Abstract: Metal halide perovskite (MHP) quantum dots (QDs) offer immense potential for several areas of photonics research due to their easy and low-cost fabrication and excellent optoelectronic properties. However, practical applications of MHP QDs are limited by their poor stability and, in particular, their tendency to aggregate. Here, we develop a two-step double-solvent strategy to grow and confine CsPbBr3 QDs within the three-dimensional (3D) cavities of a mesoporous SBA-16 silica scaffold (CsPbBr3@SBA-16). Strong confinement and separation of the MHP QDs lead to a relatively uniform size distribution, narrow luminescence, and good ambient stability over 2 months. In addition, the CsPbBr3@SBA-16 presents a high activity and stability for visible-light-driven photocatalytic toluene C(sp(3))-H bond activation to produce benzaldehyde with similar to 730 mu mol g(-1) h(-1) yield rate and near-unity selectivity. Similarly, the structural stability of CsPbBr3@SBA-16 QDs is superior to that of both pure CsPbBr3 QDs and those confined in MCM-41 with 1D channels.

Abstract: Climate warming is severely affecting high-latitude regions. In the Arctic tundra, it may lead to enhanced soil nutrient availability and interact with simultaneous changes in grazing pressure. It is presently unknown how these concurrently occurring global change drivers affect the root-associated fungal communities, particularly mycorrhizal fungi, and whether changes coincide with shifts in plant mycorrhizal types. We investigated changes in root-associated fungal communities and mycorrhizal types of the plant community in a 10-yr factorial experiment with warming, fertilisation and grazing exclusion in a Finnish tundra grassland. The strongest determinant of the root-associated fungal community was fertilisation, which consistently increased potential plant pathogen abundance and had contrasting effects on the different mycorrhizal fungal types, contingent on other treatments. Plant mycorrhizal types went through pronounced shifts, with warming favouring ecto- and ericoid mycorrhiza but not under fertilisation and grazing exclusion. Combination of all treatments resulted in dominance by arbuscular mycorrhizal plants. However, shifts in plant mycorrhizal types vs fungi were mostly but not always aligned in their magnitude and direction. Our results show that our ability to predict shifts in symbiotic and antagonistic fungal communities depend on simultaneous consideration of multiple global change factors that jointly alter plant and fungal communities.

Abstract: Aim: We aimed to assess the impact of road disturbances on the dominant mycorrhizal types in ecosystems at the global level and how this mechanism can potentially lead to lasting plant community changes. Location: Globally distributed mountain regions Time Period: 2007-2018 Taxa studied: Plants (linked to their associated mycorrhizal fungi) Methods: We used a database of coordinated plant community surveys following mountain roads from 894 plots in 11 mountain regions across the globe in combination with an existing database of mycorrhizal-plant associations in order to approximate the relative abundance of mycorrhizal types in natural and disturbed environments. Results: Our findings show that roadside disturbance promotes the cover of plants associated with arbuscular mycorrhizal (AM) fungi. This effect is especially strong in colder mountain environments and in mountain regions where plant communities are dominated by ectomycorrhizal (EcM) or ericoid-mycorrhizal (ErM) associations. Furthermore, non-native plant species, which we confirmed to be mostly AM plants, are more successful in environments dominated by AM associations. Main Conclusions: These biogeographical patterns suggest that changes in mycorrhizal types could be a crucial factor in the worldwide impact of anthropogenic disturbances on mountain ecosystems. Indeed, roadsides foster AM-dominated systems, where AM-fungi might aid AM-associated plant species while potentially reducing the biotic resistance against invasive non-native species, often also associated with AM networks. Restoration efforts in mountain ecosystems will have to contend with changes in the fundamental make-up of EcM- and ErM plant communities induced by roadside disturbance.

