Influence of Field Effects on the Performance of InGaAs-Based Terahertz Radiation Detectors

A detailed electrical characterization of high-performance bow-tie InGaAs-based terahertz detectors is presented along with simulation results. The local surface potential and tunnelling current were scanned over the surfaces of the detectors by means of Kelvin probe force microscopy (KPFM) and scanning tunnelling microscopy (STM), which also enabled the determination of the Fermi level. Current-voltage curves were measured and modelled using the Synopsys Sentaurus TCAD package to gain deeper insight into the processes involved in detector operation. In addition, we performed finite-difference time-domain (FDTD) simulations to reveal features related to changes in the electric field due to the metal detector contacts. The investigation revealed that field-effect-induced conductivity modulation is a possible mechanism contributing to the high sensitivity of the studied detectors.     

Electrochemical gold deposition from sulfite solution: application for subsequent polyaniline layer formation

Electrochemical gold deposition from sulfite solutions was studied by means of voltammetry, EIS and EQCM. A gold film electrode was used for polyaniline layer formation by electrochemical oxidation of aniline. The standard electrochemical reduction potential of the reaction [Au(SO₃)₂]³⁻ + e⁻ = Au + 2 SO₃²⁻ was determined, and is equal to 0.116 V (vs. NHE). Both solution stirring and temperature increase accelerate the electrochemical reduction of gold, when the electrode potential is below −0.55 V. When the potential is above −0.55 V the electrochemical reduction proceeds via passive layer formation. Our study suggests that the passive layer consists of chemically adsorbed sulfite ions and sulfur. The gold film deposited from sulfite solution is a high quality substrate suitable for conducting polymer layer formation. This technique, where a polymer layer electrode is prepared by thin gold film deposition onto a metal surface and by subsequent polymer layer formation, can be applied in sensor research and technology.     

Tissue-Based Markers as a Tool to Assess Response to Neoadjuvant Radiotherapy in Rectal Cancer—Systematic Review

According to current guidelines, the current treatment for locally advanced rectal cancer is neoadjuvant therapy, followed by a total mesorectal excision. However, radiosensitivity tends to differ among patients due to tumor heterogeneity, making it difficult to predict the possible outcomes of the neoadjuvant therapy. This review aims to investigate different types of tissue-based biomarkers and their capability of predicting tumor response to neoadjuvant therapy in patients with locally advanced rectal cancer. We identified 169 abstracts in NCBI PubMed, selected 48 reports considered to meet inclusion criteria and performed this systematic review. Multiple classes of molecular biomarkers, such as proteins, DNA, micro-RNA or tumor immune microenvironment, were studied as potential predictors for rectal cancer response; nonetheless, no literature to date has provided enough sufficient evidence for any of them to be introduced into clinical practice.     

Modelling of activation processes for GR-280 graphite at Ignalina NPP

Ignalina Nuclear Power Plant (INPP) operates two RBMK-1500 water-cooled graphite-moderated channel-type power reactors. The total mass of graphite in the cores of both units at INPP is about 3600 tons. Modelling of activation processes in the reactor's structural materials is necessary for decommissioning planning, because large amounts of activated structural materials (graphite, stainless steel, concrete, etc.) should be managed as radioactive waste. Knowledge of radiological characteristics and a radioactive inventory of irradiated materials are essential in planning of the decommissioning processes. The purpose of this work was to perform conservative neutron activation analysis for decommissioning purposes of INPP. ORIGEN computer code was used for the calculations. Activity levels were calculated for different nuclides present in the graphite and estimates were made how these activity levels depend on irradiation time, neutron flux value and other parameters. Obtained results were compared with the data available from other investigations for GR-280 graphite.     

Mechanical relaxation phenomena in polyimide and poly(2,6-dimethyl-p-phenylene oxide) from 100°K to 700°K

Existing dynamic mechanical relaxation data on two polymers containing aromatic groups in the backbone chain, viz., polyimide PI, and poly(2,6-dimethyl-p-phenylene oxide), PDMPO, are reviewed and new data bearing on specimen purity and water content are presented. It is demonstrated that three separate relaxation processes are normally present in both polymers in the temperature range from about 100–400°K. The lowest temperature relaxation, designated γ, occurs in the 100–180°K range and is considered to arise from limited rotational oscillation of some phenylene rings about the 1,4 axis. Another relaxation process, designated β arises from the presence of water in the polymer. Its strength increases with increase of water content, its activation energy is about 10–12 kcal/mole, and it occurs in the 180–190°K range at 1 Hz. A higher strength secondary glass relaxation process, designated β*, occurs in the 280–400°K range at usual measuring frequencies (1 Hz to 10⁴ Hz). This relaxation is thought to be associated with the combined reorientational motion, of rings and connecting atoms of the monomer unit in “defect” regions, or regions of poor chain packing. As such, its position is affected by sample history. Both polymers also show a rise in damping in the high temperature region indicative of additional main chain motions. In addition to the above relaxations, PDMPO shows a δ-relaxation below liquid nitrogen temperatures, associated with onset of Me rotation and PI shows an additional small relaxation near 500°K.     

Diphenylamine‐Substituted Carbazole‐Based Hole Transporting Materials for Perovskite Solar Cells: Influence of Isomeric Derivatives

A series of new branched hole transporting materials (HTMs) containing two diphenylamine‐substituted carbazole fragments linked by a nonconjugated methylenebenzene unit is synthesized and tested in perovskite solar cells. Synthesis of the investigated materials is performed by a simple two‐step synthetic procedure providing a target product in high yield. The isolated materials demonstrate good thermal stability and majority of the investigated compounds exist in an amorphous state, which is advantageous as there is no risk of crystallization directly in the film. The highest charge drift mobility of µ₀ = 4 × 10^?4 cm² V^?1 s^?1, measured at weak electric fields, is by ca. one order of magnitude higher than that of Spiro‐OMeTAD under identical conditions. From the perovskite solar cell testing results, it can be seen that performance of two new HTMs ( V885 and V911 ) is on a par with Spiro‐OMeTAD. Due to the ease of synthesis, good thermal, optical and photophysical properties, this type of molecules hold great promise for practical application in commercial perovskite solar cells.