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Keywords = ultrathin oxide layers

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15 pages, 2310 KB  
Article
Time-Domain Simulation and Optimization of the Memory Window for HZO-Based FeFETs Using the NLS Model
by Shangda Han, Weifeng Lü, Yekun Liang and Tianyu Dai
Micromachines 2026, 17(7), 828; https://doi.org/10.3390/mi17070828 - 10 Jul 2026
Viewed by 386
Abstract
Hafnium-zirconium oxide (HZO)-based ferroelectric field-effect transistors (FeFETs) are expected to become core devices for new embedded memory and compute-in-memory systems. However, existing simulations rely on finite-element-based TCAD tools, which are computationally intensive and time-consuming, and they struggle to account for the dynamic flipping [...] Read more.
Hafnium-zirconium oxide (HZO)-based ferroelectric field-effect transistors (FeFETs) are expected to become core devices for new embedded memory and compute-in-memory systems. However, existing simulations rely on finite-element-based TCAD tools, which are computationally intensive and time-consuming, and they struggle to account for the dynamic flipping of ferroelectric domains. This paper utilizes a time-domain simulation framework based on the nucleation-limited switching (NLS) model coupled with the surface potential of a MOSFET, enabling a self-consistent solution for polarization and electrical characteristics; a Monte Carlo method is employed to simulate device variability, and Shmoo plots are used to identify optimal programming and erasure process windows; an integrated solution is proposed for 22 nm FDSOI devices, addressing geometric scaling, modification of the Landau–Khalatnikov (L-K) dynamic model for ultrathin ferroelectric layers, and suppression of short-channel effects. Model validation is limited to selected operating metrics, and predictive accuracy outside the calibrated cases requires additional independent datasets. This method enables end-to-end simulation of FeFETs, from material polarization and device electrical characteristics to performance optimization, thereby providing model-based analytical and design support for the development of advanced, ultra-low-power FeFETs. Full article
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11 pages, 1340 KB  
Article
Ion-Gel-Assisted MoS2 Transfer Method for Low-Voltage, High-Performance MoS2/ITZO Heterojunction Phototransistor Application
by Soobin Lee, Jidong Jin, Zhenyuan Xiao, Wensi Cai, Zhigang Zang, Hyun Seok Lee and Jaekyun Kim
Micromachines 2026, 17(5), 574; https://doi.org/10.3390/mi17050574 - 7 May 2026
Viewed by 711
Abstract
Molybdenum disulfide (MoS2) is a compelling candidate for visible-light detection due to its strong optical absorption and tunable bandgap, yet the development of high-performance MoS2 photodetectors remains limited by challenges in scalable integration, low-voltage operation, and efficient photoresponse. Here, we [...] Read more.
Molybdenum disulfide (MoS2) is a compelling candidate for visible-light detection due to its strong optical absorption and tunable bandgap, yet the development of high-performance MoS2 photodetectors remains limited by challenges in scalable integration, low-voltage operation, and efficient photoresponse. Here, we report an ion-gel-assisted transfer strategy that enables the fabrication of large-area MoS2/ion gel films that are suitable for low-power phototransistor applications. The transferred MoS2/ion gel stack is laminated onto an indium-tin-zinc-oxide (ITZO) layer on a glass substrate to fabricate a MoS2/ITZO heterojunction phototransistor, with the ion gel serving as an ultrathin, high-capacitance gate dielectric. The resulting phototransistor exhibits a field-effect mobility of 4.12 cm2/Vs, an on/off current ratio of 4.9 × 105, and a subthreshold swing of 0.17 V/dec. Under 635, 520, and 405 nm illumination with a power density of 4.5 mW/cm2, it achieves responsivities of 0.58, 1.82, and 5.56 A W−1 and detectivities of 5.90 × 109, 1.86 × 1010, and 5.68 × 1010 Jones, respectively. These findings demonstrate that the ion-gel-assisted transfer process offers a robust route to high-performance, low-voltage photodetection and provides a promising platform for next-generation optoelectronic technologies. Full article
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12 pages, 6551 KB  
Article
Thermal Stability and Microstructural Evolution of Cu Joints with an Ultra-Thin Sintered Layer
by Siwen Shao, Chenghao Zhang, Wei Jiang, Chun Li, Xiaoqing Si, Zongjing He, Jian Cao and Yang Liu
Appl. Sci. 2026, 16(9), 4108; https://doi.org/10.3390/app16094108 - 22 Apr 2026
Viewed by 521
Abstract
Low-temperature Cu sintering is used as a die-bonding strategy for the third-generation power device, and the Cu-sintered joints require long-term stability at elevated temperature. In this work, we investigate the thermal stability and microstructural evolution of the Cu interconnect joints with an ultra-thin [...] Read more.
