Irradiation Step Research Articles

Degradation of thermoplastic polymers for fused filament fabrication under (S)TEM electron beam irradiation

The structural characterization of polymers and, in particular, of those used in Additive Manufacturing (AM) technologies, is essential to improve the understanding of their structure-property relationship for promising high-performance applications. For this, (scanning) transmission electron microscopy-electron energy loss spectroscopy, (S)TEM-EELS is an outstanding tool for exploring materials chemical and structural characteristics at high spatial resolution. However, the high beam-sensitivity of soft materials, such as polymers, hinders the possibility of probing in-depth analysis provided by (S)TEM-EELS. In this work, we analyse the electron beam irradiation damage of four polymers commonly used in Fused Filament Fabrication (FFF), namely polylactic acid (PLA), polycaprolactone (PCL), acrylonitrile butadiene styrene (ABS) and acrylonitrile styrene acrylate (ASA). For this, sequential low-loss and core-loss EEL spectra have been recorded, and the related signals have been monitored as a function of the accumulated dose. Our results show that the critical electron doses using the specimen thickness variations are larger for polymers containing aromatic groups (ABS and ASA) than for aliphatic polymers (PLA and PCL). Regarding the different elements, a larger sensitivity to the electron beam of oxygen regarding carbon and nitrogen is also evidenced. Our results have shown that polymer degradation occurs to a larger extent in the initial steps of electron irradiation, for very low accumulated electron doses, meaning that care should be taken in the selection of the microscopy settings to avoid artefacts produced by the electron beam. Degradation pathways for the four polymers studied are discussed.

Nanosilicon Stabilized With Ligands: Effect of High‐Energy Proton Beam on Luminescent Properties

ABSTRACTSilicon nanopowders with nitrogen heterocyclic carbene (NHC) and butyl as stabilizing ligands were synthesized by bottom‐up chemical methods. Transmission electron microscopy (TEM) was used to obtain nanoparticle size distribution with 1.8–2.5‐nm average diameter. Optical characteristics (photoluminescence [PL] and infrared [IR] absorption spectra) of samples were investigated as fabricated and on different steps of irradiation by high‐energy 22.5‐MeV protons. The PL spectral changes are slightly different for two cases, but in general, we can see a decrease in luminescence amplitude with fluence growth up to 4·1014 cm−2, mainly for NHC‐stabilized nanosilicon. Main mechanisms of radiation‐induced changes in nanosilicon sample optical properties are discussed by the joint use of PL and IR spectra analysis.

Radiation Damage on Silicon Photomultipliers from Ionizing and Non-Ionizing Radiation of Low-Earth Orbit Operations.

Silicon Photomultipliers (SiPMs) are single photon detectors that gained increasing interest in many applications as an alternative to photomultiplier tubes. In the field of space experiments, where volume, weight and power consumption are a major constraint, their advantages like compactness, ruggedness, and their potential to achieve high quantum efficiency from UV to NIR makes them ideal candidates for spaceborne, low photon flux detectors. During space missions however, SiPMs are usually exposed to high levels of radiation, both ionizing and non-ionizing, which can deteriorate the performance of these detectors over time. The goal of this work is to compare process and layout variation of SiPMs in terms of their radiation damage effects to identify the features that helps reduce the deterioration of the performance and develop the next generation of more radiation-tolerant detectors. To do this, we used protons and X-rays to irradiate several Near Ultraviolet High-Density (NUV-HD) SiPMs with small areas (single microcell, 0.2 × 0.2 mm2 and 1 × 1 mm2) produced at Fondazione Bruno Kessler (FBK), Italy. We performed online current-voltage measurements right after each irradiation step, and a complete functional characterization before and after irradiation. We observed that the main contribution to performance degradation in space applications comes from proton damage in the form of an increase in primary dark count rate (DCR) proportional to the proton fluence and a reduction in activation energy. In this context, small active area devices show a lower DCR before and after irradiation, and we propose light or charge-focusing mechanisms as future developments for high-sensitivity radiation-tolerant detectors.

