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Grady Jacobs posted an update 2 months ago
An investigation into the structural and physical characteristics of armchair MoSi2N4 nanoribbons, substitutionally doped with 3d transition metals (TM) at Mo sites, was performed using density functional theory in conjunction with the non-equilibrium Green’s function approach. Doping of nonmagnetic direct semiconductors with TM elements can produce diverse device materials, including indirect semiconductors, semimetals, metallic materials, and half-metals. Anticipated are 100% spin filtering effects in spin-up and spin-down half metals, along with a negative differential resistance having a peak-to-valley ratio greater than 140 and a rectification effect with a ratio exceeding 130. Also predicted is high spin polarization in the semiconductor behavior.
With the development of the Internet of Things (IoT), numerous electronic gadgets are interconnected and exchange a great deal of data through the internet. The expanding realm of linked devices has brought about an increase in security concerns. As a potential security solution, hardware intrinsic physical unclonable functions (PUFs) are semiconductor devices exploiting inherent randomness generated during manufacturing. By employing a physically unclonable function (PUF), unclonable security keys are generated, effectively addressing the inherent limitations of conventional electronic systems that solely depend on software. Proposed physical unclonable functions (PUFs) that leverage emerging memory devices requiring switching procedures are plentiful; nevertheless, the creation of a hardware-intrinsic PUF with low power consumption still represents a major hurdle. The nonlinear conductance changes in oxide semiconductor-based Schottky diodes, resulting from the fabrication process, are shown to be a sufficient source of entropy for the construction of a PUF, dispensing with switching operations. Through the use of a mild oxygen plasma treatment, the naturally occurring surface electron accumulation layer in oxide semiconductor films is partially removed, leading to a large variation in nonlinearity and acting as an exotic entropy source. Schottky diodes treated with a mild plasma process demonstrated a near-ideal 50% average uniformity and uniqueness, and possessed an ideal entropy value, avoiding extra hardware area and power consumption. The introduction of hardware-intrinsic PUFs for energy-efficient cryptographic hardware will be catalyzed by these findings.
Although colorectal cancer (CRC) responds well to surgical treatment and can be further aided by postoperative chemotherapy, its five-year survival rate is still not particularly positive. In order to facilitate early colorectal cancer diagnosis, the development of a sensitive, efficient, and compliant detection system is indispensable, thereby improving the potential for effective interventions and treatment. Currently, common clinical CRC detection strategies involve endoscopy, stool tests, imaging, and tumor biomarker analysis. Blood-based biomarkers, a non-invasive approach for screening, show considerable potential for early cancer diagnosis, predictive factors, prognosis, and cancer stage determination. Recent studies highlight electrochemical biosensors’ growing appeal in blood biomarker detection, owing to their affordability, high sensitivity, adaptability, excellent selectivity, and rapid response. For improved sensor performance, nano-conductive polymer materials, particularly polypyrrole (PPy), are frequently employed due to their superior electrical properties, flexible surfaces, straightforward preparation, functionalization potential, and favorable biocompatibility. This review delves into the distinguishing features of PPy-based biosensors, their synthesis procedures, and their application in the detection of colorectal cancer (CRC) biomarker. In closing, the implications and difficulties of implementing PPy-based sensors for the diagnosis of CRC are examined.
The application of light to photosensitive molecules within photodynamic therapy (PDT) prompts the creation of highly cytotoxic reactive oxygen species (ROS), showcasing its effectiveness as a cancer treatment modality. Nonetheless, its implementation has been significantly limited to superficial tissues and those easily accessible through either endoscopic or laparoscopic procedures, owing to the inherent scattering and absorption of photons by intervening tissues. Recent advancements in nanoparticle-based X-ray scintillator and photosensitizer design have facilitated the combination of these components into single, nanocomposite particles. X-ray irradiation of these nanoplatforms generates substantial ROS quantities, enabling, for the first time, non-invasive deep-tissue PDT of tumors, mitigating many of the therapeutic limitations and side effects characteristic of conventional PDT. XCT790 This review investigates the fundamental precepts and development of PDT, transitioning from its traditional, dominant technique using light-activated, small molecule photosensitizers that passively accumulate in tumors, to its newest approach employing X-ray-activated, scintillator-photosensitizer hybrid nanoplatforms for active cancer biomarker targeting. This paper details the hurdles and possible treatments for the clinical implementation of these hybrid nanoplatforms and X-ray PDT.
