Ms Time Research Articles

Physics and Technology Research for Liquid-Metal Divertor Development, Focused on a Tin-Capillary Porous System Solution, at the OLMAT High Heat-Flux Facility

The operation of the Optimization of Liquid Metal Advanced Targets (OLMAT) facility began in April 2021 with the scientific objective of exposing liquid-metal plasma facing components (PFCs) to the particle and power fluxes provided by one of the hydrogen neutral beam injectors of the TJ-II stellarator. The system can deliver heat fluxes from 5 to 58 MW m−2 of high energy hydrogen neutral particles (≤ 33 keV) with fluxes up to 1022 m2 s−1 (containing an ion fraction ≤ 33% in some instances), pulsed operation of 30–150 ms duration and repetition rates up to 2 min−1. These characteristics enable OLMAT as a high heat flux (HHF) facility for PFC evaluation in terms of power exhaust capabilities, thermal fatigue and resilience to material damage. Additionally, the facility is equipped with a wide range of diagnostics that includes tools for analyzing the thermal response of the targets as well as for monitoring atomic/plasma physics phenomena. These include spectroscopy, pyrometry, electrical probing and visualization (fast and IR cameras) units. Such particularities make OLMAT a unique installation that can combine pure technological PFC research with the investigation of physical phenomena such as vapor shielding, thermal sputtering, the formation/characterization of plasma plumes with significant content of evaporated metal and the detection of impurities in front of the studied targets. Additionally, a myriad of surface characterization techniques as SEM/EDX for material characterization of the exposed PFC prototypes are available at CIEMAT. In this article, first we provide an overview of the current facility upgrade in which a high-power CW laser, that can be operated in continuous and pulsed modes (0.2–10 ms), dump and electrical (single Langmuir) probe embedded on the target surface have been installed. This laser operation will allow simulating more relevant heat loading scenarios such as nominal steady-state divertor heat fluxes (10–20 MW m−2 in continuous mode) and transients including ELM loading and disruption-like events (ms time scales and power densities up to GW m−2 range). The work later focuses on the more recent experimentation (2022 fall campaign) where a 3D printed Tungsten (W) Capillary Porous System (CPS) target, with approximated 30 μm pore size and a 37% porosity and filled with liquid tin. This porous surface was a mock-up of the PFC investigated in the ASDEX Upgrade divertor manipulator. The target composed with this element was eventually exposed to a sequence of shots with the maximum heat flux that OLMAT provides (58 ± 14 MWm−2). Key questions as resilience to dry-out and particle ejection of the liquid metal layer, its refilling, the induced damage/modification of the porous W matrix and the global performance of the component are addressed, attempting to shed light on the issues encountered with the PFC at tokamak scale testing.

(Invited) Understanding Oxygen Transport in Polymer Electrolyte Membrane Water Electrolyzers Using X-Ray Computed Tomography

This study aims to understand the fundamental processes that affect catalyst utilization and gas transport through the porous media in polymer electrolyte water electrolyzers (PEWEs) to optimize porous transport layers (PTLs) and flow-fields. We designed a novel operando x-ray computed tomography (CT) cell that can resolve oxygen transport along a 10 cm x 1 cm membrane electrode assembly (MEA) active area. The flow field with two straight channels was designed for this operando cell. X-ray CT with the field of view (FOV) of about 3 mm x 2 mm and resolution of 0.7 um allowed visualizing MEA and flow channels of operando PEWEs. The cell features three observation windows that are transparent to x-rays. These are located near the inlet, in the middle of the flow-channels and at the outlet. In addition, thermocouples are embedded in various locations in the cell to measure temperature profiles of the cell. Oxygen content in the flow-channels was observed for various current densities using 2D radiography technique, with 5 ms time resolution step size. The cell morphology and steady-state oxygen distribution in the PTL were observed using stained water (stained with NaI). The results show significant oxygen enrichment in the channels near the outlet, as well as higher oxygen presence in the PTLs near the outlet. This new cell design can enable simultaneous heat and mass transport measurements along the flow channels. Inlet-outlet variations in oxygen content at scale of 10 cm is of relevant to single cell testing in the laboratory.

