Strong Carbon Layer-Encapsulated Cobalt Tin Sulfide-Based Nanoporous Material as a Bifunctional Electrocatalyst for Zinc-Air Batteries.

Global demands for cost-effective, durable, highly active, and bifunctional catalysts for metal-air batteries are tremendously increasing in scientific research fields. In this work, a strategy for the rational fabrication of carbon layer-encapsulated cobalt tin sulfide nanopores (CoSnOH/S@C NPs) material as a bifunctional electrocatalyst for rechargeable zinc (Zn)-air batteries by a cost-effective and facile two-step hydrothermal method is reported. Moreover, the effect of metal elements on the morphology of CoSnOH nanodisks material via the hydrothermal method is investigated. Owing to its excellent nanostructure, exclusive porous network, and high specific surface area, the optimized CoSnOH/S@C NPs material reveals superior catalytic properties. The as-prepared CoSnOH/S@C NPs electrocatalyst reveals better properties of oxygen reduction reaction (half-wave potential of -0.88 V vs reversible hydrogen electrode) and oxygen evolution reaction (overpotential of 137 mV at 10 mA cm-2) when compared with commercial Pt/C and IrO2 catalyst materials. Most significantly, the CoSnO/S@C NPs-based Zn-air battery exhibits more excellent cycling stability than the Pt/C+IrO2 catalyst-based one. Consequently, the proposed material provides a new route for fabricating more active and stable multifunctional catalyst materials for energy conversion and storage systems.

Wireless Alerts and Data Monitoring from BNNO-MWCNTs/PDMS Composite Film-Based TENG Integrated Inhaler for Smart Healthcare Application.

In recent years, the implementation of energy-harvesting technology in medical equipment has attracted significant interest owing to its potential for self-powered and smart healthcare systems. Herein, the integration of a triboelectric nanogenerator (TENG) is proposed into an inhaler for energy-harvesting and smart inhalation monitoring. For this initially, barium sodium niobium oxide (Ba2NaNb5O15) microparticles (BNNO MPs) are synthesized via a facile solid-state synthesis process. The BNNO MPs with ferroelectricity and high dielectric constant are incorporated into polydimethylsiloxane (PDMS) polymer to make BNNO/PDMS composite films (CFs) for TENG fabrication. The fabricated TENG is operated in a contact-separation mode, and its electrical output performance is compared to establish the optimal BNNO MPs concentration. Furthermore, multi-wall carbon nanotubes (MWCNTs), a conductive filler material, are used to enhance the electrical conductivity of the CFs, thereby improving the electrical output performance of the TENG. The robustness/durability of the proposed BNNO-MWCNTs/PDMS CF-based TENG are investigated. The proposed TENG device is demonstrated to harvest electrical energy from mechanical motions via regular human activities and power portable electronics. The TENG is integrated into the inhaler casing to count the number of sprays remaining in the canister, send the notification to a smartphone via Bluetooth, and harvest energy.

Multistage SrBaTiO3 /PDMS Composite Film-Based Hybrid Nanogenerator for Efficient Floor Energy Harvesting Applications.

Triboelectric nanogenerators are an emerging energy-scavenging technology that can harvest kinetic energy from various mechanical moments into electricity. The energy generated while humans walk is the most commonly available biomechanical energy. Herein, a multistage consecutively-connected hybrid nanogenerator (HNG) is fabricated and combined with a flooring system (MCHCFS) to efficiently harvest mechanical energy while humans walk. Initially, the electrical output performance of the HNG is optimized by fabricating a prototype device using various strontium-doped barium titanate (Ba1- x Srx TiO3 , BST) microparticles loaded polydimethylsiloxane (PDMS) composite films. The BST/PDMS composite film acts as a negative triboelectric layer that operates against aluminum. Single HNG operated in contact-separation mode could generate an electrical output of ≈280 V, ≈8.5 µA, and ≈90 µC m-2 . The stability and robustness of the fabricated HNG are confirmed and eight similar HNGs are assembled in a 3D-printed MCHCFS. The MCHCFS is specifically designed to distribute applied force on the single HNG to four nearby HNGs. The MCHCFS can be implemented in real-life floors with an enlarged surface area to harvest energy generated while humans walk into direct current electrical output. The MCHCFS is demonstrated as a touch sensor that can be utilized in sustainable path lighting to save enormous electricity waste.

Mechanical and Acoustic-Driven BiFeO3 Composite Films-Based Hybrid Nanogenerator for Energy Harvesting and Sensing Applications.

