Anodic TiO2 Nanotubes Research Articles

Glucose Oxidation Performance of Zinc Nano-Hexagons Decorated on TiO2 Nanotube Arrays

Electrochemically anodized TiO2 nanotube arrays (NTAs) were used as a support material for the electrodeposition of zinc nanoparticles. The morphology, composition, and crystallinity of the materials were examined using scanning electron microscopy (SEM). Electrochemical impedance spectroscopy (EIS) was performed to evaluate the electrochemical properties of TiO2 NTAs. Annealing post-anodization was shown to be effective in lowering the impedance of the TiO2 NTAs (measured at 1 kHz frequency). Zinc nanohexagons (NHexs) with a mean diameter of ~300 nm and thickness of 10–20 nm were decorated on the surface of TiO2 NTAs (with a pore diameter of ~80 nm and tube length of ~5 µm) via an electrodeposition process using a zinc-containing deep eutectic solvent. EIS and CV tests were performed to evaluate the functionality of zinc-decorated TiO2 NTAs (Zn/TiO2 NTAs) for glucose oxidation applications. The Zn/TiO2 NTA electrocatalysts obtained at 40 °C demonstrated enhanced glucose sensitivity (160.8 μA mM−1 cm−2 and 4.38 μA mM−1 cm−2) over zinc-based electrocatalysts reported previously. The Zn/TiO2 NTA electrocatalysts developed in this work could be considered as a promising biocompatible electrocatalyst material for in vivo glucose oxidation applications.

A Study on Cu Decorated Anodic TiO2 Nanotubes for Non-Enzymatic Glucose Sensing and Photoelectrochemical Water Splitting Application

Free-standing, surface-modified TiO2 nanotubes(TNTs) decorated with copper nanostructures have been extensively studied as promising materials for their application in biosensing and photo-electrochemical splitting of water. Here, the TNTs are prepared by electrochemical anodization followed by modification with copper nanostructures via UV-assisted photo-reduction technique. Field-emission scanning electron microscopy and X-ray diffraction studies confirmed the structural and morphological properties of the TNTs, along with their tubular architecture and mixed-phase composition of Anatase-Rutile. Energy-dispersive spectroscopic analysis verified the successful deposition of copper. Diffuse reflectance spectroscopy revealed an electronic band gap of 3.2 eV. The copper-modified TNTs showed an enhanced sensitivity in the sensing of glucose to the tune of 0.52 mA mM−1 cm−2 with a high linear range of 0.5 to 7 mM and showed superior selectivity against interferents. It was found that the modified TNTs exhibited a higher photocurrent response of 1.09 mA cm−2 compared with pristine TNTs (0.69 mA cm−2). These findings indicate the promising potential of copper-modified TNTs for continuous glucose monitoring and photo-electrochemical applications.

Enhanced Photocatalytic Paracetamol Degradation by NiCu-Modified TiO2 Nanotubes: Mechanistic Insights and Performance Evaluation.

Anodic TiO2 nanotube arrays decorated with Ni, Cu, and NiCu alloy thin films were investigated for the first time for the photocatalytic degradation of paracetamol in water solution under UV irradiation. Metallic co-catalysts were deposited on TiO2 nanotubes using magnetron sputtering. The influence of the metal layer composition and thickness on the photocatalytic activity was systematically studied. Photocatalytic experiments showed that only Cu-rich co-catalysts provide enhanced paracetamol degradation rates, whereas Ni-modified photocatalysts exhibit no improvement compared with unmodified TiO2. The best-performing material was obtained by sputtering a 20 nm thick film of 1:1 atomic ratio NiCu alloy: this material exhibits a reaction rate more than doubled compared with pristine TiO2, enabling the complete degradation of 10 mg L-1 of paracetamol in 8 h. The superior performance of NiCu-modified systems over pure Cu-based ones is ascribed to a Ni and Cu synergistic effect. Kinetic tests using selective holes and radical scavengers unveiled, unlike prior findings in the literature, that paracetamol undergoes direct oxidation at the photocatalyst surface via valence band holes. Finally, Chemical Oxygen Demand (COD) tests and High-Resolution Mass Spectrometry (HR-MS) analysis were conducted to assess the degree of mineralization and identify intermediates. In contrast with the existing literature, we demonstrated that the mechanistic pathway involves direct oxidation by valence band holes.