Abstract: In a world increasingly reliant on alternative energy sources, the quest for efficient and secure storage solutions is paramount. This doctoral thesis explores the exciting potential of a familiar material – water – to act as a vault for next-generation energy sources like hydrogen (H2) and methane (CH4). Nature offers a solution in the form of clathrate hydrates, fascinating cage-like structures formed from water molecules that can trap these gas molecules within their framework. This research investigates on improving the formation kinetics and gas storage capabilities of clathrate hydrates utilizing porous materials and the interstitial space between non-porous materials to augment the contact between gas and water thereby catalysing the growth of hydrates and unlocking their full potential as efficient and secure energy storage reservoirs. A key outcome of this research is the formulation of an empirical correlation, offering predictive insights into CH4 hydrate phase equilibrium conditions. Innovative approaches utilizing thermally conductive beads have yielded substantial enhancements in CH4 uptake. Furthermore, the identification of optimal water content within porous materials showcases a pathway to maximize CH4 storage capacity and hydrate growth kinetics. In the domain of hydrogen storage, attention is also directed towards unstirred systems, where the integration of functionalized porous materials has demonstrated a significant improvement in the rate of hydrate formation and the overall H2 storage capacity. A noteworthy achievement of this research lies in the successful storage of H2 within confined CH4 hydrates through a gas exchange process and the preliminary results show the potential for safer and more sustainable method for H2 storage at mild thermodynamic conditions, offering promising prospects for future energy systems.

Abstract: Cu is one of the most promising materials as an electrocatalyst for the nitrate reduction reaction (NO3RR) to ammonia, a reaction that can simultaneously remove nitrates from wastewater and produce ammonia, a high-value commodity chemical. However, a rational approach to catalyst design is lacking, limiting efficient catalyst optimization. In this work, we propose a way to synthesize monodisperse, polycrystalline Cu NPs with small variances in size by changing the carbon chain length of the phosphonic acid-based ligand. Cu NPs with 8.3, 10.0, and 11.9 nm diameters are successfully synthesized, and high-resolution electron microscopy and tomography are used to characterize these NPs in depth. By isolating Cu NP size as a parameter, we can unequivocally establish its effect on electrochemical performance for the NO3RR to ammonia under optimal operating conditions for the catalyst (0.1 M KOH electrolyte at -1.25 V vs RHE, as established in the first phase). The smallest Cu NPs (8.3 nm with a TDPA ligand) perform best, achieving Faradaic efficiencies (FEs) of 85.4% and absolute current densities of similar to 250 mA cm(-2), with increasing current densities and constant FEs as the particle size decreases. To allow for a rational approach to Cu-based catalyst design from a stability perspective, this work completed a first study of the main degradation pathway that the Cu NPs undergo during NO3RR. High-resolution electron microscopy and tomography are used to characterize the particles at various stages of the reaction. The NPs undergo agglomeration, pulverization, and particle detachment due to the reaction, starting at a particle size of 8.3 nm and progressively getting smaller, but leveling off, until a NP size of 2.6 nm is reached after 2 h of electrolysis. This decrease in NP size goes paired with a decrease in FE from 83% after the first 15 min to 74% after 2 h at -0.75 V vs RHE, despite the increase in active surface area. These insights into the most prominent degradation mechanisms allow for rational adjustments to future catalysts to combat these changes; for example, by embedding NPs in a tailored support, morphological degradation could be impeded. Therefore, these insights allow for a rational approach to the improvement of the stability of Cu-based catalysts for the NO3RR, a very important but often an overlooked aspect of catalyst design.

Abstract: LaMnO 3 (LMO) thin films epitaxially grown on SrTiO 3 (STO) usually exhibit ferromagnetism above a critical layer thickness. We report the use of scanning SQUID microscopy (SSM) to study the suppression of the ferromagnetism in STO / LMO / metal structures. By partially covering the LMO surface with a metallic layer, both covered and uncovered LMO regions can be studied simultaneously. While Au does not significantly influence the ferromagnetic order of the underlying LMO film, a thin Ti layer induces a strong suppression of the ferromagnetism, over tens of nanometers, which increases with time on a timescale of days. Detailed electron energy loss spectroscopy analysis of the Ti-LaMnO 3 interface reveals the presence of Mn 2 + and an evolution of the Ti valence state from Ti 0 to Ti 4 + over approximately 5 nm. Furthermore, we demonstrate that by patterning Ti / Au overlayers, we can locally suppress the ferromagnetism and define ferromagnetic structures down to sub -micrometer scales.

