Design of multi-layer anti-reflection coating for terrestrial solar panel glass

To date, there is no ideal anti-reflection (AR) coating available on solar glass which can effectively transmit the incident light within the visible wavelength range. However, there is a need to develop multifunctional coating with superior anti-reflection properties and self-cleaning ability meant to be used for solar glass panels. In spite of self-cleaning ability of materials like TiO₂ and ZnO, these coatings on glass substrate have tendency to reduce light transmission due to their high refractive indices than glass. Thus, to infuse the anti-reflective property, a low refractive index, SiO₂ layer needs to be used in conjunction with TiO₂ and ZnO layers. In such case, the optimization of individual layer thickness is crucial to achieve maximum transmittance of the visible light. In the present study, we propose an omni-directional anti-reflection coating design for the visible spectral wavelength range of 400–700 nm, where the maximum intensity of light is converted into electrical energy. Herein, we employ the quarter wavelength criteria using SiO₂, TiO₂ and ZnO to design the coating composed of single, double and triple layers. The thickness of individual layers was optimized for maximum light transmittance using essential Mcleod simulation software to produce destructive interference between reflected waves and constructive interference between transmitted waves.     

Novel construction of CdS-encapsulated TiO2 nano test tubes corked with ZnO nanorods

A novel TiO₂ nanotube array/CdS nanoparticle/ZnO nanorod (TiO₂ NT/CdS/ZnO NR) photocatalyst was constructed by chemical assembling CdS into the TiO₂ NTs, and then laying ZnO NRs on the surface. The SEM results showed that the TiO₂ NTs looked like many “nano test tubes” and the ZnO NRs served as the corks to seal the nozzle. This photocatalyst exhibited a wide absorption range (200-535 nm) in both ultraviolet and visible regions (UV-vis region), and maintained very high photoelectrocatalytic (PEC) activities. The maximum photoelectric conversion efficiencies (η) of TiO₂ NT/CdS/ZnO NRs are 31.8 and 5.98% under UV light (365 nm) and visible light (420-800 nm), respectively.     

CdS-sensitized ZnO nanorod arrays coated with TiO2 layer for visible light photoelectrocatalysis

A novel ZnO/CdS/TiO₂ nanorod array composite structure was fabricated by depositing CdS-sensitized layer onto ZnO nanorod arrays via chemical bathing deposition and subsequently coated by TiO₂ protection layer via a vacuum dip-coating process. The films were characterized by x-ray diffraction, field emission scanning electron microscopy, energy dispersive spectrum, and UV–Vis diffuse reflectance spectroscopy. For the films severed as the photoanodes, linear sweep voltammetry and transient photocurrent (i _ph) were investigated in a three-electrode system. The photoelectrocatalytic activity was evaluated by the degradation of methylene blue (MB) under visible light irradiation. The results show that the oriented ZnO nanorods are adhered by relatively uniform CdS-sensitized layer and coated with TiO₂ layer. Both the coated and uncoated CdS-sensitized ZnO nanorod arrays exhibit the visible light response and the photoelectrocatalytic activity on the degradation of MB under visible light irradiation. The ZnO/CdS/TiO₂ nanorod array film possesses stable and superior photoelectrocatalytic performance owing to the TiO₂ thin layer protecting the CdS from photocorrosion.     

Fabrication of patterned CdS/TiO2 heterojunction by wettability template-assisted electrodeposition

A wettability template-assisted process was applied to selectively deposit cadmium sulfide (CdS) nanospheres on TiO₂ nanotube layers to form uniformly coupled CdS/TiO₂ semiconductor heterojunction micropatterns. The effect of deposition time on the size and morphology of the as-prepared CdS/TiO₂ array patterns was investigated. It is shown that the CdS nanocrystals with a highly ordered, hierarchically porous structure in nano-micro dual scales could be selectively grown within the superhydrophilic regions. The patterned CdS/TiO₂ heterojunctions have demonstrated enhanced photo-response under both UV and visible light irradiation. This novel template patterning technique, which is based on wettability contrast, can be applied to a broad range of technological areas, such as sensor arrays and optoelectronic devices.     