Nanocrystalline NaBiF4 particles, doped with lanthanide ions, were synthesized via a facile precipitation route to investigate upconversion emission characteristics. By precisely controlling the concentration of the Yb³⁺-Ho³⁺-Ce³⁺ triad, near-infrared pumping can be converted into visible light, offering the potential to tune the emission color in accordance with the Ce³⁺ doping amount. Experimentation with Ce3+ concentrations up to 20 atomic percent in the NaBiF4Yb3+/Ho3+ structure demonstrated a chromatic evolution, moving from green for the Ce3+ deficient sample to a red color. A theoretical rate equation model details the impact of cross-relaxation mechanisms between Ho3+ and Ce3+ ions on the relative efficiency of upconversion pathways. Results of experiments suggest that illuminating intra-4f Ho3+ transitions with light near the ultraviolet-visible edge promotes the downconversion of near-infrared Yb3+ emission through quantum cutting, driven by energy transfer between Ho3+ and Yb3+. The developed NaBiF4 particles, as demonstrated in this study, exhibit promise for applications leveraging lanthanide-based light frequency conversion and the fine-tuning of multicolored emission.
PCRAM, a next-generation non-volatile memory, has the capability to fill the performance void between DRAM and NAND flash in the computer’s storage architecture. One of the promising materials for high-speed PCRAM, Sb2Te3, displays a swift crystallization process but demonstrates a lack of thermal resilience. We explored the impact carbon doping has on the characteristics of Sb2Te3. The research indicated the appearance of the FCC phase in C-doped Sb2Te3 at 200 degrees Celsius, which then progressed to the HEX phase at the notably lower temperature of 25 degrees Celsius. This departure from earlier findings where no FCC phase was observed in carbon-doped Sb2Te3 compounds is noteworthy. Density functional theory calculations, performed using first-principles methods and supported by experimental results, indicate a gradual decrease in the formation energy of the FCC-Sb2Te3 structure as carbon doping concentration rises. Sp2-hybridized carbon molecular clusters are a common feature of doped carbon atoms within the grain boundaries of Sb2Te3, exhibiting a structural resemblance to the layered arrangement of graphite. Subsequent to the doping of carbon atoms, the thermal stability of Sb2Te3 is enhanced. A 5 nanosecond operating speed, combined with a remarkable 10-year data retention capability at 1381 degrees Celsius, and a low power consumption of 0.057 picojoules, are characteristics of the C-Sb2Te3 alloy PCRAM device cell array we have fabricated. Furthermore, the resistance value is continuously adjustable and exhibits a very low drift coefficient.
The preparation methodology plays a considerable role in shaping the structural, morphological, and gas-sensing properties of mixed-oxide materials, frequently demonstrating heightened photocatalytic and sensing capabilities when compared to single-metal oxides. This work details the preparation of TiO2 and ZnO-based semiconductor nanomaterial hybrids using laser ablation of Zn and Ti plates in water, followed by their evaluation as chemiresistive gas sensors for volatile organic compounds (2-propanol, acetaldehyde, ethanol, methanol) and ammonia. Zinc and titanium metal targets were ablated under the influence of an infrared millisecond pulsed laser, delivering 20 joules per pulse at a frequency of 5 hertz, resulting in the formation of two nano-hybrids: TiO2/ZnO and ZnO/TiO2, each created via specific ablation sequences. Tuning the gas-sensing characteristics of the prepared hybrids was found to be linked to variations in their surface chemistry, morphology, crystallinity, and phase composition. In the assessment of various tested gases, the TiO2/ZnO sample exhibited preferential sensitivity to ethanol, whereas the ZnO/TiO2 sample showed a response to 2-propanol at ambient conditions, both with a detection limit around 50 ppm. At room temperature, 100 ppm of the target gas prompted a response time of 24 seconds and a recovery time of 607 seconds for the TiO2/ZnO sensor, contrasted by the ZnO/TiO2 sensor’s response and recovery times of 54 and 50 seconds, respectively.
Employing the Material Extrusion (MEX) Additive Manufacturing (AM) process, specifically Fused Filament Fabrication (FFF), Acrylonitrile Butadiene Styrene (ABS) nanocomposites were developed. To probe the effect of Titanium Nitride (TiN) nanoparticles on the mechanical properties of thermoplastic polymers, a range of mechanical tests was meticulously performed on the 3D-printed structures. Detailed morphological analysis of the produced filaments and 3D-printed specimens was carried out using Atomic Force Microscopy (AFM) and Scanning Electron Microscopy (SEM) techniques. High-magnification images revealed a direct link between TiN concentration and the nanocomposites’ surface characteristics, indicating a clear correlation with their mechanical strength.