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CSIC

Spanish National Research Council
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2,446 Projects, page 1 of 490
  • Funder: European Commission Project Code: 323316
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  • Funder: European Commission Project Code: 706094
    Overall Budget: 170,122 EURFunder Contribution: 170,122 EUR

    The European commission recognizes the importance of nanotechnology, semiconductors and advanced materials as key enabling technologies. The application of functional nanostructured materials in industrial processes and advanced science is of capital and strategic importance for the European economy and society. Their inclusion as reliable, standard and affordable components will boost the competitiveness of European industry, specifically in the fabrication of 4th generation solar cells. Sensitized Perovskites Solar cells (PSC) represent advantages in terms of cost manufacturing, energy generation and integration in flexible and semitransparent devices. However, the viability of their mass scale fabrication is hindered by economic and technical difficulties. Some of these technical issues arise from inefficient infiltration of the perovskite absorber into a fragile mesoporous (mp) TiO2 layer. My project addresses these problems applying a recently developed straightforward method for secure TiO2 nanotube layers (TNL) to commodity thermoplastic polymers. This novel method combined with optimized solution synthesized perovskites will result in the production of flexible and pliable PSC. Specifically, I propose to produce a step change in the standardization and fabrication of functional nanostructured materials, and its implementation in optimized PSCs. Lastly, the study on the life cycle management and viability of the industrial production of these PSC will be evaluated in an innovative photovoltaic manufacture company, ONYX SOLAR. Hence, the project is designed to generate disruptive, but easily scalable technology that may be rapidly adopted by European industry to boost its competitiveness in functional nanostructured composites and 4th generation solar cells.

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  • Funder: European Commission Project Code: 625997
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  • Funder: European Commission Project Code: 219811
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  • Funder: European Commission Project Code: 101107228
    Funder Contribution: 165,313 EUR

    Antimicrobial resistance is on the rise and it is predicted to become the first cause of death by 2050. One of the characteristic bacteria phenotypes of antibiotic resistance (and more generally of a stress response) is filamentation, which has been linked to survival strategies and virulence and is present in the most common form of bacteria in nature: biofilms. Thus, characterizing the filamentation phenotype opens the door to understanding the physiology and adaptation of bacterial cells under stress and during colonization processes. Filamentation results from a coordination of growth and division which are driven by the assembly machinery of the Fts system, the Min oscillatory system, and the nuclear occlusion system. In particular, Fts participates in the septum assembly, a ring-forming cell wall that will separate the daughter cells, whereas the Min oscillatory system restricts the assembly of the division machinery at specific locations to avoid nucleoid cleavage. When bacteria grow regularly, a single septum forms by the middle (symmetric division) to separate the nucleoids of daughter cells. However, when bacteria grow anomalously longer (filamentation), multiple nucleoids continue to segregate along the cell at regular intervals and several putative septa are created. Yet, filamentous bacteria do not grow indefinitely, and division events occur “randomly” (in terms of their timing and the selected septum). This raises the unexplored question of how size is regulated during filamentation processes. In this context, we hypothesize that the interplay between mechanical cues (e.g., filament bending) and changes in the bacteria membrane potential play a key role to regulate bacterial filamentation. Thus, the main objective of this project is determining how mechanosensitive and electrical properties of the division/growth machinery in E. coli regulate its filamentation.

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