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1.
Nanoscale ; 15(3): 1145-1153, 2023 Jan 19.
Article in English | MEDLINE | ID: mdl-35903972

ABSTRACT

Nanowire geometry allows semiconductor heterostructures to be obtained that are not achievable in planar systems, as in, for example, axial superlattices made of large lattice mismatched materials. This provides a great opportunity to explore new optical transitions and vibrational properties resulting from the superstructure. Moreover, superlattice nanowires are expected to show improved thermoelectric properties, owing to the dominant role of surfaces and interfaces that can scatter phonons more effectively, reducing the lattice thermal conductivity. Here, we show the growth of long (up to 100 repetitions) GaAs/GaP superlattice nanowires with different periodicities, uniform layer thicknesses, and sharp interfaces, realized by means of Au-assisted chemical beam epitaxy. By optimizing the growth conditions, we obtained great control of the nanowire diameter, growth rate, and superlattice periodicity, offering a valuable degree of freedom for engineering photonic and phononic properties at the nanoscale. As a proof of concept, we analyzed a single type of superlattice nanowire with a well-defined periodicity and we observed room temperature optical emission and new phonon modes. Our results prove that high-quality GaAs/GaP superlattice nanowires have great potential for phononic and optoelectronic studies and applications.

2.
Chempluschem ; 79(2): 184, 2014 Feb.
Article in English | MEDLINE | ID: mdl-31986582

ABSTRACT

Invited for this month's cover are the three collaborating groups from the University of Stuttgart and the Fraunhofer Institute for Applied Polymer Research in Potsdam, both from Germany as well as the University of Windsor, Canada. The cover picture shows the shift of frontier orbital energies and symmetries upon excitation with light for three different chromophore lengths. Read the full text of the article at 10.1002/cplu.201300308.

3.
Chempluschem ; 79(2): 223-232, 2014 Feb.
Article in English | MEDLINE | ID: mdl-31986584

ABSTRACT

Three series of rigidified tri-, penta- and heptamethine merocyanine dyes were synthesised. A piperidyl moiety was chosen as the electron-donating substituent while the electron-accepting group was varied from ketones to malononitriles and cyanoacetates. The structures of the compounds in the solid state and in solution were elucidated by X-ray diffraction and NMR spectroscopy, respectively, while optical properties were investigated by absorption and emission spectroscopy. As a general trend, the acceptor properties decrease in the series malononitrile>cyanoacetate>ketone based on the analysis of their solvatochromic behaviour. The experimental results were further supported by calculations at the B3LYP 6-311+G(d) level of theory.

4.
Beilstein J Org Chem ; 8: 371-8, 2012.
Article in English | MEDLINE | ID: mdl-22509205

ABSTRACT

4-Cyano-1,1'-biphenyl derivatives bearing ω-hydroxyalkyl substituents were reacted with methyl 3-chloro-3-oxopropionate or cyanoacetic acid, giving liquid-crystalline linear malonates and cyanoacetates. These compounds formed monotropic nematic phases at 62 °C down to ambient temperature upon cooling from the isotropic liquid. The mesomorphic properties were investigated by differential scanning calorimetry, polarizing optical microscopy and X-ray diffraction (WAXS).

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