Low-temperature Cu sintering is used as a die-bonding strategy for the third-generation power device, and the Cu-sintered joints require long-term stability at elevated temperature. In this work, we investigate the thermal stability and microstructural evolution of the Cu interconnect joints with an ultra-thin sintered layer at the temperature of 250 °C in air. The as-prepared joint shows a dense well-bonded interface with low porosity before the thermal aging test. The average shear strength of the joints increases from 85.5 MPa to 91.3 MPa after aging up to 300 h. With further increase in aging time, the shear strength begins to decrease. However, the strength remains at a high level of 69.8 MPa even after 500 h of aging, satisfying the requirements for high-temperature stability. At short aging times, the porosity within the interface reduces slightly, and the fracture exhibits distinct ductile characteristics. When the aging time exceeds 300 h, the oxide content at the interface increases from the outer region toward the inner part, and aging cracks eventually appear at the edge of the sintered layer. Therefore, it is demonstrated that the dense and thin sintered layer limits oxygen diffusion, guaranteeing the high-temperature stability of the sintered joint. Full article
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18 pages, 3552 KB  
Article
Exceptional Specific Shielding Effectiveness of TOCNFs@MXene Hybrid Films via Densification Engineering
by Beibei Wang, Licheng Zhou, Sentao Wei, Jian Wang, Qun Wu, Chuan Cao and Kushairi Mohd Salleh
Polymers 2026, 18(8), 999; https://doi.org/10.3390/polym18080999 - 20 Apr 2026
Cited by 1 | Viewed by 1062
Abstract
The rapid advancement of communication technologies exacerbates severe electromagnetic interference (EMI) pollution. Conventional flexible shielding materials rely heavily on non-degradable petroleum-based polymers, aggravating the electronic waste crisis. To address this dual challenge, sustainable biomass-derived TEMPO-oxidized cellulose nanofibrils (TOCNFs) emerge as ideal structural substrates. [...] Read more.
The rapid advancement of communication technologies exacerbates severe electromagnetic interference (EMI) pollution. Conventional flexible shielding materials rely heavily on non-degradable petroleum-based polymers, aggravating the electronic waste crisis. To address this dual challenge, sustainable biomass-derived TEMPO-oxidized cellulose nanofibrils (TOCNFs) emerge as ideal structural substrates. However, their intrinsic electrical insulation necessitates integrating conductive two-dimensional (2D) MXene, which suffers from severe self-restacking and brittleness. Herein, TOCNFs@MXene hybrid films are manufactured via vacuum filtration and hot-pressing densification. TOCNFs inhibit MXene self-restacking, constructing a highly ordered layered architecture via a dense hydrogen-bonded network. The optimized ultrathin film T5@M20 (~4.92 μm) exhibits an electrical conductivity of 1.09 × 106 ± 5.06 × 104 s m−1 and an X-band shielding effectiveness (SETotal) of 25.55 dB. Demonstrating an ultrahigh thickness-normalized specific shielding effectiveness (SSE/t) of 51,934.72 dB·cm2·g−1, this sustainable architecture shows exceptional potential for next-generation flexible electronics. Full article
(This article belongs to the Section Polymer Membranes and Films)
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17 pages, 2620 KB  
Article
Characterization of an Ultra-Thin Silicon Strain Gauge Exposed to Gamma Ray Irradiation
by Fan Yang, Hao Liu, Masahito Takakuwa, Tomoyuki Yokota, Takao Someya, Jarred W. Fastier-Wooller, Shun Muramatsu, Michitaka Yamamoto, Kenta Murakami, Toshihiro Itoh and Seiichi Takamatsu
Sensors 2026, 26(8), 2514; https://doi.org/10.3390/s26082514 - 19 Apr 2026
Viewed by 769
Abstract
Microelectromechanical systems are being increasingly deployed in nuclear industry robotics, where their great sensitivity and mechanically stable silicon structures enable reliable sensing in radiation-exposed environments. An ultra-thin silicon strain gauge without an oxide substrate layer designed for robotic electronic skin is evaluated under [...] Read more.
