Hierarchies of Hofstadter butterflies in 2D covalent organic frameworks

The Hofstadter butterfly is one of the first and most fascinating examples of the fractal and self-similar quantum nature of free electrons in a lattice pierced by a perpendicular magnetic field. However, the direct experimental verification of this effect on single-layer materials is still missing as very strong and inaccessible magnetic fields are necessary. For this reason, its indirect experimental verification has only been realized in artificial periodic 2D systems, like moiré lattices. The only recently synthesized 2D covalent organic frameworks might circumvent this limitation: Due to their large pore structures, magnetic fields needed to detect most features of the Hofstadter butterfly are indeed accessible with today technology. This work opens the door to make this exotic and theoretical issue from the 70s measurable and might solve the quest for the experimental verification of the Hofstadter butterfly in single-layer materials. Moreover, the intrinsic hierarchy of different pore sizes in 2D covalent organic framework adds additional complexity and beauty to the original butterflies and leads to a direct accessible playground for new physical observations

Hierarchies of Hofstadter butterflies in 2D covalent-organic frameworks

The Hofstadter butterfly is one of the first and most fascinating examples of the fractal and self-similar quantum nature of free electrons in a lattice pierced by a perpendicular magnetic field. However, the direct experimental verification of this effect on single-layer materials is still missing as very strong and inaccessible magnetic fields are necessary. For this reason, its indirect experimental verification has only been realized in artificial periodic 2D systems, like moir\'e lattices. The only recently synthesized 2D covalent-organic frameworks might circumvent this limitation: Due to their large pore structures, magnetic fields needed to detect most features of the Hofstadter butterfly are indeed accessible with today's technology. This work opens the door to making this exotic and theoretical issue from the 70s measurable and might solve the quest for the experimental verification of the Hofstadter butterfly in single-layer materials. Moreover, the intrinsic hierarchy of different pore sizes in a 2D covalent-organic framework adds additional complexity and beauty to the original butterflies and leads to a directly accessible playground for new physical observations

Control of Crystallinity of Vinylene-Linked Two-Dimensional Conjugated Polymers by Rational Monomer Design

The interest in two-dimensional conjugated polymers (2D CPs) has increased significantly in recent years. In particular, vinylene-linked 2D CPs with fully in-plane sp2-carbon-conjugated structures, high thermal and chemical stability, have become the focus of attention. Although the Horner-Wadsworth-Emmons (HWE) reaction has been recently demonstrated in synthesizing vinylene-linked 2D CPs, it remains largely unexplored due to the challenge in synthesis. In this work, we reveal the control of crystallinity of 2D CPs during the solvothermal synthesis of 2D-poly(phenylene-quinoxaline-vinylene)s (2D-PPQVs) and 2D-poly(phenylene-vinylene)s through the HWE polycondensation. The employment of fluorinated phosphonates and rigid aldehyde building blocks is demonstrated as crucial factors in enhancing the crystallinity of the obtained 2D CPs. Density functional theory (DFT) calculations reveal the critical role of the fluorinated phosphonate in enhancing the reversibility of the (semi)reversible C−C single bond formation

Structural Reinforcement in Mechanically Interlocked Two-Dimensional Polymers by Suppressing Interlayer Sliding

Preserving the superior mechanical properties of monolayer two-dimensional (2D) materials when transitioning to bilayer and layer-stacked structures poses a great challenge, primarily arising from the weak van der Waals (vdW) forces that facilitate interlayer sliding and decoupling. Here, we discover that mechanically interlocked 2D polymers (2DPs) offer a means for structural reinforcement from monolayer to bilayer. Incorporating macrocyclic molecules with one and two cavities into 2DPs backbones enables the precision synthesis of mechanically interlocked monolayer (MI-M2DP) and bilayer (MI-B2DP). Intriguingly, we have observed an exceptionally high effective Young's modulus of 222.4 GPa for MI-B2DP, surpassing those of MI-M2DP (130.1 GPa), vdW-stacked MI-M2DPs (2 MI-M2DP, 8.1 GPa) and other reported multilayer 2DPs. Modeling studies demonstrate the extraordinary effectiveness of mechanically interlocked structures in minimizing interlayer sliding (~0.1 {\AA}) and energy penalty (320 kcal/mol) in MI-B2DP compared to 2 MI-M2DP (~1.2 {\AA}, 550 kcal/mol), thereby suppressing mechanical relaxation and resulting in prominent structural reinforcement

