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Ohne ZusammenfassungMitteilung aus dem Chemischen Untersuchungsamte der Stadt Dresden.  相似文献   
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The non-orthogonal multiple access (NOMA) wireless networks are a robust multi-access mechanism that serves multiple clients accessing the same resource block simultaneously. The fifth-generation wireless networks offer huge efficiency in spectrum utilization, which can be exploited to deploy NOMA for LOS communication of unmanned aerial vehicles (UAVs). Previous research has extensively analyzed various aspects of NOMA-UAV communication systems, including user access fairness, coverage, maximizing system capacity, and total energy efficiency. However, only a few researchers have focused on maximizing the EE of NOMA-UAV wireless networks with user quality of service (QoS) constraints. This paper proposes a fuzzy logic-based crossover-based coati optimization algorithm for maximizing the energy efficiency of NOMA-UAV, along with user scheduling. The main objective of this model is to offer a solution to the joint energy efficiency and user QoS scheduling problem. The fuzzy decision-making strategy optimizes the energy efficiency (EE) of NOMA-UAV by selecting appropriate power and time resources. Additionally, the crossover-based coati optimization algorithm transforms the subchannel allocation problem into a two-sided matching procedure. The efficiency of the proposed algorithm is evaluated concerning overall residual energy, number of remaining nodes, and time consumption. The experimental outcomes demonstrate the capability of the proposed model in optimizing the energy efficiency of the NOMA-UAV network by identifying the optimal resource set in terms of time and power while satisfying the clients' QoS.  相似文献   
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This work investigates the radiation resistance of high-performance multi-component perovskite solar cells (PSCs) for the first time under extreme short-pulse proton irradiation conditions. The devices are subjected to high-intensity 170 keV pulsed (150 ns) proton irradiation, with a fluence of up to 1013 p cm−2, corresponding to ≈30 years of operation at low Earth orbit. A complex material characterization of the perovskite active layer and device physics analysis of the PSCs before and after short-pulse proton irradiation is conducted. The obtained results indicate that the photovoltaic performance of the solar cells experiences a slight deterioration up to 20 % and 50 % following the low 2 × 1012 p cm−2 and high 1 × 1013 p cm−2 proton fluences, respectively, due to increased non-radiative recombination losses. The findings reveal that multi-component PSCs are immune even to extreme high-intense short-pulse proton irradiation, which exceeds harsh space conditions, including intense coronal ejection events usually associated with solar flares.  相似文献   
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Assessment of T-cell response to the tumor is important for diagnosis of the disease and monitoring of therapeutic efficacy. For this, new non-destructive label-free methods are required. Fluorescence lifetime imaging (FLIM) of metabolic coenzymes is a promising innovative technology for the assessment of the functional status of cells. The purpose of this work was to test whether FLIM can resolve metabolic alterations that accompany T-cell reactivation to the tumors. The study was carried out on C57Bl/6 FoxP3-EGFP mice bearing B16F0 melanoma. Autofluorescence of the immune cells in fresh lymphatic nodes (LNs) was investigated. It was found that fluorescence lifetime parameters of nicotinamide adenine dinucleotide (phosphate) NAD(P)H are sensitive to tumor development. Effector T-cells in the LNs displayed higher contribution of free NADH, the form associated with glycolysis, in all tumors and the presence of protein-bound NADPH, associated with biosynthetic processes, in the tumors of large size. Flow cytometry showed that the changes in the NADH fraction of the effector T-cells correlated with their activation, while changes in NADPH correlated with cell proliferation. In conclusion, FLIM of NAD(P)H in fresh lymphoid tissue is a powerful tool for assessing the immune response to tumor development.  相似文献   
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