Microelectromechanical systems are being increasingly deployed in nuclear industry robotics, where their great sensitivity and mechanically stable silicon structures enable reliable sensing in radiation-exposed environments. An ultra-thin silicon strain gauge without an oxide substrate layer designed for robotic electronic skin is evaluated under Co-60 γ irradiation, representative of nuclear decommissioning conditions. The sensor performance is evaluated based on electrical measurements conducted before and after irradiation, focusing on cumulative radiation-induced effects. The results show that silicon strain gauge signal maintains a high linearity (R2 > 0.99) under strain. Across an accumulated dose range up to approximately 15 Gy, only minor variations are observed, including a resistance increase within 1.3% and a reduction in gauge factor within 5% for most specimens. The radiation-induced resistance increases and sensitivity degradation results in a maximum strain estimation error of approximately 22.5 με (≈3.5%) within the tested operating range below 700 με. Full article
(This article belongs to the Special Issue Motor Control and Remote Handling in Robotic Applications)
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12 pages, 6355 KB  
Article
Comparison of Oxide Scale Morphology on FeAl-Based Alloy After Long-Term Oxidation in Air and Water Vapor at 700 °C
by Janusz Cebulski, Dorota Pasek, Maria Sozańska, Magdalena Popczyk, Jadwiga Gabor and Andrzej Swinarew
Materials 2026, 19(7), 1459; https://doi.org/10.3390/ma19071459 - 5 Apr 2026
Viewed by 627
Abstract
The present study investigates the morphology, chemical composition, and phase constitution of oxide scales formed on the Fe40Al5Cr0.2TiB intermetallic alloy after long-term oxidation at 700 °C for 2000 h in air and water vapor environments. The results demonstrate the formation of an extremely [...] Read more.
The present study investigates the morphology, chemical composition, and phase constitution of oxide scales formed on the Fe40Al5Cr0.2TiB intermetallic alloy after long-term oxidation at 700 °C for 2000 h in air and water vapor environments. The results demonstrate the formation of an extremely thin oxide scale (≈300 nm), composed predominantly of α-Al2O3, which provides effective protection against further oxidation. The oxide layer exhibits locally heterogeneous morphology, including whisker-like structures and fine crystallites. Due to the very limited thickness of the oxide scale, significant challenges arise in the interpretation of microanalytical data. It is shown that the accelerating voltage strongly influences the effective information depth in SEM-EDS analysis, leading to a substantial contribution from the substrate even at low voltages. Monte Carlo simulations were used to support the interpretation of electron–matter interactions and to explain the observed discrepancies in chemical analysis. The study demonstrates that reliable characterization of ultrathin oxide scales requires careful optimization of SEM parameters and the combined use of complementary techniques, including EDS/WDS, XRD, and EBSD. The findings highlight the importance of methodological considerations in the analysis of thin oxide layers and provide guidance for the correct interpretation of experimental data in similar systems. Full article
(This article belongs to the Special Issue Achievements in Foundry Materials and Technologies (Second Edition))
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16 pages, 3762 KB  
Article
Numerical Analysis and Design of an Ultra-Thin Flexible Transparent Metasurface for Broadband Radar-Infrared Compatible Stealth
by Liang Xu, Yijia Li, Xingyuan Wang, Jingxuan Sun and Zhixun Yang
Micromachines 2026, 17(3), 277; https://doi.org/10.3390/mi17030277 - 24 Feb 2026
Cited by 2 | Viewed by 1761
Abstract
In response to the significant challenges posed by the rapid progress of multi-spectral detection technologies to traditional stealth techniques, this paper presents a flexible transparent metasurface structure that is compatible with radar and infrared stealth. It consists of multi-layer functional patterned indium tin [...] Read more.
