Highly selective chemosensor for repetitive detection of Fe3+ in pure water and bioimaging.

Combining octavinyl-polyhedral oligomeric silsesquioxane (OV-POSS) with amine-containing polyacrylamide (OV-POSS co-poly(acrylamide)) gives a new fluorescent polymeric chemo-sensor with complete water solubility. It shows better selectivity for Fe3+ in water over a wide detection range (pH = 4-10). The incorporation of Fe3+ into OV-POSS co-poly(acrylamide) results in a significant fluorescence enhancement in water over other metal ions. The bound ratio of OV-POSS co-poly(acrylamide)-Fe3+ complex was determined to be 1 : 2 according to the Job's plot. The association constant (Ka) of Fe3+ binding with the chemosensor was 7.416 × 107, and the detection limit was 0.9 × 10-9 M. Moreover, it was found that the system possessed low cytotoxicity, good permeability, high stability, and compatibility. Hence, it can be successfully applied in bio-imaging with bright blue fluorescence. In addition, a visible color change to the naked eye from colorless to bright yellow could be directly observed when Fe3+ was added into the chemosensor OV-POSS co-poly(acrylamide) compared with other metal ions.

Chemical Decoration of Perovskites by Nickel Oxide Doping for Efficient and Stable Perovskite Solar Cells.

Crystal engineering of CH3NH3PbI3- xCl x perovskite films through modification by decoration with p-type semiconductor materials was proposed as an efficient method for obtaining good-quality crystalline films. A simple method is demonstrated to improve the quality of perovskite films by adding nickel oxide (NiO x) nanoparticles into the precursor solution. The addition of NiO x brings about high-quality crystals and convenient photo-generated charge transport with reduced defect density owing to efficient control of the preferred nucleation and crystal growth. The sufficient contact between CH3NH3PbI3- xCl x-NiO x and the electron-transport layer can contribute to photo-generated carrier lifetime and transport through the optimized interface. Moreover, it is demonstrated that a strong chemical bonding interaction between MAPbI3- xCl x and NiO x could protect perovskite materials from oxygen and humidity corrosion, showing remarkable stability holding ∼81% of the initial power conversion efficiency (PCE) after 50 days. The device with the best PCE of 19.34% is achieved because of the improved short-circuit current from 22.23 to 23.01 mA cm-2 and fill factor from 68.97 to 75.06%. The results certify that this p-type charge transport material decoration method for the optimization of perovskite films is an efficient way to optimize the performance.

Data analysis between controllable variables and the performance of CuS crackle based electrode.

In this article, we provide the data analysis between controllable variables and the performance of CuS crackle based electrode, there are four important factors which could influence the formation of cracks, the colloid concentration, drying temperature, colloid dosage and ambient humidity. We carried out and summed nineteen controlled data experiments below and other variates which could affect the performance were discussed in this article.

Highly flexible, transparent and conducting CuS-nanosheet networks for flexible quantum-dot solar cells.

The rapid development of modern electronics has given rise to a higher demand for flexible and wearable energy sources. Flexible transparent conducting electrodes (TCEs) are one of the essential components of flexible/wearable thin-film solar cells (SCs). In this regard, we present highly transparent and conducting CuS-nanosheet (NS) networks with an optimized sheet resistance (Rs) as low as 50 Ω sq-1 at 85% transmittance as a counter electrode (CE) for flexible quantum-dot solar cells (QDSCs). The CuS NS network electrode exhibits remarkable mechanical flexibility under bending tests compared to traditional ITO/plastic substrates and sputtered CuS films. Herein, CuS NS networks not only served as conducting films for collecting electrons from the external circuit, but also served as superior catalysts for reducing polysulfide (S2-/Sx2-) electrolytes. A power conversion efficiency (PCE) up to 3.25% was achieved for the QDSCs employing CuS NS networks as CEs, which was much higher than those of the devices based on Pt networks and sputtered CuS films. We believe that such CuS network TCEs with high flexibility, transparency, conductivity and catalytic activity could be widely used in making wearable electronic products.