Abstract: Steel shipwrecks buried along the Belgian and French North Sea coast have proven to show very low corrosion rates due to concretion. This work aims to provide an in-depth analysis of the formed concretion layers and gain a more complete understanding of the gradual deposition processes in the North Sea. Detailed microstructural characterization by scanning electron microscopy, energy dispersive x-ray spectroscopy, and x-ray diffraction of two different specimens demonstrates that the concretion includes a complex structure of multiple layers. Closest to the metal surface, a layer of 100% akaganeite is found. It forms from corrosion products exhibiting high Cl- ions concentrations at the metal surface. Next, other iron oxides, such as goethite, lepidocrocite, and magnetite, are observed. Then, layers that both contain corrosion products and compounds from the environment are present. These layers contain calcium carbonates (calcite and aragonite), calcium sulfate (gypsum), and quartz (sand). Moreover, due to a displacement of calcium by iron, an additional phase is formed consisting out of hard, dense siderite mixed into calcite. Finally, the surface of the concretion is covered by a biofilm.

Abstract: We investigated the electron-phonon ( e -ph ) coupling and vibrational thermal conductivity in the representative MAB compounds, namely MoAlB, WAlB, Tc 2 AlB 2 , and Cr 2 AlB 2 . The spectral distribution functions of e -ph interaction, obtained through ab initio linear-response calculations, reveal that the electron-phonon coupling values range from low (0.15) to moderate (0.58). With such e -ph coupling, out of the considered compounds, only Tc 2 AlB 2 exhibits a superconducting transition, at 4 K. We further evaluated the thermal conductivity and associated properties like scattering rates, obtained using ab initio and other methodologies. The latter included the iterative solution of the Peierls-Boltzmann transport equation, using HIPHIVE package for advanced optimization and machine learning techniques, and employing maximum likelihood estimation to approximate scattering rates from a limited set of scattering processes. We found that these methods yield nearly identical predictions for thermal conductivity values, with a significant decrease in the computational cost compared to the first-principles methods. We examined interactions arising from both three-phonon (3 ph ) and four -phonon (4 ph ) scattering processes. The 4 ph interactions demonstrated a smaller yet significant impact on the overall vibrational thermal conductivity, most notably in Tc 2 AlB 2 . Our findings indicate that Cr 2 AlB 2 has the highest thermal conductivity across all considered crystal directions, with the thermal conductivity being spatially anisotropic, most pronouncedly in Tc 2 AlB 2 . Finally, we show that empirical expressions based on Slack models are well suited for screening the thermal conductivity properties of MAB phases, and can be employed to establish upper and lower limits of their thermal conductivity.

Abstract: We present a detailed theoretical investigation on the electronic transport properties of n-type monolayer (ML) transition metal dichalcogenides (TMDs) at low temperature in the presence of proximity-induced interactions such as Rashba spin-orbit coupling (RSOC) and the exchange interaction. The electronic band structure is calculated by solving the Schr & ouml;dinger equation with a k <middle dot> p Hamiltonian, and the electric screening induced by electron-electron interaction is evaluated under a standard random phase approximation approach. In particular, the longitudinal and transverse or Hall mobilities are calculated by using a momentum-balance equation derived from a semiclassical Boltzmann equation, where the electron-impurity interaction is considered as the principal scattering center at low temperature. The obtained results show that the RSOC can induce the in-plane spin components for spin-split subbands in different valleys, while the exchange interaction can lift the energy degeneracy for electrons in different valleys. The opposite signs of Berry curvatures in the two valleys would introduce opposite directions of Lorentz force on valley electrons. As a result, the transverse currents from nondegenerate valleys can no longer be canceled out so that the transverse current or Hall mobility can be observed. Interestingly, we find that at a fixed effective Zeeman field, the lowest spin-split conduction subband in ML-TMDs can be tuned from one in the K'-valley to one in the K-valley by varying the Rashba parameter. The occupation of electrons in different valleys also varies with changing carrier density. Therefore, we can change the magnitude and direction of the Hall current by varying the Rashba parameter, effective Zeeman field, and carrier density by, e.g., the presence of a ferromagnetic substrate and/or applying a gate voltage. By taking the ML-MoS2 as an example, these effects are demonstrated and examined. The important and interesting theoretical findings can be beneficial to experimental observation of the valleytronic effect and to gaining an in-depth understanding of the ML-TMD systems in the presence of proximity-induced interactions.

