Search Results (226)

Recently, a new class of materials with very high porosity and ultra-lightweight, namely, semiconductor aero-materials, has attracted the attention of many researchers. Semiconductor aero-materials, due to their special properties, can be used in the development of devices applied in biomedical, electronics, optoelectronic, energy conversion and storage, sensors, biosensors, catalysis, automotive, and aeronautic industries. Although aero-materials and aerogels are similar, different methods of obtaining them are used. Aerogels are synthesized from organic, inorganic, or hybrid precursors, the main characteristic being that they are gel-like solids with a high air content (99.9%) in the structure. Thus, three-dimensional (3D) interconnected porous network chains are formed, resulting in light solid-state structures with very high porosity due to the large number of air pores in the network. On the other hand, to obtain aero-materials with controlled properties such as morphology, shape, or the formation of 3D hollow structures, sacrificial templates are used. Thus, sacrificial structures (which can be easily removed) can be obtained depending on the morphology of the 3D structure to be obtained. Therefore, this review paper offers a comprehensive coverage of the synthesis methods of different types of semiconductor aero-materials that use ZnO tetrapod, ZnO(T), as a sacrificial template, related to the present and future perspectives. These ZnO(T) sacrificial substrates offer several advantages, including diverse synthesis processes and easy removal methods that occur simultaneously with the growth of the desired aero-materials. Full article

Photocatalytic hydrogen (H₂) production offers a promising solution to energy shortages and environmental challenges by converting solar energy into chemical energy. Hydrogen, as a versatile energy carrier, can be generated through photocatalysis under sunlight or via electrolysis powered by solar or wind energy. However, the advancement of photocatalysis is hindered by the limited availability of effective visible light-responsive semiconductors and the challenges of charge separation and transport. To address these issues, researchers are focusing on the development of novel nanostructured semiconductors and composite materials that can enhance photocatalytic performance. In this paper, we provide an overview of the advanced photocatalytic materials prepared so far that can be activated by sunlight, and their efficiency in H₂ production. One of the key strategies in this research area concerns improving the separation and transfer of electron–hole pairs generated by light, which can significantly boost H₂ production. Advanced hybrid materials, such as organic–inorganic hybrid composites consisting of a combination of polymers with metal oxide photocatalysts, and the creation of heterojunctions, are seen as effective methods to improve charge separation and interfacial interactions. The development of Schottky heterojunctions, Z-type heterojunctions, p–n heterojunctions from nanostructures, and the incorporation of nonmetallic atoms have proven to reduce photocorrosion and enhance photocatalytic efficiency. Despite these advancements, designing efficient semiconductor-based heterojunctions at the atomic scale remains a significant challenge for the realization of large-scale photocatalytic H₂ production. In this review, state-of-the-art advancements in photocatalytic hydrogen production are presented and discussed in detail, with a focus on photocatalytic nanostructures, heterojunctions and hybrid composites. Full article

This paper proposes a structural silicon heterojunction photosensitive element with a simple form, low manufacturing cost, and efficient performance, which has a high-intensity photoelectric effect and a high frequency range of use. It can be applied as microwave switches to active frequency selective surfaces (AFSSs) to replace PIN diodes. Meanwhile, we explore the crucial role of pentacene/silicon heterojunction in the photoelectric conversion process. It is found that due to the inherent photovoltaic effect and the built-in electric field interaction between the two materials, the insertion loss of the heterojunction formed is reduced to 4.5 dB, which is 2.5 dB lower than that of the high-resistivity silicon wafer. In order to further reduce the insertion loss, the surface of the silicon wafer is etched and then heterojunction is prepared, which can further reduce insertion loss to within 2.5 dB, and the bandwidth difference between the presence and absence of pump excitation exceeds 10 dB extends to 12 GHz, indicating that the light collecting ability of structural silicon significantly enhances its photoelectric effect. The research results demonstrate the potential of using structural silicon heterojunctions in photoelectric devices, providing new technology for high-performance microwave switches and implementing optically controlled FSSs. Full article