A novel Ti³⁺-mediated approach for supporting palladium on anodic TiO2 nanotubes: Toward efficient and recyclable catalysis in the heck reaction

A simple electrochemical reduction technique was employed to generate Ti3+ with strong reducing property on the anodic TiO2 nanotubes (ATNTs). Utilizing Ti3+ as the reducing agent, Pd2+ was successfully reduced in situ to Pd0 on the anodic TiO2 nanotubes (Pd@ATNTs). Various characterization methods were employed to confirm that the proportion of Ti3+ and the size of Pd nanoparticles could be controlled by adjusting the electrochemical reduction voltage. The obtained Pd@ATNTs-2.5 exhibited satisfactory catalytic efficiency (TOF: 1302 h−1) in the Heck reaction between various aryl halides and olefins. Furthermore, Pd@ATNTs-2.5 demonstrated high stability, with no significant loss of catalytic activity observed even after six cycles.

Totally Tubular TiO2 Nanotubes as Semiconducting Material for Dye-Sensitized Photoelectrodes

The use of chemical bonds to store solar energy is a promising approach to address the intermittency of the sun by harnessing sunlight to drive chemical transformations. One strategy to drive these processes is to use a bespoke semiconductor surface implemented in a photoelectrode to absorb light and generate charge carriers that can drive redox reactions such as the direct oxidation of adsorbed species on the photoanode. To minimize recombination of photogenerated electron-hole pairs, molecular donor-chromophore-acceptor (D-C-A) systems can be used to sensitize wide bandgap semiconductors for visible light absorption and to generate (high energy) long-living charge separated states. Such assemblies represent a photoelectrode for dye-sensitized photoelectrochemical cells (DS-PECs). Presented here are recent findings using molecularly sensitized TiO2 nanotubes as a nanohybrid architecture for DS-PECs. The highly ordered and oriented 1D-nanostructures are purpose-grown using a self-organizing electrochemical anodization approach. The nanotube mouth is functionalized with a Cu(I)-based donor-chromophore-acceptor system by direct assembly at the surface. The resulting photoanodes are investigated against different water oxidation catalysts (e.g., [Cp*Ir(pyalk)OH], pyalk = 2-(pyridine-2-yl)propan-2-ol; CoOx) for their ability to generate oxidizing equivalents that can subsequently drive follow-on oxidation reactions. A more common TiO2 nanostructure morphology (e.g., nanospheres) and simpler Cu(I)-based chromophores are also examined for comparative purposes to highlight the advantages of the proposed assembly.It is well understood that the role of the semiconductor is to connect the molecular components and transfer/store charge carriers from the excited dye to drive redox processes. The TiO2 nanotubes used here are synthesized by self-organized electrochemical anodization (SOA); a process Involving an anode/cathode arrangement where Ti is used as the anode. This process is a balance between the electrochemical formation of TiO2 and simultaneous chemical dissolution in fluoride-containing electrolytes. The resulting semiconducting film is found to be a vertically oriented, size-controlled, and back-contacted nanostructured array of TiO2 on a foil of titanium. In addition to this composition inheriting high chemical stability, the morphology can grant added benefits such as two-dimensional confinement, directional charge transport and orthogonal charge separation.[1]A crucial limiting factor for the performance of this system is the recombination of the electron-hole pairs. By using a transition metal complex or chromophore (C) that is covalently linked with electron donating (D) and electron accepting (A) moieties, the energy levels can be aligned for charge-transfer processes between the electroactive groups for directional electron transport and formation of a charge-separated state.[2] Copper(I) D-C-A assemblies are also of interest when taking into consideration the low-cost and photophysical properties when compared to typical ruthenium(II) polypyridine chromophores used in these types of cells. Transient photocurrent measurements of the photoelectrode suggest that the TiO2 nanotubes’ mouths generate a base photocurrent, which could be associated with graphitic-like carbon impurities extending light absorption for photoactivity. Furthermore, once the surface is decorated with the copper(I) D-C-A assembly, the photocurrent is significantly increased, enabling light-driven oxidation of CoOx photoelectrochemically deposited on the surface of the photoelectrode.REFERENCES[1] Nguyen, N. T.; Altomare, M.; Yoo, J. E.; Taccardi, N.; Schmuki, P. Noble Metals on Anodic TiO2 Nanotube Mouths: Thermal Dewetting of Minimal Pt Co-Catalyst Loading Leads to Significantly Enhanced Photocatalytic H2 Generation. Adv. Energy Mater. 2016, 6, 1501926. DOI: 10.1002/aenm.201501926[2] Singh, Z.; Kamal, S.; Majewski, M. B. Copper(I) Donor−Chromophore−Acceptor Assembly for Light-Driven Oxidation on a Zinc Oxide Nanowire Electrode. J. Phys. Chem. C. 2022, 126, 39, 16732-16743. DOI: 10.1021/acs.jpcc.2c04652 Figure 1

In situ Ion Pumping Anodization to Confine Single‐Atom Fe onto TiO2 Nanotubes for Enhanced Noble‐Metal‐Free Photocatalytic Hydrogen Generation