High-performance amorphous carbon/PDMS flexible strain sensors by introducing low interfacial mismatch

It is important and challenging to develop environment-tolerant stretchable strain sensors under some harsh environments. Here, amorphous carbon (a-C)/Polydimethylsiloxane (PDMS) sensors were fabricated with the direct-current magnetron sputtering technology, their sensing performances were optimized by adjusting the elastic mismatch between the top a-C film and used PDMS substrate, and their application under a simulated marine atmospheric environment was evaluated. The results showed that the combination of low stress a-C and low elastic modulus PDMS was favorable to improve the sensing performance, the optimal sensor exhibited the maximum gauge factor (GF) of 3026.9, large tensile strain range to 50 %, rapid response (loading delay time 92.3 ms and unloading delay time 24.6 ms), as well as high durability (>5000 cycles). After 120 h salt spray test, the sensor was quite stable and can detect various human movements with both high sensitivity and stability, such as wrist pulse, wrist bending, and finger bending. This work pioneers the elastic mismatch strategy for high-performance a-C/PDMS sensors and confirms their great potential in the practical applications under harsh environments.

Exceeding 100 µs Charge Carrier Separation in Perovskite Mediated by Rhodamine 6G

AbstractHalide perovskite colloidal nanocrystals (NCs) have enabled considerable progress in light conversion applications. However, the presence of unavoidable defect states and phase transition effects can accelerate undesirable rapid charge recombination of the photogenerated charge carriers. To address this issue, chromophores with an anchoring moiety are often used to modify the surface of the NCs, promoting prolonged charge separation through electron or energy transfer processes for optoelectronic applications. Here, steady‐state and time‐resolved spectroscopy methods are combined with density functional theory (DFT) calculations to explore and decipher the excited‐state interaction in colloidal CsPbX3 (X = Br, I) NCs with a rhodamine 6G (Rh6G) hybrid assembly. The results show that Rh6G dimerizes even at low concentrations, as evidenced by DFT calculations. The binding of Rh6G on the NC surface is confirmed by FTIR and NMR spectroscopy techniques. In addition, transient absorption spectroscopy reveals directional sub‐ps electron transfer from Rh6G to CsPbI3 NCs, whereas energy transfer occurs from CsPbBr3 to Rh6G, which ultimately recombines in the µs time regime. The findings highlight the simplest and most practical approaches for studying and tailoring the excited‐state interaction in colloidal perovskite NCs and chromophore assembly.

Fast backward steps and detachment of single kinesin molecules measured under a wide range of loads.

To understand force generation under a wide range of loads, the stepping of single kinesin molecules was measured at loads from -20 to 42 pN by optical tweezers with high temporal resolution. The optical trap has been improved to halve positional noise and increase bandwidth by using 200-nm beads. The step size of the forward and backward steps was 8.2 nm even over a wide range of loads. Histograms of the dwell times of backward steps and detachment fit well to two independent exponential equations with fast (~0.4 ms) and slow (>3 ms) time constants, indicating the existence of a fast step in addition to the conventional slow step. The dwell times of the fast steps were almost independent of the load and ATP concentration, while those of the slow backward steps and detachment depended on those. We constructed the kinetic model to explain the fast and slow steps under a wide range of loads.

Comparing the effects of dietary sugars on cognitive performance and reaction time: A randomized, placebo- controlled and double-blind experimental trial

The aim of the study was to compare the effects of acute intake dietary sugars on cognitive performance and reaction time. This study was, randomized, placebo-controlled, double-blind experimental design, conducted with 75 healthy adults. At the beginning of the study, the participants (36 male, 39 female; 21.6 ± 1.3 years of age; body mass index: 21.59 ± 1.94 kg/m2) were randomly divided into equal five groups (n:15) (glucose (10 g), fructose (10 g), sucrose (10 g), saccharin (0.24 g), placebo), and received dietary sugars dissolved in 200 mL of water. Cognitive performance was determined with Cancelation Test, and the Simple Response Time and Ruler Drop Tests were used in order to response and reaction time of participants, respectively. General score of cognitive performance (0.93 ± 0.1), reaction (295 ± 20 ms), and response (204 ms) were highest in glucose and lowest in placebo (0.63 ± 0.1; 368 ± 22 ms; 251 ms, respectively) (p < .001). Saccharin groups had a higher reaction (312 ± 22 ms) and response (216 ms) time score compared to consumed fructose (316 ± 39; 227 ms), sucrose (354 ± 26; 246 ms), and placebo (368 ± 22; 251 ms) groups, respectively (p < .001). These findings show that differences in the absorption pattern and sweetness levels of sugar types may have different effects on cognitive performance and reaction time.