Photoelectrochemical (PEC) sensors have emerged as potential analysis techniques in recent years due to PEC’s benefits, which include straightforward operation, quick response times, and basic equipment. In this work, a new PEC sandwich immunoassay was fabricated, which was based on low-toxicity BiOI/BiOCl composites accompanied by enhanced signal detection via AgI-conjugated antibodies (Ab₂-AgI). Specifically, the low-toxicity inorganic semiconductor BiOI/BiOCl composites were first utilized in PEC bioanalysis. Owing to the unique configuration of energy levels between BiOI and BiOCl, the photoelectric response was more excellent than those of BiOI or BiOCl alone. Moreover, the Ab₂-AgI conjugates were utilized as signal amplification components through the specific antibody–antigen immunoreaction. In the presence of target Ag, the immobilized Ab₂-AgI conjugates clearly improve the steric hindrance of the sensing electrode and effectively hinder the transfer of photo-induced holes; meanwhile, AgI NPs can competitively absorb excitation light. A new PEC immunosensing platform for detecting tumor markers at 0 V under visible light excitation was developed, and using carcinoembryonic antigen (CEA) as a model analyte demonstrated an ultra-low detection limit of 4.9 fg·mL⁻¹. Meanwhile, it demonstrated excellent specificity and stability, potentially opening up a novel and promising platform for detecting other critical biomarkers. Full article

The wastewater from Chemical Mechanical Polishing (CMP) generated in the semiconductor industry contains a significant concentration of suspended particles and necessitates rigorous treatment to meet environmental standards. Ceramic ultrafiltration membranes offer significant advantages in treating such high-solid wastewater, including a high separation efficiency, environmental friendliness, and straightforward cleaning and maintenance. However, the preparation of high-precision ceramic ultrafiltration membranes with a smaller pore size (usually <20 nm) is very complicated, requiring the repeated construction of transition layers, which not only increases the time and economic costs of manufacturing but also leads to an elevated transport resistance. In this work, halloysite nanotubes (HNTs), characterized by their high aspect ratio and lumen structure, were utilized to create a high-porosity transition layer using a spray-coating technique, onto which a γ-Al₂O₃ ultrafiltration selective layer was subsequently coated. Compared to the conventional α-Al₂O₃ transition multilayers, the HNTs-derived transition layer not only had an improved porosity but also had a reduced pore size. As such, this strategy tended to simplify the preparation process for the ceramic membranes while reducing the transport resistance. The resulting high-flux γ-Al₂O₃ ultrafiltration membranes were used for the high-efficiency treatment of CMP wastewater, and the fouling behaviors were investigated. As expected, the HNTs-mediated γ-Al₂O₃ ultrafiltration membranes exhibited excellent water flux (126 LMH) and high rejection (99.4%) of inorganic particles in different solvent systems. In addition, such membranes demonstrated good operation stability and regeneration performance, showing promise for their application in the high-efficiency treatment of CMP wastewater in the semiconductor industry. Full article

In this study, the effects of various moisture pretreatment devices (MPDs) on the analytical process of trichloroethylene (TCE) and nitrous oxide (N₂O), which are representative organic and inorganic compounds emitted from semiconductor industries, were investigated. Three types of MPDs—a KPASS (MPD_K), a Nafion™ dryer (MPD_N), and a cooler (MPD_C)—were evaluated for their performance under sample gas conditions of 25 °C and 150 °C at various flow rates. MPD modification was also carried out to improve their performance at high loading capacities. The results indicated that humidity introduced significant bias in the measurement of TCE and N₂O according to the analyzers explored in this study. At a flow rate of 1 L/min, among the MPDs, MPD_N exhibited the highest moisture removal efficiency, followed by MPD_K and MPD_C. In terms of analyte recovery rates, MPD_K achieved the highest TCE recovery, followed by MPD_N and MPD_C, across all tested conditions. Conversely, MPD_C resulted in the lowest N₂O recovery rates, whereas MPD_K and MPD_N maintained over 95% recovery rates. At a flow rate of 4 L/min, MPD_N and MPD_C did not work at high temperatures. In contrast, the modified MPD_K, which received less investment compared to many other membranes, showed an acceptable moisture removal efficiency (>85%) and analyte recovery (>98%). Therefore, modified KPASS is recommended as a useful moisture pretreatment device for the analytical process of TCE and N₂O at both normal and high loading capacities. Full article