Abstract: The stability of the dumbbell structure has been confirmed by previous theory and experiment. Based on firstprinciples calculations, we proposed hexagonal dumbbell graphene (HDB C10) and rectangular dumbbell graphene (RDB C10) monolayers containing periodically raised C (CR) atoms. They turn out to have high mobility semiconductor properties. By adsorbing H atoms on these CR atoms, their band structures can be widely tuned from semiconductor to semimetal. When considering adsorption of two/four H atoms on the unit cell of the dumbbell structure, the bandgap can be increased, and isolated flat band structures can be obtained by further adding or removing H atoms. Remarkably, two different Dirac band structures can be found in the HDB/RDB C10H2-I monolayers. The HDB C10H2-I shows a Dirac cone with isotropic Fermi velocities, while the RDB C10H2-I monolayer exhibits a quasi-one-dimensional Dirac nodal line with varying Fermi velocities along the XS path. Tight-binding (TB) models are constructed including nearest neighbor (NN) and next NN hopping in order to understand our DFT results. These TB models are related to the Su-Schrieffer-Heeger model, and are able to explain the tunable topological properties of the RDB C10H2-I monolayer. They not only are able to explain the different kinds of Fermi velocity, but also can predict the emergence of topological edge states, providing a good platform for research on Dirac fermions. The HDB/RDB C10 monolayer exhibits more freedom of tunable band structures and more stable hydrogen storage capacity, making it superior to graphene. Finally, possible experimental synthesis paths of these DB monolayers are provided.

Abstract: We detail the magnetic properties of monolayer CrX2 and its Janus counterparts CrXY (X, Y = S, Se, Te, with X not equal Y) using ab initio methods and Landau-Lifshitz-Gilbert magnetization dynamics, and uncover the pronouncedly strong interplay between their structure symmetry and the magnetic order. The relaxation of nonmagnetic chalcogen atoms, that carry large spin-orbit coupling, changes the energetically preferential magnetic order between in-plane antiferromagnetic and tilted ferromagnetic one. The considered Janus monolayers exhibit sizable Dzyaloshinskii-Moriya interaction, in some cases above 20% of the isotropic exchange, and critical temperature of the long-range magnetic order in the vicinity or even significantly above the room temperature.