In response to the significant challenges posed by the rapid progress of multi-spectral detection technologies to traditional stealth techniques, this paper presents a flexible transparent metasurface structure that is compatible with radar and infrared stealth. It consists of multi-layer functional patterned indium tin oxide (ITO) films and a flexible polydimethylsiloxane (PDMS) substrate. The metasurface uses a high-duty-cycle multi-scale circular ring to achieve a microwave absorption bandwidth of 30 GHz and low infrared emissivity of 0.33 in an optimized ultra-thin 2.65 mm thickness system. The simulation results show that the metasurface achieves absorption exceeding 90% in the frequency range of 10.8–40.8 GHz, which covers common radar bands like X, Ku, K, and Ka. Furthermore, the structure exhibits polarization insensitivity and sustains stable absorption in a wide range of 60 degrees of transverse magnetic (TM) fields. Meanwhile, it decreases the radar cross-section (RCS) by more than 10 dB over a wide angular range even when bent. This study presents a feasible metasurface with ultra-thin, flexible, transparent, and multi-spectral compatibility for the next generation of stealth systems. Full article
(This article belongs to the Section E:Engineering and Technology)
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15 pages, 5266 KB  
Article
Design and Evaluation of a Laboratory-Scale Thermal ALD System: Case Study of ZnO
by J. Navarro-Rodríguez, D. Mateos-Anzaldo, J. Martínez-Castelo, R. Ramos-Irigoyen, A. Pérez-Sánchez, O. Pérez-Landeros, M. Curiel-Álvarez, E. Martínez-Guerra, H. Tiznado-Vázquez and N. Nedev
Processes 2026, 14(3), 399; https://doi.org/10.3390/pr14030399 - 23 Jan 2026
Viewed by 1897
Abstract
Atomic Layer Deposition (ALD) is a key thin-film fabrication technique that enables the growth of ultra-thin, conformal, and compositionally controlled layers for applications in nanoelectronics, optoelectronics, and energy devices. However, the high cost and operational complexity of commercial ALD systems limit their accessibility [...] Read more.
Atomic Layer Deposition (ALD) is a key thin-film fabrication technique that enables the growth of ultra-thin, conformal, and compositionally controlled layers for applications in nanoelectronics, optoelectronics, and energy devices. However, the high cost and operational complexity of commercial ALD systems limit their accessibility in academic and emerging research environments. In this work, a low-cost, automated thermal ALD system is designed, assembled, and experimentally validated for the deposition of zinc oxide (ZnO) thin films. The developed system enables precise control of precursor dosing, purge sequences, and substrate temperature via an integrated LabVIEW–Arduino control architecture, allowing reproducible and stable thin-film growth. The design allows the use of various precursors through high-precision three-way diaphragm valves. In addition, the system allows continuous purge gas flow in the reaction chamber, which enhances the drag velocity of the precursor gas, reducing dosage requirement, accelerating chamber saturation time and lowering the total consumption of precursors per deposition cycle. ZnO thin films were successfully grown on silicon and glass substrates at 200 °C using diethylzinc (DEZ) as the metal precursor and hydrogen peroxide (H2O2) as the oxidant. The process exhibited self-limiting growth characteristics typical of ALD, yielding a growth per cycle of approximately 0.8 Å. The deposited ZnO films exhibited optical transparency of 70–80% in the visible region, a refractive index of approximately 1.9, and an optical bandgap close to 3.4 eV, which are consistent with values reported for high-quality ZnO films grown in commercial ALD systems. These results demonstrate that the proposed low-cost platform is capable of producing functional ZnO thin films with properties comparable to those obtained with conventional commercial reactors. Overall, this work presents an accessible and scalable thermal ALD system that significantly reduces equipment costs while maintaining reliable process control and film quality, offering a practical framework for expanding thin-film research capabilities across microelectronics, optoelectronics, and nanotechnology laboratories. Full article
(This article belongs to the Special Issue Recent Progress in Thin Film Processes and Engineering)
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17 pages, 15287 KB  
Article
Tuning Optical Absorption and Device Performance in P3HT:PCBM Organic Solar Cells Using Annealed Silver Thin Films
by Alaa Y. Mahmoud
Polymers 2026, 18(2), 254; https://doi.org/10.3390/polym18020254 - 17 Jan 2026
Viewed by 1341
Abstract
In this study, we investigated the effect of annealing ultrathin silver (Ag) films of varying thicknesses (1–6 nm) on both their optical absorption and the performance of poly(3-hexylthiophene-2,5-diyl) (P3HT) and [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) organic solar cells (OSCs). The Ag [...] Read more.
