Фотоиндуцированный перенос заряда в слоистых 2D наноструктурах PbSe-MoS-=SUB=-2-=/SUB=-

Semiconductor 2D nanostructures are a new platform for the creation of modern optoelectronic devices. Layered 2D PbSe-MoS2 nanostructures with efficient photoinduced charge transfer from PbSe nanoplatelets (NPLs) to MoS2 were created. When PbSe NPLs with short organic ligands are deposited onto a thin layer of MoS2 NPLs, a decrease in their photoluminescence intensity and a decrease in the average photoluminescence lifetime are observed. When a layered 2D PbSe-MoS2 nanostructure is illuminated with IR radiation, a photocurrent appears, which indicates the contribution of PbSe NPLs to the electrical response of the system. Ultrathin layers of transition metal dichalcogenides sensitized with nanostructures based on lead chalcogenides can be used in photodetectors with a spectral sensitivity region extended to the near-IR range.

Ag/MgO Nanoparticles via Gas Aggregation Nanocluster Source for Perovskite Solar Cell Engineering

Nanocluster aggregation sources based on magnetron-sputtering represent precise and versatile means to deposit a controlled quantity of metal nanoparticles at selected interfaces. In this work, we exploit this methodology to produce Ag/MgO nanoparticles (NPs) and deposit them on a glass/FTO/TiO2 substrate, which constitutes the mesoscopic front electrode of a monolithic perovskite-based solar cell (PSC). Herein, the Ag NP growth through magnetron sputtering and gas aggregation, subsequently covered with MgO ultrathin layers, is fully characterized in terms of structural and morphological properties while thermal stability and endurance against air-induced oxidation are demonstrated in accordance with PSC manufacturing processes. Finally, once the NP coverage is optimized, the Ag/MgO engineered PSCs demonstrate an overall increase of 5% in terms of device power conversion efficiencies (up to 17.8%).

Controlled Release Utilizing Initiated Chemical Vapor Deposited (iCVD) of Polymeric Nanolayers

This review will focus on the controlled release of pharmaceuticals and other organic molecules utilizing polymeric nanolayers grown by initiated chemical vapor deposited (iCVD). The iCVD layers are able conform to the geometry of the underlying substrate, facilitating release from one- and two-dimensional nanostructures with high surface area. The reactors for iCVD film growth can be customized for specific substrate geometries and scaled to large overall dimensions. The absence of surface tension in vapor deposition processes allows the synthesis of pinhole-free layers, even for iCVD layers <10 nm thick. Such ultrathin layers also provide rapid transport of the drug across the polymeric layer. The mild conditions of the iCVD process avoid damage to the drug which is being encapsulated. Smart release is enabled by iCVD hydrogels which are responsive to pH, temperature, or light. Biodegradable iCVD layers have also be demonstrated for drug release.

Composite membranes with cellulose acetate surface layer for water treatment

Microporous composite membranes containing from one to three ultrathin layers were obtained by multistage immersion of a paper base in a solution of cellulose acetate in acetone. The physicochemical properties of membranes have been studied and the parameters of membrane separation of heavy metal ions from tap water have been determined. An increase in the particle size and a decrease in the absolute value of the ζ-potential with an increase in the concentration of cellulose acetate in acetone were revealed. It was found that the porosity of the membranes increased from 47 % to 51 % depending on the number of ultrathin cellulose acetate layers on the substrate surface. A decrease in the moisture absorption of composite membranes and an increase in the contact angle of wetting with distilled water from 30.0° to 68.8°, depending on the number of ultrathin layers, were noted. Microscopic examination of the membrane surface showed that the ultrathin layer consists of many pores with sizes less than 1 micron. The absorption bands in the IR spectra of cellulose acetate and the surface of the composite microporous cellulose acetate (MAC) membrane are identical. The retention capacity of MAC composite membranes, determined by iron ions from an iron (III) chloride solution, ranged from 47.5 to 97.4 % depending on the number of cellulose acetate layers on the substrate surface with a specific productivity of 27.9 to 7399 dm3/(m2·h) and a pressure of 0.35 MPa. A high selectivity of a microporous membrane of three layers of cellulose acetate (MAC3) with respect to heavy metal ions contained in tap water was established: Cr3+ (96 %) > Cu2+ (92 %) > Fe3+ (90 %) > Mn2+ (45 %).