Nanogenerators for acoustic energy harvesting are still in the early stage of development, and many challenges such as the optimization of device structure and the design of efficient and sensitive materials need to be addressed. To solve the above-mentioned problems, herein, advancement in synthesized multiferroic material for hybridizing the nanogenerator and efficient harvesting of various energies such as acoustic, mechanical, and vibrational energies is reported. Initially, bismuth ferrate (BiFeO3 , BFO)-based composite films are prepared with high ferroelectric and dielectric coefficients. The hybrid nanogenerator (HNG) based on a 3D-printed structure has the highest electrical output which is further improved depending on the BFO loading concentration in the composite film. The 0.5 wt% BFO-loaded PVDF-based HNG offers the enhanced open circuit voltage, short circuit current, and charge density values of ≈30 V, ≈1 µA, and ≈10 µC/m2 , respectively. The optimized HNG is employed to harvest mechanical energy from everyday human life. Furthermore, the HNG layers are used in the fabrication of a multi-energy harvester/sensor (MEH/S) which can harvest/sense various vibrational and acoustic energies under different acoustic frequencies and amplitudes, respectively. The harvested energy from the MEH/S is tested to power portable electronics.

Prussian-Blue Analogue-Derived Hollow Structured Co3 S4 /CuS2 /NiS2 Nanocubes as an Advanced Battery-Type Electrode Material for High-Performance Hybrid Supercapacitors.

The facile and cost-effective fabrication of hybrid nanostructures comprised of hollow mixed metallic chalcogenides has attracted growing interest in the development of high-performance energy storage devices. Herein, multi-component (nickel-cobalt-copper-sulfides/selenides (NCCS/NCCSe)) hollow nanocubes (HNCs) are prepared via a single-step sulfurization/selenization process. The NCCS material shows interior HNCs, and the NCCSe material exhibits slightly formed porous cubes. Both the prepared materials demonstrate higher charge storage performance than the precursor NCC NCs owing to the improved surface morphology and addition of sulfur and selenium ions. Particularly, the NCCS HNCs electrode reveals superior specific capacity (capacitance) (70.32 mAh g-1 (666.20 F g-1 ) at 5 mA cm-2 ) along with excellent cycling stability of 108.6% even after 10 000 cycles. Interestingly, the electrode delivers a good rate capability of 83.5% at a high current density of 20 mA cm-2 . The feasibility of the battery-type NCCS HNCs as a positive electrode is explored by constructing an aqueous electrochemical hybrid capacitor (AEHC). The AEHC exhibits maximum energy and power densities of 23.15 Wh kg-1 and 7899.08 W kg-1 , respectively. Remarkably, it demonstrates superior long-life cycling stability even after 10 000 cycles (120.6% retention). The suitability of AEHC for practical application is also tested by driving electronic devices.

High-Efficiency Poly(Vinylidene Fluoride-Co-Hexafluoropropylene) Loaded 3D Marigold Flower-Like Bismuth Tungstate Triboelectric Films for Mechanical Energy Harvesting and Sensing Applications.

Triboelectric nanogenerators (TENGs) are one of the most trending energy harvesting devices because of their efficient and simple mechanism in harvesting mechanical energy from the environment into electricity. Herein, ferroelectric and dielectric bismuth tungstate (Bi2 WO6 (BWO)) with a marigold flower-like structure is prepared via a hydrothermal method, which is embedded in poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP), forming a PVDF-HFP/BWO composite polymer film (CPF) to fabricate TENGs. Generally, the ferroelectric materials exhibit a large piezoelectric coefficient, high electrostatic dipole moment, and high dielectric constant. The prepared PVDF-HFP/BWO CPF reveals a high polar crystalline ß-phase which leads to enhanced piezoelectric and ferroelectric properties of the CPF, thus resulting in the increased electrical performance of the fabricated TENG. The electrical output performance of the proposed TENG is systematically investigated by varying the amount of BWO material embedded in the PVDF-HFP polymer. The fabricated PVDF-HFP/2.5 wt% BWO CPF-based TENG device exhibits the highest electrical output performance. Additionally, the robust test of the TENG device is conducted to investigate the electrical performance for long-term durability and mechanical stability. Finally, the proposed TENG is operated as a self-powered sensor, harvesting mechanical energy from daily life human activities, and powering various low-power portable electronics.

Recent Advanced Development of Artificial Interphase Engineering for Stable Sodium Metal Anodes.