Thirty years of forest productivity in a mountainous landscape: The Yin and Yang of topography

AbstractWe measured light‐related patterns of primary productivity within a topographically complex Oregon watershed over a 30‐year period. Second‐growth conifer densities were experimentally altered in 1981. Plots receiving at least 3434 MJ m−2 over a 6‐month growing season averaged 40% greater aboveground net primary productivity (ANPP) than those receiving less light (p = 0.000). Unthinned stands potentially built enough LAI to compensate for low light, but risked mortality that exceeded resilience. The two light levels acted as basins of attraction for other physiological and ecological processes, including size–density relationships and limiting foliar nutrients. Initial (1981) LAI and the irradiation step (above or below 3434 MJ m−2) explained 60% of variation in a 30‐year ANPP. Irradiation within each light group did not affect ANPP. At high irradiation, foliar N/Ca and slope steepness (both negative) explained 58% of the variation in residuals from the initial models, while at low irradiation on north, east, and west aspects, 83% of residual variation was explained by foliar Mg (+), understory cover (+), and 30‐year mortality (−). Light use efficiency (LUE) of fully stocked stands correlated with LAI and foliar N/K. Results suggest that understory influence on tree foliar N (+ or −) enhances ANPP by regulating critical nutrient ratios. Mortality reduced or eliminated differences among thinning levels, which did not vary at low light and only between unthinned and heavily thinned at high light. Values associated with relatively open forests (biodiversity, resilience) may be attained without large sacrifice of long‐term carbon sinks. In our study, light interacts with topography to produce nonlinear dynamics in which small changes in irradiation can have large consequences. Reduced sunlight has been suggested as a geoengineering option to combat global warming. Ecological changes out of proportion to lowered irradiation are a distinct possibility, including sharp reductions in terrestrial carbon sinks.

Extending the ESR and OSL dating comparison on coastal dune deposits from the Wilderness-Knysna area (South Africa)

Our work follows up on the initial methodological ESR dating study by Ben Arous et al. (2022) on several quartz samples from the Plio-Pleistocene to Holocene aeolian coastal dune deposits of the Wilderness-Knysna area (South Africa) that were previously dated by optically stimulated luminescence (OSL). Here, we extend this first ESR-OSL comparison with five additional optically-bleached quartz samples. We used the Multiple Aliquot Additive Dose (MAAD) method to specifically (i) evaluate the influence of the irradiation dose steps on the determination of low De values (<100 Gy) and (ii) obtain finite ESR ages for older samples that sometimes show saturated OSL signals. Following the Multiple Centre ESR dating approach, the Aluminium (Al) and Titanium (Ti) signals (Ti–H and Ti–Li–H, the latter resulting from a mixture of Ti centres) were systematically measured in all samples, and resulting De values and age estimates were compared with the corresponding OSL data. Our results show that for young samples (<50 ka) showing De values of a few tens of Grays (Gy), the use of smaller irradiation steps spaced by < 100 Gy has a noticeable impact on the MAAD dose evaluation from the Ti centres, usually leading to De results closer to the expected values (for 2/3 samples). However, this also makes the ESR measurements somewhat more challenging, with higher experimental uncertainties, lower measurement repeatability and lower goodness-of-fit resulting from the relatively weak Ti ESR intensities, ultimately impacting the robustness of the ESR data collected. In this sense, our study illustrates the limitations of the ESR method to detect very low dose irradiation values < 30 Gy with our experimental conditions (i.e., using MAAD procedure, a standard resonator and a measurement temperature of ∼90 K). On the contrary, it also highlights the greater potential of the Ti–H signal to date Late Pleistocene samples, confirming previous studies. Moreover, our results suggest that the transport and bleaching conditions of these aeolianite deposits may not be ideal for the reset of the radiation-induced Al and Ti ESR signals, which is consistent with the very few existing studies specifically focused on this type of samples, but contrasts with other previous dating applications centered on fluvial environments. Finally, we also provide additional chronological constraints to the Landward barrier complex and Coversands deposits, two of the oldest Plio-Quaternary formations in the Wilderness-Knysna area.