In this study, we investigated the effect of annealing ultrathin silver (Ag) films of varying thicknesses (1–6 nm) on both their optical absorption and the performance of poly(3-hexylthiophene-2,5-diyl) (P3HT) and [6,6]-phenyl-C61-butyric acid methyl ester (PCBM) organic solar cells (OSCs). The Ag films were deposited on indium tin oxide (ITO) anodes and annealed at 300 °C for 1–2 h to modify the anodic interface. The optical and electrical properties of the resulting devices were systematically characterized and optimized. The results revealed that a 1 nm AgO layer annealed for 2 h significantly enhanced the device performance, yielding a 6% increase in power conversion efficiency compared to the standard configuration. This improvement is attributed to two main factors: (i) a 25% increase in light absorption of the AgO/P3HT:PCBM film due to localized surface plasmon resonance of Ag nanoparticles and (ii) an 11% reduction in series resistance resulting from the favorable alignment of the Ag work function with the ITO anode and the polymer HOMO, which facilitates efficient hole extraction. These findings highlight the potential of ultrathin, annealed Ag/AgO interfacial layers as an effective strategy to enhance light absorption and charge transport in OSCs. Full article
(This article belongs to the Special Issue Advances in Polymeric Organic Optoelectronic Materials and Devices)
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14 pages, 16690 KB  
Article
Experimental Study on Thermal Oxidative Aging Effects on the Performance and Compatibility of Different Types of Waterproofing Membranes
by Shaochun Li, Yang Du, Wenbin Geng, Ruiyun Zhang, Guojun Sun and Xingpeng Ma
Polymers 2026, 18(2), 162; https://doi.org/10.3390/polym18020162 - 7 Jan 2026
Cited by 2 | Viewed by 884
Abstract
As urbanization and extreme weather conditions intensify, the comprehensive performance requirements for building waterproofing systems are becoming more demanding. Single-layer waterproof membranes often struggle to meet usage requirements in complex environments, leading to the gradual rise of composite waterproof systems. This paper selects [...] Read more.
