Stability of Cubic FAPbI3_3 from X-ray Diffraction, Anelastic, and Dielectric Measurements

Among the hybrid metal-organic perovskites for photovoltaic applications FAPbI_3 (FAPI) has the best performance regarding efficiency and the worst regarding stability, even though the reports on its stability are highly contradictory. In particular, since at room temperature the cubic alpha phase, black and with high photovoltaic efficiency, is metastable against the yellow hexagonal delta phase, it is believed that alpha-FAPI spontaneously transform into delta-FAPI within a relatively short time. We performed X-ray diffraction and thermogravimetric measurements on loose powder of FAPI, and present the first complete dielectric and anelastic spectra of compacted FAPI samples under various conditions. We found that alpha-FAPI is perfectly stable for at least 100 days, the duration of the experiments, unless extrinsic factors induce its degradation. In our tests, degradation was detected after exposure to humidity, strongly accelerated by grain boundaries and the presence of delta phase, but it was not noticeable on the loose powder kept in air under normal laboratory illumination. These findings have strong implications on the strategies for improving the stability of FAPI without diminishing its photovoltaic efficiency through modifications of its composition

Titanium and Ruthenium Phthalocyanines for NO2 Sensors: A Mini-Review

This review presents studies devoted to the description and comprehension of phenomena connected with the sensing behaviour towards NO2 of films of two phthalocyanines, titanium bis-phthalocyanine and ruthenium phthalocyanine. Spectroscopic, conductometric, and morphological features recorded during exposure to the gas are explained and the mechanisms of gas-molecule interaction are also elucidated. The review also shows how X-ray reflectivity can be a useful tool for monitoring morphological parameters such as thickness and roughness that are demonstrated to be sensitive variables for monitoring the exposure of thin films of sensor materials to NO2 gas

Nonlinear Optical Characterization of CsPbBr3 Nanocrystals as a Novel Material for the Integration into Electro-Optic Modulators

The present work is concerned with the investigation of the nonlinear optical response of green emissive CsPbBr3 nanocrystals, in the form of colloidal dispersions in toluene, synthesized via a room-temperature ligand-assisted supersaturation recrystallization (LASR) method. After carrying out a preliminary characterization via X-Ray Diffraction (XRD) and Absorption and Photoluminescence (PL) Spectroscopies, the optical nonlinearity of the as-obtained colloids is probed by means of a single-beam Z-scan setup. Results show that the material in question, within the sensitivity of the experimental apparatus, exhibits a nonlinear refractive index n2 that is the order of 10-15 cm2/W. Moreover, a three-photon absorption mechanism (3PA) is postulated, according to the fitting of the recorded Z-scan traces and the fundamental absorption threshold, which turns out to be off resonance with twice the energy of the laser radiation. A figure of merit is, then, calculated as an indicator of the quality of the CsPbBr3 nanocrystals as a candidate material for photonic devices, for instance, Kerr-like electro-optic modulators (EOMs)

Stability Enhancement in OPV: In-Situ Studies of Plasmonic Devices

Extended Abstract Bulk heterojunction (BHJ) organic photovoltaic (OPV) devices attracted considerable research interest due to several significant characteristics, such as their flexibility, lightweight, low environmental impact and reduced cost of large-scale production. A key aspect in OPVs is improving the device long-term stability: in this contest, novel organic materials and cell architectures are developed and a significant task is played by the development of in-situ diagnostics able to detect the driving mechanisms of device degradation, considering that the optical and transport properties of the device active elements depend on the structural, morphological and interfacial characteristics. In this work we discuss our recent results on devices incorporating metallic nanoparticles (NPs) in the photoactive layer, in order to take advantage of the ability of the metallic NPs to rise the BHJ optical absorption by the excitation of Localized Surface Plasmon Resonance. Both plasmonic and reference systems are studied and a powerful approach for addressing the role of structural/morphological and interface properties of the different layers and their interfaces is used: time-resolved Energy Dispersive X-ray Reflectivity/Diffraction (EDXR/EDXD) techniques are applied jointly with in-situ atomic force microscopy (AFM). The results of such unconventional approach, based on time-resolved EDXR/AFM cross-monitoring, showed that incorporating metallic NPs allowed to control both the bulk and the interface morphological degradation pathways References [1] B. Paci, A. Generosi, V. Rossi Albertini, G.Spyropoulos, E. Stratakis, E. Kymakis, "Enhancement of photo/thermal stability of organic bulk heterojunction photovoltaic devices via gold nanoparticles doping of the active layer,&quot