Mitigating Gas Evolution in Electron Beam-Induced Gel Polymer Electrolytes Through Bi-Functional Cross-Linkable Additives.

The current high-capacity lithium-ion batteries (LIBs), reliant on flammable liquid electrolytes (LEs) and nickel-rich cathodes, are plagued by safety hazards, especially the risk of hazardous gas release stemming from internal side reactions. To address these safety concerns, an electron beam (E-beam)-induced gel polymer electrolyte (E-Gel) is introduced, employing dipentaerythritol hexaacrylate (DPH) as a bi-functional cross-linkable additive (CIA). The dual roles of DPH are exploited through a strategically designed E-beam irradiation process. Applying E-beam irradiation on the pre-cycled cells allows DPH to function as an additive during the initial cycle, establishing a protective layer on the surface of the anode and cathode and as a cross-linker during the E-beam irradiation step, forming a polymer framework. The prepared E-Gel with CIA has superior interfacial compatibility, facilitating lithium-ion diffusion at the electrode/E-Gel interface. The electrochemical assessment of 1.2 Ah pouch cells demonstrates that E-Gel substantially reduces gas release by 2.5 times compared to commercial LEs during the initial formation stage and ensures superior reversible capacity retention even after prolonged cycling at 55°C. The research underscores the synergy of bifunctional CIA with E-beam technology, paving the way for large-scale production of safe, high-capacity, and commercially viable LIBs.

Dynamic response characteristics and economic analyses of two solar-assisted multi-generation systems

Efficient use of solar energy can alleviate the depletion of fossil energy and global warming. In this paper, two solar-aided combined cooling, heating and power systems are proposed and dynamically modeled. The main difference between the two systems is whether the solar energy is stored. A rotor speed-temperature-fuel control system is established, which is suitable for both systems. A control system for solar heat collection process is developed. Energy, exergy and techno-economic analyses are carried out to evaluate the thermodynamic and economic performances. The dynamic responses under direct normal irradiation perturbation and load perturbation are also investigated. The result shows that compared with the system without energy storage, the system with energy storage has higher primary energy utilization rate, exergy efficiency and fuel saving rate, but the economic performance is poorer. The rotor speed-temperature-fuel control system can guarantee a short equilibrium time and a small overshoot for power generation process. When electrical load disturbance occurs, the stabilization times of the output power, cooling energy supply and thermal energy supply are 30 s, 675 s and 770 s, respectively. Under the regulation of the solar heat collection control system, the maximum overshoot of the outlet thermal oil temperature of the parabolic trough solar collector is 2.6 % with a stabilization time of 83 s when the direct normal irradiation step disturbance occurs.

Surface chemical reactions of etch stop prevention in plasma-enhanced atomic layer etching of silicon nitride

Molecular dynamics (MD) simulations were performed to examine the influence of oxygen (O) ion irradiation at the end of each cycle of plasma-enhanced atomic layer etching (PE-ALE) of silicon nitride (SiN). The main concern during the SiN PE-ALE process is that it can lead to an etch stop due to excessive hydrofluorocarbon (HFC) polymer accumulation, which hinders ion impact in the desorption step. Such an etch stop can be avoided by incorporating an oxygen (O2) plasma irradiation step after the desorption step of a conventional two-step PE-ALE process of SiN. In this study, the differences between the two- and three-step PE-ALE processes of SiN with and without O2 plasma irradiation are discussed. In the simulations of this study, low-energy CH2F radicals are deposited on a SiN surface in the adsorption step, and the modified surface is then irradiated with energetic Ar+ ions and removed in the desorption step. In the O2 plasma irradiation step, the resulting surface is irradiated with low-energy O species, and excess carbon (C) atoms are removed. It has been found that the O irradiation step effectively prevents the accumulation of C atoms by promoting the formation of volatile CO molecules.