Photoinduced Nonthermal Reduction of the Coercive Field in FePt and FePt0.84Rh0.16 Epitaxial Thin Films in the L10 Phase

The time-resolved magneto-optical Kerr effect in epitaxial thin films of the FePt compound and the FePt0.84Rh0.16 solid solution with the perpendicular magnetic anisotropy on MgO (001) substrates has been studied. The evolution of hysteresis loops at short (100 fs–1 ns) and long (1–20 ms) time scales after the excitation by a femtosecond light pulse has been studied. Long-lived nonthermal reduction of the coercive field has been detected. The coercive field is recovered in several milliseconds. It has been proposed to explain the observed phenomenon by the excitation of high-Q-factor acoustic resonances in the substrate/film system and to the strong magnetoelastic interaction in FePt and FePt0.84Rh0.16 films.

Difluoromethylborates and Muonium for the Study of Isonitrile Insertion Affording Phenanthridines via Imidoyl Radicals.

The 6-(difluoromethyl)phenanthridine unit is a highly attractive fluoroalkyl-substituted planar nitrogen heterocycle in pharmaceutical and agrochemical research. In this paper, we report that difluoromethylborates can be used as a source of difluoromethyl radicals for isonitrile insertion, leading to 6-(difluoromethyl)phenanthridines. Tuning the aryl substituents in the difluoromethylborates and oxidizing reagents enabled the synthesis of 6-(difluoromethyl)phenanthridines through the generation of difluoromethyl radical and spontaneous intramolecular cyclization of the CF2H-imidoyl radical intermediates. The presence of difluoromethyl radicals was experimentally confirmed, and the reaction mechanisms including imidoyl radical and prompt cyclization reactions could be supported theoretically. Furthermore, we obtained valuable information about the imidoyl radical intermediate by performing transverse-field muon spin rotation (TF-μSR) measurements of 2-isocyano-4'-methoxy-1,1'-biphenyl and using density functional theory (DFT) calculations to interpret the spectra. Muonium, a simple free radical, preferentially adds to the carbon atom of the isonitrile unit, yielding the corresponding imidoyl radical. The temperature dependence of the muon hyperfine coupling constant and the spin relaxation of the muoniated radical signal are compatible with the intramolecular cyclization of biaryl-substituted imidoyl radicals on the μs time scale.

Effect of polymer host matrix on multi-stage isomerization kinetics of DASA photochromes

Molecular photoswitches provide a means for imparting synthetic structures with intrinsically logical and highly tunable photoresponsive properties. One variety of organic photoswitches known as Donor-Acceptor Stenhouse Adducts, or DASAs, are promising candidates for next generation light responsive materials because of their unique ability to stabilize three photochemically distinct isomeric states in solution, while their counterparts are strictly limited to binary state behavior. In this work, we show how polymethacrylate host matrices shift the energetic landscape of DASA relative to solution, prohibiting accumulation of an intermediate third isomeric state by decelerating critical steps in the photoswitching mechanism. Specifically, we employ a dual-wavelength, phase locked detection scheme to probe thermal isomerizations in the switching process that occur at fast (∼ms) time scales that are inaccessible by standard UV–Vis spectroscopic techniques. The results of this study provide valuable insight into the mechanism of multistate DASA reactivity and establish the foundation necessary to guide future efforts in offsetting kinetic matrix effects to enable dynamic, three state photoswitching in polymeric hosts.

