Enhanced Oxygen Evolution Electrocatalysis in Strained A-Site Cation Deficient LaNiO3 Perovskite Thin Films.

As the BO6 octahedral structure in perovskite oxide is strongly linked with electronic behavior, it is actively studied for various fields such as metal-insulator transition, superconductivity, and so on. However, the research about the relationship between water-splitting activity and BO6 structure is largely lacking. Here, we report the oxygen evolution reaction (OER) of LaNiO3 (LNO) by changing the NiO6 structure using compositional change and strain. The 5 atom % La deficiency in LNO resulted in an increase of the Ni-O-Ni bond angle and an expansion of bandwidth, enhancing the charge transfer ability. In-plane compressive strain derives the higher dz2 orbital occupancy, leading to suitable metal-oxygen bond strength for OER. Because of the synergistic effect of A-site deficiency and compressive strain, the overpotential (η) of compressively strained L0.95NO film is reduced to 130 mV at j = 30 µA/cm2 compared with nonstrained LNO (η = 280 mV), indicating a significant enhancement in OER.

Fabrication and Analysis of Perovskite Solar Cells (PSCs) by Using Phosphor and TiO2 Photoelectrode.

In this work, to explore the influence of phosphor additives on the conversion efficiency of perovskite solar cells (PSC), we introduce a Y3Al5O12:Ce3+ (YAG:Ce3+) phosphor layer. The YAG:Ce3+ nanophosphor acts as a light down-converting material to absorb high energy photons and emit lower energy photons that match well with the absorption of the perovskite layer, yielding more excited photo-generated electron-hole pairs. Therefore, the incident solar light can be harvested more effectively. We used 8 mg/ml of TiO2 mixed with YAG:Ce3+ in the PSCs and realized a light-to-electric energy conversion efficiency of 13.34%, a short circuit current density of 21.23 mA/cm², an open circuit voltage of 0.97 V, and a FF of 55.96%. Higher efficiencies were achieved for PSCs with phosphor-mixed TiO2 than for cells with pure TiO2 nanoparticles. The samples were characterized by XRD, SEM, UV-vis, PL, and IV-curves. Photoelectrode DSSC with light-to-electric energy conversion efficiency was achieved under a simulated solar light irradiation of 100 mW/cm² (AM 1.5).

High-Throughput Analysis of New Bone Formation and Bone Substitutes After Maxillary Sinus Floor Elevation Using Synchrotron Radiation Micro-Computed Tomography.

This study addresses the usability of synchrotron radiation micro-computed tomography (SR-µCT) for the high-throughput examination of bone biopsy specimens harvested from maxillary sinus floor elevation (MSFE) patients. The experimental procedure devised for efficient data acquisition and volume analysis of bone biopsy specimens of sinus lift using SR-µCT is presented. The measuring was done in approximately one minute per field of view; 3D image visualization and volume analysis could be performed in one hour. Six months after the sinus floor augmentation procedure, bone biopsy specimens were collected. Six specimens were studied. The percentages of bone measured by 3D volumetric analysis using SR-µCT and 2D area analysis using conventional histomorphometry were compared. A specimen was measured in any cross section, and the analysis was readily extended to the entire volume of the specimen. Significant differences between the 2D and the 3D measurement results were revealed. Based on our observations, we report structural inhomogeneity in the grafted volume of the MSFE site. The new bone volume assessed by SR-µCT correlates with the percentage of bone as assessed by conventional 2D histologic photomicrographs. SR-µCT is thus a reliable technique to determine the volume of newly formed bone at the MSFE.

Effects of Enhanced Hydrophilic Titanium Dioxide-Coated Hydroxyapatite on Bone Regeneration in Rabbit Calvarial Defects.

