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The main aim of this paper is to introduce a solution for network analysis based on pgRouting to resolve the bicycle accessibility of forested green spaces. The proposed application uses open-source software tools such as PostgreSQL with PostGIS extension. The solution includes a complete description of how to perform network analysis using a spatial database with SQL and pgRouting. The implemented functionalities consist of solutions for finding the equidistance or isochrone area for any selected point location. The method is tested on case study data drawn from a total of 9,500 km of roads suitable for cyclists in the Poznań Metropolitan Area, located in western Poland. The results of the analysis were isochrones determining the bicycle accessibility of forested areas. The accessibility analysis was performed considering an urbanised residential area. As a result of the analysis, locations with the best and limited access to forested green areas were identified. Moreover, the described methodology is ready to be used to solve various accessibility problems.

Solid-state batteries possess the potential to significantly impact energy storage industries by enabling diverse benefits, such as increased safety and energy density. However, challenges persist with physicochemical properties and processes at electrode/electrolyte interfaces. Thus, there is great need to characterize such interfaces in situ, and unveil scientific understanding that catalyzes engineering solutions. To address this, we conduct multiscale in situ microscopies (optical, atomic force, and infrared near-field) and Fourier transform infrared spectroscopies (near-field nanospectroscopy and attenuated total reflection) of intact and electrochemically operational graphene/solid polymer electrolyte interfaces. We find nanoscale structural and chemical heterogeneities intrinsic to the solid polymer electrolyte initiate a cascade of additional interfacial nanoscale heterogeneities during Li plating and stripping; including Li-ion conductivity, electrolyte decomposition, and interphase formation. Moreover, our methodology to nondestructively characterize buried interfaces and interphases in their native environment with nanoscale resolution is readily adaptable to a number of other electrochemical systems and battery chemistries. Solid-state batteries remain promising but essential insights into electrode-electrolyte interface are required. Here, the authors report in situ infrared nanospectroscopy of the lithium-polymer-electrolyte interface to reveal its intrinsic molecular, structural, and chemical heterogeneities.

The main aim of the study was to introduce a spatial database application for the estimation of changes in shoreline position. The open-source PostgreSQL database system with the PostGIS spatial extension was used as the data store for digitalised shorelines. The solution to calculations of the shoreline changes was based on the functions written in the PL/SQL language and geospatial functions provided by the PostGIS extension. The traditional method was used to quantify the distances and rate of shoreline movement. Outputs of the calculations were stored in the database table and simply visualised using graphical functions in the R software environment or in GIS Desktop software. The advantage of presented method is the application of SQL language in the analysis of the relation between the geometry of shorelines stored in the database table, which, compared to other similar solutions, gives the user fully open, simple analytical code and enable selecting custom parameters of analysis, modifying code and performing additional calculations.

Herein, we present a scalable approach for the synthesis of a hydrogen-bonded organic–inorganic framework via coordination-driven supramolecular chemistry, for efficient remediation of trace heavy metal ions from water. In particular, using copper as our model ion of interest and inspired by nature’s use of histidine residues within the active sites of various copper binding proteins, we design a framework featuring pendant imidazole rings and copper-chelating salicylaldoxime, known as zinc imidazole salicylaldoxime supramolecule. This material is water-stable and exhibits unprecedented adsorption kinetics, up to 50 times faster than state-of-the-art materials for selective copper ion capture from water. Furthermore, selective copper removal is achieved using this material in a pH range that was proven ineffective with previously reported metal–organic frameworks. Molecular dynamics simulations show that this supramolecule can reversibly breathe water through lattice expansion and contraction, and that water is initially transported into the lattice through hopping between hydrogen-bond sites. Heavy metals and metalloids pose major threats to health and environmental ecosystems, thus systems for low-cost remediation are needed. Here the authors report the scalable design of a hydrogen-bonded organic–inorganic framework for selective removal of trace heavy metal ions from water.

C–H bond activation enables the facile synthesis of new chemicals. While C–H activation in short-chain alkanes has been widely investigated, it remains largely unexplored for long-chain organic molecules. Here, we report light-driven C–H activation in complex organic materials mediated by 2D transition metal dichalcogenides (TMDCs) and the resultant solid-state synthesis of luminescent carbon dots in a spatially-resolved fashion. We unravel the efficient H adsorption and a lowered energy barrier of C–C coupling mediated by 2D TMDCs to promote C–H activation and carbon dots synthesis. Our results shed light on 2D materials for C–H activation in organic compounds for applications in organic chemistry, environmental remediation, and photonic materials. C–H activation in long-chain organic molecules remains largely unexplored. Here, the authors report light-driven C–H activation mediated by 2D TMDCs and the resultant synthesis of luminescent carbon dots.