Pyro-Photoelectric Effect Enhanced Dual-Mode Self-Powered ITO/ZnO:Ga Microwire/AlGaN Thin-Film Heterojuncted Ultraviolet Imaging Photodetector

Ultraviolet (UV) photodetectors have received a significant amount of attention in a variety of areas; especially, self-powered photodetectors are anticipated to address the energy-saving demand in the astronautics under the photovoltaic effect. In this work, a ZnO:Ga/Al <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">0.1</sub> Ga <sub xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">0.9</sub> N heterojunction is introduced for performing UV photodetector, which is enhanced by the pyro-photoelectric effect coupling of pyroelectric and photovoltaic effects. The heterojunction UV photodetector can operate in a self-powered mode with responsivity of 0.063 mA W <sup xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">-1</sup> under the illumination of 135 μW cm <sup xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">-2</sup> . More importantly, after pyro-photoelectric enhancement, the photocurrent is effectively increased from 13 pA to 45 pA. Additionally, under the illumination of 493 μW cm <sup xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">-2</sup> , the photo-to-dark-current ratio ( <italic xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">PDCR</i> ) of 80 and 1.7 × 10 <sup xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">4</sup> are obtained at reverse bias of -10 V and forward bias of +10 V, respectively, indicating that the heterojunction UV photodetector can be regarded as a dual-mode photodetector since it can operate in both forward-biased photoconductive mode and reverse-biased depletion mode. Moreover, the UV photodetector exhibits a fast temporal pulsed laser response with a rising time of 0.79 ms and decay time of 9.4 ms. In all, this work presents a novel strategy for the advancement of UV detection.

COUNTERPOINT: the Seductive Trap of Relying on Exaggerated Effects in Short-Term Heart Failure Trials to Predict Benefits and Risks in Patients With Long-Term Disease

COUNTERPOINT: the Seductive Trap of Relying on Exaggerated Effects in Short-Term Heart Failure Trials to Predict Benefits and Risks in Patients With Long-Term Disease

Host Surface-Induced Excitation Wavelength-Dependent Organic Afterglow.

The design and construction of organic afterglow materials is an attractive but formidably challenging task due to the low intersystem crossing efficiency and nonradiative decay. Here, we developed a host surface-induced strategy to achieve excitation wavelength-dependent (Ex-De) afterglow emission through a facile dropping process. The prepared PCz@dimethyl terephthalate (DTT)@paper system exhibits a room-temperature phosphorescence afterglow, with the lifetime up to 1077.1 ± 15 ms and duration time exceeding 6 s under ambient conditions. Furthermore, we can switch the afterglow emission on and off by adjusting the excitation wavelength below or above 300 nm, showing a remarkable Ex-De behavior. Spectral analysis demonstrated that the afterglow originates from the phosphorescence of PCz@DTT assemblies. The stepwise preparation process and detailed experiments (XRD, 1H NMR, and FT-IR analysis) proved the presence of strong intermolecular interactions between the carbonyl groups on the surface of DTT and the entire frame of PCz, which can inhibit the nonradiative processes of PCz to achieve afterglow emission. Theoretical calculations further manifested that DTT geometry alteration under different excitation beams is the main reason for the Ex-De afterglow. This work discloses an effective strategy for constructing smart Ex-De afterglow systems that can be fully exploited in a range of fields.

A robust-switchable poly(vinyl alcohol) gel with adjustable multiple hydrogen bonding interactions

It is highly desirable to develop gels possessing exceptional and adjustable mechanical properties, self-healing performance, recycling behavior, etc., simultaneously. In this study, a poly(vinyl alcohol)/tannic acid (PVA/TA) gel with extraordinary mechanical properties (∼4.9 MPa, ∼950%) was prepared by forming crystalline regions and multiple hydrogen bonds. More interestingly, the strength/elongation and shape of the gel could be continuously and regularly regulated. Take the 15% PVA/TA gel as an example, its mechanical strength can be freely and consecutively converted between about 0.36 MPa and around 0.80 MPa. Besides, the PVA/TA gel can be served as a sensor with rapid responsiveness (Response time ∼ 165 ms and recovery time ∼ 151 ms) to monitor the changes of strain in real time when ferric chloride is added. Specifically, the gel can still effectively monitor the human motions after self-healing and recycling. This study provides an important reference value for the preparation of gels with high and adjustable mechanical properties, self-healing performance, recycling behavior, etc.

