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Showing 1–12 of 12 results
Advanced filters: Author: Natalie Stingelin Clear advanced filters
  • Further achievements in the realm of organic and molecular electronics — even at the level of device applications — requires greater understanding of the materials at a fundamental level. This insight can only come with input from researchers in several disciplines working together on the materials from different perspectives.

    • Natalie Stingelin
    News & Views
    Nature Materials
    Volume: 8, P: 858-860
  • Direct visualization of polymer semiconductor structure in electrolyte environments and across length scales facilitates mechanistic understanding of this versatile but complex class of materials.

    • Erin Ratcliff
    • Natalie Stingelin
    News & Views
    Nature Materials
    Volume: 24, P: 10-11
  • Simplification in large-area manufacturing of complex organic electronics is a critical step towards ubiquitous, flexible, portable applications; why not make the molecules do the work?

    • Natalie Stingelin-Stutzmann
    News & Views
    Nature Materials
    Volume: 7, P: 171-172
  • Charge generation and transport are crucial to the performance of organic solar cells, but the mechanism remains controversial. Causa’ et al. show that the phase morphology of polymer:fullerene blends determines the exciton dissociation at femtoseconds, although the spatial separation can occur at picoseconds.

    • Martina Causa'
    • Jelissa De Jonghe-Risse
    • Natalie Banerji
    ResearchOpen Access
    Nature Communications
    Volume: 7, P: 1-10
  • Photocarrier generation at organic semiconductor heterojunctions is a crucial process, yet its mechanism and dynamics remain unclear. Here, Provencher et al.show little change in polymer structure following the charge-transfer process and interpret the observation in terms of unbounded electron-hole pairs.

    • Françoise Provencher
    • Nicolas Bérubé
    • Sophia C. Hayes
    Research
    Nature Communications
    Volume: 5, P: 1-11
  • Though solution-processed conjugated polymers with inverted temperature activated transport have been reported, the origin of this behaviour is unclear. Here, the authors realize temperature-independent electron transport above 280 K in a donor-acceptor copolymer through microstructural engineering.

    • Alessandro Luzio
    • Fritz Nübling
    • Mario Caironi
    ResearchOpen Access
    Nature Communications
    Volume: 10, P: 1-13
  • The field of organic electronics has acknowledged that the key to process and device optimization is to elucidate the correlation between the active layer morphology and performance. This Review outlines how this can be achieved using accessible approaches from materials science and classical polymer thermodynamics.

    • Zhengxing Peng
    • Natalie Stingelin
    • Jasper J. Michels
    Reviews
    Nature Reviews Materials
    Volume: 8, P: 439-455
  • The recent demonstration that highly disordered polymer films can transport charges as effectively as polycrystalline semiconductors has called into question the relationship between structural order and mobility in organic materials. It is now shown that, in high-molecular-weight polymers, efficient charge transport is allowed due to a network of interconnected aggregates that are characterized by short-range order.

    • Rodrigo Noriega
    • Jonathan Rivnay
    • Alberto Salleo
    Research
    Nature Materials
    Volume: 12, P: 1038-1044
  • Difficulties in controlling the nucleation and growth of thin films of organic semiconductors have impaired progress in organic electronics. Now, efficient control of the crystallite nucleation and microstructure of a broad range of organic semiconductors without detriment to their electronic properties has been achieved through the addition of small quantities of additives—a widely used strategy in bulk polymer crystallization.

    • Neil D. Treat
    • Jennifer A. Nekuda Malik
    • Natalie Stingelin
    Research
    Nature Materials
    Volume: 12, P: 628-633