AbstractAchieving a high dispersity of deposited transition metal is crucial in the anodization preparation of noble‐metal‐free composites for photocatalytic hydrogen generation. Herein, for the first time, an in situ ion pumping anodization method is proposed to confine single‐atom Fe within the spatially ordered structure of anodized TiO2 nanotubes (TNT), assisted by ferric sodium salt of ethylenediaminetetraacetic acid (EDTA) as an “ion pump” to deliver Fe3+ toward anodes. Both experimental and theoretical calculations confirm that highly dispersed single‐atom Fe can interact with single‐electron‐trapped oxygen vacancies (SETOV), effectively reducing the oxygen vacancy concentration in TiO2 nanotubes. This reduction promotes efficient charge carrier separation through the Fe(III)/Fe(II) pathway and enhances hydrogen desorption, ultimately boosting the photocatalytic hydrogen evolution performance.

Fast Response UV Photodetector Based on Aligned Arrays of Anodic Anatase TiO2 Nanotubes

Fast Response UV Photodetector Based on Aligned Arrays of Anodic Anatase TiO2 Nanotubes

Structural evolution of anodized TiO2 nanotubes and their solar energy applications

Structural evolution of anodized TiO2 nanotubes and their solar energy applications

A three-layer zirconia structure composed of nanotubes, dense layer and nanotubes: Evidence against the FADT

Porous anodic oxides have become a research hotspot, but their formation mechanisms are still controversial. The classical field-assisted dissolution theory (FADT) is a theory of top-down dissolution to form nanotubes. However, certain key problems such as the three-stage current-time curve in anodizing process cannot be explained by this theory. The oxygen bubble mold (OBM) is a new mechanism of bottom-up growth of nanotubes, which can explain the phenomenon that cannot be explained by the FADT. Compared to the anodic TiO2 nanotubes, ZrO2 nanotubes have a more complex anodizing current-time curve which is not studied sufficiently. Under certain conditions, there are double complete three-stage current-time curves and two-layer nanotubes. In this study, to explore the formation mechanism of anodic ZrO2 nanotubes, the current-time curve and the interesting morphology were analyzed, after zirconium anodizing and SEM characterizing. An interesting three-layer structure composed of upper nanotubes, dense layer and lower nanotubes formed by zirconium anodizing is reported for the first time. The lower nanotubes and the dense layer are tightly bonding, which strongly refutes the FADT. The OBM was used to explain this phenomenon, which promoted the development of the formation mechanism of anodic ZrO2 nanotubes.

Surface modification of TiO2 nanotubes via pre-loaded hydroxyapatite towards enhanced bioactivity

Anodic TiO2 nanotubes (NTs) are widely established in biomedical applications, as the sub-100 nm morphology significantly impacts their biological activity. In this study, we examine the use and surface functionalization of TiO2 nanotube layers on titanium substrates to facilitate the formation of hydroxyapatite, a crucial ability for implant applications. TiO2 NT layers are grown by electrochemical anodization and the focus is on as-formed and anatase NTs with 100- and 15-nm-diameters, the latter amorphous and available in double-wall (DT) or single-wall (ST) structures. Surface modification of the TiO2 NTs is achieved through an alternate immersion method (AIM) or a simple CaCl2 immersion. The former deposits hydroxyapatite (HA) coatings on/in the NT layers, while the latter forms a thin Ca-surface-modified layer on the TiO2 surface. Both methods effectively induce the formation of an HA layer on 100-nm-diameter NTs after five days of immersion in simulated body fluid (SBF). The chemical composition of NTs is a deciding factor, as the 100-nm-diameter NTs that already contain phosphates (from the anodizing electrolyte) also lead to HA formation by modification via Ca-functionalization (CaCl2 immersion). Whereas, for smaller diameter NTs, the surface nanotopography of the DT and ST NTs is key for the HA nucleation and formation via the AIM approach, but not via immersion in a calcium-containing solution. This promising approach accelerates the growth of HA on TiO2 nanomaterials by initiating apatite nucleation on TiO2 NTs and, thus, has significant implications for increasing their bioactivity in biomedical applications.

Free-standing arrays of BaTiO3 nanotubes for non-enzymatic glucose sensing & hydrophobic coating applications

BaTiO3 nanostructures have been considered as a promising candidates in recent past for energy and biomedical sectors owing to their excellent physiochemical properties, such as high dielectric constant, excellent piezoelectric property, good biocompatibility, non-linear optical characteristics etc. Present study reveals on free-standing arrays of BaTiO3 nanostructures, were fabricated by hydrothermal conversion of anodic TiO2 nanotubes. Morphological and structural information of the BaTiO3 nanotubes were done using FESEM and XRD studies. FESEM analysis revealed that the fabricated samples were having tubular morphology of average length and pore diameter of 4.63 μm and 290 nm respectively. Cubical perovskite crystalline phase of BaTiO3 was confirmed through XRD analysis. The BaTiO3 nanotube samples had shown a higher sensitivity of 44.43 μA mM−1 cm−2 and a faster response of 0.1 s for glucose detection. The fabricated BaTiO3 nanotubes film also showed a higher contact angle of 122.70°. Therefore, our present fabrication on Titanium foil study emphasizes on arrays of BaTiO3 nanotubes which will open up a new window in the development of various types of sensing and hydrophobic coating applications.

