Tunable Near-Infrared Localized Surface Plasmon Resonance of F, In-Codoped CdO Nanocrystals

Nanocrystals (NCs) of transparent conducting oxides with a localized surface plasmon resonance (LSPR) in the near-infrared (NIR) spectral region show promising electrochromic properties for the development of a new generation of dynamic "smart windows". In this regard, we exploit thin films of F, In-codoped CdO (FICO) NCs as active coatings for electrochromic devices. The control over the dopants concentration in FICO NCs results in fine tuning of their LSPR across the NIR region of the electromagnetic spectrum. Highly transparent mesoporous electrodes were prepared from colloidal FICO NCs by in situ ligand exchange of the pristine organic capping ligands. This approach preserves the optical and electrical properties of native NCs and delivers highly homogeneous, nonscattering films with a good electronic coupling between the NCs. We achieved a dynamic control over the LSPR frequency by reversible electrochemical doping, hence a spectrally selective modulation of the optical transmittance in the NIR region of the solar spectrum, which carries nearly 50% of the whole solar heat. Spectroelectrochemical characterization, coloration efficiency, and switching kinetics results indicate that thin film based on FICO NCs are potential candidates for plasmonic electrochromic applications. Moreover, the high electron mobility and wide optical bandgap of FICO makes NCs of this material suitable for large-area devices capable of dynamically controlling the heat load coming from the solar infrared radiation, without affecting the visible light transmittance

MAPLE deposition of nanomaterials

The matrix-assisted pulsed laser evaporation (MAPLE) has been recently exploited for depositing films of nanomaterials by combining the advantages of colloidal inorganic nanoparticles and laser-based techniques. MAPLE-deposition of nanomaterials meeting applicative purposes demands their peculiar properties to be taken into account while planning depositions to guarantee a congruent transfer (in terms of crystal structure and geometric features) and explain the deposition outcome. In particular, since nanofluids can enhance thermal conductivity with respect to conventional fluids, laser-induced heating can induce different ablation thermal regimes as compared to the MAPLE-treatment of soft materials. Moreover, nanoparticles exhibit lower melting temperatures and can experience pre-melting phenomena as compared to their bulk counterparts, which could easily induce shape and or crystal phase modification of the material to be deposited even at very low fluences. In this complex scenario, this review paper focuses on examples of MAPLE-depositions of size and shape controlled nanoparticles for different applications highlights advantages and challenges of the MAPLE-technique. The influence of the deposition parameters on the physical mechanisms which govern the deposition process is discussed

Transforming colloidal Cs4PbBr6 nanocrystals with poly(maleic anhydride-alt -1-octadecene) into stable CsPbBr3 perovskite emitters through intermediate heterostructures

The preparation of strongly emissive CsPbBr3 perovskite nanocrystals with robust surface passivation is a challenge in the field of lead halide perovskite nanomaterials. We report an approach to prepare polymer-capped CsPbBr3 perovskite nanocrystals by reacting oleylammonium/oleate-capped Cs4PbBr6 nanocrystals with poly(maleic anhydride-alt-1-octadecene) (PMAO). PMAO contains succinic anhydride units that are reactive towards the oleylamine species present on the Cs4PbBr6 nanocrystals' surface and produces polysuccinamic acid, which, in turn, triggers the Cs4PbBr6 to CsPbBr3 conversion. The transformation occurs through the formation of Cs4PbBr6-CsPbBr3 heterostructures as intermediates, which are captured because of the mild reactivity of PMAO and are investigated by high-resolution electron microscopy. The Cs4PbBr6-CsPbBr3 heterostructures demonstrate a dual emission at cryogenic temperature with an indication of the energy transfer from Cs4PbBr6 to CsPbBr3. The fully-transformed CsPbBr3 NCs have high photoluminescence quantum yield and enhanced colloidal stability, which we attribute to the adhesion of polysuccinamic acid to the NC surface through its multiple functional groups in place of oleate and alkylammonium ligands. The PMAO-induced transformation of Cs4PbBr6 NCs opens up a strategy for the chemical modification of metal halide NCs initially passivated with nucleophilic amines

Electrochromic evaluation of airbrushed water-dispersible W18O49 nanorods obtained by microwave-assisted synthesis

Motivated by the technological relevance of tungsten oxide nanostructures as valuable materials for energy saving technology, electrochemical and electrochromic characteristics of greener processed nanostructured W18O49-based electrodes are discussed in this work. For the purpose, microwave-assisted water-dispersible W18O49 nanorods have been synthesized and processed into nanostructured electrodes. An airbrushing technique has been adopted as a cost-effective large-area scalable methodology to deposit the W18O49 nanorods onto conductive glass. This approach preserves the morphological and crystallographic habit of native nanorods and allows highly homogeneous transparent coating where good electronic coupling between nanowires is ensured by a mild thermal treatment (250 °C, 30 min). Morphological and structural characteristics of active material were investigated from the synthesis to the nanocrystal deposition process by transmission and scanning electron microscopy, x-ray diffraction, atomic force microscopy and Raman spectroscopy. The as-obtained nanostructured film exhibited good reversible electrochemical features through several intercalation-deintercalation cycles. The electrochromic properties were evaluated on the basis of spectro-electrochemical measurements and showed significant optical contrast in the near-infrared region and high coloration efficiency at 550 nm