Search Results (195)

The phototherapeutic applications of porphyrin-based nanoscale metal–organic frameworks (nMOFs) are limited by the poor penetration of conventional excitation light sources into biological tissues. Radiodynamic therapy (RDT), which directly excites photosensitizers using X-rays, can overcome the issue of tissue penetration. However, RDT faces the problems of low energy conversion efficiency, requiring a relatively high radiation dose, and the potential to cause damage to normal tissues. Researchers have found that by using some metals with high atomic numbers (high Z) as X-ray scintillators and coordinating them with porphyrin photosensitizers to form MOF materials, the excellent antitumor effect of radiotherapy (RT) and RDT can be achieved under low-dose X-ray irradiation, which can not only effectively avoid the penetration limitations of light excitation methods but also eliminate the defect issues associated with directly using X-rays to excite photosensitizers. This review summarizes the relevant research work in recent years, in which researchers have used metal ions with high Z, such as Hf⁴⁺, Th⁴⁺, Ta⁵⁺, and Bi³⁺, in coordination with carboxyl porphyrins to form MOF materials for combined RT and RDT toward various cancer cells. This review compares the therapeutic effects and advantages of using different high-Z metals and introduces the application of the heavy atom effect. Furthermore, it explores the introduction of a chemodynamic therapy (CDT) mechanism through iron coordination at the porphyrin center, along with optimization strategies such as oxygen delivery using hemoglobin to enhance the efficacy of these MOFs as radiosensitizers. This review also summarizes the potential of these materials in preclinical applications and highlights the current challenges they face. It is expected that the summary and prospects outlined in this review can further promote preclinical biomedical research into and the development of porphyrin-based nMOFs. Full article

Developing high-performance photocatalysts for solar hydrogen production requires the synergistic modulation of chemical composition, nanostructure, and charge carrier transport pathways. Herein, we report a Cs and P co-doped tubular graphitic carbon nitride (Cs/PTCN-x) photocatalyst synthesized via a strategy that integrates elemental doping with morphological engineering. Structural characterizations reveal that phosphorus atoms substitute lattice carbon to form P-N bonds, while Cs⁺ ions intercalate between g-C₃N₄ layers, collectively modulating surface electronic states and enhancing charge transport. Under visible-light irradiation (λ ≥ 400 nm), the optimized Cs/PTCN-3 catalyst achieves an impressive hydrogen evolution rate of 8.085 mmol·g⁻¹·h⁻¹—over 33 times higher than that of pristine g-C₃N₄. This remarkable performance is attributed to the multidimensional synergy between band structure tailoring and hierarchical porous tubular architecture, which together enhance light absorption, charge separation, and surface reaction kinetics. This work offers a versatile approach for the rational design of g-C₃N₄-based photocatalysts toward efficient solar-to-hydrogen energy conversion. Full article

Exposure to high-linear energy transfer (LET) heavy ions, such as ²⁸Si, poses a significant cancer risk for astronauts. While previous studies have linked high-LET radiation exposure to persistent oxidative stress and dysregulated stress responses in intestinal crypt cells with an increased risk of tumorigenesis, the relationship between IR-induced oxidative DNA damage and intestinal cancer risk remains incompletely understood. Here, we investigated the time-dependent effects of ²⁸Si-ion radiation on intestinal tumorigenesis and oxidative DNA damage in Apc^1638N/+ mice, a model for human intestinal cancer predisposition. Male Apc^1638N/+ mice were exposed to 10 cGy of either γ-rays (low-LET) or ²⁸Si-ions (high-LET), and intestinal tumor burden was assessed at 60 and 150 days post-irradiation. While both radiation groups showed modest, non-significant tumor increases at 60 days, ²⁸Si-irradiated mice exhibited an approximately 2.5-fold increase in tumor incidence by 150 days, with a higher incidence of invasive carcinomas compared to γ and sham groups. Serum 8-OxodG levels, a marker of systemic oxidative stress, were significantly elevated in the ²⁸Si-ion group, correlating with increased intestinal 8-OxodG staining. Additionally, assessment of the proliferation marker Cyclin D1 and metaplasia marker Guanylyl Cyclase C (GUCY2C) also revealed significant crypt cell hyperproliferation accompanied by increased metaplasia in ²⁸Si-exposed mouse intestines. Positive correlations between serum 8-OxodG and tumor-associated endpoints provide compelling evidence that exposure to ²⁸Si-ions induces progressive intestinal tumorigenesis through sustained oxidative DNA damage, crypt cell hyperproliferation, and metaplastic transformation. This study provides evidence in support of the radiation quality-dependent progressive increase in systemic and intestinal levels of 8-OxodG during intestinal carcinogenesis. Moreover, the progressive increase in oxidative DNA damage and simultaneous increase in oncogenic events after ²⁸Si exposure also suggest that non-targeted effects might be a significant player in space radiation-induced intestinal cancer development. The correlation between serum 8-OxodG and oncogenic endpoints supports its potential utility as a predictive biomarker of high-LET IR-induced intestinal carcinogenesis, with implications for astronaut health risk monitoring during long-duration space missions. Full article