Abstract: In the context of global challenges such as climate change and environmental pollution, photocatalysis evolved as one of the promising strategies for sustainable energy conversion and pollutant degradation. In this thesis, photocatalysis using gas phase deposited bimetallic nanoclusters (BNCs) on TiO2 supports is studied in the context of self-cleaning surfaces and photoelectrochemical (PEC) water splitting applications. Thanks to their plasmonic properties, BNCs made of coinage metals can serve as efficient cocatalysts for the degradation of organic pollutants and surface contaminants under light irradiation. They also hold great promise for PEC water splitting, a promising pathway for renewable hydrogen production, which can be used in hydrogen fuel cells or for the environmentally friendly production of fuels in, for example, CO2 hydrogenation processes. The small size and high surface-to-volume ratio of plasmonic BNCs play pivotal roles in influencing the efficiency and selectivity of photocatalytic processes. BNCs have unique optical, physical, chemical, and structural properties distinctly different from their bulk and monometallic counterparts. These properties can be fine-tuned at the single particle level by their size, composition, and atomic arrangement, but also by interaction with other particles through the coverage and through interaction with the support. To design better photocatalysts it is crucial to carefully understand the BNCs’ characteristic properties, especially at the atomic level where synergies between different elements are sought. To achieve this objective, BNCs with well-defined sizes and compositions are deposited on TiO2 supports and we studied their structural properties and their influence on the photocatalytic activity. The general procedure followed in this thesis is the production and deposition of BNCs on TiO2 by the cluster beam deposition (CBD) technique, followed by structural and optical characterization to understand their tailored properties, and photocatalytic testing either for photodecomposition of organic molecules or PEC water splitting. In a first study, AuxAg1-x (x = 1, 0.9, 0.7, 0.5, 0.3, and 0) alloy BNCs with different compositions are synthesized in the gas phase and deposited from a molecular beam on TiO2 P25 supports. The photocatalytic self-cleaning activity of as-prepared samples is tested under UV and visible light towards stearic acid (SA) degradation. SA is a widely accepted model contaminant, which represents the group of organic fouling compounds that typically contaminates glass surfaces. A composition-dependent activity is observed with the Au0.3Ag0.7 nanocluster modified TiO2 exhibiting the highest photoactivity. Scanning transmission electron microscopy (STEM) measurements reveal that, for a mass loading corresponding to an equivalent of 4 atomic monolayers (MLs), the BNCs are uniformly distributed over the surface. The clusters have an average size of 3.5 ± 0.5 nm and are crystalline in nature. The atomic structure is characterized by X-ray absorption fine structure (XAFS) spectroscopy and their electronic structure by X-ray photoelectron spectroscopy (XPS). These measurements demonstrate a charge redistribution between the Ag and Au atoms when alloyed at the nanoscale. The effect of this charge redistribution is likely the stabilization of Ag against oxidation and directly affects the catalytic properties of the clusters. It is suggested that the highest photoactivity of 4 ML loaded Au0.3Ag0.7 under solar light results from a combination of four main possible contributing factors: (i) injection in TiO2 of excited carriers that are generated by the localized surface plasmon resonance (LSPR) effect of the BNCs in the visible light wavelength range which overlaps with the sun’s irradiance spectrum. (ii) a strong near-field enhancement that increases the photoabsorption by the TiO2 for photons that have enough energy to overcome the high bandgap, (iii) the optimized total metal loading of 4 ML leaves enough of the TiO2 surface accessible for light absorption, and finally (iv) an effective charge distribution between Au and Ag. This study demonstrates that CBD is an efficient approach for fabricating well-defined, tunable AuAg plasmon-based photocatalysts for self-cleaning applications, outperforming their monometallic counterparts as well as bimetallic alternatives obtained through colloidal methods. In a second study, titania nanotubes (TNTs) are modified with a series of AuxCu1-x (x = 1, 0.75, 0.5, 0.25, and 0) BNCs using the CBD technique. Based on the results of the first study, we opted again for a loading of 4 ML. TNTs are known for their high surface area, fast charge transfer, and corrosion resistance, while keeping the inherent strengths of traditional TiO2 materials. They prove to be promising photoanodes, enhancing photocurrent in PEC applications for water oxidation. In this work the TNTs are grown via anodic oxidation of a titanium metal foil. The crystalline anatase phase of the grown TNTs is confirmed by the X-ray diffraction technique (XRD), while transmission electron microscopy (TEM) provides information about the size and composition of the deposited BNCs. XAFS provides further structural information, while XPS measurements reveal charge redistribution between Au and Cu, which can aid in the enhancement of the PEC activity. Oxidation of as-prepared electrodes over the time results in structural changes with CuxO at the outer shell functioning as a protective layer, while the majority of the core is an alloy. The optical properties, studied through UV-Vis spectroscopy confirm the extended absorption range of the cluster-modified TNTs towards the visible region. The charge carrier recombination rate is derived from photoluminescence (PL) measurements. The as-prepared electrodes are tested photoelectrochemically for the generation of an anodic photocurrent using simulated sunlight. It is found that the AuxCu1-x (x = 1, 0.75, 0.5, 0.25 and 0) BNC modified TNTs show a remarkable enhancement in the anodic photocurrent relative to pristine TNTs, with Au0.25Cu0.75 exhibiting the highest photocurrent. This is due to the combination of many possible factors. Firstly, the charge redistribution between Au and Cu and increase stability of the Au0.25Cu0.75 electrode as observed in XAFS, indicates that the electronic effect in the cluster is also one of the governing factors for PEC activity. Secondly, formation of a surface CuOx layer, protects against further corrosion of the metallic AuCu BNCs cores. Third, reduced recombination of charge carriers is indicated by lower photoluminescent (PL) intensity compared to pristine TNTs and all other electrodes except pure gold, as observed in PL spectra. This implies that the generated charge carriers are efficiently separated by Au0.25Cu0.75 NCs acting as electron sinks and easily available for redox reactions. Fourth, the highest interfacial charge transfer efficiency is evidenced by the electrochemical impedance spectroscopy (EIS), leading to more efficacious charge migration and separation, facilitating the water oxidation surface reaction. A final beneficial factor is the uniform deposition of well-defined, size- and composition-controlled, ligand-free BNCs. Such BNCs provide more effective surface sites to the reaction medium, in contrast to electrodes synthesized by e.g. sol-gel methods, where (in)organic residues on metal surfaces may decrease the efficiency.