As urbanization and extreme weather conditions intensify, the comprehensive performance requirements for building waterproofing systems are becoming more demanding. Single-layer waterproof membranes often struggle to meet usage requirements in complex environments, leading to the gradual rise of composite waterproof systems. This paper selects three different types of waterproof membranes, ultra-thin reinforced self-adhesive polymer-modified bitumen waterproof membrane, polymer self-adhesive waterproof membrane, and polymer-modified bitumen root penetration-resistant waterproof membrane, and conducts a systematic study on their compatibility and durability. Through tensile performance, low-temperature flexibility, and peel compatibility tests, combined with thermal oxidative aging experiments at different aging times, the mechanical behavior, low-temperature adaptability, and interfacial bonding characteristics of the membranes were analyzed. The results show that the three membranes differ significantly in tensile performance. The root penetration-resistant membrane has the highest strength but is more brittle, the polymer self-adhesive membrane has lower strength but better stability, and the ultra-thin reinforced membrane performs better initially but lacks durability. In terms of low-temperature flexibility, the root penetration-resistant membrane demonstrates superior crack resistance and aging resistance. These divergent aging responses are closely related to differences in reinforcement structure, polymer modification, and the thermal–oxidative sensitivity of the bituminous adhesive layers. Peel compatibility tests show that the peel strength of the composite membranes of the ultra-thin reinforced and polymer self-adhesive membranes is significantly improved, indicating a good synergistic effect and compatibility. Overall, different waterproof membranes exhibit distinct compatibility mechanisms and aging patterns in composite applications, providing a scientific basis for the design and optimization of composite waterproof systems. Full article
(This article belongs to the Section Polymer Membranes and Films)
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43 pages, 3884 KB  
Review
Advanced Layer Fabrication Technologies in Solid Oxide Fuel Cells: From Traditional Methods to Additive and Thin-Film Strategies
by Serikzhan Opakhai, Asset Kabyshev, Marzhan Kubenova, Zhassulan Zeinulla, Bakytbek Mauyey and Saira Sakhabayeva
Nanoenergy Adv. 2026, 6(1), 2; https://doi.org/10.3390/nanoenergyadv6010002 - 25 Dec 2025
Cited by 3 | Viewed by 2774
Abstract
This review examines modern approaches to layer formation in solid oxide fuel cells (SOFCs), focusing on traditional, thin-film, and additive manufacturing methods. A systematic comparison of technologies, including slip casting, screen printing, CVD, PLD, ALD, HiPIMS, inkjet, aerosol, and microextrusion printing, is provided. [...] Read more.
This review examines modern approaches to layer formation in solid oxide fuel cells (SOFCs), focusing on traditional, thin-film, and additive manufacturing methods. A systematic comparison of technologies, including slip casting, screen printing, CVD, PLD, ALD, HiPIMS, inkjet, aerosol, and microextrusion printing, is provided. It is shown that traditional methods remain technologically robust but are limited in their capabilities for miniaturization and interfacial architecture design. Modern thin-film and additive approaches provide high spatial accuracy, improved ion-electron characteristics, and flexibility in the design of multilayer structures; however, they require addressing issues related to scalability, ink stability, interfacial compatibility, and reproducibility. Particular attention is paid to interfacial engineering methods, such as functionally graded layers, nanostructured infiltration, and temperature-controlled 3D printing. Key challenges are discussed, including thermal instability of materials, the limited gas impermeability of ultra-thin electrolytes, and degradation during long-term operation. Development prospects lie in the integration of hybrid methods, the digitalization of deposition processes, and the implementation of intelligent control of printing parameters. The presented analysis forms the basis for further research into the scalable and highly efficient production of next-generation SOFCs designed for low-temperature operation and long-term operation in future energy systems. Full article
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16 pages, 1803 KB  
Article
Layer-by-Layer Hybrid Film of PAMAM and Reduced Graphene Oxide–WO3 Nanofibers as an Electroactive Interface for Supercapacitor Electrodes
by Vanderley F. Gomes Junior, Danilo A. Oliveira, Paulo V. Morais and José R. Siqueira Junior
Nanoenergy Adv. 2025, 5(4), 22; https://doi.org/10.3390/nanoenergyadv5040022 - 12 Dec 2025
Viewed by 806
Abstract
Tungsten oxide (WO3) nanostructures have emerged as promising electroactive materials due to their high pseudocapacitance, structural versatility, and chemical stability, while reduced graphene oxide (rGO) provides excellent electrical conductivity and surface area. The strategic combination of these nanomaterials in hybrid electrodes [...] Read more.
