Search Results (123)

Background/Objectives: Boron-dipyrromethene (BODIPY) derivatives are a superior class of fluorophores prized for their exceptional photostability and tunable photophysical properties. While ideal for imaging, their translation to photodynamic therapy (PDT) has been hampered by excitation in the visible range, leading to poor tissue penetration. To overcome this, intense research has focused on developing near-infrared (NIR)-absorbing BODIPY photosensitizers (PS). This review aims to systematically summarize the hierarchical design strategies, from molecular engineering to advanced nanoplatform construction, that underpin the recent progress of NIR-BODIPY PS in therapeutic applications. Methods: We conducted a comprehensive literature review using PubMed, Scopus, and Web of Science databases. The search focused on keywords such as “BODIPY”, “aza-BODIPY”, “near-infrared”, “photodynamic therapy”, “photothermal therapy”, “nanocarriers”, “hypoxia”, “immuno-phototherapy”, and “antibacterial.” This review analyzes key studies describing molecular design, chemical modification strategies (e.g., heavy-atom effect, π-extension), nanoplatform formulation, and therapeutic applications in vitro and in vivo. Results: Our analysis reveals a clear progression in design complexity. At the molecular level, we summarize strategies to enhance selectivity, including active targeting, designing “smart” PS responsive to the tumor microenvironment (TME) (e.g., hypoxia or low pH), and precise subcellular localization (e.g., mitochondria, lysosomes). We then detail the core chemical strategies for achieving NIR absorption and high singlet oxygen yield, including π-extension, the internal heavy-atom effect, and heavy-atom-free mechanisms (e.g., dimerization). The main body of the review categorizes the evolution of advanced theranostic nanoplatforms, including targeted systems, stimuli-responsive ‘smart’ systems, photo-immunotherapy (PIT) platforms inducing immunogenic cell death (ICD), hypoxia-overcoming systems, and synergistic chemo-phototherapy carriers. Finally, we highlight emerging applications beyond oncology, focusing on the use of NIR-BODIPY PS for antibacterial therapy and biofilm eradication. Conclusions: NIR-BODIPY photosensitizers are a highly versatile and powerful class of theranostic agents. The field is rapidly moving from simple molecules to sophisticated, multifunctional nanoplatforms designed to overcome key clinical hurdles like hypoxia, poor selectivity, and drug resistance. While challenges in scalability and clinical translation remain, the rational design strategies and expanding applications, including in infectious diseases, confirm that NIR-BODIPY derivatives will be foundational to the next generation of precision photomedicine. Full article

Lead halide perovskites, exemplified by methylammonium (MA) lead iodide (MAPbI₃), combine strong optical absorption, long carrier diffusion lengths, and defect-tolerant electronic structure with facile processing, making them attractive for photovoltaics and radiation detection. Yet, their behavior under electron irradiation remains insufficiently understood, limiting deployment in space and dosimetry contexts. Here, we employ Monte Carlo simulations (Geant4) to model electron interactions with MAPbI₃ across energies from 0.1 to 100 MeV and absorber thicknesses from 10 μm to 1 cm. We quantify deposited energy, event statistics, energy per interaction, non-ionizing energy loss, and dominant radiation effects. The results reveal strong thickness-dependent regimes: thin photovoltaic-type layers (~hundreds of nanometers) are largely transparent to MeV electrons, minimizing bulk damage but allowing localized ionization, exciton self-trapping, and photoexcitation-driven ion migration. Although localized excitations can temporarily improve carrier collection under short-term exposure, their cumulative effect drives ionic rearrangement and defect growth, ultimately reducing device stability. In contrast, thicker detector-type films (10–100 μm) sustain multiple scattering and ionization cascades, enhancing sensitivity but accelerating defect accumulation. At centimeter scales, energy deposition saturates, enabling bulk-like absorption for high-flux dosimetry. Overall, electron irradiation in MAPbI₃ is dominated by electronic excitation rather than ballistic displacements, underscoring the need to optimize thickness and composition to balance efficiency, sensitivity, and durability. Full article

