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Currently, there is growing interest in wearable and biocompatible smart computing and information processing systems that are safe for the human body. Memristive devices are promising for solving such problems due to a number of their attractive properties, such as low power consumption, scalability, and the multilevel nature of resistive switching (plasticity). The multilevel plasticity allows memristors to emulate synapses in hardware neuromorphic computing systems (NCSs). The aim of this work was to study Cu/poly-p-xylylene(PPX)/Au memristive elements fabricated in the crossbar geometry. In developing the technology for manufacturing such samples, we took into account their characteristics, in particular stable and multilevel resistive switching (at least 10 different states) and low operating voltage (<2 V), suitable for NCSs. Experiments on cycle to cycle (C2C) switching of a single memristor and device to device (D2D) switching of several memristors have shown high reproducibility of resistive switching (RS) voltages. Based on the obtained memristors, a formal hardware neuromorphic network was created that can be trained to classify simple patterns.

Nanoparticles based on biocompatible methoxy poly(ethylene glycol)-b-poly(D,L-lactide) (mPEG113-b-P(D,L)LAn) copolymers as potential vehicles for the anticancer agent oxaliplatin were prepared by a nanoprecipitation technique. It was demonstrated that an increase in the hydrophobic PLA block length from 62 to 173 monomer units leads to an increase of the size of nanoparticles from 32 to 56 nm. Small-angle X-ray scattering studies confirmed the “core-corona” structure of mPEG113-b-P(D,L)LAn nanoparticles and oxaliplatin loading. It was suggested that hydrophilic oxaliplatin is adsorbed on the core-corona interface of the nanoparticles during the nanoprecipitation process. The oxaliplatin loading content decreased from 3.8 to 1.5% wt./wt. (with initial loading of 5% wt./wt.) with increasing PLA block length. Thus, the highest loading content of the anticancer drug oxaliplatin with its encapsulation efficiency of 76% in mPEG113-b-P(D,L)LAn nanoparticles can be achieved for block copolymer with short hydrophobic block.

The effect of the hydrophobic block length in diblock (PLLA x -b-PEO113, x = 64, 166, 418) and triblock (PLLA y -b-PEO91-b-PLLA y , y = 30, 52, 120) copolymers of l-lactic acid and ethylene oxide on the structure of micelles prepared by dialysis was studied by wide- and small-angle X-ray scattering in dilute aqueous solution, dynamic light scattering, transmission electron microscopy, atomic force microscopy, and force spectroscopy. It was found that the size of the crystalline PLLA core is weakly dependent on the PLLA block length. In addition to individual micelles, a number of their micellar clusters were detected with characteristic distance between adjacent micelle cores decreasing with an increase in PLLA block length. This effect was explained by the change in the conformation of PEO chains forming the micellar corona because of their overcrowding. Force spectroscopy experiments also reveal a more stretched conformation of the PEO chains for the block copolymers with a shorter PLLA block. A model describing the structure of the individual micelles and their clusters was proposed.

In this study, wide-angle X-ray diffraction, X-ray absorption spectroscopy, and transmission electron microscopy were employed to address the crystalline structure and morphology of poly(p-xylylene)−PbS nanocomposite thin films prepared by vapor deposition polymerization as well as their evolution upon thermal annealing. It was found that as-synthesized samples with different PbS contents demonstrate similar diffraction patterns that cannot be fully ascribed to a decrease in crystallite size, indicating distorted crystal structure of PbS nanoparticles compared to the bulk PbS. X-ray absorption spectroscopy reveals wide distribution of Pb−S bond lengths with a minimum value of 2.67 Å, which can be attributed to the presence of molecular (PbS) n clusters in the studied films. It was shown that thermal annealing can be used to control the size of PbS nanoparticles and, as a consequence, optical properties of the composite films. The UV−vis absorption spectra demonstrate pronounced red shift of the absorption edge correlated with the growth of PbS nanoparticles upon annealing. Comprehensive analysis of several theoretical models describing the effect of nanoparticles size on optical band gap of the composite material has been performed and compared with the experimental data.

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