The Fricke gel dosimeter, a hydrogel-based chemical dosimeter containing dissolved ferrous sulfate, measures 3D radiation dose distributions by oxidizing Fe²⁺ to Fe³⁺ upon irradiation. This study investigates the variation in Fricke yield, G(Fe³⁺), from a radiation–chemical perspective in both standard and gel-like Fricke systems of varying viscosities, under low- and high-linear energy transfer (LET) conditions. We employed our Monte Carlo track chemistry code IONLYS-IRT, using protons of 300 MeV (LET~0.3 keV/µm) and 1 MeV (LET~25 keV/µm) as radiation sources. To assess the impact of viscosity on G(Fe³⁺), we systematically varied the diffusion coefficients of all radiolytic species in the Fricke gel, including Fe²⁺ and Fe³⁺ ions. Increasing gel viscosity reduces Fe³⁺ diffusion and stabilizes spatial dose distributions but also lowers G(Fe³⁺), compromising measurement accuracy and sensitivity—especially under high-LET irradiation. Our results show that an optimal Fricke gel dosimeter must balance these competing factors. Simulations with lower sulfuric acid concentrations (e.g., 0.05 M vs. 0.4 M) further revealed that G(Fe³⁺) values at ~100 s are nearly identical for both low- and high-LET conditions. This study underscores the utility of Monte Carlo simulations in modeling viscosity effects on Fricke gel radiolysis, guiding dosimeter optimization to maximize sensitivity and accuracy while preserving spatial dose distribution integrity. Full article

Thin amorphous oxide films (a-SiO₂, a-Al₂O₃, a-MgO) were prepared by magnetron sputtering deposition. Their response to high-energy heavy ion beams (23 MeV I, 18 MeV Cu, 2.5 MeV Cu) and gamma-ray (1.25 MeV) irradiation was studied by elastic recoil detection analysis and infrared spectroscopy. It was established that their high radiation hardness is due to a high level of disorder, already present in as-prepared samples, so the high-energy heavy ion irradiation cannot change their structure much. In the case of a-SiO₂, this resulted in a completely different response to high-energy heavy ion irradiation found previously in thermally grown a-SiO₂. In the case of a-MgO, only gamma-ray irradiation was found to induce significant changes. Full article

This study presents a comprehensive analysis of the modifications in electronic structure and magnetism resulting from electronic excitation in pulsed laser-deposited Ba_0.7Sr_0.3Fe_xTi_(1−x)O₃ thin films, specifically for compositions with x = 0, 0.1, and 0.2. To investigate the effects of electronic energy loss (S_e) within the lattice, we performed 120 MeV Ag ion irradiation at varying fluences (1 × 10¹² ions/cm² and 5 × 10¹² ions/cm²) and compared the results with those of the pristine sample. The S_e induces lattice damage by generating ion tracks along its trajectory, which subsequently leads to a reduction in peak intensity observed in X-ray diffraction patterns. Atomic force microscopy micrographs indicate that irradiation resulted in a decrease in average grain height, accompanied by a more homogeneous grain distribution. X-ray photoelectron spectroscopy reveals a significant increase in oxygen vacancy (V_O) concentration as ion fluence increases. Ferromagnetism exhibits progressive deterioration with rising irradiation fluence. Due to the high S_e and multiple ion impact processes, cation interstitial defects are highly likely, which may overshadow the influence of V_O in inducing ferromagnetism, thereby contributing to an overall decline in magnetic properties. Furthermore, the elevated S_e potentially disrupts bound magnetic polarons, leading to a degradation of long-range ferromagnetism. Collectively, this investigation elucidates the electronic excitation-induced modulation of ferromagnetism, employing Fe impurity incorporation and irradiation techniques for precise defect engineering. Full article