Further improvements to lithium-ion and emerging battery technologies can be enabled by an improved understanding of the chemistry and working mechanisms of interphases that form at electrochemically active battery interfaces. However, it is difficult to collect and interpret spectra of interphases for several reasons, including the presence of a variety of compounds. To address this challenge, we herein present a vibrational spectroscopy and X-ray diffraction data library of ten compounds that have been identified as interphase constituents in lithium-ion or emerging battery chemistries. The data library includes attenuated total reflectance Fourier transform infrared spectroscopy, Raman spectroscopy, and X-ray diffraction data, collected in inert atmospheres provided by custom sample chambers. The data library presented in this work (and online repository) simplifies access to reference data that is otherwise either diffusely spread throughout the literature or non-existent, and provides energy storage researchers streamlined access to vital interphase-relevant data that can accelerate battery research efforts.

Electrochemical technologies add a unique dimension for ore refinement, representing tunable methods that can integrate with renewable energy sources and existing downstream process flows. However, the development of electrochemical extraction technologies has been impeded by the technological maturity of hydro- and pyro-metallurgy, as well as the electrical insulating properties of many metal oxide ores. The fabrication and use of carbon/insulating material composite electrodes has been a longstanding method to enable electrochemical activation. Here, using real hectorite ore, we employ this technical approach to fabricate hectorite-carbon black composite electrodes (HCCEs) and achieve electrochemical activation of hectorite. Anodic polarization results in lithium-ion release through a multi-step chemical and electrochemical mechanism that results in 50.7 ± 4.4% removal of lithium from HCCE, alongside other alkaline ions. This technical proof-of-concept study underscores that electrochemical activation of ores can facilitate lattice deterioration and ion removal from ores. Electrochemical technologies for ore refinement provide a unique opportunity to integrate with renewable energy sources but are impeded by the insulating properties of many ores. Here, the authors take inspiration from the lithium-ion battery field and fabricate hectorite–carbon black composite electrodes to enhance electron percolation into hectorite enabling lithium-ion release through a multi-step (electro)chemical mechanism.

Al-substituted Li 7 La 3 Zr 2 O 12 samples processed under argon show enhanced Li-ion transport and interfacial properties in symmetrical cells with lithium electrodes, compared to those prepared in air. In particular, the samples prepared under argon have higher ionic conductivities and lower interfacial impedances in symmetrical lithium cells, and show better DC cycling characteristics. The electronic conductivities are also somewhat higher. Pellets subjected to thermal treatment under the two types of atmospheres have different colors but exhibit similar microstructures. X-ray diffraction experiments suggest that there are slight structural differences between the two types of samples, but few dissimilarities were observed in elemental composition, distribution of ions, oxidation states, or bond lengths using laser-induced breakdown spectroscopy (LIBS), x-ray photoelectron spectroscopy (XPS), and extended x-ray absorption fine structure spectroscopy (EXAFS) to analyze the materials. Additionally, there was no evidence that La or Zr were reduced during the processing under Ar. Possible explanations for the improved electrochemical properties of the sample prepared under Ar compared to the one prepared in air include differences in grain boundary chemistries and conductivities and/or a small concentration of oxygen vacancies in the former.

Demand for lithium for batteries and other green technologies is exploding. The industry must develop sustainable methods to remove and process the element from ores and brines to avoid environmental damage. Demand for lithium for batteries and other green technologies is exploding. The industry must develop sustainable methods to remove and process the element from ores and brines to avoid environmental damage. Two workers wearing yellow overalls in a lithium evaporation pond in the Atacama desert, Chile

Foraminiferal assemblages were analyzed in a 620-cm long core retrieved from the central part of the Mecklenburg Bay (MB, south-western Baltic Sea) to aid in the reconstruction of environmental changes occurring in the area during the Holocene and to complement a set of previously investigated palaeoenvironmental proxies. A total of five foraminifera-based stratigraphic units were identified, including an initial 80-cm thick layer devoid of foraminifera. The next two units featured an increasing abundance of the foraminiferal assemblage dominated by the calcareous group species. Nearly all the calcareous foraminifera found in the core were decalcified. Following the maximum abundance within the 470–410 cm layer, the foraminiferal abundance declined sharply and the assemblage’s dominance structure changed to domination of the agglutinated foraminiferal species, , which continued up to the top of the core and marked a pronounced shift in environmental conditions (shallower depth, lower salinity, more dynamic sedimentation conditions). The foraminifera-based stratigraphy of the core proved to be complementary to that emerging from previous analyses of diatoms and sediment geochemistry.