Predictors of atrial fibrillation post coronary artery bypass graft surgery: new scoring system

BackgroundAtrial fibrillation (AF) following coronary artery bypass graft surgery (CABG) is common and results in significant increases in hospital stay and financial encumbrance.ObjectiveDetermine and use the predictors of postoperative AF...

Photoimaging with Color-Sensing Abilities by Tuning the Band Gap of a Single-Crystal Lead-Free Perovskite.

Photodetectors (PDs) composed of lead-free metal halide perovskites have been a shining topic in optoelectronics. However, it is debatable whether perovskites are an n-type or p-type semiconductor with a direct or indirect band gap. Furthermore, to date, little research has been conducted on lead-free metal halide perovskites with color-sensing abilities. Herein, for the first time, single-crystal MA3Bi2I3xBr9-3x (x = 0, 1, 2, and 3) perovskites were systematically studied, and the results showed that MA3Bi2I9 is a p-type direct-band-gap semiconductor, whereas MA3Bi2Br9 is an n-type indirect-band-gap semiconductor. Furthermore, the band gap of MA3Bi2I3xBr9-3x (x = 0, 1, 2, and 3) perovskites can be systematically tuned from 2.06 to 2.55 eV, affording it with color-sensing abilities from 450 to 580 nm, respectively. The representative Au-MA3Bi2I9-ITO (ITO = indium tin oxide) PD exhibits a superior self-powered photodetecting performance with a high responsivity (15.8 mA W-1; 580 nm, 1.0 mW cm-2), detectivity (8.1 × 1011 Jones), an on/off ratio (4231), LDR (72.5 dB) and a fast response speed (rise time of 2 μs and decay time of 29 μs). This study not only facilitates the theoretical understanding of the band gap of perovskite materials but also sheds light on the application of lead-free perovskites in object interaction and color perception.

Ultra-high throughput dual channel liquid chromatography with tandem mass spectrometry for quantification of four immunosuppressants in whole blood for therapeutic drug monitoring

Liquid chromatography with tandem mass spectrometry (LC-MS/MS) is the golden standard for immunosuppressants analyses, where optimising throughput by parallel chromatography can reduce costs and turnaround time. We aimed to double our system throughput using a dual LC-MS/MS setup. Therefore, two independent UPLC systems were hyphenated to one triple quadrupole MS, with staggered injections from one autosampler on alternating columns. The method simultaneously measured the analytes tacrolimus, sirolimus, everolimus, and cyclosporin A in whole blood using isotope dilution, with a run time of 1.5 min. Using the dual LC-MS/MS system, net run-to-run time improved from 2.3 to 0.98 min per injection, where throughput increased from 26 to 61 injections per hour. For Performance Qualification, 1101 clinical samples were measured on the dual LC-MS/MS system in addition to the standard system, during a period of one month, and the results were compared using Passing Bablok regression and Bland Altman analysis. There was excellent agreement for all four analytes, with regression slopes of 0.98–1.02x and intercepts of -0.11–0.88 µg/L. Minor bias was demonstrated between the systems with mean differences from -0.93 to 1.43%. In conclusion, the throughput was doubled and idle MS time was reduced with good agreement to the standard system. Currently, the method is applied for clinical routine with frequent peak intensities of >180 injections per day.

Predicting the Three-Dimensional Structure of the c-KIT Proto-Oncogene Promoter and the Dynamics of Its Strongly Coupled Guanine Quadruplexes.

Guanine quadruplexes (G4s) play essential protective and regulatory roles within cells, influencing gene expression. In several gene-promoter regions, multiple G4-forming sequences are in close proximity and may form three-dimensional arrangements. We analyze the interplay among the three neighboring G4s in the c-KIT proto-oncogene promoter (WK1, WSP, and WK2). We highlight that the three G4s are structurally linked and their cross-talk favors the formation of a parallel structure for WSP. Relying on all-atom molecular dynamic simulations exceeding the μs time scale and using enhanced sampling methods, we provide the first computationally resolved structure of a well-organized G4 cluster in the promoter of a crucial gene involved in cancer development. Our results indicate that neighboring G4s influence their mutual three-dimensional arrangement and provide a powerful tool to predict and interpret complex DNA structures that can ultimately be used as a starting point for drug discovery.