In this paper, we design a self-powered photoelectrochemical (PEC)-type photodetector based on a hybridization of two-dimensional (2D) few-layer antimony (Sb) nanosheets (NSs) and reduced graphene oxide (rGO). The few-layer Sb NSs obtained by liquid-phase exfoliation can be anchored on the surface of rGO through hydrothermal treatment. Specifically, during photoexcitation, the electron–hole pairs photogenerated on the surface of Sb NSs can be well stimulated and transferred by rGO, reducing the photogenerated carriers recombine on Sb NSs. The excellent electrochemical performance is confirmed by PEC tests. The photobehavior performance of the Sb NSs-rGO composite is significantly improved; its photocurrent density reaches 48.830 nA/cm² at zero potential, approximately twice that of pure Sb NSs. The hybrid exhibits a faster photoresponse speed, with the response time and recovery time being 0.140 s and 0.163 s, respectively. This enhancement arises from the conductive role of rGO as a conductive channel, and as a result, the efficient separation of photoinduced electron–hole pairs is facilitated. This study is a further exploration of hybrid engineering of 2D materials in photochemical photodetectors and demonstrates significant progress in this field. Full article

Monolayer (ML) molybdenum disulfide (MoS₂) is a typical valleytronic material which has important applications in, for example, polarization optics and information technology. In this study, we examine the effect of continuous wave (CW) laser pumping on the basic optoelectronic properties of ML MoS₂ placed on a sapphire substrate, where the pump photon energy is larger than the bandgap of ML MoS₂. The pump laser source is provided by a compact semiconductor laser with a 445 nm wavelength. Through the measurement of THz time-domain spectroscopy, we obtain the complex optical conductivity for ML MoS₂, which are found to be fitted exceptionally well with the Drude–Smith formula. Therefore, we expect that the reduction in conductivity in ML MoS₂ is mainly due to the effect of electronic backscattering or localization in the presence of the substrate. Meanwhile, one can optically determine the key electronic parameters of ML MoS₂, such as the electron density n_e, the intra-band electronic relaxation time τ, and the photon-induced electronic localization factor c. The dependence of these parameters upon CW laser pump intensity is examined here at room temperature. We find that 445 nm CW laser pumping results in the larger n_e, shorter τ, and stronger c in ML MoS₂ indicating that laser excitation has a significant impact on the optoelectronic properties of ML MoS₂. The origin of the effects obtained is analyzed on the basis of solid-state optics. This study provides a unique and tractable technique for investigating photo-excited carriers in ML MoS₂. Full article

This work presents a novel approach to investigating epitaxial GaAsN layers and GaAsN-based p-i-n solar cell structures using light-assisted scanning capacitance microscopy (SCM) and spectroscopy. Due to the technological challenges in growing high-quality GaAsN with controlled nitrogen incorporation, the epitaxial layers often exhibit inhomogeneity in their opto-electrical properties. By combining localized cross-section SCM measurements with wavelength-tunable optical excitation (800–1600 nm), we resolved carrier concentration profiles, internal electric fields, and deep-level transitions across the device structure at a nanoscale resolution. A comparative analysis between electrochemical capacitance–voltage (EC-V) profiling and photoluminescence spectroscopy confirmed multiple localized transitions, attributed to compositional fluctuations and nitrogen-induced defects within GaAsN. The SCM method revealed spatial variations in energy states, including discrete nitrogen-rich regions and gradual variations in the nitrogen content throughout the layer depth, which are not recognizable using standard characterization methods. Our results demonstrate the unique capability of the photo-scanning capacitance microscopy and spectroscopy technique to provide spatially resolved insights into complex dilute nitride structures, offering a universal and accessible tool for semiconductor structures and optoelectronic devices evaluation. Full article

