Seed Power: Natural Seed and Electrospun Poly(vinyl difluoride) (PVDF) Nanofiber Based Triboelectric Nanogenerators with High Output Power Density.

A triboelectric nanogenerator (TENG) based on natural seeds and electrospun poly(vinyl difluoride) (PVDF) fibers is reported. The nanofibers are specifically used to enhance the triboelectric effects. A mustard (flax) seed based TENG renders an impressively high electrical output with an average open circuit voltage of 84 V (126 V) and maximum power density 334 mW m (324 mW m) under an impact force of 40 N at 25 Hz.

Inducing Isotropic Growth in Multidimensional Cesium Lead Halide Perovskite Nanocrystals.

A new two-step synthetic protocol to yield monodisperse spherical zero-dimensional (0D) Cs PbX nanocrystals (NCs) and three-dimensional (3D) CsPbX NCs is described. The first step of the reaction involves the colloidal synthesis of spherical PbX seed NCs, which are subsequently converted to Cs PbX and CsPbX NCs through hot injection of a Cs precursor at the desired reaction temperatures. By employing less reactive Pb and halide precursors, the reaction time was extended from several seconds to about five minutes, thereby allowing greater control during the crystallization and growth stages.

Enhanced Exciton and Photon Confinement in Ruddlesden-Popper Perovskite Microplatelets for Highly Stable Low-Threshold Polarized Lasing.

At the heart of electrically driven semiconductors lasers lies their gain medium that typically comprises epitaxially grown double heterostuctures or multiple quantum wells. The simultaneous spatial confinement of charge carriers and photons afforded by the smaller bandgaps and higher refractive index of the active layers as compared to the cladding layers in these structures is essential for the optical-gain enhancement favorable for device operation. Emulating these inorganic gain media, superb properties of highly stable low-threshold (as low as ≈8 µJ cm ) linearly polarized lasing from solution-processed Ruddlesden-Popper (RP) perovskite microplatelets are realized.

Photoluminescence Quenching in Self-Assembled CsPbBr Quantum Dots on Few-Layer Black Phosphorus Sheets.

An ordered self-assembly of CsPbBr quantum dots (QDs) was generated on the surface of few-layer black phosphorus (FLBP). Strong quenching of the QD fluorescence was observed, and analyzed by time-resolved photoluminescence (TR-PL) studies, DFT calculations, and photoconductivity measurements. Charge transfer by type I band alignment is suggested to be the cause of the observed effects.

Benzyl Alcohol-Treated CHNHPbBr Nanocrystals Exhibiting High Luminescence, Stability, and Ultralow Amplified Spontaneous Emission Thresholds.

We report the high yield synthesis of about 11 nm sized CHNHPbBr nanocrystals with near-unity photoluminescence quantum yield. The nanocrystals are formed in the presence of surface-binding ligands through their direct precipitation in a benzyl alcohol/toluene phase. The benzyl alcohol plays a pivotal role in steering the surface ligands binding motifs on the NC surface, resulting in enhanced surface-trap passivation and near-unity PLQY values.

Modulating Excitonic Recombination Effects through One-Step Synthesis of Perovskite Nanoparticles for Light-Emitting Diodes.

The primary advantages of halide perovskites for light-emitting diodes (LEDs) are solution processability, direct band gap, good charge-carrier diffusion lengths, low trap density, and reasonable carrier mobility. The luminescence in 3 D halide perovskite thin films originates from free electron-hole bimolecular recombination. However, the slow bimolecular recombination rate is a fundamental performance limitation.

Highly stable, luminescent core-shell type methylammonium-octylammonium lead bromide layered perovskite nanoparticles.

A new protocol for the synthesis of a highly stable (over 2 months under ambient conditions) solution-processed core-shell type structure of mixed methylammonium-octylammonium lead bromide perovskite nanoparticles (5-12 nm), having spherical shape, color tunability in the blue to green spectral region (438-521 nm) and a high photoluminescence quantum yield (PLQY) of up to 92% is described. The color tunability, high PLQY and stability are due to the quantum confinement imparted by the crystal engineering associated with core-shell nanoparticle formation during growth.

Understanding the Origins of Nucleophilic Hydride Reactivity of a Sodium Hydride-Iodide Composite.

Sodium hydride (NaH) has been commonly used as a Brønsted base in chemical syntheses, while it has rarely been employed to add hydride (H(-) ) to unsaturated electrophiles. We previously developed a procedure to activate NaH through the addition of a soluble iodide source and found that the new NaH-NaI composite can effect even stereoselective nucleophilic hydride reductions of nitriles, imines, and carbonyl compounds. In this work, we report that mixing NaH with NaI or LiI in tetrahydrofuran (THF) as a solvent provides a new inorganic composite, which consists of NaI interspersed with activated NaH, as revealed by powder X-ray diffraction, and both solid-state NMR and X-ray photoelectron spectroscopies.

Enhancing electrocatalytic hydrogen evolution by nickel salicylaldimine complexes with alkali metal cations in aqueous media.

New salicylaldimine nickel complexes, comprising only earth-abundant elements, have been developed for electrocatalytic hydrogen evolution in aqueous media. The second-sphere ether functionalities on the periphery of the complexes enhance the electrocatalytic activity in the presence of alkali metal cations. The electrocatalysts demonstrate improved performances especially in the economical and sustainable seawater reaction medium.

Mesoporous cerium oxide nanospheres for the visible-light driven photocatalytic degradation of dyes.

A facile, solvothermal synthesis of mesoporous cerium oxide nanospheres is reported for the purpose of the photocatalytic degradation of organic dyes and future applications in sustainable energy research. The earth-abundant, relatively affordable, mixed valence cerium oxide sample, which consists of predominantly Ce7O12, has been characterized by powder X-ray diffraction, X-ray photoelectron and UV-vis spectroscopy, and transmission electron microscopy. Together with N2 sorption experiments, the data confirms that the new cerium oxide material is mesoporous and absorbs visible light.

Enhanced conversion efficiency in dye-sensitized solar cells based on hydrothermally synthesized TiO2-MWCNT nanocomposites.

A 50% enhancement in the conversion efficiency (4.9-7.37%) is realized in dye-sensitized solar cells using hydrothermally synthesized TiO(2)-multiwalled carbon nanotube (MWCNT) nanocomposites as compared to hydrothermally synthesized TiO(2) without MWCNT and Degussa P25.