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Janina Fischer

Researcher at Max Planck Society

Publications -  5
Citations -  142

Janina Fischer is an academic researcher from Max Planck Society. The author has contributed to research in topics: Plasmon & Hydrogen bond. The author has an hindex of 4, co-authored 5 publications receiving 138 citations.

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Plasmon hybridization in stacked double crescents arrays fabricated by colloidal lithography.

TL;DR: A plasmon hybridization model is applied to explain the spectral differences of all polarization dependent resonances and use geometric arguments to explain some of the respective shifts of the resonances.
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Plasmon hybridization and strong near-field enhancements in opposing nanocrescent dimers with tunable resonances.

TL;DR: Plasmon hybridization theory is applied to explain the spectral shifts between coupled and uncoupled crescent nanostructures based on simple geometric arguments for all polarization-dependent resonances.
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Near-Field-Mediated Enhancement of Two-Photon-Induced Fluorescence on Plasmonic Nanostructures

TL;DR: In this article, the authors investigated two-photon-induced fluorescence for organic chromophores next to elongated gold disks which support plasmonic resonances and found that the measured fluorescence is always accompanied by an autoluminescence from the gold, which is of similar intensity.
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The influence of sodium ethene sulphonate comonomer on the film formation process of poly(vinyl acetate) dispersions

TL;DR: In this article, various latex dispersions from vinyl acetate/sodium ethene sulphonate copolymers, stabilised by a constant amount of Hostapal BV, a surfactant with poly(ethylene oxide) groups, were investigated by a variety of solid and liquid state nuclear magnetic resonance methods.
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Stereoselective aggregation of chiral complexes with threefold-symmetric pendant carboxyl groups: an example of “perfect” self-assembly not seen in the crystalline state?

TL;DR: In this article, the self-assembly of tris(bidentate) chiral complexes with a threefold-symmetric array of peripheral carboxyl groups is detailed. And a model for the structure of the aggregate is proposed on the basis of the observed stereoselectivity of the aggregation process and the spectral changes.