A solid electrolyte interphase (SEI) on a sodium (Na) metal anode strongly affects the Na deposition morphology and the cycle life of Na metal batteries (SMBs). SMB applications are hindered by an unstable SEI and dendrite growth on the Na anode surface, which directly cause low coulombic efficiency and can even lead to safety issues. An artificial interface layer can stabilize Na metal anodes, be easily tailored, and is barely affected by electrochemical processes. In this review, recent advances that support the stability of working Na metal anodes are focused via artificial interphase engineering of inorganic materials, organic materials, and organic-inorganic composite materials, with an emphasis on the significance of interface engineering in SMBs. Fundamental investigations of artificial interphase engineering are also discussed on Na metal anodes and some recent research is summarized to enhance the interface between Na metal and electrolytes using an artificial interface layer. The prospects for interphase chemistry for Na metal anodes are provided to open a way to safe, high-energy, next-generation SMBs.

Metal-Organic Framework-Derived Co3 V2 O8 @CuV2 O6 Hybrid Architecture as a Multifunctional Binder-Free Electrode for Li-Ion Batteries and Hybrid Supercapacitors.

Metal-organic frameworks (MOFs) are promising materials in diverse fields because of their constructive traits of varied structural topologies, high porosity, and high surface area. MOFs are also an ideal precursor/template to derive porous and functional morphologies. Herein, Co3 V2 O8 nanohexagonal prisms are grafted on CuV2 O6 nanorod arrays (CuV-CoV)-grown copper foam (CF) using solution-processing methods, followed by thermal treatment. Direct preparation of active material on CF can potentially eliminate electrochemically inactive and non-conductive binders, leading to improved charge-transfer rate. Furthermore, solution-processing methods are simple and cost-effective. Owing to versatile valence states and good redox activity, the vanadium-incorporated mixed metal oxides (CuV-CoV) exhibited superior electrochemical performance in lithium (Li)-ion battery and supercapacitor (SC) studies. Furthermore, hollow carbon particles (HCPs) derived from MOF particles (MOF-HCPs) are used as the anode material in SCs. A hybrid SC (HSC) fabricated with CuV-CoV and MOF-HCP materials exhibited noteworthy electrochemical properties. Moreover, a solid-state HSC (SSHSC) is constructed and its real-time feasibility is investigated by harvesting the dynamic energy of a bicycle with the help of a direct current generator. The charged SSHSCs potentially powered various electronic components.

Nucleation promoted synthesis of large-area ReS2 film for high-speed photodetectors.

Rhenium disulfide (ReS2) is a transition metal dichalcogenide with a layer-independent direct bandgap. Notably, the weak interlayer coupling owing to its T-phase structure enables multi-layer ReS2 to behave similarly to decoupled monolayers. This inherent characteristic makes continuous multilayer ReS2 film a unique platform for large-area electronic applications. To date, the bulk of work on ReS2 has been conducted using mechanically exfoliated samples or small size flakes (<1 mm2) with no potential for large-scale electronics. A chemical vapor deposition (CVD) synthesis of a large area, continuous ReS2 film directly on a SiO2 substrate is also known to be more challenging compared with that of other 2D materials, such as MoS2 and WS2. This is partly due to its tendency to grow into discrete dendritic structures. In this study, a large-area (>1 cm2), continuous multilayer ReS2 film is directly synthesized on a SiO2 substrate without any transfer process. The polycrystalline ReS2 film synthesized by this method exhibits one of the fastest photoresponse speeds (0.03 s rise time and 0.025 s decay time) among the reported CVD films. The photoresponsivity R λ was also the highest among large-area CVD films. The synthesis method for a continuous multilayer ReS2 film is amenable to large-scale integration and will pave the way for practical optoelectronic applications based on 2D layered materials.

An Integrated Approach Toward Renewable Energy Storage Using Rechargeable Ag@Ni0.67 Co0.33 S-Based Hybrid Supercapacitors.