Sustainable design of high-performance multifunctional carbon electrodes by one-step laser carbonization for supercapacitors and dopamine sensors.

Laser carbonization is a rapid method to produce functional carbon materials for electronic devices, but many typical carbon precursors are not sustainable and/or require extensive processing for electrochemical applications. Here, a sustainable concept to fabricate laser patterned carbon (LP-C) electrodes from biomass-derived sodium lignosulfonate, an abundant waste product from the paper industry is presented. By introducing an adhesive polymer interlayer between the sodium lignosulfonate and a graphite foil current collector, stable, abrasion-resistant LP-C electrodes can be fabricated in a single laser irradiation step. The electrode properties can be systematically tuned by controlling the laser processing parameters. The optimized LP-C electrodes demonstrate a promising performance in supercapacitors and electrochemical dopamine biosensors. They exhibit high areal capacitances of 38.9 mF cm-2 in 1 M H2SO4 and high energy and power densities of 4.3 μW h cm-2 and 16 mW cm-2 in 17 M NaClO4, showing the best performance among biomass-derived LP-C materials reported so far. After 20 000 charge/discharge cycles, they retain a high capacitance of 81%. Dopamine was linearly detected in the range of 0.1 to 20 μM with an extrapolated limit of detection of 0.5 μM (S/N = 3) and high sensitivity (13.38 μA μM-1 cm-2), demonstrating better performance than previously reported biomass-derived LP-C dopamine sensors.

Holographic fabrication of reconfigurable diffractive elements

The fabrication of Diffractive Optical Elements (DOEs) involves the analog patterning of material surfaces on the scale of light wavelength. This typically requires multi-step lithographic processes. Differently from the photoresists of standard lithography, thin films of amorphous azobenzene-containing polymers (azopolymers) can directly produce a structured surface using a single irradiation step with structured light. The resulting surface reliefs can be used directly as planar phase-modulating DOEs without the need for any post-exposure process. Additionally, the surface geometry and its optical functionality can be reconfigured at will. Here, we demonstrate reprogrammable and ready-to-use azopolymer diffractive gratings, lenses, and holographic projectors, produced by grayscale digital holographic patterns. By exploiting the all-optical scheme based of computer-generated holography, the diffraction behavior of the DOEs is optimized during the developing of structured surfaces. Full all-optical reconfigurability of the fabricated devices is also achieved. Our approach provides a versatile, efficient, and all-optical reversible fabrication framework for DOEs, making it a promising option to overcome the demanding, cumbersome, and irreversible fabrication processes typically involved in the realization of planar diffractive optical devices.

Reduction of EpCAM-Positive Cells from a Cell Salvage Product Is Achieved by Leucocyte Depletion Filters Alone.

Intraoperative cell salvage reduces the need for allogeneic blood transfusion in complex cancer surgery, but concerns about the possibility of it re-infusing cancer cells have hindered its application in oncology. We monitored the presence of cancer cells on patient-salvaged blood by means of flow cytometry; next, we simulated cell salvage, followed by leucodepletion and irradiation on blood contaminated with a known amount of EpCAM-expressing cancer cells, assessing also residual cancer cell proliferation as well as the quality of salvaged red blood cell concentrates (RBCs). We observed a significant reduction of EpCAM-positive cells in both cancer patients and contaminated blood, which was comparable to the negative control after leucodepletion. The washing, leucodepletion and leucodepletion plus irradiation steps of cell salvage were shown to preserve the quality of RBCs in terms of haemolysis, membrane integrity and osmotic resistance. Finally, cancer cells isolated from salvaged blood lose their ability to proliferate. Our results confirm that cell salvage does not concentrate proliferating cancer cells, and that leucodepletion allows for the reduction of residual nucleated cells, making irradiation unnecessary. Our study gathers pieces of evidence on the feasibility of this procedure in complex cancer surgery. Nevertheless, it highlights the necessity of finding a definitive consensus through prospective trials.

