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Tailoring Photoluminescence Properties in Ionic Nanoparticle Networks
Author(s) -
Kronstein Martin,
Akbarzadeh Johanna,
Drechsel Christina,
Peterlik Herwig,
Neouze MarieAlexandra
Publication year - 2014
Publication title -
chemistry – a european journal
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.687
H-Index - 242
eISSN - 1521-3765
pISSN - 0947-6539
DOI - 10.1002/chem.201400392
Subject(s) - photoluminescence , stacking , luminescence , materials science , pyridinium , nanoparticle , small angle x ray scattering , ionic bonding , linker , steric effects , chemical physics , scattering , crystallography , photochemistry , nanotechnology , optoelectronics , chemistry , organic chemistry , optics , ion , physics , computer science , operating system
To investigate the original and promising luminescence properties of ionic nanoparticle networks (INN), various material compositions were investigated. In this work, the linker used to network the silica nanoparticles was varied; numerous substituted or non‐substituted imidazolium, pyrazolium and pyridinium linkers are presented. Photoluminescence experiments on the INN hybrid materials revealed strong emission bands over a broad range in the visible region of the light spectrum. Varying the aromatic linker between the imidazolium units induced clear shifts of the emission maxima up to 100 nm, as a consequence of π–π stacking interactions. Steric hindrance and inductive effects of the substituents, introduced on the aromatic units, also strongly influenced the luminescence properties of the materials by modifying the π–π stacking between the imidazolium rings. Small and wide‐angle X‐ray scattering (SAXS, WAXS) experiments revealed a clear trend between the obtained structural parameters (short‐range order parameter and distance of the aromatic units within the hybrid material) and the luminescence quantum yields of the INN materials.