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University of Freiburg

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366 Projects, page 1 of 74
  • Funder: European Commission Project Code: 101125948
    Overall Budget: 2,676,880 EURFunder Contribution: 2,676,880 EUR

    The transition towards a society based on 100% renewable energy requires massive deployment of photovoltaics of 30-70 TW until 2050. This requires huge amounts of resources, while their limited availability is already becoming apparent. A major lever to reduce resource consumption is to increase the solar cell efficiency. As best single junction solar cells approach their fundamental limits, higher efficiency can only be reached with so-called tandem solar cells, made of two or more subcells. All tandem technologies so far are based on relatively thick absorber layers, reducing resource demand compared to single junction devices by efficiency increase. There, light trapping strategies are used to maximize absorptance close to the band gap of the materials and improve efficiency by few percent relative. However, by applying advanced light trapping techniques such as nanophotonic metasurfac-es, ultrathin single junction devices with a 5-10-fold decrease in semiconductor material were realized. To reduce resource demand further, the concept of ultrathin solar cells must be extended to tandem devices. This introduces severe challenges, as not only absorption needs to be maximized within the active part, but a spectrally dependent light guiding strategy is required. Metasurfaces have shown the ability to manipulate light e.g. spectrally dependent; however, they have never been implemented into tandem solar cells. Thus, the overarching goal of PHASE is to generate a deep physical understanding of metasurfaces for ultrathin tandem solar cells and to develop process flows to implement nanopho-tonic structures into such devices with efficiencies above 30%. This will proof that the chosen tech-nology pathway can support the urgently needed energy transition. More specific, the goal of PHASE is to realize tandem solar cells, where the resource demanding semiconductor part is 10 times thinner (and thus needs 10 times less semiconductor material) than similar existing devices.

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  • Funder: European Commission Project Code: 864246
    Overall Budget: 2,000,000 EURFunder Contribution: 2,000,000 EUR

    The abusive use of antibiotics has led to multidrug-resistant bacteria and the acute threat of a post-antibiotic era. However, apart from resisters, there is a subgroup of bacteria called persisters that surviveby recalcitrance to antibiotic treatment. Persisters are not resistant to antibiotics but simply survive by metabolic shutdown. Upon withdrawal of antibiotics, these persisters resuscitate and regenerate the colony. They are heavily involved in failure of antibiotic treatment and the development of chronic infections. Bacterial persistence is controlled by the stringent response, which itself is mediated by hyperphosphorylated nucleotides, known as the magic spot (MS) nucleotides or (p)ppGpp. The importance of the stringent response, its omnipresence in the domain of bacteria, its connection to persister formation and tolerance to (antibiotic) stress, and its absence in mammals has led to significant research in microbiology. However, until recently these activities have not been paralleled by the development of chemical biology approaches. The current proposal aims to fill this gap by research into (1) synthetic methodology targeting the magic spot nucleotides and their analogs, (2) tools to identify target proteins of (p)ppGpp, and more generally (p)ppNpp (3) analytical approaches to extract, resolve, and quantify (p)ppGpp, (4) strategies to control the stringent response and persister formation with light (5) inhibitors of the stringent response. These new tools will enable a detailed understanding of the stringent response and thus ultimately help in the design of new antibiotics effective against persisters. The goal is to develop methods to force bacteria into the persistent state or inversely wake them up by using light and small molecules. Forcing bacteria out of persistence and blocking their entry into this state in combination with antibiotic treatment is a highly promising strategy to avoid the development of chronic bacterial infections.

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  • Funder: European Commission Project Code: 101124519
    Overall Budget: 2,000,000 EURFunder Contribution: 2,000,000 EUR

    Why are contemporary readers so fascinated by retellings of the Iliad or Beowulf? And why have retellings of premodern – ancient and medieval – texts not been taken seriously as a literary practice to date? In DERIVATE, I investigate the striking surge of retellings in contemporary English literature by setting the contemporary texts in a productive dialogue with practices of writing in the Middle Ages. The medieval period offers a perfect point of departure for theorizing retellings as medieval literature was inherently derivative and medieval authors had developed a system for being inventive within a system of derivations. Taking issue with the privileging of that which is new in literary history, I propose a new paradigm for literary history: literary history as a history of derivations. Starting from the premise that retelling is a transhistorical concept, the project sheds new light on the processes of reception that find their expression in the current interest in and relevance of premodern material. The project triangulates (classical) reception studies, medieval literary studies as well as literary theory, especially postmodernist theory, and scrutinizes the practice of retelling premodern (ancient and medieval) texts in contemporary English literature. DERIVATE thus develops a theory of retelling based on the intense engagement and critical comparison with medieval practices of retelling in order to map the wider cultural, historical, and literary contexts and implications of the current trend in retellings of classical and medieval texts (audiences, canon, literary market) as a springboard for developing a literary history of derivations.

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  • Funder: European Commission Project Code: 754340
    Overall Budget: 4,743,600 EURFunder Contribution: 2,371,800 EUR

    The Freiburg Institute for Advanced Studies (FRIAS) is an internationally renowned university-based institute for advanced studies that offers time-limited fellowship stays for excellent junior and senior researchers from around the world. The Institute is part of the University of Freiburg, one of the leading research universities in Europe. FRIAS is applying for a FRIAS COFUND Fellowship Programme (FCFP, phase 2) which will target experienced researchers at both the junior and senior level and offer them fellowship stays of up to one year to work on their own research project. Over the course of the FCFP (2017-24), 6 yearly calls for the academic years 2018/19 to 2023/24 will be issued, and a total of 804 fellowship months will be awarded, evenly split between Junior and Senior Fellowships. The proposed programme is an optimised continuation of the Institute’s current very successful COFUND project (FCFP, phase 1). If continued, the FCFP will form a central element of the Institute’s activities. The FCFP is open to researchers from all disciplines and nationalities. It features a transparent, merit-based selection process and offers internationally competitive employment conditions. Improvements of the FCFP (phase 2) with respect to phase 1 concern: the selection procedure, employment conditions, intersectoral networking and mobility, outreach activities, career development and alumni activities. The outstanding feature of FRIAS is its internationally diverse community of Junior and Senior Fellows from a wide spectrum of disciplines. Fellows pursue their project within the stimulating atmosphere of permanent academic exchange. Junior Fellows in particular profit from the dedicated support arrangements. The FCFP, phase 2, will continue to attract outstanding researchers from all over the world, thereby making significant contributions to world-class research, to individual researchers’ careers and thus to the European Research Area in general.

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  • Funder: European Commission Project Code: 253075
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