Co-MOF-74 rod like crystals with a length of several hundred micrometers are synthesized by a solvothermal procedure and their interaction with different gases is evaluated for selective gas sensing. We show strongly anisotropic absorption behavior of the Co-MOF-74 crystals when illuminated with polarized light. The interactions of guests (CO , propane, propene, Ar, MeOH, H O) with Co-MOF-74, is studied by various spectroscopic techniques. Vis/NIR shows peak shifts of Co-MOF-74 depending on the interaction with the guest. In the visible and the NIR the maximum absorbance is shifted selectively corresponding to the intensity of the Co -guest interaction. Even propene and propane could be distinguished at room temperature by their different interactions with Co-MOF-74. Raman spectroscopy was used to detect a modified vibrational behavior of Co-MOF-74 upon gas adsorption. We show that the adsorption of H O leads to a characteristic shift of the peak maxima in the Raman spectra.
A synthetic route to prepare metal-semiconductor hybrid nanoparticles is presented, along with the possibility to tune the ratio of primary to secondary nucleation and the morphology of the semiconductor material grown on the metal nanoparticle seeds. Gold and cobalt-platinum nanoparticles are employed as metal seeds, on which CdS or CdSe is grown. Using transmission electron microscopy, absorption spectroscopy (UV-vis), and powder X-ray diffraction as characterization techniques, a significant influence of chloride ions on the type of nucleation (that is, secondary or primary nucleation) as well as on the shape of the resulting heterostructures is observed. Partially replacing the commonly used cadmium precursor CdO by varying amounts of CdCl2 opens access to rod-like, multiarmed, flower-like, and bullet-like structures. The results suggest that neither pure CdO nor pure CdCl2 as precursors but only a mixture of both make these structures obtainable. In this article, the influence of the chloride ion concentration during semiconductor growth on metal seeds is investigated in depth. The morphology of the resulting heterostructures is characterized carefully, and a growth mechanism is suggested. Furthermore, it is shown that this synthetic approach can be transferred to seeds of various metals such as platinum, gold, and cobalt platinum.
We report the synthesis of plasmonic Cu2-x Se@ZnS core@shell nanoparticles (NPs). We used a shell growth approach, starting from Cu2-x Se NPs that have been shown before to exhibit a localized surface plasmon resonance (LSPR). By careful synthesis planning we avoided cation exchange reactions and received core@shell nanoparticles that, after oxidation under air, exhibit a strong LSPR in the NIR. Interestingly, the crystalline, closed ZnS shell that we grew with variable thickness still allowed a slow oxidation of the core under ambient conditions, while the core was effectively protected from reduction, even in the presence of reducing agents such as borane tert-butyamine complex and diisobutylaluminum hydride, giving rise to a stable particle LSPR, also under strongly reducing conditions.
In
this work, we investigate the occurrence of localized surface
plasmon resonances (LSPRs) in different nickel sulfide nanostructures.
Therefore, spherical and anisotropic nickel sulfide nanoparticles
(NPs) are synthesized and analyzed regarding their optical properties
by UV/vis/NIR and transient absorption spectroscopy. Furthermore,
new pathways for the synthesis of spherical Ni3S2 nanodots with an extremely narrow size distribution, as well as
Au–Ni3S2 core–shell NPs with controllable
shell thickness, are presented. Our results show that NPs of different
metallic nickel sulfide phases like Ni3S2 and
Ni3S4 exhibit LSPR bands in the visible regime
of the electromagnetic spectrum, which possibly makes them a comparably
cheaper alternative to NPs consisting of noble metals like Au and
Ag. In case of the presented plasmonic core–shell particles,
the resonance frequency of the plasmon can be tuned between those
of pure gold and pure Ni3S2 NPs by varying the
Ni3S2 shell thickness.
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