This review examines the distinct advantages of organic semiconductors over conventional insulating polymers as optically active materials in photonic applications. We analyze the fundamental principles governing their unique optical and electronic properties, from basic conjugated polymer systems to advanced molecular architectures. The review systematically explores key material classes, including polyfluorenes, polyphenylene vinylenes, and polythiophenes, highlighting their dual electrical–optical functionality unavailable in passive polymer systems. Particular attention is given to polymer blends, composites, and hybrid organic–inorganic systems, demonstrating how semiconductor properties enable enhanced performance through materials engineering. We contrast passive components with active photonic devices, illustrating how the semiconductor nature of these polymers facilitates novel functionalities beyond simple light guiding. The review explores emerging applications in neuromorphic photonics, quantum systems, and bio-integrated devices, where the combined electronic–optical properties of organic semiconductors create unique capabilities impossible with insulating polymers. Finally, we discuss design strategies for optimizing these distinctive properties and present perspectives on future developments. This review establishes organic semiconductors as transformative materials for advancing photonic technologies through their combined electronic–optical functionality. Full article

The continuous growth of energy-efficient electronic devices and compact systems has motivated researchers to develop TFTs based on p-type semiconductors. This review examines the developments in p-type thin-film transistors (TFTs) processed using solution methods to achieve integration with complementary metal–oxide–semiconductor technology. Improving organic p-type materials is critical for achieving advanced mobility and stability characteristics with suitable process integration. Scientists study these materials for use in wearable devices which display mechanical strength when fitted onto a curve. This review presents an exclusive discussion about the wide spectrum of applications which involve flexible displays and sensors, together with upcoming technologies such as artificial skin and flexible integrated circuits. The article examines present material challenges, along with device reliability and large-scale production methods, to give a thorough analysis of solution-processed p-type TFTs toward their broad implementation in upcoming electronic devices. By summarizing the developments and most recent studies in the field, this review aims to provide useful information regarding current research into and future trends of p-type TFTs. Full article

Today, flexible and lightweight electronics are regarded as a viable alternative to conventional rigid and heavy devices in various application fields. In the optoelectronic area, organic semiconductors offer advantages such as high absorption coefficients, low processing temperatures, mechanical flexibility and compatibility with plastic substrates, while inorganic nanostructures provide good electronic properties and high thermal stability. Thus, composite films with enhanced properties can be achieved by inserting inorganic nanostructures within organic layers. In this research work, CuS nanoparticles were prepared by wet chemical precipitation and then added to an organic mixture containing poly(3-hexylthiophene) (P3HT) and N,N-bis-(1-dodecyl)perylene-3,4,9,10 tetracarboxylic diimide (AMC14), a chemically synthesized semiconductor, for fabricating hybrid composite films by matrix assisted pulsed laser evaporation (MAPLE) on indium tin oxide/poly(ethylene terephthalate) (ITO/PET) flexible substrates. A comparative assessment of the morphological, compositional, optical and electrical properties of the composite (P3HT:AMC14:CuS) and organic (P3HT:AMC14) layers was performed to evaluate their applicability in the photovoltaic cells. The transmission and emission spectra of the composite films are dominated by the optical features of AMC14, a perylene diimide derivative compound used as acceptor. In the case of devices based on MAPLE deposited composite layer fabricated on ITO/PET substrates, the electrical measurements carried under illumination revealed an improvement in the open circuit voltage parameter emphasizing their potential applications in the flexible device area. Full article

Charge transfer dynamics fundamentally influence energy conversion efficiency in excited electronic states, directly impacting photoelectric conversion, molecular electronics, and catalysis. The core hole clock (CHC) technique enables the precise measurement of interfacial charge transfer time, providing insights into the electronic structure and dynamics of organic and inorganic coupled systems. Among these materials, poly(3-hexylthiophene) (P3HT), a p-type semiconductor known for its high charge mobility, serves as an ideal model for charge transfer studies. This review discusses recent advancements in understanding charge transfer dynamics in P3HT-based composites through the application of the CHC technique. The studies are categorized into two main areas: (1) P3HT combined with carbon-based nanomaterials and (2) P3HT combined with 2D materials. These findings highlight the effectiveness of the CHC technique in probing interfacial charge transfer and emphasize the critical role of nanomaterial interfaces in modulating charge transfer, which is essential for advancing organic electronic devices and energy conversion systems. Full article