Self-powered charging systems in conjunction with renewable energy conversion and storage devices have attracted promising attention in recent years. In this work, a prolific approach to design a wind/solar-powered rechargeable high-energy density pouch-type hybrid supercapacitor (HSC) is proposed. The pouch-type HSC is fabricated by engineering nature-inspired nanosliver (nano-Ag) decorated Ni0.67 Co0.33 S forest-like nanostructures on Ni foam (nano-Ag@NCS FNs/Ni foam) as a battery-type electrode and porous activated carbon as a capacitive-type electrode. Initially, the core-shell-like NCS FNs/Ni foam is prepared via a single-step wet-chemical method, followed by a light-induced growth of nano-Ag onto it for enhancing the conductivity of the composite. Utilizing the synergistic effects of forest-like nano-Ag@NCS FNs/Ni foam as a composite electrode, the fabricated device shows a maximum capacitance of 1104.14 mF cm-2 at a current density of 5 mA cm-2 and it stores superior energy and power densities of 0.36 mWh cm-2 and 27.22 mW cm-2 , respectively along with good cycling stability, which are higher than most of previous reports. The high-energy storage capability of HSCs is further connected to wind fans and solar cells to harvest renewable energy. The wind/solar charged HSCs can effectively operate various electronic devices for a long time, enlightening its potency for the development of sustainable energy systems.

Real-time detection of the nanoparticle induced phytotoxicity in rice root tip through the visible red emissions of Eu3+ ions.

Phytotoxicity is one of the most important factors involved in the reduction of crop production. With the introduction of NaBiF4 nanoparticles, the effect of the particle size (>50 nm) on rice development was systematically studied. Through the exogenous treatment of multiple concentrations of nanoparticles, the primary root length, lateral root number, and lateral root length were significantly inhibited under higher content of nanoparticles, but more crown root formation was induced, which might be due to phytotoxicity. With the help of the red emission of the Eu3+-activated NaBiF4 nanoparticles, we could infer that the nanoparticles were accumulated in the root tip cells in the division and elongation zone but not in the mature region. Additionally, the investigation on the influence of the studied nanoparticles on the gene level and the expression of phytotoxicity related genes was performed to further identify the effect of the nanoparticles on the rice root development. These results potentially explain the effect of larger nanoparticles on phytotoxicity in the plant roots.

Achieving a High Areal Capacity with a Binder-Free Copper Molybdate Nanocone Array-Based Positive Electrode for Hybrid Supercapacitors.

Herein, we develop a binder-free copper molybdate nanocone array with a prism-like morphology on nickel foam (Cu3Mo2O9 NCAs/Ni foam) using a single-step hydrothermal method. With an optimal growth time (10 h) under hydrothermal conditions, the prism-like Cu3Mo2O9 NCAs are uniformly decorated on Ni foam with good adhesion and crystallinity. The prepared Cu3Mo2O9 NCAs/Ni foam has been directly used as a binder-free electrode to examine its suitability as a positive electrode in hybrid supercapacitors. In an aqueous 1 M KOH electrolyte, the binder-free Cu3Mo2O9 NCAs/Ni foam showed battery-type behavior with a high areal capacity of 449.5 µAh cm-2 at a discharge current density of 2 mA cm-2 and also exhibited a good cycling stability. In addition, the pouch-type hybrid supercapacitor is assembled using the prism-like Cu3Mo2O9 NCAs/Ni foam as a positive electrode and the activated carbon as a negative electrode in a 1 M KOH electrolyte. The hybrid supercapacitor achieves a maximum cell potential of 1.6 V with superior energy storage properties, including a high areal capacitance of 609.7 mF cm-2 at 3.5 mA cm-2, a high areal energy (0.21 mWh cm-2), and a high power density (2.73 mW cm-2). The obtained results suggest that the facilely synthesized Cu3Mo2O9 NCAs/Ni foam electrode has great potential in high-performance energy storage devices.

Synthesis of Er(III)/Yb(III)-doped BiF3 upconversion nanoparticles for use in optical thermometry.

The authors describe an ethylene glycol assisted precipitation method for synthesis of Er(III)/Yb(III)-doped BiF3 nanoparticles (NPs) at room temperature. Under 980-nm light irradiation, the NPs emit upconversion (UC) emission of Er(III) ions as a result of a two-photon absorption process. The temperature-dependent green emissions (peaking at 525 and 545 nm) are used to establish an unambiguous relationship between the ratio of fluorescence intensities and temperature. The NPs have a maximum sensitivity of 6.5 × 10-3 K-1 at 619 K and can be applied over the 291-691 K temperature range. The results indicate that these NPs are a promising candidate for optical thermometry. Graphical abstract Schematic of the room-temperature preparation of Er(III)/Yb(III)-doped BiF3 nanoparticles with strongly temperature-dependent upconversion emission.

Preparation of Eu3+ ions activated Ca2La8(SiO4)6O2 oxyapatite nanophosphors through two-step surfactant-free method and their optical and electrical properties.