Preparation of Fe-doped TiO2 nanotube arrays and their photocatalytic activities under visible light

Fe-doped TiO₂ nanotube arrays have been prepared by the template-based liquid phase deposition method. Their morphologies, structures and optical properties were investigated by scanning electron microscopy, transmission electron microscopy, X-ray diffraction and UV-vis absorption spectroscopy. Their photocatalytic activities were evaluated by the degradation of methylene blue under visible light. The UV-vis absorption spectra of the Fe-doped TiO₂ nanotube arrays showed a red shift and an enhancement of the absorption in the visible region compared to the undoped sample. The Fe-doped TiO₂ nanotube arrays exhibited good photocatalytic activities under visible light irradiation, and the optimum dopant amount was found to be 5.9 at% in our experiments.     

Preparation and photocatalytic activity of N-doped TiO2 nanotube array films

The N-doped TiO₂ nanotube array films were fabricated directly by one-step electrochemical anodic oxidation of Ti foils in an HF electrolyte containing ammonium and nitrate ions. The as-prepared samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), energy dispersive spectrometer (EDX), and ultraviolet–visible (UV–vis) absorption spectroscopy, respectively. The photocatalytic activities were evaluated by the degradation of methyl orange (MO) under visible light irradiation. The results showed that N dopant was successfully introduced into the TiO₂ nanotube array films. The N-doped TiO₂ nanotube array films showed a red shift and an enhancement of the absorption in the visible light region compared to the undoped sample. The photocatalytic activities of the N-doped TiO₂ samples were much higher than those of the undoped sample. A maximum enhancement of photocatalytic activity was achieved for the N-doped TiO₂ sample prepared in 0.07 M HF electrolyte containing 1.0 M NH₄NO₃, and 81% of MO was degraded in 150 min under visible light irradiation.     

ZnO Film UV Photodetector with Enhanced Performance: Heterojunction with CdMoO4 Microplates and the Hot Electron Injection Effect of Au Nanoparticles

A novel CdMoO₄–ZnO composite film is prepared by spin‐coating CdMoO₄ microplates on ZnO film and is constructed as a heterojunction photodetector (PD). With an optimized loading amount of CdMoO₄ microplates, this composite film PD achieves a ≈18‐fold higher responsivity than pure ZnO film PD at 5 V bias under 350 nm (0.15 mW cm⁻²) UV light illumination, and its decay time shortens to half of the original value. Furthermore, Au nanoparticles are then deposited to modify the CdMoO₄–ZnO composite film, and the as‐constructed photodetector with an optimized deposition time of Au nanoparticles yields an approximately two‐fold higher photocurrent under the same condition, and the decay time reduces by half. The introduced CdMoO₄ microplates form type‐II heterojunctions with ZnO film and improve the photoelectric performance. The hot electrons from Au nanoparticles are injected into the CdMoO₄–ZnO composite film, leading to the increased photocurrent. When the light is off, the Schottky barriers formed between Au nanoparticles and CdMoO₄–ZnO composite film block the carrier transportation and accelerate the decay process of current. The study on Au‐nanoparticle‐modified CdMoO₄–ZnO composite film provides a facile method to construct ZnO film based PD with novel structure and high photoelectric performance.     

Rapid synthesis, characterization and optical properties of TiO2 coated ZnO nanocomposite particles by a novel microwave irradiation method

A novel and rapid microwave method was used to prepare TiO₂ coated ZnO nanocomposite particles. The resulted particles were characterized by X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), high resolution transmission electron microscopy (HR-TEM) and X-ray photoelectron spectroscopy (XPS). Results show that ZnO nanoparticles were coated with 6-10 nm amorphous TiO₂ layers. In addition, zeta potential analysis demonstrated the presence of TiO₂ layer on the surface of ZnO nanoparticles. Photoluminescence (PL) spectroscopy and UV-visible spectroscopy were used to investigate the optical properties of the nanoparticles. Compared to uncoated ZnO nanoparticles, the TiO₂ coated ZnO nanoparticles showed enhanced UV emission. The UV-visible diffuse reflectance study revealed the significant UV shielding characteristics of the nanocomposite particles. Moreover, amorphous TiO₂ coating effectively reduced the photocatalytic activity of ZnO nanoparticles as evidenced by the photodegradation of Orange G with uncoated and TiO₂ coated ZnO nanoparticles under UV radiation.     