The regeneration of bone defects caused by periodontal disease or trauma is an important goal. Porous hydroxyapatite (HA) is an osteoconductive graft material. However, the hydrophobic properties of HA can be a disadvantage in the initial healing process. HA can be coated with TiO2 to improve its hydrophilicity, and ultraviolet irradiation (UV) can further increase the hydrophilicity by photofunctionalization. This study was designed to evaluate the effect of 5% TiO2-coated HA on rabbit calvarial defects and compare it with that of photofunctionalization on new bone in the early stage. The following four study groups were established, negative control, HA, TiO2-coated HA, and TiO2-coated HA with UV. The animals were sacrificed and the defects were assessed by radiography as well as histologic and histomorphometric analyses. At 2 and 8 weeks postoperatively, the TiO2-coated HA with UV group and TiO2-coated HA group showed significantly higher percentages of new bone than the control group (p < 0.05). UV irradiation increased the extent of new bone formation, and there was a significant difference between the TiO2-coated HA group and TiO2-coated HA with UV group. The combination of TiO2/HA and UV irradiation in bone regeneration appears to induce a favorable response.

Broadband terahertz generation and detection at 10 nm scale.

Terahertz (0.1-30 THz) radiation reveals a wealth of information that is relevant for material, biological, and medical sciences with applications that span chemical sensing, high-speed electronics, and coherent control of semiconductor quantum bits. To date, there have been no methods capable of controlling terahertz (THz) radiation at molecular scales. Here we report both generation and detection of broadband terahertz field from 10 nm scale oxide nanojunctions. Frequency components of ultrafast optical radiation are mixed at these nanojunctions, producing broadband THz emission. These same devices detect THz electric fields with comparable spatial resolution. This unprecedented control, on a scale of 4 orders of magnitude smaller than the diffraction limit, creates a pathway toward THz-bandwidth spectroscopy and control of individual nanoparticles and molecules.

Anomalous high mobility in LaAlO3/SrTiO3 nanowires.

Nanoscale control of the metal-insulator transition at the interface between LaAlO(3) and SrTiO(3) provides a pathway for reconfigurable, oxide-based nanoelectronics. Four-terminal transport measurements of LaAlO(3)/SrTiO(3) nanowires at room temperature (T = 300 K) reveal an equivalent 2D Hall mobility greatly surpassing that of bulk SrTiO(3) and approaching that of n-type Si nanowires of comparable dimensions. This large enhancement of mobility is relevant for room-temperature device applications.

A self-powered photodetector through facile processing using polyethyleneimine/carbon quantum dots for highly sensitive UVC detection.

Ultraviolet C (UVC) photodetectors have garnered considerable attention recently because the detection of UVC is critical for preventing skin damage in humans, monitoring environmental conditions, detecting power aging in facilities, and military applications. As UVC detectors are "solar-blind", they encounter less interference than other environmental signals, resulting in low disturbance levels. This study employed a natural precursor (glucose) and a one-step ultrasonic reaction procedure to prepare carbon quantum dots (CQDs), which served as a convenient and environmentally friendly material to combine with polyethyleneimine (PEI). The prepared materials were used to develop a self-powered, high-performance UVC photodetector. The thickness of the constitutive film was investigated in detail based on the conditions of the electron transport pathway and trap positions to further improve the performance of the PEI/CQD photodetectors. Under the optimized conditions, the photodetector could generate a strong signal (1.5 mA W-1 at 254 nm) and exhibit high detectability (1.8 × 1010 Jones at 254 nm), an ultrafast response, and long-term stability during the power supply sequence. The developed solar-blind UVC photodetector can be applied in various ways to monitor UVC in an affordable, straightforward, and precise manner.

Polymer-Doped SnO2 as an Electron Transport Layer for Highly Efficient and Stable Perovskite Solar Cells.

To produce highly efficient and repeatable perovskite solar cells (PSCs), comprehending interfacial loss and developing approaches to ameliorate interfacial features is essential. Nonradiative recombination at the SnO2-perovskite interface in SnO2-based perovskite solar cells (PSCs) leads to significant potential loss and variability in device performance. To improve the quality of the SnO2 electron transport layer, a novel polymer-doped SnO2 matrix, specifically using polyacrylic acid, was developed. This matrix is formed by spin-coating a SnO2 colloidal solution that includes polymers. The polymer aids in dispersing nanoparticles within the substrate and is evenly distributed in the SnO2 solution. As a result of the polymer addition, the density and wetting properties of the SnO2 layer substantially improved. Subsequently, perovskite-based photovoltaic devices comprising SnO2 and Spiro-OMeTAD layers and using (FAPbI3)0.97(MAPbBr3)0.03 perovskite are constructed. These optimized devices exhibited an increased efficiency of 17.2% when compared to the 15.7% power conversion efficiency of the control device. The incorporation of polymers in the electron transport layer potentially enables even better performance in planar perovskite solar cells.