Eu3+ ions activated Ca2La8(SiO4)6O2 (CLSO):Eu3+ nanophosphor samples were synthesized by a mixed solvothermal and hydrothermal method. The samples were carefully studied using various characterization techniques. The XRD patterns of CLSO:Eu3+ and CLSO confirmed that the samples were crystallized in hexagonal phase with a space group of P63/m (176). The morphology of the nanoparticles was studied by varying the reaction parameters such as growth, temperature and time. The photoluminescence (PL) excitation and PL emission spectra exhibited the typical Eu3+ bands in the wavelength range of 200-550 nm and 400-750 nm, respectively. The intensity of the [Formula: see text] electric dipole (ED) transition peak was strong in the PL emission spectrum which imparts the red color when observed under ultraviolet light. The ED transition peak intensity increased when the sample was calcined at an elevated temperature of 700 °C, indicating improved asymmetry ratio and good chromaticity coordinates. The electrical properties of the prepared materials were studied by spin-coating the powder dispersed solutions on the silica substrate. The output current values were also measured for the CLSO nanoparticles prepared under different growth conditions. These results showed the advantages of CLSO nanoparticles for their application in optics and feasibility in nanoelectronic and energy harvesting devices.

Photoluminescence, cathodoluminescence and thermal stability of Sm3+ -activated Sr3 La(VO4 )3 red-emitting phosphors.

A series of Sm3+ -activated Sr3 La(VO4 )3 phosphors were synthesized by a facile sol-gel method. X-ray diffraction patterns and photoluminescence (PL)/cathodoluminescence (CL) spectra as well as PL decay curves were employed to characterize the obtained samples. Upon 402 nm light excitation, the characteristic emissions of Sm3+ ions corresponding to 4 G5/2 →6 HJ transitions were observed in all the as-prepared products. The PL emission intensity was increased with increase in Sm3+ ion concentration, while concentration quenching occurred when the doping concentration was over 4 mol%. The non-radiative energy transfer mechanism for concentration quenching of Sm3+ ions was dominated by dipole-dipole interaction and the critical distance was around 21.59 Å. Furthermore, temperature-dependent PL emission spectra revealed that the obtained phosphors possessed good thermal stability with an activation energy of 0.19 eV. In addition, the CL spectra of the samples were almost the same as the PL spectra, and the CL emission intensity showed a tendency to increase with increase in accelerating voltage and filament current. These results suggest that the Sm3+ -activated Sr3 La(VO4 )3 phosphors with good color coordinates, high color purity and superior thermal stability may be a potential candidate for applications in white light-emitting diodes and field-emission displays as red-emitting phosphors.

Improvement in light harvesting of dye-sensitized solar cells with antireflective and hydrophobic textile PDMS coating by facile soft imprint lithography.

We demonstrated the improved conversion efficiency (η) of dye-sensitized solar cells (DSSCs) using the textile-patterned polydimethylsiloxane (PDMS) antireflection layers prepared by metal-coated textile master molds by a simple soft imprint lithography. When light propagates through the textile-patterned surface of PDMS (i.e., textile PDMS) laminated on the outer glass surface deposited with fluorine-doped tin oxide (i.e., FTO/glass), both the transmitted and diffused lights into the photo-anode of DSSCs were simultaneously enhanced. Compared to the bare FTO/glass, the textile PDMS increased the total transmittance from 82.3 to 85.1% and its diffuse transmittance was significantly increased from 5.9 to 78.1% at 550 nm of wavelength. The optical property of textile PDMS was also theoretically analyzed by the finite-difference time-domain simulation. By laminating the textile PDMS onto the outer glass surface of DSSCs, the η was enhanced from 6.04 to 6.51%. Additionally, the fabricated textile PDMS exhibited a hydrophobic surface with water contact angle of ~123.15°.

Inverted tetrahedron-pyramidal micropatterned polymer films for boosting light output power in flip-chip light-emitting diodes.

We report the improved light output power in gallium nitride-based green flip-chip light-emitting diodes (FCLEDs) employed with inverted tetrahedron-pyramidal micropatterned polydimethylsiloxane (ITPM PDMS) films as an encapsulation and protection layer. The micropatterns are transferred into the surface of PDMS films from the sapphire substrate master molds with two-dimensional periodic hexagonal TPM arrays by a soft imprint lithography method. The ITPM PDMS film laminated on the sapphire dramatically enhances the diffuse transmittance (T(D)) in a wavelength (λ) range of 400-650 nm, exhibiting the larger T(D) value of ~53% at λ = 525 nm, (cf., T(D) ~1% for planar sapphire). By introducing the ITPM PDMS film on the outer surface of sapphire in FCLEDs, the light output power is enhanced, indicating the increment percentage of ~11.1% at 500 mA of injection current compared to the reference FCLED without the ITPM PDMS film, together with better electroluminescence intensity and far-field radiation pattern.