Exceptional structural and functional stability of Zr-doped REBaCuO tapes with respect to neutron irradiation and overheating

The impact of neutron irradiation on the properties of second-generation REBaCuO tapes was studied. The main aim of the present study was to identify the fast neutrons irradiation fluence threshold, φ th, at which the high-field critical current at low temperatures, I c (10 K, 8 T), starts degrading. Following up on our previous publication for low irradiation fluences, two new irradiation steps were added. Up to the last but one irradiation step, the T c in all samples followed a linear dependence on the fast neutrons irradiation fluence, T c(φ) ≈ T c(0) − τφ (τ being a numerical constant in units of K/1022 m−2 and φ in 1022 m−2). In parallel, I c (10 K, 8 T) continuously grew with φ up to the threshold fluence, φ th ≈ 3× to 4.3 × 1022 m−2. The last gradual irradiation by φ≈ 1.83 × 1022 m−2 brought a severe degradation both in T c and I c (10 K, 8 T) in most samples, irrespective of their irradiation history. This effect was attributed to radiation overheating. Annealing of pristine tapes in dilute Ar confirmed this scenario. Two of the SuperPower tapes, doped by Zr, appeared to be exceptionally stable against both types of overheating. The tape doped with 7.5% Zr, T c(φ) followed the linear dependence up to the highest cumulative fluence φ =6.16 × 1022 m−2, while the I c (10 K, 8 T) drop was several orders of magnitude lower than in the samples without Zr. TEM study found that the Zr-doped tapes survived the overheating during the last irradiation step in a crystalline form, while all other samples were amorphized.

Enabling Logic Computation Between Ta/CoFeB/MgO Nanomagnets

Dipolar coupled magnets proved to have the potential to be capable of successfully performing digital computation in a highly parallel way. For that, nanomagnet-based computation requires precise control of the domain wall nucleation from a well-localized region of the magnet. Co/Pt and Co/Ni multilayer stacks were successfully used to demonstrate a variety of computing devices. However, Ta/CoFeB/MgO appears more promising thanks to the lower switching field required to achieve a full magnetization reversal, reduced thickness (less than 10 nm), and its compatibility with magnetic tunnel junctions. In this work, the switch of the information is achieved through the application of a magnetic field, which allows to scale more the nanomagnets with respect to current-driven magnetization reversal-based devices and to go towards 3D structures. We experimentally demonstrate that Ga <sup xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">+</sup> ions can be used to tune the energy landscape of the structured magnets to provide signal directionality and achieve a distinct logic computation. We prove that it is possible to define the artificial nucleation center in different structures with two irradiation steps and that this approach can enable logic computation in ultra-thin films by dipolar interaction. Moreover, different from previous studies, the results coming from the irradiation analysis are then used for real logic devices. We present the experimental demonstration of a set of fully working planar inverters, showing that it is possible to reach a coupling field between input and output, which is strong enough to reliably implement logic operations. Micromagnetic simulations are used to study the nucleation center’s effectiveness with respect to its position in the magnet and to support the experiments. Our results open the path to the development of more efficient nanomagnet-based logic circuits.