Photodegradation is a sustainable green technology that has been studied worldwide, especially for wastewater treatment. The calcination temperature has an important impact on the physicochemical properties of the prepared photocatalysts. In this study, a ternary photocatalyst of Cu₂O/WO₃/TiO₂ (CWT) was successfully synthesized using an ultrasonic-assisted hydrothermal technique, and the calcination temperature was varied from 500 to 800 °C. The characterization outcomes proved that the anatase phase titanium dioxide (TiO₂) in the CWT composite transformed to rutile phase TiO₂ when the calcination temperature reached 700 °C and 800 °C. The surface area of the CWT composite decreased from 35.77 to 8.09 m².g⁻¹ and the particle size of the CWT composite increased from 39.11 to 180.25 nm with an increasing calcination temperature from 500 to 800 °C. Photoelectrochemical (PEC) studies showed the charge-transfer resistance of 208.10 Ω, electron lifetime of 32.48 ms, current density of 1.40 mA.cm⁻², transient photovoltage of 0.53 V, and p-n heterojunction properties for CWT-500. Reactive Black 5 (RB5) was used as the model pollutant to examine the photodegradation performance. The photodegradation rate of CWT-500 was the highest (0.70 × 10⁻² min⁻¹) due to its large surface area, effective separation of photoexcited electron-hole pairs, and low photoexcited charge carrier recombination rate. Full article

To extend the spectral utilisation of In₂S₃, an In₂S₃/C₃N₄ nanocomposite was prepared. The effects of different sulphur sources, electrodes, and bias voltages on the optoelectronic performance were examined. Photoelectric properties in response to light sources with wavelengths of 405, 532, 650, 780, 808, 980, and 1064 nm were investigated using Au electrodes and the carbon electrodes with 5B pencil drawings. This study shows that the aggregation states of the In₂S₃/C₃N₄ nanocomposite possess photocurrent switching responses in the broadband region of the light spectrum. Combining two types of partially visible light-absorbing material extends utilisation to the near-infrared region. Impurities or defects embody an electron-donating effect. Since the energy levels of defects or impurities with an electron-donating effect are close to the conduction band, low-energy lights (especially NIR) can be utilised. The non-equilibrium carrier concentration (photogenerated electrons) of the nanocomposites increases significantly under NIR photoexcitation conditions. Thus, photoconductive behaviour is manifested. A good photoelectric signal was still measured when zero bias was applied. This demonstrates self-powered photoelectric response characteristics. Different sulphur sources significantly affect the photoelectric performance, suggesting that they create different defects that affect charge transport and base current noise. It is believed that interfacial interactions in the In₂S₃/C₃N₄ nanocomposite create a built-in electric field that enhances the separation and transfer of electrons and holes produced by light stimulation. The presence of the built-in electric field also leads to energy band bending, which facilitates the utilisation of the light with longer wavelengths. This study provides a reference for multidisciplinary applications. Full article

Photothermal catalytic CO₂ conversion into chemicals that provide added value represents a promising strategy for sustainable energy utilization, yet the development of highly efficient, stable, and selective catalysts remains a significant challenge. Herein, we report a rationally designed p-n junction heterostructure, T-CZ-PBA (SC), synthesized via controlled pyrolysis of high crystalline Prussian blue analogues (PBA) precursor, which integrates CuCo alloy, ZnO, N-doped carbon (NC), and Zn^II-Co^IIIPBA into a synergistic architecture. This unique configuration offers dual functional advantages: (1) the abundant heterointerfaces provide highly active sites for enhanced CO₂ and H₂ adsorption/activation, and (2) the engineered energy band structure optimizes charge separation and transport efficiency. The optimized T-C₃Z₁-PBA (SC) achieves exceptional photothermal catalytic performance, demonstrating a CO₂ conversion rate of 126.0 mmol gcat⁻¹ h⁻¹ with 98.8% CO selectivity under 350 °C light irradiation, while maintaining robust stability over 50 h of continuous operation. In situ diffuse reflectance infrared Fourier transform spectroscopy (in situ DRIFTS) investigations have identified COOH* as a critical reaction intermediate and elucidated that photoexcitation accelerates charge carrier dynamics, thereby substantially promoting the conversion of key intermediates (CO₂* and CO*) and overall reaction kinetics. This research provides insights for engineering high-performance heterostructured catalysts by controlling interfacial and electronic structures. Full article