Improved biomolecular detection based on a plasmonic nanoporous gold film fabricated by oblique angle deposition.

We demonstrated an enhanced surface plasmon resonance (SPR) detection by incorporating a nanoporous gold film on a thin gold substrate. Nanoscale control of thickness and roughness of the nanoporous layer was successfully accomplished by oblique angle deposition. In biosensing experiments, the results obtained by biotin-streptavidin interaction showed that SPR samples with a nanoporous gold layer provided a notable sensitivity improvement compared to a conventional bare gold film, which is attributed to an excitation of local plasmon field and an increased surface reaction area. Imaging sensitivity enhancement factor was employed to estimate an overall sensor performance of the fabricated samples and an optimal SPR structure was determined. Our approach is intended to show the feasibility and extend the applicability of the nanoporous gold film-mediated SPR biosensor to diverse biomolecular binding events.

Broadband high-reflective distributed Bragg reflectors based on amorphous silicon films for semiconductor laser facet coatings.

We fabricated amorphous silicon (a-Si)-based distributed Bragg reflectors (DBRs) consisting of alternating dense/porous films (i.e., pair) for a center wavelength (λ(c)) of 0.96 µm by oblique angle deposition (OAD) technique using an electron-beam evaporation system. The dense (high refractive index, i.e., high-n) and porous (low-n) a-Si films were deposited at two incident vapor flux angles of 0° and 80° in the OAD, respectively. Their optical reflectance characteristics were investigated in the wavelength range of 0.6-1.5 µm, including theoretical comparison using a rigorous coupled-wave analysis method. Above three pairs, the reflectivity (R) of a-Si DBRs was almost saturated at wavelengths around 0.96 µm, exhibiting R values of >97%. For the a-Si DBR with only three pairs, a broad normalized stop bandwidth (Δλ/λ(c)) of ∼22.5% was obtained at wavelengths of ∼0.87-1.085 µm, keeping high R values of >95%. To simply demonstrate the feasibility of device applications, the a-Si DBR with three pairs was coated as a high-reflection layer at the rear facet of GaAs/InGaAs quantum-well laser diodes (LDs) operating at λ=0.96 µm. For the LDs coated with three-pair a-Si DBR, external differential quantum efficiency (η(d)) was nearly doubled compared to the uncoated LDs, indicating the η(d) value of ∼50.6% (i.e., η(d)∼25.5% for the uncoated LDs).

Tunable distributed Bragg reflectors with wide-angle and broadband high-reflectivity using nanoporous/dense titanium dioxide film stacks for visible wavelength applications.

Highly-tolerant distributed Bragg reflectors (DBRs) based on the same materials consisting of nanoporous/dense titanium dioxide (TiO2) film pair structures with wide-angle and broadband highly-reflective properties at visible wavelengths are reported. For a high refractive index contrast, the two dense and nanoporous TiO2 film stacks are alternatingly deposited on silicon (Si) substrates by a oblique angle deposition (OAD) method at two vapor flux angles (θα) of 0 and 80° for high and low refractive indices, respectively. For the TiO2 DBRs at a center wavelength (λ(c)) of 540 nm, the maximum level in reflectance (R) band is increased with increasing the number of pairs, exhibiting high R values of > 90% for 5 pairs, and the normalized stop bandwidth (∆λ/λ(c)) of ~17.8% is obtained. At λ(c) = 540 nm, the patterned TiO2 DBR with 5 pairs shows an uniform relative reflectivity over a whole surface of 3 inch-sized Si wafer and a large-scalable fabrication capability with any features. The angle-dependent reflectance characteristics of TiO2 DBR at λ(c) = 540 nm are also studied at incident angles (θ(inc)) of 20-70° for p-, s-, and non-polarized lights in the wavelength region of 350-750 nm, yielding high R values of > 70.4% at θ(inc) values of 20-70° for non-polarized light. By adjusting the λ(c)/4 thicknesses of nanoporous and dense films, for λ(c) = 450, 540, and 680 nm, tunable broadband TiO2 DBRs with high R values of > 90% at wavelengths of 400-800 nm are realized.