Aluminum (Oxy)nitride thin films grown by fs-PLD as electron emitters for thermionic applications

Thin films based on aluminum nitride were obtained by fs-laser assisted Pulsed Laser Deposition (fs-PLD) at room temperature on tantalum substrates for studying the electron emission performance in the temperature range 700- 1600 °C, so to investigate the possibility of their exploitation as thermionic cathodes. Results of structural, chemical and morphological analyses show the growth of nanostructured thin films with a significant oxygen contamination, forming a mixture of crystalline aluminum nitride and aluminum oxide as well as metallic aluminum inclusions. Despite the considerable presence of oxygen, the developed cathodes demonstrate to possess promising thermionic emission characteristics, with a work function of 3.15 eV, a valuable Richardson constant of 20.25 A/(cm²K²), and a highly thermo-electronic stability up to operating temperatures of 1600 °C

Conjugates of Gold Nanoparticles and Antitumor Gold(III) Complexes as a Tool for Their AFM and SERS Detection in Biological Tissue

Citrate-capped gold nanoparticles (AuNPs) were functionalized with three distinct antitumor gold(III) complexes, e.g., [Au(N,N)(OH)2][PF6], where (N,N)=2,2′-bipyridine; [Au(C,N)(AcO)2], where (C,N)=deprotonated 6-(1,1-dimethylbenzyl)-pyridine; [Au(C,N,N)(OH)][PF6], where (C,N,N)=deprotonated 6-(1,1-dimethylbenzyl)-2,2′-bipyridine, to assess the chance of tracking their subcellular distribution by atomic force microscopy (AFM), and surface enhanced Raman spectroscopy (SERS) techniques. An extensive physicochemical characterization of the formed conjugates was, thus, carried out by applying a variety of methods (density functional theory—DFT, UV/Vis spectrophotometry, AFM, Raman spectroscopy, and SERS). The resulting gold(III) complexes/AuNPs conjugates turned out to be pretty stable. Interestingly, they exhibited a dramatically increased resonance intensity in the Raman spectra induced by AuNPs. For testing the use of the functionalized AuNPs for biosensing, their distribution in the nuclear, cytosolic, and membrane cell fractions obtained from human lymphocytes was investigated by AFM and SERS. The conjugates were detected in the membrane and nuclear cell fractions but not in the cytosol. The AFM method confirmed that conjugates induced changes in the morphology and nanostructure of the membrane and nuclear fractions. The obtained results point out that the conjugates formed between AuNPs and gold(III) complexes may be used as a tool for tracking metallodrug distribution in the different cell fractions

Gas sensing (RuPc)(2) thin films: Electrical response to NO2 gas and morphological changes induced by external moisture

The morphological changes induced in (RuPc)(2) gas sensing thin films by hydration and de-hydration processes were investigated. Prior to this study a preliminary characterization was performed by conductivity measurements upon exposure to NO2 gas fluxes, to verify the electrical sensing response of the films. This response was correlated to the bulk morphological modification of the films. Subsequently, the effect of external moisture on the morphological stability of the films was addressed. This morphological characterization of the films was performed by using the energy dispersive X-ray reflectivity (EDXR) and atomic force microscopy (AFM) techniques, both ex situ and in situ, i.e. under operating conditions, during exposure of these films to 100% of relative humidity. The measurements allowed an accurate observation of both the surface morphology(i.e. its roughness obtained independently by EDXR and AFM). Moreover bulk evolution of the films was obtained by in situ EDXR and the morphological changes allowed to retrieve information on the water uptake dynamics. Moreover, the reversibility of the water/film interaction was studied and correlated to the sensing properties of the (RuPc)(2). (C) 2008 Elsevier B.V. All rights reserved