Exciton generation and separation play an important role in the photoelectric properties and the luminescence performance of materials. In order to tailor the defects and grain boundaries and improve the exciton separation and light harvesting of the graphitic carbon nitride (g-C₃N₄) nanosheets, a C₃N₄/bismuth sulfide (Bi₂S₃) nanocomposite was synthesized. The photoelectric properties of the 405, 532, 650, 780, 808, 980 and 1064 nm light sources were studied using Au electrodes and graphite electrodes with 4B and 5B pencil drawings. The results indicate that the C₃N₄/Bi₂S₃ nanocomposite exhibited photocurrent switching behavior in the broadband light spectrum range. It is noted that even with zero bias applied, a good photoelectric signal was still measured. The resulting nanocomposite exhibited good photophysical stability. Physical mechanisms are discussed herein. It is suggested that the interfacial interaction of C₃N₄ and Bi₂S₃ in the nanocomposite creates a strong built-in electric field, which accelerates the separation of excitons. Therefore, as a dynamic process of photoexcitation, fluorescence, the photoelectric effect, and scattering are three main competing processes; the separation of excitons and the extraction of free photogenerated charge can be used as a reference for the fluorescent materials or other photoelectric materials studies as photophysical properties. This study also serves as an important reference for the design, defect and grain boundary modulation or interdisciplinary application of functional nanocomposites, especially for the bandgap modulation and suppression of photogenerated carrier recombination. Full article

Vacancy defect graphitic carbon nitride (g-C₃N₄) and conjugated polyimide (PI) polymer photocatalysts have become increasingly recognized as metal-free photocatalysts featuring an appropriate bandgap. The narrow absorption spectrum of visible light and the rapid recombination rate of the photoexcited charge carriers in PI polymers and g-C₃N₄ impede its photocatalytic performance. The presence of oxygen vacancies (OVs) in PI polymer photocatalysts, as well as nitrogen vacancies (NVs) and carbon vacancies (CVs) in g-C₃N₄, can significantly enhance the migration of photogenerated electrons. Adding vacancies to improve the electronic structure and band gap width can greatly enhance the photocatalytic efficiency of PI polymers and g-C₃N₄. Defect engineering is important for increasing the photocatalytic ability of PI-polymer and g-C₃N₄. There remains a notable absence of thorough review papers covering the synthesis, characterization, and applications of vacancy-rich PI-polymer and g-C₃N₄ in photocatalysis. This review paper examines the roles of OVs in PI-polymer, NVs, and CVs in g-C₃N₄ and thoroughly summarizes the preparation approaches employed before and after, as well as during polymerization. This review scrutinizes spectroscopic characterization techniques, such as EPR, XPS, PAS, XRD, FTIR, and NMR, for vacancy defect analysis. We also reviewed the role of vacancies, which include light absorption, photogenerated charge carrier separation, and transfer dynamics. This review could serve as a comprehensive understanding, a vacancy-engineered design framework, and a practical guide for synthesizing and characterizing. Full article

The interfacial energy level alignment in the copper phthalocyanine/SiO₂/p-Si(100) heterojunction has been studied in dark conditions and under illumination. The element-sensitivity of the time-resolved X-ray photoemission provides a real-time picture of the photoexcited carrier dynamics at the interface and within the film, enabling one to distinguish between substrate and molecular contributions. We observe a molecule-to-substrate charge transfer under photoexcitation, which is directly related to the transient modification of the band bending in the substrate due to the surface photovoltage effect. Our results show that charge generation in the heterojunction is driven by the molecular layer in contact with the substrate. The different molecular orientation at the interface creates a new channel for charge injection in the substrate under photoexcitation. Full article

When a sample of semiconducting material is illuminated by monochromatic light, in which the photon energy is higher than the energy gap of the semiconductor, part of the absorbed electromagnetic energy is spent on the generation of pairs of quasi-free charge carriers that are bound by Coulomb attraction. Photo-generated pairs diffuse through the material as a whole according to the density gradients established, carrying part of the excitation energy and charge through the semiconducting sample. This energy is indirectly transformed into heat, where the excess negatively charged electron recombines with a positively charged hole and causes additional local heating of the lattice. The dynamic of the photoexcited charge carrier is described by a non-linear partial differential equation of ambipolar diffusion. In moderate doped semiconductors with a low-level injection of charge carriers, ambipolar transport can be reduced to the linear parabolic partial differential equation for the transport of minority carriers. In this paper, we calculated the spectral function of the photoinduced charge carrier distribution based on an approximation of low-level injection. Using the calculated distribution and inverse Laplace transform, the dynamics of recombination photoinduced heat sources at the surfaces of semiconducting samples were studied for pulse optical excitations of very short and very long durations. It was shown that the photoexcited charge carriers affect semiconductor heating depending on the pulse duration, velocity of surface recombination, lifetime of charge carriers, and their diffusion coefficient. Full article