Tungsten oxide (WO3) nanostructures have emerged as promising electroactive materials due to their high pseudocapacitance, structural versatility, and chemical stability, while reduced graphene oxide (rGO) provides excellent electrical conductivity and surface area. The strategic combination of these nanomaterials in hybrid electrodes has gained attention for enhancing the energy storage performance of supercapacitors. In this work, we report the fabrication and electrochemical performance of nanostructured multilayer films based on the electrostatic Layer-by-Layer (LbL) self-assembly of poly (amidoamine) (PAMAM) dendrimers alternated with tungsten oxide (WO3) nanofibers dispersed in reduced graphene oxide (rGO). The films were deposited onto indium tin oxide (ITO) substrates and subsequently subjected to electrochemical reduction. UV-Vis spectroscopy confirmed the linear growth of the multilayers, while atomic force microscopy (AFM) revealed homogeneous surface morphology and thickness control. Electrochemical characterization by cyclic voltammetry (CV) and galvanostatic charge–discharge (GCD) revealed a predominantly electrical double-layer capacitive (EDLC) behavior. From the GCD measurements (PAMAM/rGO-WO3)20 films achieved an areal capacitance of ≈2.20 mF·cm−2, delivering an areal energy density of ≈0.17 µWh·cm−2 and an areal power density of ≈2.10 µW·cm−2, demonstrating efficient charge storage in an ultrathin electrode architecture. These results show that the synergistic integration of PAMAM dendrimers, reduced graphene oxide, and WO3 nanofibers yields a promising strategy for designing high-performance electrode materials for next-generation supercapacitors. Full article
(This article belongs to the Special Issue Hybrid Energy Storage Systems Based on Nanostructured Materials)
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14 pages, 4228 KB  
Article
Room Temperature UV Photodetector Based on Aero-Titania
by Mircea Nicolaescu, Tudor Braniste, Corina Orha, Mina-Ionela Morariu, Sebastian Lehmann, Kornelius Nielsch, Ion M. Tiginyanu, Raluca Faur, Victor Zalamai, Carmen Lazau and Cornelia Bandas
Int. J. Mol. Sci. 2025, 26(22), 11035; https://doi.org/10.3390/ijms262211035 - 14 Nov 2025
Cited by 1 | Viewed by 1072
Abstract
This research demonstrates, for the first time, the integration of aero-titania material in sensor devices. An innovative approach for the practical application of aero-titania (aero-TiO2) materials in photodetectors and the characterization under ultraviolet irradiation was assessed. The fabrication of aero-materials was [...] Read more.
This research demonstrates, for the first time, the integration of aero-titania material in sensor devices. An innovative approach for the practical application of aero-titania (aero-TiO2) materials in photodetectors and the characterization under ultraviolet irradiation was assessed. The fabrication of aero-materials was carried out through the atomic layer deposition (ALD) of titanium dioxide ultrathin layers on a sacrificial network consisting of zinc oxide micro-tetrapods. This process was followed by a selective etching of the sacrificial ZnO template and formation of aero-titania hollow micro-tetrapods. The obtained material has been characterized using UV-Vis spectroscopy, scanning electron microscopy (SEM), and X-ray diffraction (XRD) analysis. The development of photodetectors was achieved through the sequential spin-coating deposition of aero-TiO2 onto an interdigitated ceramic electrode. The obtained results show that, for high-intensity ultraviolet, the maximum sensitivity was reached for the two-deposited-layer aero-TiO2 sensor at about 23, since for the low-intensity UV the highest sensitivity was recorded for the one-deposited-layer aero-TiO2 sensor at about 12. In terms of the responsivity, the highest response was obtained for the one-deposited-layer aero-TiO2 sensor under low-intensity illumination, reaching about 1.23 × 10−4 A W−1 cm−2. Thus, the aero-TiO2 structure demonstrates the practical viability and application potential of this emerging class of materials in advanced sensing technologies. Full article
(This article belongs to the Special Issue State-of-the-Art Electrochemical Reaction Technologies)
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13 pages, 2257 KB  
Article
Scalable High-Yield Exfoliation of Hydrophilic h-BN Nanosheets via Gallium Intercalation
by Sungsan Kang, Dahun Kim, Seonyou Park, Sung-Tae Lee, John Hong, Sanghyo Lee and Sangyeon Pak
Inorganics 2025, 13(10), 314; https://doi.org/10.3390/inorganics13100314 - 25 Sep 2025
Cited by 5 | Viewed by 3162
Abstract
Hexagonal boron nitride (h-BN) possesses a unique combination of a wide bandgap, high thermal conductivity, and chemical inertness, making it a key insulating and thermal management material for advanced electronics and nanocomposites. However, its intrinsic hydrophobicity and strong interlayer van der Waals forces [...] Read more.
