Local and landscape factors shape alpha and beta trophic interaction diversity in urban gardens.

Promoting urban green spaces is an effective strategy to increase biodiversity in cities. However, our understanding of how local and landscape factors influence trophic interactions in these urban contexts remains limited. Here, we sampled cavity-nesting bees and wasps and their natural enemies within 85 urban gardens in Zurich (Switzerland) to identify factors associated with the diversity and dissimilarity of antagonistic interactions in these communities. The proportions of built-up area and urban green area at small landscape scales (50 m radius), as well as the management intensity, sun exposure, plant richness and proportion of agricultural land at the landscape scale (250 m radius), were key drivers of interaction diversity. This increased interaction diversity resulted not only from the higher richness of host and natural enemy species, but also from species participating in more interactions. Furthermore, dissimilarity in community structure and interactions across gardens (beta-diversity) were primarily influenced by differences in built-up areas and urban green areas at the landscape scale, as well as by management intensity. Our study offers crucial insights for urban planning and conservation strategies, supporting sustainability goals by helping to understand the factors that shape insect communities and their trophic interactions in urban gardens.

Vertically oriented low-dimensional perovskites for high-efficiency wide band gap perovskite solar cells.

Controlling crystal growth alignment in low-dimensional perovskites (LDPs) for solar cells has been a persistent challenge, especially for low-n LDPs (n < 3, n is the number of octahedral sheets) with wide band gaps (>1.7 eV) impeding charge flow. Here we overcome such transport limits by inducing vertical crystal growth through the addition of chlorine to the precursor solution. In contrast to 3D halide perovskites (APbX3), we find that Cl substitutes I in the equatorial position of the unit cell, inducing a vertical strain in the perovskite octahedra, and is critical for initiating vertical growth. Atomistic modelling demonstrates the thermodynamic stability and miscibility of Cl/I structures indicating the preferential arrangement for Cl-incorporation at I-sites. Vertical alignment persists at the solar cell level, giving rise to a record 9.4% power conversion efficiency with a 1.4 V open circuit voltage, the highest reported for a 2 eV wide band gap device. This study demonstrates an atomic-level understanding of crystal tunability in low-n LDPs and unlocks new device possibilities for smart solar facades and indoor energy generation.

Responsive Optical Materials Based on Ligand-Free Perovskite Quantum Dots Embedded in Mesoporous Scaffolds.

Herein we show that dispersing inorganic cesium lead bromide (CsPbBr3) perovskite quantum dots (QDs) in optical quality films, possessing an accessible and controlled pore size distribution, gives rise to fluorescent materials with a controlled and highly sensitive response to ambient changes. A scaffold-based synthesis approach is employed to obtain ligand-free QDs, whose pristine surface endows them with high sensitivity to the presence of different vapors in their vicinity. At the same time, the void network of the host offers a means to gradually expose the embedded QDs to such vapors. Under these conditions, the luminescent response of the QDs is mediated by the mesostructure of the matrix, which determines the rate at which vapor molecules will adsorb onto the pore walls and, eventually, condensate, filling the void space. With luminescence quantum yields as high as 60%, scaffold-supported ligand-free perovskite nanocrystals display intense photoemission signals over the whole process, as well as high photo- and chemical stability, which allows illuminating them for long periods of time and recovering the original response upon desorption of the condensed phase. The results herein presented open a new route to explore the application of perovskite QD-based materials in sensing.

Enhancing charge extraction in inverted perovskite solar cells contacts via ultrathin graphene:fullerene composite interlayers.

Improving the perovskite/electron-transporting layer (ETL) interface is a crucial task to boost the performance of perovskite solar cells (PSCs). This is utterly fundamental in an inverted (p-i-n) configuration using fullerene-based ETLs. Here, we propose a scalable strategy to improve fullerene-based ETLs by incorporating high-quality few-layer graphene flakes (GFs), industrially produced through wet-jet milling exfoliation of graphite, into phenyl-C61-butyric acid methyl ester (PCBM). Our new composite ETL (GF:PCBM) can be processed into an ultrathin (∼10 nm), pinhole-free film atop the perovskite. We find that the presence of GFs in the PCBM matrix reduces defect-mediated recombination, while creating preferential paths for the extraction of electrons towards the current collector. The use of our GF-based composite ETL resulted in a significant enhancement in the open circuit voltage and fill factor of triple cation-based inverted PSCs, boosting the power conversion efficiency from ∼19% up to 20.8% upon the incorporation of GFs into the ETL.