The increasing concentration of antibiotics in natural water poses a significant threat to society’s sustainable development due to water pollution. Photocatalytic technology is an efficient and environmentally friendly approach to environmental purification, offering great potential for addressing pollution and attracting significant attention from scholars worldwide. TiO₂, as a representative semiconductor photocatalytic material, exhibits strong oxidation ability and excellent biocompatibility. However, its wide band gap and the rapid recombination of photo-generated electron–hole pairs significantly limit its photocatalytic applications. Recent studies indicate that constructing heterojunctions with synergistic plasmonic effects is an effective strategy for developing high-performance photocatalysts. In this study, Bi metal nanoparticles and (BiO)₂CO₃ nanosheets were simultaneously grown on TiO₂ nanofibers via an in situ hydrothermal method, successfully forming a Bi@(BiO)₂CO₃/TiO₂ composite fiber photocatalyst with synergistic plasmonic effects. The surface plasmon resonance (SPR) effect of Bi nanoparticles combined with the (BiO)₂CO₃/TiO₂ heterojunction enhances sunlight absorption, facilitates efficient separation of photo-generated carriers, and significantly strengthens the photo-oxidation and reduction abilities. This system effectively generates abundant hydroxyl (·OH) and superoxide (·O²⁻) radicals under sunlight excitation. Consequently, Bi@(BiO)₂CO₃/TiO₂ exhibited outstanding photocatalytic performance. Under simulated sunlight for 60 min, the photodegradation efficiencies of the quinolone antibiotics lomefloxacin, ciprofloxacin, and norfloxacin reached 93.2%, 97.5%, and 100%, respectively. Bi@(BiO)₂CO₃/TiO₂ also demonstrates excellent stability and reusability. This study represents a significant step toward the application of TiO₂-based photocatalyst materials in environmental purification. Full article

Electrochemical polymerization of 3,4-ethylenedioxythiophene in the presence of water-soluble fullerene derivatives was investigated. The electronic structure, morphology, spectroelectrochemical, electrochemical properties and near-IR photoconductivity of composite films of poly(3,4-ethylenedioxythiophene) with fullerenes were studied for the first time. It was shown that fullerene with hydroxyl groups creates favorable conditions for the formation of PEDOT chains and more effectively compensates for the positive charges on the PEDOT chains. The near-IR photoconductivity results from the generation of charge carriers due to electron transfer from the photoexcited PEDOT molecule to the fullerene acceptor. Full article

The rational design of heterojunction photocatalysts enabling fast transportation and efficient separation of photoexcited charge carriers is the key element in visible light-driven photocatalyst systems. Herein, we develop a unique Z-scheme heterojunction consisting of NiMoO₄ microflowers (NMOF) and ZIF67, referred to as ZINM (composite), for the purpose of antibiotic degradation. ZIF67 was produced by a solution process, whereas NMOF was synthesized via coprecipitation with a glycine surfactant. The NMOF exhibited a monoclinic phase with a highly oriented, interconnected sheet-like morphology. The ZINM showed better optical and charge transfer characteristics than its constituents, ZIF67 and NiMoO₄. Consequently, the developed heterojunction photocatalysts exhibited superior photocatalytic redox capability; the ZINM30 (the composite with 30 wt.% of NiMoO₄ loaded) could degrade 91.67% of tetracycline and 86.23% of norfloxacin within 120 min. This enhanced photocatalytic activity was attributable to the reduced bandgap (E_gap = 2.01 eV), unique morphology, high specific surface area (1099.89 m²/g), and intimate contact between ZIF67 and NiMoO₄, which facilitated the establishment of the Z-scheme heterojunction. Active species trapping tests verified that •O₂⁻ and h⁺ were the primary species, supporting the proposed degradation mechanism. This work highlights a valid Z-scheme ZIF67/NiMoO₄ heterojunction system for efficient carrier separation and, therefore, enhanced photocatalytic degradation of antibiotics. Full article