Abstract: Transmission electron microscopy is an important technique in the exploration of materials’ structures. This is especially true since the development of electron optical aberration correctors greatly facilitated atomic resolution imaging. We are currently experiencing an ongoing revolution in electron microscopy with the widespread adoption of direct electron detectors. Scientists have reported a lot of key scientific findings facilitated by direct electron detectors. One particular research domain is electron ptychography, which holds promise for unraveling the intricate structures of highly beam-sensitive materials like bio samples and achieving super-resolution without the limitation of aperture in the condenser lens system. Nevertheless, challenges persist both in experimental setups and algorithmic processes. Issues such as the comparatively sluggish scanning speed of cameras and contrast reversals of the reconstructed phase for relatively thick specimens, disrupting phase or weak phase approximations, remain noteworthy limitations. This thesis addresses these challenges by the event-driven Timepix3 detector, presenting a viable solution to the speed bottleneck. Moreover, innovative approaches for applying electron ptychography to relatively thick samples, employing a middle focusing strategy, are proposed. This research aims to push the boundaries of electron microscopy, offering solutions to existing limitations and advancing the field towards more efficient and accurate imaging techniques.

Abstract: In the pursuit of higher critical temperature of superconductivity, quasiflat electronic bands and Van Hove singularities in two dimensions (2D) have emerged as a potential approach to enhance Cooper pairing on the basis of mean-field expectations. However, these special electronic features suppress the superfluid stiffness and, hence, the Berezinskii-Kosterlitz-Thouless (BKT) transition in 2D superconducting systems, leading to the emergence of a significant pseudogap regime due to superconducting fluctuations. In the strong-coupling regime, one finds that superfluid stiffness is inversely proportional to the superconducting gap, which is the predominant factor contributing to the strong suppression of superfluid stiffness. Here we reveal that the aforementioned limitation is avoided in a 2D superconducting electronic system with a quasiflat electronic band with a strong pairing strength coupled to a deep band with weak electronic pairing strength. Owing to the multiband effects, we demonstrate a screening-like mechanism that circumvents the suppression of the superfluid stiffness. We report the optimal conditions for achieving a large enhancement of the BKT transition temperature and a substantial shrinking of the pseudogap regime by tuning the intraband couplings and the pair-exchange coupling between the two band-condensates.