ERP evidence for emotion-specific congruency effects between sentences and new words with disgust and sadness connotations.

The present study investigated how new words with acquired connotations of disgust and sadness, both negatively valenced but distinctive emotions, modulate the brain dynamics in the context of emotional sentences. Participants completed a learning session in which pseudowords were repeatedly paired with faces expressing disgust and sadness. An event-related potential (ERP) session followed the next day, in which participants received the learned pseudowords (herein, new words) combined with sentences and were asked to make emotional congruency judgment. Sad new words elicited larger negative waveform than disgusting new words in the 146-228 ms time window, and emotionally congruent trials showed larger positive waveform than emotionally incongruent trials in the 304-462 ms time window. Moreover, the source localization in the latter suggested that congruent trials elicited larger current densities than incongruent trials in a number of emotion-related brain structures (e.g., the orbitofrontal cortex and cingulate gyrus) and language-related brain structures (e.g., the temporal lobe and the lingual gyrus). These results suggested that faces are an effective source for the acquisition of words' emotional connotations, and such acquired connotations can generate semantic and emotional congruency effects in sentential contexts.

Integrating laboratory acoustic measurements, deep neural networks, and micro-CT imaging for characterizing rock brittle deformation

Brittle deformation is prevalent in both geological processes and engineered structures, so probing its actions is an important task as much for Earth materials and engineered ones. To characterize brittle deformation, acoustic waves are especially useful in revealing deformation processes. To promote the use of acoustic techniques, we present an integrated characterization approach that includes both acoustic data collection and analysis. By customizing a rock sample and acoustic sensor assembly, we incorporate acoustic data acquisition into a core holder system that accommodates relatively small samples (2.54 cm diameter) under triaxial loading. Along with fast and high-resolution acoustic waveform recording, the compact design facilitates convenient collection of high-quality acoustic data. To meet the challenge of efficiently and accurately picking P-wave arrivals for hundreds of thousands of acoustic waveforms, we modified and implemented a deep neural network model from the seismology literature called PhaseNet. After training with an augmented dataset of manually-picked arrivals (a total of around 50,000 waveforms), the modified PhaseNet model achieved more than 88% (96%) picking accuracy within ±1 μs (±2 μs) time residual relative to manual picks. This demonstrates the potential of integrating deep learning techniques into the workflow of acoustic data analysis for rapid and accurate extraction of valuable information from a large acoustic dataset. Finally, we conducted high-resolution micro-computed tomography (micro-CT) to inform and complement acoustic characterization at micron- and centimeter-scales. Microscopic observations validate the spatial development of two macroscopic fractures, and suggest that deformation-induced changes in velocity need to be incorporated for accurately locating microcracking events. Thus, integrating acoustic monitoring, a deep neural network, and micro-CT imaging offers an effective means to understand brittle deformation from micro to centimeter scales.

V3O7·H2O Nanowire Film/Td-MoTe2 Flake Mixed-dimensional Van der Waals Heterostructure for Photodetection

A novel van der Waals (vdWs) heterostructure composed of V3O7·H2O nanowire film and Td-MoTe2 flake is presented for photodetection for the first time. The vdWs heterojunction device demonstrated more efficient photodetection performance with higher responsivity of 76.89 mA/W, superior specific detectivity of 1.22 × 1010 Jones, higher external quantum efficiency of 10.61% and fast response (rise time = 27.0 ms and fall time = 27.2 ms). A van der Waals heterostructure composed of V3O7·H2O nanowire film and Td-MoTe2 flake for NIR photodetection with responsivity of 76.89 mA/W, specific detectivity of 1.22 × 1010 Jones, external quantum efficiency of 10.61% and fast response speed (rise time = 27.0 ms and fall time = 27.2 ms).