Formamidinium lead halide (FAPbX3) has attracted greater attention and is more prominent recently in photovoltaic devices due to its broad absorption and higher thermal stability in comparison to more popular methylammonium lead halide MAPbX3. Herein, a simple and highly reproducible room temperature synthesis of device grade high quality formamidinium lead bromide CH(NH2)2PbBr3 (FAPbBr3) colloidal nanocrystals (NC) having high photoluminescence quantum efficiency (PLQE) of 55–65% is reported. In addition, we demonstrate high brightness perovskite light emitting device (Pe-LED) with these FAPbBr3 perovskite NC thin film using 2,2′,2″-(1,3,5-Benzinetriyl)-tris(1-phenyl-1-H-benzimidazole) commonly known as TPBi and 4,6-Bis(3,5-di(pyridin-3-yl)phenyl)-2-methylpyrimidine (B3PYMPM) as electron transport layers (ETL). The Pe-LED device with B3PYMPM as ETL has bright electroluminescence of up to 2714 cd/m2, while the Pe-LED device with TPBi as ETL has higher peak luminous efficiency of 6.4 cd/A and peak luminous power efficiency of 5.7 lm/W. To our knowledge this is the first report on high brightness light emitting device based on CH(NH2)2PbBr3 widely known as FAPbBr3 nanocrystals in literature.
The aim of this study was to reproduce the physico-mechanical antibacterial effect of the nanocolumnar cicada wing surface for metallic biomaterials by fabrication of titanium (Ti) nanocolumnar surfaces using glancing angle sputter deposition (GLAD). Nanocolumnar Ti thin films were fabricated by GLAD on silicon substrates. S. aureus as well as E. coli were incubated with nanostructured or reference dense Ti thin film test samples for one or three hours at 37 °C. Bacterial adherence, morphology, and viability were analyzed by fluorescence staining and scanning electron microscopy and compared to human mesenchymal stem cells (hMSCs).
Bacterial adherence was not significantly different after short (1 h) incubation on the dense or the nanostructured Ti surface. In contrast to S. aureus the viability of E. coli was significantly decreased after 3 h on the nanostructured film compared to the dense film and was accompanied by an irregular morphology and a cell wall deformation. Cell adherence, spreading and viability of hMSCs were not altered on the nanostructured surface. The results show that the selective antibacterial effect of the cicada wing could be transferred to a nanostructured metallic biomaterial by mimicking the natural nanocolumnar topography.
Scalable fabrication of spherical particles at both the micro-and nanoscales is of significant importance for applications spanning optical devices, electronics, targeted drug delivery, biodevices, sensors, and cosmetics. However, current top-down and bottom-up fabrication methods are unable to provide the full spectrum of uniformly sized, well-ordered, and high-quality spheres due to their inherent restrictions. Here, a generic, scalable, and precisely controllable fabrication method is demonstrated for generating spherical particles in a full range of diameters from microscale to nanoscale. This method begins with a macroscopic composite multimaterial solid-state preform drawn into a fiber that defines precisely the initial conditions for the process. It is then followed by CO 2 laser heating to enable the transformation from a continuous fiber core into a series of homogeneous spheres via Plateau-Rayleigh capillary instability inside the fiber. This physical breakup method applies to a wide range of functional materials with different melting temperatures from 400 to 2400 K and 10 orders of difference in fiber core/cladding viscosity ratio. Furthermore, an ordered array of silicon-based whispering-gallery mode resonators with the Q factor as high as 7.1 × 10 5 is achieved, owing to the process induced ultrasmooth surface and highly crystalline nature.
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