Nonmonotonic Photostability of BA2MAn-1PbnI3n+1 Homologous Layered Perovskites.

Layered lead halide perovskites (2D LHPs) are attracting considerable attention as a promising material for a new generation of solar cell devices. LHPs have been presented as a more stable alternative to the more widespread 3D bulk perovskite materials; however, a critical analysis of their photostability is still lacking. In this work, we perform a comparative study between BA2MAn-1PbnI3n+1 (BA─butylammonium and MA─methylammonium) 2D LHPs with different dimensionalities (n = 1-3) and MAPbI3 3D perovskites. We compare different stability testing protocols including photometrical determination of iodine-containing products in nonpolar solvents, X-ray diffraction, and photoluminescence (PL) spectroscopy. The resulting trends of the photostability in an inert atmosphere based on PL spectroscopy measurements demonstrate a nonmonotonic dependence of the degradation rate on the perovskite layer thickness n with a "stability island" at n ≥ 3, which is caused by a combination of antibate factors of electronic structures and chemical compositions in the family of 2D perovskites. We also identify a critical oxygen concentration in the surrounding environment that affects the mechanism and strongly enhances the rate of layered perovskite photodegradation.

Manipulating Color Emission in 2D Hybrid Perovskites by Fine Tuning Halide Segregation: A Transparent Green Emitter.

Halide perovskite materials offer an ideal playground for easily tuning their color and, accordingly, the spectral range of their emitted light. In contrast to common procedures, this work demonstrates that halide substitution in Ruddlesden-Popper perovskites not only progressively modulates the bandgap, but it can also be a powerful tool to control the nanoscale phase segregation-by adjusting the halide ratio and therefore the spatial distribution of recombination centers. As a result, thin films of chloride-rich perovskite are engineered-which appear transparent to the human eye-with controlled tunable emission in the green. This is due to a rational halide substitution with iodide or bromide leading to a spatial distribution of phases where the minor component is responsible for the tunable emission, as identified by combined hyperspectral photoluminescence imaging and elemental mapping. This work paves the way for the next generation of highly tunable transparent emissive materials, which can be used as light-emitting pixels in advanced and low-cost optoelectronics.

Litter decomposition driven by soil fauna, plant diversity and soil management in urban gardens.

In the face of growing urban densification, green spaces in cities, such as gardens, are increasingly important for biodiversity and ecosystem services. However, the influences of urban green space management on biodiversity and ecosystem functioning (BEF) relationships is poorly understood. We investigated the relationship between soil fauna and litter decomposition in 170 urban garden sites along a gradient of urbanisation intensity in the city of Zurich, CH. We used litter bags of 1 and 4 mm mesh size to evaluate the contribution of soil meso- and macrofauna on litter decomposition. By using multilevel structural equation models (SEM), we investigated direct and indirect environmental effects and management practices on litter decomposition and litter residue quality. We evaluated the role of taxonomic, functional and phylogenetic diversity of soil fauna species on litter decomposition, based on a sample of 120 species (81,007 individuals; 39 collembola, 18 earthworm, 16 isopod, 47 gastropod species). We found highest litter decomposition rates using 4 mm mesh size litter bags, highlighting the importance of soil macrofauna. Urban warming, a proxy for urbanisation intensity, covaried positively, whereas soil disturbances, such as intensive soil and crop management, were negatively correlated with decomposition rates. Interestingly, soil fauna species richness decreased, with the exception of gastropods, and soil fauna abundance increased with urban warming. Our data also show that plant species richness positively affected litter decomposition by increasing soil fauna species richness and microbial activity. A multivariate analysis of organic compounds in litter residues confirmed the importance of soil fauna species richness and garden management on litter decomposition processes. Overall, we showed, that also in intensively managed urban green spaces, such as gardens, biodiversity of plants and soil fauna drives key ecosystem processes. Urban planning strategies that integrate soil protecting management practices may help to maintain important ecosystem services in this heavily used urban environment.