Scaffold-Guided Crystallization of Oriented α-FAPbI Nanowire Arrays for Solar Cells.

Perovskite nanowire arrays with large surface areas for efficient charge transfer and continuous highly crystalline domains for efficient charge transport exhibit ideal morphologies for solar-cell active layers. Here, we introduce a room temperature two-step method to grow dense, vertical nanowire arrays of formamidinium lead iodide (FAPbI). PbI nanocrystals embedded in the cylindrical nanopores of anodized titanium dioxide scaffolds were converted to FAPbI by immersion in a FAI solution for a period of 0.

The synthesis of Pt doped WO nanosheets and application on colorimetric detection of cysteine by naked eye using response surface methodology for optimization.

We present a simple, sensitive, and specific colorimetric using the peroxidase properties method based on Pt doped WO nanosheets to detect the cysteine. Pt@WONSs were synthesized by hydrothermal method and characterized by Fourier transform infrared (FTIR), Transmission electron microscopy (TEM), energy-dispersive X-ray spectroscopy (EDX), and X-ray diffraction patterns (XRD) methods. The response surface methodology (RSM) method based on the central composite design (CCD) was used to optimize test parameters such as pH, nanosheet concentration, and temperature.

Nanoconfining solution-processed organic semiconductors for emerging optoelectronics.

Solution-processable organic materials for emerging electronics can generally be divided into two classes of semiconductors, organic small molecules and polymers. The theoretical thermodynamic limits of device performance are largely determined by the molecular structure of these compounds, and advances in synthetic routes have led to significant progress in charge mobilities and light conversion and light emission efficiencies over the past several decades. Still, the uncontrolled formation of out-of-equilibrium film microstructures and unfavorable polymorphs during rapid solution processing remains a critical bottleneck facing the commercialization of these materials.

Orienting and shaping organic semiconductor single crystals through selective nanoconfinement.

For organic semiconductor crystals exhibiting anisotropic charge transport along different crystallographic directions, nanoconfinement is a powerful strategy to control crystal orientation by aligning the fast crystallographic growth direction(s) with the unconfined axis(es) of nanoconfining scaffolds. Here, design rules are presented to relate crystal morphology, scaffold geometry, and orientation control in solution-processed small-molecule crystals. Specifically, organic semiconductor triisopropylsilylethynyl pyranthrene needle-like crystals with a dimensionality of n = 1 and perylene platelike crystals with n = 2 were grown from solution within nanoconfining scaffolds comprising cylindrical nanopores with a dimensionality of m = 1, representing one unconfined dimension along the cylinder axis, and those comprising nanopillar arrays with a dimensionality of m = 2.