Complete removal of CO at ambient conditions using copper manganese oxide (CuMnOx) catalysts synthesised via co-precipitation with ultrasonic irradiation

This present work investigates the novel method of synthesising copper manganese oxide (Hopcalite) catalysts with a Cu:Mn ratio of 1:2 by using a facile ultrasound-assisted co-precipitation synthesis technique. The CuMnOx catalysts were synthesised using an ultrasonic bath or an ultrasonic probe with varying ultrasonic powers. The catalysts were further characterised and evaluated for the oxidation of carbon monoxide (CO). Characterisation results revealed that samples prepared using the ultrasonic method exhibited enhanced physical properties, such as highly dispersed particles with a larger surface area and pore size. Besides, the presence of mixed copper and manganese oxide phases was detected, which provided synergistic interactions to facilitate and enhance CO oxidation. The amorphicity and reducibility of the catalysts were also improved, thus indicating the presence of more active sites. Furthermore, the catalyst prepared using the ultrasonic probe at a power of 23.3 W with a 15 min sonication time was found to be the most active, with the capability of oxidising CO to CO2 to completion (100 %) at ambient conditions. It also possessed high catalytic stability, in which catalytic activity was not compromised for as long as 200 min. On the whole, this work has ascertained that by incorporating a simple ultrasonic irradiation step into the synthesis procedure of copper manganese oxide catalysts, the overall performance of the catalyst can be greatly improved compared to those already found in the literature, which demonstrates the potential application of this new method on a wider, commercial scale for carbon monoxide removal.

Near-room temperature synthesis of Zn&lt;sup&gt;2+&lt;/sup&gt;-doped γ-Ga&lt;sub&gt;2&lt;/sub&gt;O&lt;sub&gt;3&lt;/sub&gt; nanoparticles via direct oxidation of Zn–Ga alloy by ultrasound

This study used ultrasound irradiation to fabricate Zn2+-doped γ-Ga2O3 nanoparticles (NPs) from Zn–Ga alloy at near-room temperature (60 °C). The Zn2+-doped γ-Ga2O3 NPs were obtained at 60 °C after two steps of ultrasound irradiation (miniaturization and oxidation of Zn–Ga alloy). The specific surface area of Zn2+-doped γ-Ga2O3 NPs with a zinc content of 4 at.% was 90.4 m2/g. The oxidation behavior of Zn–Ga liquid alloy significantly differed from that of liquid Ga. X-ray photoelectron spectroscopy spectrum and lattice constant of Zn2+-doped γ-Ga2O3 confirmed Zn2+-doping into the γ-Ga2O3 crystal structure. By annealing at 900 °C, the obtained Zn2+-doped γ-Ga2O3 did not transform to Zn2+-doped β-Ga2O3 but to the mixed phase of β-Ga2O3 and ZnGa2O4. The results indicate that Zn2+ cations, with larger ionic radii than Ga3+ cations, are more difficult to be introduced into the β-Ga2O3 crystal lattice. Thus, this ultrasound process can potentially synthesize various metal cations-doped γ-Ga2O3 NPs without using high temperatures and pressures.

Influence of ultraviolet and chemical treatment on the biodegradation of low-density polyethylene and high-density polyethylene by Cephalosporium strain.

In the present work, the potential of Cephalosporium strain in degrading the pre-treated (ultraviolet irradiation followed by nitric acid treatment) low-density polyethylene and high-density polyethylene films was investigated. Our observations revealed a significant weight reduction of 24.53 ± 0.73% and 18.22 ± 0.31% in pre-treated low-density polyethylene and high-density polyethylene films respectively, after 56days of incubation with the Cephalosporium strain. Changes in the physicochemical properties of the mineral salt medium (MSM) were studied to assess the extent of biodegradation. The pH of the MSM decreased gradually during the incubation period, whereas its total dissolved solids and conductivity values increased steadily. Fourier transform infrared spectroscopy (FTIR) indicated the formation of hydroxyl and C = C groups in biodegraded low-density polyethylene films, while in the case of biodegraded high-density polyethylene films it indicated the [Formula: see text]CH2 stretching. Furthermore, the thermogravimetric analysis (TGA) revealed an enhancement in the thermal stabilities of both the LDPE and HDPE films post the biodegradation. Modifications in the polymer surface morphologies after UV irradiation, chemical treatment, and biodegradation steps were visualized via scanning electron microscopy (SEM) analysis. All our observations confirm the ability of the Cephalosporium strain in biodegrading the pre-treated LDPE and HDPE films.