The dependence of polyethylene deformation on applied mechanical stress under varying load conditions and radiation doses was investigated experimentally. Obtained results reveal significant alterations in the mechanical properties of polyethylene following irradiation with krypton ions at doses of 1.5 × 10⁶, 1.6 × 10⁷, 5.0 × 10⁸, and 1.0 × 10⁹ ions/s. The stress–strain curves obtained for both the unirradiated and irradiated samples are numerically modeled using frameworks developed by the authors. The findings indicate that irradiation with krypton ions at an energy level of 147 MeV exerts a pronounced impact on the deformation and strength characteristics of polyethylene. Notably, increasing the radiation dose to 10⁹ particles/s results in a 2.5-fold increase in the rate of mechanical stress. Furthermore, the degree of deformation distortions in molecular chains induced by high-energy Kr¹⁵⁺ ion irradiation has been quantified as a function of irradiation fluence. Increasing the irradiation fluence from 10⁶ ion/cm² to 10⁷ ion/cm² causes only minor variations in deformation distortions, which are attributed to the localized isolation of latent tracks and associated changes in electron density. A comparative analysis of the mechanical behavior of irradiated polymer materials further revealed differences between ion and electron irradiation effects. It was observed that Teflon films lose their plasticity after irradiation, whereas polyethylene films exhibit enhanced elongation and tearing performance at higher strain values relative to their non-irradiated counterparts. This behavior was consistently observed for films irradiated with both ions and electrons. However, an important distinction was identified: high-energy electron irradiation degrades the strength of polyethylene, whereas krypton ion irradiation at 147 MeV does not result in strength reduction. Full article

A straightforward chemical polymerization process was used to create the polyaniline/LiClO₄/CuO nanoparticle (PLC) nanocomposite, which was then exposed to varying doses of electron beam (EB) radiation and studied. The FESEM, XRD, FTIR, DSC, TG/DTA, and electrochemical measurements with higher EB doses showed clear changes. The FTIR spectra of the PLC nanocomposite showed variations in the C-N and carbonyl groups at 1341 cm⁻¹ and 1621 cm⁻¹, respectively. After a 120 kGy EB dose, the shape changed from a smooth, uneven surface to a well-connected, nanofiber-like structure, creating pathways for electricity to flow through the polymer matrix. The EB irradiation improved the thermal stability by decreasing the melting temperature, and the XRD and DSC studies reveal that the decrease in crystallinity is attributed to the dominant chain scission mechanism. The enhanced absorption and red shift in the wavelength (from 374 nm to 400 nm) observed in the UV-Visible spectroscopy were caused by electrons transitioning from a lower to a higher energy state, with a progressive drop in the band gaps (E_g) from 2.15 to 1.77 eV following irradiation. The dielectric parameters increased with the temperature and electron beam doses because of the dissociation of the ion aggregates and the emergence of defects and/or disorders in the polymer band gaps. This was triggered by chain scission, discontinuity, and bond breaking in the molecular chains at elevated levels of radiation energy, leading to an augmented charge carrier density and, subsequently, enhanced conductivity. The cyclic voltammetry study revealed an enhanced electrochemical stability at a high scan rate of about 600 mV/s for the PLC nanocomposite with the increase in the EB doses. The I-V characteristics measured at room temperature exhibited nonohmic behavior with an expanded current range, and the electrical conductivity was estimated, using the I-V curve, to be around 1.05 × 10⁻⁴ S/cm post 20 kGy EB irradiation. Full article

We perform the numerical study of the response of the media with golden nanoantennas upon irradiation by intense ~10¹⁷–10¹⁸ W/cm² short 0.1 ps laser pulses. We study the influence of resonant nanoantennas on the ionization process and on the ions’ energy evolution at various intensities of laser pulses. Numerical modeling is performed with the help of EPOCH software using the “particle-in-cell” numeral method. The response of resonating nanoantennas of dipole and crossed shapes, embedded in dense media, is studied. The dynamics of ionization and the energies of ions acquired during the passage of the laser pulse are studied. The differences in the ionization energies for nanoantennas of dipole and crossed shapes are explored. The ionization dynamics in the matter doped with nanoantennas is examined; crossed-shaped antennas are identified for the best energy absorption in high-intensity fields. Full article

