Ecofriendly Green Synthesis of Copper (II) Oxide Nanoparticles Using Leaves (Molokhaia) Extract and Their Application for the Environmental Remediation of Direct Violet Dye via Advanced Oxidation Process.

In this research, copper (II) oxide nanoparticles were prepared by an ecofriendly green method using the extract of leaves (Molokhaia) as a surfactant, capping and anti-agglomeration agent. The ecofriendly green CuO NPs were characterized using different chemical and physical techniques and the results confirmed the formation of monoclinic tenorite CuO nanoparticles with an average particle size of 12 nm and BET surface area of 11.1 m/g.

Photo-oxidative Decolorization of Brilliant Blue with AgNPs as an Activator in the Presence of KSO and NaBH.

The decolorization of brilliant blue (E133) in aqueous solution by KSO and NaBH with AgNPs as an activator was studied spectrophotometrically under normal laboratory conditions. Batch experiments were performed to investigate the effects of reaction time, initial dye concentration, activator concentration, solution pH, and temperature on the decolorization of E133. KSO and NaBH did not decolorize the dye E133 in the absence of AgNPs.

Betanin assisted synthesis of betanin@silver nanoparticles and their enhanced adsorption and biological activities.

Natural red purple dye, Betanin, was extracted from the beetroot, purified by aqueous two- phase extraction and gel permeation column chromatography, and used as a reducing agent for the synthesis of silver-betanin core-shell triangular nanodisks for the first time. Spectroscopic data show that the nanoparticle structure is core@shell like with Ag as core and betanin as shell. Langmuir monolayer model (q = 32.

Donor-π-donor type hole transporting materials: marked π-bridge effects on optoelectronic properties, solid-state structure, and perovskite solar cell efficiency.

Donor-π-bridge-donor type oligomers (D-π-D) have been studied intensively as active materials for organic optoelectronic devices. In this study, we introduce three new D-π-D type organic semiconductors incorporating thiophene or thienothiophene with two electron-rich TPA units, which can be easily synthesized from commercially available materials. A thorough comparison of their optoelectronic and structural properties was conducted, revealing the strong influence of the extent of longitudinal π-bridge conjugation on both the solid structure of the organic semiconductive materials and their photovoltaic performance when applied as hole transporting materials (HTM) in perovskite solar cells.

Perovskite Solar Cells: Influence of Hole Transporting Materials on Power Conversion Efficiency.

The recent advances in perovskite solar cells (PSCs) created a tsunami effect in the photovoltaic community. PSCs are newfangled high-performance photovoltaic devices with low cost that are solution processable for large-scale energy production. The power conversion efficiency (PCE) of such devices experienced an unprecedented increase from 3.

A dual-functional asymmetric squaraine-based low band gap hole transporting material for efficient perovskite solar cells.

We demonstrate for the first time an asymmetric squaraine-based low band-gap hole transporting material, which acted as both light harvesting and hole transporting layers in methylammonium lead triiodide perovskite solar cells. Opto-electrochemical characterization revealed extremely high molar extinction coefficients of the absorption bands in the low energy region and prominent space charge delocalization due to its electronically asymmetric nature. A suitable band alignment of the squaraine HOMO level with the valence band edge of the perovskite, and the conduction band of the TiO2 with LUMO of the perovskite allowed a cascade of hole extraction and electron injection, respectively.

Deuterium isotope effect on bulk heterojunction solar cells. Enhancement of organic photovoltaic performances using monobenzyl substituted deuteriofullerene acceptors.

A series of novel monobenzyl-substituted deuteriofullerenes (BnDCs) were synthesized efficiently through Co-catalyzed selective monofunctionalization of C60. Bulk heterojunction solar cells, based on poly(3-hexylthiophene) as the donor and BnDCs as the acceptors, exhibited higher photovoltaic performances as compared to the corresponding protonated BnHCs devices.

Photoelectrocatalytic disinfection of E. coli suspensions by iron doped TiO2.

Photoelectrocatalytic disinfection of E. coli by an iron doped TiO(2) sol-gel electrode is shown to be more efficient than disinfection by the corresponding undoped electrode. Thus, the improvements in photocatalytic efficiency associated with selective doping have been combined with the electric field enhancement associated with the application of a small positive potential to a UV irradiated titanium dioxide electrode.