Oxide-based platform for reconfigurable superconducting nanoelectronics.

We report quasi-1D superconductivity at the interface of LaAlO3 and SrTiO3. The material system and nanostructure fabrication method supply a new platform for superconducting nanoelectronics. Nanostructures having line widths w ~ 10 nm are formed from the parent two-dimensional electron liquid using conductive atomic force microscope lithography. Nanowire cross-sections are small compared to the superconducting coherence length in LaAlO3/SrTiO3, placing them in the quasi-1D regime. Broad superconducting transitions versus temperature and finite resistances in the superconducting state well below Tc ≈ 200 mK are observed, suggesting the presence of fluctuation- and heating-induced resistance. The superconducting resistances and V-I characteristics are tunable through the use of a back gate. Four-terminal resistances in the superconducting state show an unusual dependence on the current path, varying by as much as an order of magnitude. This new technology, i.e., the ability to 'write' gate-tunable superconducting nanostructures on an insulating LaAlO3/SrTiO3 'canvas', opens possibilities for the development of new families of reconfigurable superconducting nanoelectronics.

Recent Advances of Doped SnO2 as Electron Transport Layer for High-Performance Perovskite Solar Cells.

Perovskite solar cells (PSCs) have garnered considerable attention over the past decade owing to their low cost and proven high power conversion efficiency of over 25%. In the planar heterojunction PSC structure, tin oxide was utilized as a substitute material for the TiO2 electron transport layer (ETL) owing to its similar physical properties and high mobility, which is suitable for electron mining. Nevertheless, the defects and morphology significantly changed the performance of SnO2 according to the different deposition techniques, resulting in the poor performance of PSCs. In this review, we provide a comprehensive insight into the factors that specifically influence the ETL in PSC. The properties of the SnO2 materials are briefly introduced. In particular, the general operating principles, as well as the suitability level of doping in SnO2, are elucidated along with the details of the obtained results. Subsequently, the potential for doping is evaluated from the obtained results to achieve better results in PSCs. This review aims to provide a systematic and comprehensive understanding of the effects of different types of doping on the performance of ETL SnO2 and potentially instigate further development of PSCs with an extension to SnO2-based PSCs.

Toward Industrial Production of a High-Performance Self-Powered Ultraviolet Photodetector Using Nanoporous Al-Doped ZnO Thin Films.

Al-doped ZnO (AZO) thin films are effective n-type semiconductors for ultraviolet (UV) detection because of their low cost, high electron mobility, and high sensitivity to UV light, especially in the UVA spectrum. However, a reasonable compromise between performance (such as sensitivity, detectivity, and response time) and fabrication ease remains an obstacle to the practicability of AZO-based UV photodetectors. To address this issue, we propose an efficient strategy to achieve a large AZO photoactive area for outstanding performance, along with a facile sol-gel method. Consequently, the device exhibits a superb on/off ratio of >104, a high detectivity of 1.85 × 1012 Jones, and a fast response speed under 365 nm UVA illumination without external energy consumption. Hence, this study suggests a self-powered and high-performance nanoporous AZO-based UVA detector with an environmentally friendly scalable process that satisfies industrial production requirements for numerous practical UV-detection applications.

Deep-Ultraviolet Transparent Electrode Design for High-Performance and Self-Powered Perovskite Photodetector.

In this study, a highly crystalline and transparent indium-tin-oxide (ITO) thin film was prepared on a quartz substrate via RF sputtering to fabricate an efficient bottom-to-top illuminated electrode for an ultraviolet C (UVC) photodetector. Accordingly, the 26.6 nm thick ITO thin film, which was deposited using the sputtering method followed by post-annealing treatment, exhibited good transparency to deep-UV spectra (67% at a wavelength of 254 nm), along with high electrical conductivity (11.3 S/cm). Under 254 nm UVC illumination, the lead-halide-perovskite-based photodetector developed on the prepared ITO electrode in a vertical structure exhibited an excellent on/off ratio of 1.05 × 104, a superb responsivity of 250.98 mA/W, and a high specific detectivity of 4.71 × 1012 Jones without external energy consumption. This study indicates that post-annealed ITO ultrathin films can be used as electrodes that satisfy both the electrical conductivity and deep-UV transparency requirements for high-performance bottom-illuminated optoelectronic devices, particularly for use in UVC photodetectors.

