nbn:de:kobv:517-opus-69826}, school = {Universit{\"a}t Potsdam}, year = {2013}, abstract = {The supercapacitor is one of the most important energy storage devices as its construction allows for addressing many of the drawbacks related to batteries, but the low energy density of current systems is a major issue. In this doctoral dissertation, with a view to attaining high energy density supercapacitor systems that can be comparable to those for batteries, new heteroatom-containing carbons in the form of particles and three-dimensional films were investigated. A nitrogen-containing material, acrodam, was chosen as the carbon precursor due to the inexpensiveness, high carbonization yield, oligomerizability, etc. The carbon particles were prepared from acrodam together with caesium acetate as a meltable flux agent, and disclosed excellent properties in hydroquinone-loaded sulphuric acid electrolyte with high energy densities (up to 133.0 Wh kg-1) and sufficient cycle stabilities. These properties are already now comparable to those of batteries. Besides, conductive carbon three-dimensional films were fabricated using acrodam oligomer as the precursor by the inexpensive spin coating method. The films were found to be homogeneous, flat, void- and crack-free, and high conductivities (up to 334 S cm-1) could be obtained at the carbonization temperature of 1000 ºC. Furthermore, a porous carbon three-dimensional film could be formed using an organic template at the first attempt. This finding demonstrates the film's potentiality for various applications such as supercapacitor electrode; the essential absence of contact resistance within the network should contribute to effective transportation of electron within the electrode. The progress made in this dissertation will open a new way to further enhancement of energy density for supercapacitor as well as other applications that exceeds the current properties.}, language = {en} }