Site-selective chemical reactions by on-water surface sequential assembly

Controlling site-selectivity and reactivity in chemical reactions continues to be a key challenge in modern synthetic chemistry. Here, we demonstrate the discovery of site-selective chemical reactions on the water surface via a sequential assembly approach. A negatively charged surfactant monolayer on the water surface guides the electrostatically driven, epitaxial, and aligned assembly of reagent amino-substituted porphyrin molecules, resulting in a well-defined J-aggregated structure. This constrained geometry of the porphyrin molecules prompts the subsequent directional alignment of the perylenetetracarboxylic dianhydride reagent, enabling the selective formation of a one-sided imide bond between porphyrin and reagent. Surface-specific in-situ spectroscopies reveal the underlying mechanism of the dynamic interface that promotes multilayer growth of the site-selective imide product. The site-selective reaction on the water surface is further demonstrated by three reversible and irreversible chemical reactions, such as imide-, imine-, and 1, 3-diazole (imidazole)- bonds involving porphyrin molecules. This unique sequential assembly approach enables site-selective chemical reactions that can bring on-water surface synthesis to the forefront of modern organic chemistry

Using Image-based AI for insect monitoring and conservation - InsectAI COST Action

The InsectAI COST action will support insect monitoring and conservation at the national and continental scale in order to understand and counteract widespread insect declines. The Action will bring together a critical mass of researchers and stakeholders in image-based insect AI technologies to direct and drive the research agenda, build research capacity across Europe and support innovation and application. There is mounting evidence that populations of insects around the world are in sharp decline. Understanding trends in species and their drivers is key to knowing the size of the challenge, its causes and how to address it. To identify solutions that lead to sustainable biodiversity alongside economic prosperity, insect monitoring should be efficient and provide standardised and frequently updated status indicators to guide conservation actions. The EU Biodiversity Strategy 2030 identifies the critical challenge of delivering standardised information about the state of nature and image-based insect AI can contribute to this. Specifically, the EU Nature Restoration Law will likely set binding targets for the high resolution data that cameras can provide. Thus, outputs of the Action will contribute directly to EU policies implementation, where biodiversity monitoring is considered a key component. The InsectAI COST Action will organise workshops, conferences, short-term scientific missions, hackathons, design-sprints and much more, across four Working Groups. These groups will address how image-based insect AI technologies can best address Societal Needs, support innovation in Image Collection hardware, create standardised approaches for Image Processing and develop novel Data Analysis and Integration methods for turning data into actionable insights

Retrofitting metal-organic frameworks

AbstractThe post-synthetic installation of linker molecules between open-metal sites (OMSs) and undercoordinated metal-nodes in a metal-organic framework (MOF) — retrofitting — has recently been discovered as a powerful tool to manipulate macroscopic properties such as the mechanical robustness and the thermal expansion behavior. So far, the choice of cross linkers (CLs) that are used in retrofitting experiments is based on qualitative considerations. Here, we present a low-cost computational framework that provides experimentalists with a tool for evaluating various CLs for retrofitting a given MOF system with OMSs. After applying our approach to the prototypical system CL@Cu3BTC2 (BTC = 1,3,5-benzentricarboxylate) the methodology was expanded to NOTT-100 and NOTT-101 MOFs, identifying several promising CLs for future CL@NOTT-100 and CL@NOTT-101 retrofitting experiments. The developed model is easily adaptable to other MOFs with OMSs and is set-up to be used by experimentalists, providing a guideline for the synthesis of new retrofitted MOFs with modified physicochemical properties.</jats:p

Virtuelle PC Pools für Computerpraktika am Beispiel der Materialwissenschaften

Computerpraktika stellen einen wichtigen Bestandteil vieler Lehrveranstaltungen dar, welche die Grundlagen und Details von computergestützten Methoden vermitteln sollen. In den Materialwissenschaften spielen solche Methoden eine zunehmend wichtige Rolle. Typischerweise setzen die Praktika eine physische Präsenz in den PC Pools voraus, u.a. da eine Vielzahl von verschiedenen Programmen lokal installiert und bereitgestellt werden muss. Um Computerpraktika auch in der Online-Lehre vollumfänglich und weitestgehend unabhängig von den Gegebenheiten der Studierenden einsetzen zu können, wurde im Wintersemester 2020/21 ein virtueller PC Pool auf Basis von virtuellen Maschinen mit Web-basiertem Zugang eingerichtet. Dieser virtuelle PC Pool wurde in verschiedenen Lehrveranstaltungen erfolgreich eingesetzt und kann auch bei hybriden Lehrformaten in verschiedenen Disziplinen verwendet werden.</jats:p