Hexagonal boron nitride (h-BN) possesses a unique combination of a wide bandgap, high thermal conductivity, and chemical inertness, making it a key insulating and thermal management material for advanced electronics and nanocomposites. However, its intrinsic hydrophobicity and strong interlayer van der Waals forces severely limit exfoliation efficiency and dispersion stability, particularly in scalable liquid-phase processes. Here, we report a synergistic exfoliation strategy that integrates acid-induced hydroxylation with gallium (Ga) intercalation to achieve high-yield (>80%) production of ultrathin (<4 nm) hydrophilic h-BN nanosheets. Hydroxylation introduces abundant -OH groups, expanding interlayer spacing and significantly increasing surface polarity, while Ga intercalation leverages its native Ga2O3 shell to form strong interfacial interactions with hydroxylated basal planes. This oxide-mediated adhesion facilitates efficient layer separation under mild sonication, yielding nanosheets with well-preserved lateral dimensions and exceptional dispersion stability in polar solvents. Comprehensive characterization confirms the sequential chemical and structural modifications, revealing the crucial roles of hydroxylation-induced activation and Ga2O3 assisted wettability enhancement. This combined chemical activation–soft metallic intercalation approach provides a scalable, solution-processable route to high-quality h-BN nanosheets, opening new opportunities for their integration into dielectric, thermal interface, and multifunctional composite systems. Full article
(This article belongs to the Special Issue Physicochemical Characterization of 2D Materials)
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13 pages, 3420 KB  
Article
Semiconducting Tungsten Trioxide Thin Films for High-Performance SERS Biosensors
by Hao Liu, Liping Chen, Bicheng Li, Haizeng Song, Chee Leong Tan, Yi Shi and Shancheng Yan
Nanomaterials 2025, 15(18), 1393; https://doi.org/10.3390/nano15181393 - 10 Sep 2025
Cited by 2 | Viewed by 1375
Abstract
Surface-enhanced Raman Scattering (SERS) enables ultrasensitive detection but is often hindered by biocompatibility and sustainability concerns due to its reliance on noble metal substrates. To overcome these limitations, we develop a semiconductor-based SERS platform utilizing ultrathin tungsten trioxide (WO3) nanofilms synthesized [...] Read more.
Surface-enhanced Raman Scattering (SERS) enables ultrasensitive detection but is often hindered by biocompatibility and sustainability concerns due to its reliance on noble metal substrates. To overcome these limitations, we develop a semiconductor-based SERS platform utilizing ultrathin tungsten trioxide (WO3) nanofilms synthesized via a facile annealing process on fluorine-doped tin oxide (FTO). This system achieves an impressive Raman enhancement factor of 1.36 × 106, enabling ultrasensitive detection of rhodamine 6G (R6G) and methylene blue (MB) at ultralow concentrations, surpassing conventional metal-based SERS platforms. It is further suggested that this is a substrate that can be easily coupled to other metals. An application for the detection of adenine molecules is realized through layered WO3-Au NPs composites, where embedded gold nanoparticles act as plasma “hot spots” to amplify the sensitivity. Density functional theory (DFT) calculations and band structure analysis confirm that synergistic interface charge transfer and naturally formed oxygen vacancies enhance performance. By combining semiconductor compatibility with other metal amplification, this WO3-based SERS platform offers a sustainable and high-performance alternative to conventional substrates, paving the way for environmentally friendly and scalable Raman sensing technologies. Full article
(This article belongs to the Section Nanoelectronics, Nanosensors and Devices)
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