Self-Powered UVC Photodetector Based on Europium Metal-Organic Framework for Facile Monitoring Invisible Fire.

The effective use of a europium metal-organic framework (Eu-MOF) as a photoabsorber material has been reported. Using the advantages of Eu-MOFs including simple preparation, wide bandgap structure, and stability in the environment, a self-powered and high UVC-selectivity detector based on Eu-MOF nanoparticles was prepared with a simple device geometry. The as-fabricated photodetector was highly sensitive to 254 nm UV illumination without an external power supply. Accordingly, it exhibited a high UVC-to-UVA rejection ratio (I254/I365 ≈ 40) and UVC-to-solar rejection ratio (I254/Isolar light ≈ 34), a fast response time of 98/122 ms, a comparable on/off photocurrent ratio (107.33), and superior stability. The self-powered Eu-MOF photodetector can detect and monitor UV emission from an invisible fire in an early state at room temperature, suggesting practical use as a potential optoelectronic device.

Metal Electrode-Free Halide Perovskite-Based Flexible Ultraviolet-C Photodetector with Large Area.

Ultraviolet-C (UVC) photodetector has appealed to a numerous number of research owing to its manifold applications in wireless communication, flame monitoring, and medicine. However, in addition to superior performance and high stability of recent studies, scalability and production cost are important factors for commercialization and practical implementation. In this study, a halide perovskite-based UVC photodetector was fabricated using spin-coating process and low-temperature annealing. Corning® Willow® Glass was selected as the substrate for the bottom-illuminated device due to its flexibility and exceptional optical transmission (approximately 60%) in the deep-UV region. The device had a vertical structure with a large active area (1 cm2) owing to the judicious utilization of electrodes. Under bent state with a curvature radius of 25 mm, the as-fabricated device exhibited high response and repeatability with an on/off ratio of 9.57 × 103, a fast response speed of 45/46 ms (rise/fall times) at zero bias under the illumination of a 254-nm UV lamp. The results are based on a flexible and lightweight photodetector without the utilization of notable metal electrodes.

Recent advances in self-powered and flexible UVC photodetectors.

Ultraviolet-C (UVC) radiation is employed in various applications, including irreplaceable applications in military and civil fields, such as missile guidance, flame detection, partial discharge detection, disinfection, and wireless communication. Although most modern electronics are based on Si, UVC detection technology remains a unique exception because the short wavelength of UV radiation makes efficient detection with Si difficult. In this review, recent challenges in obtaining ideal UVC photodetectors with various materials and various forms are introduced. An ideal photodetector must satisfy the following requirements: high sensitivity, fast response speed, high on/off photocurrent ratio, good regional selectivity, outstanding reproducibility, and superior thermal and photo stabilities. UVC detection is still in its infancy compared to the detection of UVA as well as other photon spectra, and recent research has focused on different key components, including the configuration, material, and substrate, to acquire battery-free, super-sensitive, ultra-stable, ultra-small, and portable UVC photodetectors. We introduce and discuss the strategies for fabricating self-powered UVC photodetectors on flexible substrates in terms of the structure, material, and direction of incoming radiation. We also explain the physical mechanisms of self-powered devices with various architectures. Finally, we present a brief outlook that discusses the challenges and future strategies for deep-UVC photodetectors.

Nonvolatile Control of Metal-Insulator Transition in VO2 by Ferroelectric Gating.

Controlling phase transitions in correlated materials yields emergent functional properties, providing new aspects to future electronics and a fundamental understanding of condensed matter systems. With vanadium dioxide (VO2 ), a representative correlated material, an approach to control a metal-insulator transition (MIT) behavior is developed by employing a heteroepitaxial structure with a ferroelectric BiFeO3 (BFO) layer to modulate the interaction of correlated electrons. Owing to the defect-alleviated interfaces, the enhanced coupling between the correlated electrons and ferroelectric polarization is successfully demonstrated by showing a nonvolatile control of MIT of VO2 at room temperature. The ferroelectrically-tunable MIT can be realized through the Mott transistor (VO2 /BFO/SrRuO3 ) with a remanent polarization of 80 µC cm-2 , leading to a nonvolatile MIT behavior through the reversible electrical conductance with a large on/off ratio (≈102 ), long retention time (≈104 s), and high endurance (≈103 cycles). Furthermore, the structural phase transition of VO2 is corroborated by ferroelectric polarization through in situ Raman mapping analysis. This study provides novel design principles for heteroepitaxial correlated materials and innovative insight to modulate multifunctional properties.

