ERC FUNDED PROJECTS

Previous efforts to raise living standards have been based on relentlessly increasing combustion, causing environmental destruction at all scales. In addition to climate-warming CO2, fossil fuel combustion also produces a large number of organic compounds and particulate matter, which deteriorate air quality. The atmosphere is cleansed from such pollutants by gas-phase oxidation reactions, which are invariably mediated by peroxy radicals (RO2). Oxidation transforms initially volatile and water-insoluble hydrocarbons into water-soluble forms (ultimately CO2), enabling scavenging by liquid droplets. A minor but crucially important alternative oxidation pathway leads to oxidative molecular growth, and formation of atmospheric aerosols. Aerosols impart a huge influence on the atmosphere, from local air quality issues to global climate forcing, yet their formation mechanisms and structures of organic aerosol precursors remains elusive. In a paradigm change, RO2 was recently found to undergo autoxidation, enabling rapid aerosol precursor formation even at sub-second time-scales – in stark contrast to the long processing times (days - weeks) previously assumed to be necessary. We have shown how abundant biogenic hydrocarbons (BVOC) autoxidize, but due to key structural differences, the same pathways are not available for anthropogenic hydrocarbons (AVOC), and thus they were not expected to autoxidize. My preliminary experiments reveal that AVOCs do autoxidize, but the mechanism enabling this remain unknown. Crucially, the co-reactants shown to inhibit BVOC seem to enforce AVOC autoxidation – potentially explaining the recent mysterious discovery of new-particle formation in polluted megacities. In ADAPT, I will use a combination of novel mass spectrometric detection methods fortified by theoretical calculations, to solve the mechanism of AVOC autoxidation. This will directly assist both air quality management, and the design of cleaner fuels and engines.

2 689 147 €

Start date: 2021-02-01, End date: 2026-01-31

The human microbiome has been increasingly in the focus of research for its importance in human health and disease. Yet, the viruses (phages) infecting these microbiota have gained much less attention. The majority of phages reside integrated in the genomes of their microbial hosts as so called lysogenic prophages. Often, these prophages encode important toxins and other virulence related factors that, while they are beneficial to their microbial hosts, may be detrimental for the infected human. Prophages can be induced under certain conditions to resume a lytic lifestyle resulting in the production of virus particles and often in the destruction of the host cell. Frequently, however, phage induction also leads to increased production of virulence factors. In this project, we aim to uncover small molecules modulating phage induction. We will explore to what extent microbial metabolites of human microbiota act as native triggers or inhibitors of phage induction and shape the complex interspecies interactions in the microbiome. The corresponding phage inducing or dysregulating metabolites will be isolated to elucidate their chemical structure and unveil their molecular targets. We will develop chemical tools to dissect and interrogate the responsible mechanisms and finally develop customized synthetic modulators that allow us to achieve control over the activity of phage-microbe systems with specific medical relevance. The integrated approach of the CAPSID project will provide first comprehensive insights into the chemistry of microbe-phage interactions and allow to assess its role for infectious diseases and its potential for customized treatment of microbial pathogens.

1 992 240 €

Start date: 2020-10-01, End date: 2025-09-30

Since the discovery in the nineteenth century, carbonylation chemistry has found broad applicability in chemical industries and become now a key technology for bulk and fine chemical synthesis. Despite its substantial toxicity, carbon monoxide (CO) is commonly used as carbonyl source causing considerable safety issues, particularly when used on bulk scale. The replacement of this hazardous gas with more benign surrogates would be highly desirable, and recent ideas focus on the valorisation of carbon dioxide as abundant, non-toxic and renewable carbon resource. However, few industrial processes utilise carbon dioxide as a raw material, and potent catalysts are required to overcome its thermodynamic and kinetic barrier. In this regard, ionic liquids show considerable potential as cooperative media as they can solubilise large concentrations of carbon dioxide but also strongly interact and activate carbon dioxide. This project focuses on the photocatalytic reduction of carbon dioxide in ionic liquids and its successive conversion into carbonyl compounds. Several goals need to be realised, including fundamental studies and optimisation of the ionic liquid co-catalysed photocatalytic reduction of carbon dioxide to produce CO under mild conditions (Goal 1). The reactivity of formed CO in supercritical carbon dioxide with various organic substrates needs to be explored (Goal 2) before finally developing a streamlined and continuous process for the direct formation of carbonyl compounds from carbon dioxide (Goal 3). I envision that the photocatalytic activation of carbon dioxide in combination with the positive features of tailored ionic liquids as co-catalysts may overcome problems currently associated with carbon dioxide utilisation, eventually replacing the long-standing bastion of CO-based carbonylation chemistry with novel solutions.

1 963 515 €

Start date: 2021-01-01, End date: 2025-12-31

"Large bodies usually follow the classical equations of motion. Deviations from this can be called macroscopic quantum behavior. These phenomena have been experimentally verified with cavity Quantum Electro Dynamics (QED), trapped ions, and superconducting Josephson junction systems. Recently, evidence was obtained that also moving objects can display such behavior. These objects are micromechanical resonators (MR), which can measure tens of microns in size and are hence quite macroscopic. The degree of freedom is their vibrations: phonons. I propose experimental research in order to push quantum mechanics closer to the classical world than ever before. I will try find quantum behavior in the most classical objects, that is, slowly moving bodies. I will use MR's, accessed via electrical resonators. Part of it will be in analogy to the previously studied macroscopic systems, but with photons replaced by phonons. The experiments are done in a cryogenic temperature mostly in dilution refrigerator. The work will open up new perspectives on how nature works, and can have technological implications. The first basic setup is the coupling of MR to microwave cavity resonators. This is a direct analogy to optomechanics, and can be called circuit optomechanics. The goals will be phonon state transfer via a cavity bus, construction of squeezed states and of phonon-cavity entanglement. The second setup is to boost the optomechanical coupling with a Josephson junction system, and reach the single-phonon strong-coupling for the first time. The third setup is the coupling of MR to a Josephson junction artificial atom. Here we will access the MR same way as the motion of a trapped ions is coupled to their internal transitions. In this setup, I am proposing to construct exotic quantum states of motion, and finally entangle and transfer phonons over mm-distance via cavity-coupled qubits. I believe within the project it is possible to perform rudimentary Bell measurement with phonons."

2 004 283 €

Start date: 2015-01-01, End date: 2019-12-31