Novel UV–Visible Photodetector in Photovoltaic Mode with Fast Response and Ultrahigh Photosensitivity Employing Se/TiO2 Nanotubes Heterojunction

A feasible strategy for hybrid photodetector by integrating an array of self‐ordered TiO₂ nanotubes (NTs) and selenium is demonstrated to break the compromise between the responsivity and response speed. Novel heterojunction between the TiO₂ NTs and Se in combination with the surface trap states at TiO₂ help regulate the electron transport and facilitate the separation of photogenerated electron–hole pairs under photovoltaic mode (at zero bias), leading to a high responsivity of ≈100 mA W^?1 at 620 nm light illumination and the ultrashort rise/decay time (1.4/7.8 ms). The implanting of intrinsic p‐type Se into TiO₂ NTs broadens the detection range to UV–visible (280–700 nm) with a large detectivity of over 10¹² Jones and a high linear dynamic range of over 80 dB. In addition, a maximum photocurrent of ≈10⁷ A is achieved at 450 nm light illumination and an ultrahigh photosensitivity (on/off ratio up to 10⁴) under zero bias upon UV and visible light illumination is readily achieved. The concept of employing novel heterojunction geometry holds great potential to pave a new way to realize high performance and energy‐efficient optoelectronic devices for practical applications.     

Visible light photoelectrocatalysis with salicylic acid-modified TiO2 nanotube array electrode for p-nitrophenol degradation

This research focused on immersion method synthesis of visible light active salicylic acid (SA)-modified TiO₂ nanotube array electrode and its photoelectrocatalytic (PEC) activity. The SA-modified TiO₂ nanotube array electrode was synthesized by immersing in SA solution with an anodized TiO₂ nanotube array electrode. Scanning electron microscope (SEM), X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), infrared spectroscopy (IR), UV–vis diffuse reflectance spectrum (DRS), and Surface photovoltage (SPV) were used to characterize this electrode. It was found that SA-modified TiO₂ nanotube array electrode absorbed well into visible region and exhibited enhanced visible light PEC activity on the degradation of p-nitrophenol (PNP). The degradation efficiencies increased from 63 to 100% under UV light, and 79–100% under visible light (λ > 400 nm), compared with TiO₂ nanotube array electrode. The enhanced PEC activity of SA-modified TiO₂ nanotube array electrode was attributed to the amount of surface hydroxyl groups introduced by SA-modification and the extension of absorption wavelength range.     

Understanding the Enhancement Mechanisms of Surface Plasmon‐Mediated Photoelectrochemical Electrodes: A Case Study on Au Nanoparticle Decorated TiO2 Nanotubes

Surface plasmon resonance (SPR) enhancement in photocatalyst and photovoltaics has been widely studied and different enhancement mechanisms have been established based on different heterostructure interface configurations. This work is intended to unveil the mechanisms behind charge or energy transfer in different plasmonic configurations of metal particle–semiconductor interfaces, especially with a dielectric layer. For this purpose, a series of composite photoelectrodes based on anodic TiO₂ nanotube (TONT) backbones coated with Au, Al₂O_3, or both are designed and characterized systematically. In conjunction with both experimental measurements and numerical simulations, it is revealed that in the TONT‐Al₂O₃‐Au electrode system (i.e., a thin nonconductive spacer between semiconductor and metal), the enhancement is dominantly governed by SPR‐mediated hot‐electron injection rather than conventional‐thought near‐field electromagnetic enhancement. Among all configurations, the TONT‐Au‐Al₂O₃ electrode shows the best photoresponse in both UV and visible regions. The superior visible light response of the TONT‐Au‐Al₂O₃ electrode is ascribed to the Al₂O₃ intensified local electromagnetic field that enhances the hot‐electron injection through the TiO₂‐Au interface, and an effective surface passivation by the Al₂O₃ coating.     

Metal-Oxide Heterojunction Optoelectronic Synapse and Multilevel Memory Devices Enabled by Broad Spectral Photocarrier Modulation

Broad spectral response and high photoelectric conversion efficiency are key milestones for realizing multifunctional, low-power optoelectronic devices such as artificial synapse and reconfigurable memory devices. Nevertheless, the wide bandgap and narrow spectral response of metal-oxide semiconductors are problematic for efficient metal-oxide optoelectronic devices such as photonic synapse and optical memory devices. Here, a simple titania (TiO₂)/indium-gallium-zinc-oxide (IGZO) heterojunction structure is proposed for efficient multifunctional optoelectronic devices, enabling widen spectral response range and high photoresponsivity. By overlaying a TiO₂ film on IGZO, the light absorption range extends to red light, along with enhanced photoresponsivity in the full visible light region. By implementing the TiO₂/IGZO heterojunction structure, various synaptic behaviors are successfully emulated such as short-term memory/long-term memory and paired pulse facilitation. Also, the TiO₂/IGZO synaptic transistor exhibits a recognition rate up to 90.3% in recognizing handwritten digit images. Moreover, by regulating the photocarrier dynamics and retention behavior using gate-bias modulation, a reconfigurable multilevel (≥8 states) memory is demonstrated using visible light.     