Impact of 3MeV Energy Proton Particles on Mid-IR QCLs

This paper reports the results obtained for a distributed-feedback quantum cascade laser (DFB-QCL) exposed to different fluences of proton particles: 1014, 1015 and 1016 p/cm2. Dedicated laboratory setups were developed to assess the irradiation-induced changes in this device. Multiple parameters defining the QCL performances were investigated prior to and following each irradiation step: (i) voltage-driving current; (ii) emitted optical power-driving current; (iii) central emitting wavelength-driving current; (iv) emitted spectrum-driving current; (v) transversal mode structure-driving current, maintaining the system operating temperature at 20 °C. The QCL system presented, before irradiation, two emission peaks: a central emission peak and a side peak. After proton irradiation, the QCL presented a spectral shift, and the ratio between the two peaks also changed. Even though, after irradiation, the tunning spectral range was reduced, at the end of the tests, the system was still functional.

Radiation damage effects of protons and X-rays on silicon photomultipliers

Silicon photomultipliers (SiPMs) are highly-sensitive photodetectors emerging as the technology of choice for many applications. In high-energy physics experiments and as the detectors for space instruments they are often exposed to a large amount of irradiation. In recent years, there has been an increasing interest in assessing the performance deterioration of such detectors after ionizing and non-ionizing radiation, such as protons, neutrons and X or gamma rays. It is interesting to compare the radiation damage effects on several types of SiPMs, to assess the main deterioration mechanisms on SiPM performances. In this work we report on the irradiation by protons and X-rays of several types of small-area ( ∼ 1 mm 2 ) SiPMs, produced in FBK with different technologies. We show and compare the most interesting results of the online measurements, taken just after each irradiation step, for both irradiations. We performed and monitored the current variation during a room temperature annealing. Finally we characterized all the main functional performance of the irradiation SiPMs, highlighting the most interesting variations.

Influence of Bulk Doping and Halos on the TID Response of I/O and Core 150 nm nMOSFETs

The total ionizing dose sensitivity of planar 150 nm CMOS technology is evaluated by measuring the DC responses of nMOSFETs at several irradiation steps up to 125 krad(SiO2). Different TID sensitivities are measured for transistors built with different channel dimensions and operating voltages (I/O and core). The experimental results evidence strong relations between TID sensitivity and the doping profiles in the channel. I/O transistors have the highest TID sensitivity due to their thicker gate oxide and lower bulk doping compared with core devices. In general, narrow-channel devices have the worst degradation with negative threshold voltage shifts, transconductance variations and increased subthreshold leakage currents, suggesting charge trapping in shallow trench isolation (STI). The enhanced TID tolerance of short-channel core devices is most likely related to the increased channel doping induced by the overlapping of halo implantations. Finally, transistors fabricated for low-leakage applications exhibit near insensitivity to TID due to higher bulk doping used during the fabrication to minimize the drain-to-source leakage current.

Latent track PET membranes for high-performance Li+/Mg2+ selectivity assisted with trivalent ion

Selective ionic transport in sub-nanometer pores attracts strong interest. It is still limited by the difficulties in large-scale production of uniform membranes with well-defined sub-nanometer pores. The polymer membranes with latent track are excellent candidate materials. However, the Li+/Mg2+ selectivity in latent track polymer membranes is not high. Herein, we optimize the fabrication process and introduce the trivalent coexisting ions to achieve high selectivity. The polyethylene terephthalate membranes are prepared using the sequential steps of swift heavy ion irradiation, UV illumination, and DMF treatment. The DMF extraction can well control the pore diameters ranging from 2.96 to 5.19 Å as a moderate treatment of membranes. It generates high selectivity in latent track membranes. More interestingly, the ionic transport behavior can be significantly regulated by coexisting ions. By optimizing the experimental conditions, the high selectivity of Li+/Mg2+ of 773 can be achieved in the mixture solutions.