GaN-based terahertz (THz) Schottky barrier diodes (SBDs) are critical components for achieving high-power performance in THz frequency multipliers. However, the space applications of GaN-based THz SBDs are significantly constrained due to insufficient research on the effects of space irradiation. This work investigates the effects of 450 MeV Kr swift heavy ion (SHI) irradiation on the electrical characteristics and induced defects in GaN-based THz SBDs. It was found that the high-frequency performance of GaN-based THz SBDs is highly sensitive to Kr SHI irradiation, which can be attributed to defects induced in the GaN epitaxial layer by the irradiation. Low-frequency noise analysis reveals trap states located at an energy level of approximately 0.62 eV below the conduction band. Moreover, the results from SRIM calculation and photoluminescence spectra confirmed the presence of irradiation-induced defects caused by Kr SHI irradiation. Full article

The rapid rise in the power conversion efficiency (PCE) of perovskite solar cells (PSCs) has opened the door for diverse potential applications in powering indoor Internet of Things (IoT) devices. An energy harvesting system (EHS) powered by a PSC module with a backup Li-ion battery, which stores excess power at moments of high irradiances and delivers the stored power to drive the load during operation scenarios with low irradiances, has been designed. A DC-DC boost converter is engaged to match the voltage of the PSC and Li-ion battery, and maximum power point tracking (MPPT) is achieved by a perturb and observe (P&O) algorithm, which perturbs the photovoltaic (PV) system by adjusting its operating voltage and observing the difference in the output power of the PSC. Furthermore, the charging and discharging rate of the battery storage is controlled by a DC-DC buck–boost bidirectional converter with the incorporation of a proportional–integral (PI) controller. The bidirectional DC-DC converter operates in a dual mode, achieved through the anti-parallel connection of a conventional buck and boost converter. The proposed EHS utilizes DC-DC converters, MPPT algorithms, and PI control schemes. Three different case scenarios are modeled to investigate the system’s behavior under varying irradiances of 200 W/m², 100 W/m², and 50 W/m². For all three cases with different irradiances, MPPT achieves tracking efficiencies of more than 95%. The laboratory-fabricated PSC operated at MPP can produce an output power ranging from 21.37 mW (50 W/m²) to 90.15 mW (200 W/m²). The range of the converter’s output power is between 5.117 mW and 63.78 mW. This power range can sufficiently meet the demands of modern low-energy IoT devices. Moreover, fully charged and fully discharged battery scenarios were simulated to study the performance of the system. Finally, the IoT load profile was simulated to confirm the potential of the proposed energy harvesting system in self-sustainable IoT applications. Upon review of the current literature, there are limited studies demonstrating a combination of EHS with PSCs as an indoor power source for IoT applications, along with a bidirectional DC-DC buck–boost converter to manage battery charging and discharging. The evaluation of the system performance presented in this work provides important guidance for the development and optimization of new-generation PV technologies like PSCs for practical indoor applications. Full article

Microplastic pollution represents a significant global environmental issue, with cigarette filters being a major contributor due to their slow biodegradation. To address this issue while creating valuable materials, we developed a novel approach to synthesize nitrogen-doped carbon nanotubes on carbonized cigarette filter powder (NCNT@cCFP) using a microwave irradiation and nickel-catalyzed process. The successful incorporation of nitrogen (~6.6 at.%) and the enhanced graphitic structure create a hierarchical conductive network with abundant active sites for electrochemical reactions. The resulting NCNT@cCFP electrode exhibits a specific capacitance of 452 F/g at 1 A/g in a three-electrode configuration. The integrated hierarchical structure facilitates efficient electron transport and ion diffusion, leading to excellent rate capability (91.6% at 10 A/g) and cycling stability (96.5% retention after 5000 cycles). Furthermore, a symmetric supercapacitor device demonstrates promising energy storage capability with a maximum energy density of 14.0 Wh/kg at 483.1 W/kg, while maintaining 10.4 Wh/kg at a high power density of 4419.1 W/kg. This synergistic waste recycling strategy combined with microwave-driven synthesis offers a sustainable pathway for developing high-performance energy storage materials. Full article