Synthesis and enhanced light absorption of alumina matrix nanocomposites containing multilayer oxide nanorods and silver nanoparticles

In this paper, multilayer oxide nanorods were deposited in the nanopores of anodic aluminum oxide (AAO) via solution infiltration followed by heat treatment. The nanorods have a core–shell structure. First, the shell (nanotube) with the thickness of about 40 nm was made of TiO₂ through the hydrolysis of (NH₄)₂TiF₆. Second, silver nanoparticles with the diameter of about 3 nm were added into the TiO₂ layer through thermal decomposition of AgNO₃ at elevated temperatures. Then, cylindrical cores (nanorods) of CoO and ZnO with 200 nm diameter were prepared, respectively. Scanning electron microscopy (SEM) and transmission electron microscopy (TEM) were used to characterize the structure and composition of the nanorods. UV–vis light absorption measurements in the wavelength range from 350 to 1000 nm were performed to study the effect of nanorod and nanoparticle addition on the light absorption property of the alumina nanocomposites. It is found that CoO nanorods increase the light absorption of the alumina matrix composite in the wavelength range from 500 nm to 800 nm, but the TiO₂ shell does not increase the light absorption much. The ZnO nanorods do not change the light absorption either. However, the addition of silver nanoparticles significantly enhances light absorption of both AAO/TiO₂/Ag/CoO and AAO/TiO₂/Ag/ZnO nanocomposites. This increase in the visible light absorption reveals that there exists surface plasmon around the fine silver nanoparticles in the nanorods.     

Fabrication of TiO2 nanotube film by well-aligned ZnO nanorod array film and sol-gel process

High density TiO₂ nanotube film with hexagonal shape and narrow size distribution was fabricated by templating ZnO nanorod array film and sol-gel process. Well-aligned ZnO nanorod array films obtained by aqueous solution method were used as template to synthesize ZnO/TiO₂ core-shell structure through sol-gel process. Subsequently, TiO₂ nanotube array films survived by removing the ZnO nanorod cores using wet-chemical etching. Polycrystalline anatase TiO₂ nanotube films were ∼ 1.5 μm long and ∼ 100 nm in inter diameter with a wall thickness of ∼ 10 nm.     

Phosphomolybdic acid-modified highly organized TiO2 nanotube arrays with rapid photochromic performance

TiO₂ nanotube arrays were prepared by means of an electrochemical anodization technique in an organic electrolyte solution doped with polyvinyl pyrrolidone (PVP) and were subsequently modified with phosphomolybdic acid (PMoA) to obtain PMoA/TiO₂ nanotube arrays. The microstructure and photochromic properties were investigated via X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM), transmission electron microscopy (TEM), ultraviolet–visible spectroscopy (UV–vis), and X-ray photoelectron spectroscopy (XPS). The results indicated that the Keggin structure of PMoA and the nanotube structure of TiO₂ were not destroyed, and there was a strong degree of interaction between PMoA and TiO₂ at the biphasic interface with lattice interlacing during the compositing process. The XPS results further indicated that there was a change in the chemical microenvironment during the formation process of the composite, and a new charge transfer bridge was formed through the Mo-O-Ti bond. Under visible light irradiation, the colorless PMoA/TiO₂ nanotube array quickly turned blue and exhibited a photochromic response together with reversible photochromism in the presence of H₂O₂. After visible light irradiation for 60 s, the appearance of Mo⁵⁺ species in the XPS spectra indicated a photoreduction process in accordance with a photoinduced electron transfer mechanism.     

Robust and Aligned Carbon Nanotube/Titania Core/Shell Films for Flexible TCO‐Free Photoelectrodes

Carbon nanotube (CNT)/semiconducting oxide hybrids are an ideal architecture for light‐harvesting devices, in which the CNTs are expected to not only act as a scaffold but also provide fast transport paths for photogenerated charges in the oxide. However, the current potential of CNTs for charge transport is largely suppressed due to the nanotubes not being interconnected but isolated by the low conductive oxide coatings. Herein, a flexible and conductive CNT/TiO₂ core/shell heterostructure film is reported, with aligned and interconnected CNTs wrapped in a continuous TiO₂ coating. Without using additional transparent conducting oxide (TCO) substrates, this unique feature of the film boosts the incident photon‐to‐electron conversion efficiency to 32%, outperforming TiO₂ nanoparticle electrodes fabricated on TCO substrates. Moreover, the film shows high structural stability and can generate a stable photocurrent even after being bent hundreds of times.     