Silicon-Based Technologies for Flexible Photovoltaic (PV) Devices: From Basic Mechanism to Manufacturing Technologies.

Over the past few decades, silicon-based solar cells have been used in the photovoltaic (PV) industry because of the abundance of silicon material and the mature fabrication process. However, as more electrical devices with wearable and portable functions are required, silicon-based PV solar cells have been developed to create solar cells that are flexible, lightweight, and thin. Unlike flexible PV systems (inorganic and organic), the drawbacks of silicon-based solar cells are that they are difficult to fabricate as flexible solar cells. However, new technologies have emerged for flexible solar cells with silicon. In this paper, we describe the basic energy-conversion mechanism from light and introduce various silicon-based manufacturing technologies for flexible solar cells. In addition, for high energy-conversion efficiency, we deal with various technologies (process, structure, and materials).

Study on Performance Improvements in Perovskite-Based Ultraviolet Sensors Prepared Using Toluene Antisolvent and CH3NH3Cl.

In this study, a simply structured perovskite-based ultraviolet C (UVC) sensor was prepared using a one-step, low-temperature solution-processing coating method. The UVC sensor utilized CH3NH3PbBr3 perovskite as the light-absorbing layer. To improve the characteristics of CH3NH3PbBr3, an antisolvent process using toluene and the addition of CH3NH3Cl were introduced. The device with these modifications exhibited a response rise/fall time of 15.8/16.2 ms, mobility of 158.7 cm2/V·s, responsivity of 4.57 mA/W, detectivity of 1.02 × 1013 Jones, and external quantum efficiency of 22.32% under the 254-nm UV illumination. Therefore, this methodology could be a good approach in facilitating UVC detection.

Particle Size Effect of Lanthanum-Modified Bismuth Titanate Ceramics on Ferroelectric Effect for Energy Harvesting.

Piezoelectric nanogenerators (PNGs) have been studied as renewable energy sources. PNGs consisting of organic piezoelectric materials such as poly(vinylidene fluoride) (PVDF) containing oxide complex powder have attracted much attention for their stretchable and high-performance energy conversion. In this study, we prepared a PNG combined with PVDF and lanthanum-modified bismuth titanate (Bi4-XLaXTi3O12, BLT) ceramics as representative ferroelectric materials. The inserted BLT powder was treated by high-speed ball milling and its particle size reduced to the nanoscale. We also investigated the effect of particle size on the energy-harvesting performance of PNG without polling. As a result, nano-sized powder has a much larger surface area than micro-sized powder and is uniformly distributed inside the PNG. Moreover, nano-sized powder-mixed PNG generated higher power energy (> 4 times) than the PNG inserted micro-sized powder.

Enhancing Performance of Perovskite Solar Cells by TiCl4 Treatment on the Surface Roughness of the Titanium Dioxide Layer.

Perovskite solar cells have been attracting extensive attention because of their superior photovoltaic performances and lower costs as compared to those of prevailing photovoltaic technologies. There are four main interfaces in perovskite solar cells: flourine-doped tin oxide/electron transport layer, electron transport layer/perovskite layer, perovskite layer/hole transport layer, and hole transport layer/metal electrode. Among them, the interface between the perovskite layer (general formula RPbX3) and electron transport layer significantly affects the power conversion efficiency. In this study, a layer of TiO2, which is the most popular metal oxides used for perovskite solar cells applications, was deposited as the electron transport layer. To enhance the perovskite solar cells performance, surface treatment was performed with TiCl4 (80 mM). To investigate the effect of TiCl4 treatment, ultraviolet-visible spectroscopy was performed on the perovskite film. Atomic force microscopy, X-ray diffraction, scanning electron microscopy and performance of perovskite solar cells have been also evaluated in this paper. The results indicated that the TiCl4 treatment significantly improved the perovskite solar cells performance.