As the development of nuclear fusion depends on plasma-facing materials, new methods for improving the radiation resistance of tungsten are being created and tested. This paper presents the results of studying the structure, surface morphology, phase composition, and residual internal stresses in tungsten alloys modified by plasma flows and irradiated with helium ions with an energy of 40 keV and doses of (1–3) × 10¹⁷ cm⁻². It is shown that the effect of compression plasma flows on tungsten leads to the modification of its grain structure in the near-surface layer, forming dispersed cells of 220–320 nm in size due to high-speed crystallization. The results of measuring the lattice parameters and internal stresses in irradiated tungsten alloys showed that the near-surface layer accumulates radiation defects, creating internal stresses, the relaxation of which leads to local destruction of the surface. Preliminary plasma treatment creates an increased density of intergranular boundaries, which serve as sinks for radiation defects and increase the radiation resistance of tungsten alloys. Full article

The increasing presence of pollutants, including pharmaceuticals and pesticides, in water resources necessitates the development of effective remediation technologies. Zeolites are promising agents for pollutant removal due to their high surface area, ion-exchange capacity, natural abundance, and diverse tailorable porous structures. This review focuses on the efficient application of modified zeolites and mesoporous materials as photocatalysts and adsorbents for removing contaminants from water bodies. The adsorption and photodegradation of pesticides and selected non-steroidal anti-inflammatory drugs and antibiotics on various zeolites reveal optimal adsorption and degradation conditions for each pollutant. In most reported studies, higher SiO₂/Al₂O₃ ratio zeolites exhibited improved adsorption, and thus photodegradation activities, due to increased hydrophobicity and lower negative charge. For example, SBA-15 demonstrated high efficiency in removing diclofenac, ibuprofen, and ketoprofen from water in acidic conditions. Metal doped into the zeolite framework was found to be a very active catalyst for the photodegradation of organic pollutants, including pesticides, pharmaceuticals, and industrial wastes. It is shown that the photocatalytic activity depends on the zeolite-type, metal dopant, metal content, zeolite pore structure, and the energy of the irradiation source. Faujasite-type Y zeolites combined with ozone achieved up to 95% micropollutant degradation. Bentonite modified with cellulosic biopolymers effectively removed pesticides such as atrazine and chlorpyrifos, while titanium and/or silver-doped zeolites showed strong catalytic activity in degrading carbamates, highlighting their environmental application potential. Full article

In the present work, we present the process of preparing CdS nanostructures based on templating synthesis using chemical deposition (CD) on a SiO₂/Si substrate. A 0.7 μm thick silicon dioxide film was thermally prepared on the surface of an n-type conduction Si wafer, followed by the creation of latent ion tracks on the film by irradiating them with swift heavy Xe ions with an energy of 231 MeV and a fluence of 10⁸ cm⁻². As a result of etching in hydrofluoric acid solution (4%), pores in the form of truncated cones with different diameters were formed. The filling of the nanopores with cadmium sulfide was carried out via templated synthesis using CD methods on a SiO_2 nanopores/Si substrate for 20–40 min. After CdS synthesis, the surfaces of nanoporous SiO_2 nanopores/Si were examined using a scanning electron microscope to determine the pore sizes and the degree of pore filling. The crystal structure of the filled silica nanopores was investigated using X-ray diffraction, which showed CdS nanocrystals with an orthorhombic structure with symmetry group 59 Pmmn observed at 2θ angles of 61. 48° and 69.25°. Photoluminescence spectra were recorded at room temperature in the spectral range of 300–800 nm at an excitation wavelength of 240 nm, where emission bands centered around 2.53 eV, 2.45 eV, and 2.37 eV were detected. The study of the CVCs showed that, with increasing forward bias voltage, there was a significant increase in the forward current in the samples with a high degree of occupancy of CdS nanoparticles, which showed the one-way electronic conductivity of CdS/SiO₂/Si nanostructures. For the first time, CdS nanostructures with orthorhombic crystal structure were obtained using track templating synthesis, and the density of electronic states was modeled using quantum–chemical calculations. Comparative analysis of experimental and calculated data of nanostructure parameters showed good agreement and are confirmed by the results of other authors. Full article