Low‐density Polyethylene Films Loaded by Titanium Dioxide and Zinc Oxide Nanoparticles as a New Active Packaging System against Escherichia coli O157:H7 in Fresh Calf Minced Meat

Antibacterial packaging is introduced as a new method to prevent microbial food spoilage. Antibacterial effects of TiO₂, ZnO and mixed TiO₂–ZnO nanoparticle‐coated low‐density polyethylene (LDPE) films on Escherichia coli PTCC1330 were investigated. Bactericidal efficiency of 0.5%, 1% and 2% TiO₂ and ZnO nanoparticles and also 1% mixed TiO₂–ZnO nanoparticles with ratios of 25/75, 50/50 and 75/25 were tested under ultraviolet (UV) and fluorescent lights at two states: films alone and fresh calf minced meat packed. Maximum colony‐forming unit (CFU) reduction of 99.8% and 99.7% were obtained using 1% and 2% ZnO nanoparticle‐coated LDPE film under fluorescent light for films alone as well as 99.8% and 99.6% for fresh calf minced meat packed. 90.3% and 51.8% CFU reduction were recorded for 1% TiO₂ nanoparticle‐coated LDPE films in the presence of UV light at direct contact with bacteria and fresh calf minced meat packed, respectively. Maximum CFU reductions of 96% and 64.1% were obtained using 50/50 ratio of TiO₂/ZnO nanoparticles at the presence of UV light for film alone and fresh calf minced meat packed, respectively. ZnO nanoparticle‐coated LDPE films were identified as the best case to improve shelf life and prevent E. coli growth in fresh calf minced meat.     

UV and visible light photodegradation effect on Fe–CNT/TiO2 composite catalysts

Using multi-walled carbon nanotube (CNT) as an one-dimensional support, we have succeeded in uniformly anchoring of TiO₂ and Fe nanoparticles at its surface. The as-prepared Fe–CNT/TiO₂ composite photocatalysts have been investigated by degrading methylene blue (MB) under UV and differently intensified visible light irradiation. The ability of CNT to store and shuttle electrons, and Fe nanoparticles demonstrate its capability to serve as a yield and transfer electrons on demand to separate h^?+?/e^??? pairs. Moreover, the MB photodegradation increase with an increase of visible light intensity can be ascribed to the enhancement MB cationic radical. In addition, chemical oxygen demand (COD) of piggery waste and reduction efficiency of Cr (IV) was done at regular intervals, which gave a good idea about mineralization of wastewater.     

Synthesis and characterization of polythiophene-modified TiO<Subscript>2</Subscript> nanotube arrays

The highly ordered and uniform TiO₂ nanotube arrays were fabricated by anodic oxidation method and PTh(polythiophene)/TiO₂ nanotube arrays electrode were obtained by electrochemical polymerization. X-ray powder diffraction (XRD) analysis confirmed the formation of TiO₂ phase. The morphologies and optical characteristics of the TiO₂ nanotube arrays were studied by scanning electron microscope (SEM), UV-Vis absorption spectra and Raman spectra. The results demonstrate that the PTh/TiO₂ electrode could enlarge the visible light absorption region and increase the photocurrent in visible region. The modified TiO₂ electrode with light-to-electric energy conversion efficiency of 1·46%, the short-circuit current density of 4·52 mAcm^− 2, open-circuit voltage of 0·74 V and fill factor of 0·44, were obtained.     

Fabrication of periodically aligned vertical single-crystalline anatase TiO2 nanotubes with perfect hexagonal open-ends using chemical capping materials

A vertically aligned anatase TiO2 （A-TiO2） nanotube array has been fabricated by coating a ZnO nanorod （NR） template with a TiO2 precursor solution. After coating, the ZnO NR cores were selectively etched in an acidic environment to form TiO2 nanotubes （NTs）. More specifically, after growing the ZnO NRs via a hydrothermal method, one drop of the TiO2 precursor solution was cast to coat the ZnO NRs, the tops of which were previously covered with chemical capping materials by electrostatic interaction, and then the sample was sintered. Finally, the sample was immersed in an acidic solution resulting in selective etching of the ZnO NR cores. Thus, only TiO2 NTs remained on the substrate. The capping material is effectively used to create a perfect, hexagonal open-ended TiO2 NT array, which interestingly extends onset absorption towards the visible region.