The organic–inorganic hybrid (BEDT-TTF)₃[Cu₂(μ-C₂O₄)₃·CH₃CH₂OH·1.2H₂O] (I) was obtained using the electrocrystallization method. It comprises a θ²¹-phase organic donor layer and a two-dimensional inorganic antiferromagnetic honeycomb lattice. Cu(II) is octahedrally coordinated by three bisbidenetate oxalates, exhibiting Jahn–Teller distortion. CH₃CH₂OH and H₂O molecules are located within the cavities of the honeycomb lattice. The total formal charge of the three donor molecules was assigned to be +2 based on the bond lengths in the TTF core, which corresponded to the Raman spectra. It is a semiconductor with σ_rt = 0.04 S/cm and E_α = 40 meV. No long-range ordering was observed above 2 K from zero-field cooling/field cooling magnetization, as confirmed by specific heat measurements. The spin frustration with f > 10 from the antiferromagnetic copper-oxalate-framework was observed. It is a candidate quantum spin liquid. Full article

In the present work, nine ‘defect’ perovskites with the chemical formula A₂ZrX₆ have been studied, where the A-site cations are a methylammonium cation, formamidinium cation, and trimethyl-sulfonium cation and the X-site anions are halogen, X = Cl, Br, and I. We employ periodic DFT calculations using GGA-PBE, MBJ, HSEsol, and HSE06 functionals. All studied compounds exhibit a wide-bandgap energy that ranges from 5.22 eV to 2.11 eV, while for some cases, geometry optimization led to significant structural modification. It was found that the increase in the halogen size resulted in a decrease in the bandgap energy. The choice of the organic A-site cation affects the bandgap as well, which is minimal for the methylammonium cation. Such semiconductors with organic cations may be utilized in optoelectronic devices, given the substantial benefit of solution processability and thin film formation compared to purely inorganic analogs, such as Cs₂ZrX₆. Full article

The photocatalytic N₂ fixation reaction still faces high N₂ activation energy barriers and inefficient electron transfer efficiency, limiting the overall ammonia yield of semiconductors. This communication reports on the construction of an organic/inorganic g-C₃N₄/oxygen vacancy-enriched TiO₂ (g-C₃N₄/TiO₂-OV) composite system via the annealing treatment in an H₂/Ar mixed atmosphere for enhanced photocatalytic N₂ fixation activity. After illumination for 4 h, g-C₃N₄/TiO₂-OV with 1 wt% g-C₃N₄ loading demonstrates the optimal ammonia yield of 31.6 μmol L⁻¹. This study demonstrates the existence of oxygen vacancies on the TiO₂ surface through EPR while also investigating the carrier separation and transport efficiency of the material using photoelectric characterization. The experimental results indicate that the introduction of OVs into TiO₂ serves as Lewis acid sites, facilitating N₂ adsorption. Moreover, the lower onset potential and higher current density of g-C₃N₄/TiO₂-OV composites indicate that the construction of the heterojunction composite significantly decreases the interfacial charge recombination and N₂ activation energy barrier, effectively improving the ammonia yield towards N₂ photo-reduction. This work emphasizes the importance of rational tailoring of TiO₂-based photocatalysts in the field of N₂ fixation. Full article

Coupling superconducting (SC) contacts to light-emitting layers can lead to remarkable effects, as seen in inorganic quantum-well LEDs with superconducting contacts, where an enhancement in radiative recombination was observed. Additional dramatic effects were theorized if both electrodes are SC, such as correlated emission and 2-photon entanglement. Motivated by this and by the question of whether proximity induced SC is possible in organic light-emitting materials, we studied the electronic properties of stacked SC–organic–SC devices. Our structures consisted of Nb (bottom) and NbN (top) SC electrodes and a spin-coated light-emitting semiconductor polymer, MEH-PPV. Sputtering the SC directly on the polymer causes pinholes, which we prevent by ultra-slow deposition of a 5 nm aluminum film, before depositing the top SC in situ. The Al protects the organic film from damage and pinhole formation, while preserving SC in the top electrodes due to the proximity effect between Al and NbN. Electrical transport measurements of the completed junctions indicate that indeed, the top and bottom contacts are superconducting and the protected MEH-PPV layer is pinhole-free, as supported by HR-TEM and EDS. Most importantly, we find that as the temperature is decreased below the critical temperature of the SCs, the device shows evidence for the proximity effect in the MEH-PPV. Full article