ABSTRACT
A Scanning Tunneling Microscopy/Spectroscopy (STM/STS) and synchrotron X-ray diffraction study on clustered C3N4 nanoparticles (nanoflakes) is conducted on green-chemistry synthesized samples obtained from chitosan through high power sonication. Morphological aspects and the electronic characteristics are investigated. The observed bandgap of the nanoflakes reveals the presence of different phases in the material. Combining STM morphology, STS spectra and X-ray diffraction (XRD) results one finds that the most abundant phase is graphitic C3N4. A high density of defects is inferred from the XRD measurements. Additionally, STM-electroluminescence (STMEL) is detected in C3N4 nanoflakes deposited on a gold substrate. The tunneling current creates photons that are three times more energetic than the tunneling electrons of the STM sample. We ponder about the two most probable models to explain the observed photon emission energy: either a nonlinear optical phenomenon or a localized state emission.
ABSTRACT
The integrated photoluminescence intensity in thin films of 'Super Yellow' copolymer has been analyzed using a Mott-like temperature dependence. This has enabled us to observe contributions from two emission channels, indicative of exciton recombination proceeding from two distinct origins. At high temperature, interchain thermally activated exciton energy transfer and migration dominates, resulting in large scale quenching of the integrated emission intensity and hence the photoluminescence quantum yield. However, at relatively low temperature, an additional increase of the integrated emission intensity occurs. This new channel of emission has been attributed to recombination from excitons where intrachain exciton energy transfer between adjacent subunits of the copolymer backbone becomes hindered. The activation energy barriers that control both of these emission channels have been obtained and are correlated with chain backbone degrees of freedom.