Anodized TiO2 Nanotubes Sensitized with Selenium Doped CdS Nanoparticles for Solar Water Splitting

In this research, TiO2 nanotubes (NTs) were produced by electrochemical anodization of a Ti substrate where different NH4F wt.% in the electrolyte was added. NTs with diameter of 65–90 nm and 3.3–4.9 µm length were obtained and sensitized with binary cadmium chalcogenides nanoparticles, CdS and CdSe, by successive ionic layer adsorption and reaction method (SILAR). Additionally, both anions S and Se were deposited onto Cd, labeled as CdSSe and CdSeS, to evaluate the effect of the deposition order of the anion from the precursor solution to form cadmium chalcogenides. The structural, optical, and electrochemical performance were analyzed through the SEM, XRD, XPS, UV-VIS, lineal voltammetry and chronoamperometry characterizations. The increase of NH4F wt.% from 1.5% to 4.5% produced a decrement of the diameter and length attributed to the fluoride ions concentration causing solubility of the NTs. XRD confirmed the TiO2 anatase and hexagonal CdS structures. From the EDS and XPS results, the presence of small amount of Se in the sensitized samples demonstrated the doping effect of Se instead of forming ternary semiconductor. With the sensitization of the TiO2 NTs with the nanoparticles, an improved hydrogen generation was observed (reaching 1.068 mL h−1 cm−2) in the sample with CdSSe. The improvement was associated to a synergetic effect in the light absorption and higher cadmium chalcogenide amount deposited when sulfur ions were deposited before selenium.

Synthesis and Study of SrTiO3/TiO2 Hybrid Perovskite Nanotubes by Electrochemical Anodization.

Layers of TiO2 nanotubes formed by the anodization process represent an area of active research in the context of innovative energy conversion and storage systems. Titanium nanotubes (TNTs) have attracted attention because of their unique properties, especially their high surface-to-volume ratio, which makes them a desirable material for various technological applications. The anodization method is widely used to produce TNTs because of its simplicity and relative cheapness; the method enables precise control over the thickness of TiO2 nanotubes. Anodization can also be used to create decorative and colored coatings on titanium nanotubes. In this study, a combined structure including anodic TiO2 nanotubes and SrTiO3 particles was fabricated using chemical synthesis techniques. TiO2 nanotubes were prepared by anodizing them in ethylene glycol containing NH4F and H2O while applying a voltage of 30 volts. An anode nanotube array heat-treated at 450 °C was then placed in an autoclave filled with dilute SrTiO3 solution. Scanning electron microscopy (SEM) analysis showed that the TNTs were characterized by clear and open tube ends, with an average outer diameter of 1.01 μm and an inner diameter of 69 nm, and their length is 133 nm. The results confirm the successful formation of a structure that can be potentially applied in a variety of applications, including hydrogen production by the photocatalytic decomposition of water under sunlight.

Enhanced Electrocatalytic Oxygen Reduction Reaction of TiO2 Nanotubes by Combining Surface Oxygen Vacancy Engineering and Zr Doping.

This work examines the cooperative effect between Zr doping and oxygen vacancy engineering in anodized TiO2 nanotubes (TNTs) for enhanced oxygen reduction reactions (ORRs). Zr dopant and annealing conditions significantly affected the electrocatalytic characteristics of grown TNTs. Zr doping results in Zr4+ substituted for Ti4+ species, which indirectly creates oxygen vacancy donors that enhance charge transfer kinetics and reduce carrier recombination in TNT bulk. Moreover, oxygen vacancies promote the creation of unsaturated Ti3+(Zr3+) sites at the surface, which also boosts the ORR interfacial process. Annealing at reductive atmospheres (e.g., H2, vacuum) resulted in a larger increase in oxygen vacancies, which greatly enhanced the ORR activity. In comparison to bare TNTs, Zr doping and vacuum treatment (Zr:TNT-Vac) significantly improved the conductivity and activity of ORRs in alkaline media. The finding also provides selective hydrogen peroxide production by the electrochemical reduction of oxygen.

Anodic TiO2 nanotubes for hydrophobic coatings and photo-electrochemical water splitting application

In recent years, anodic TiO2 nanotubes (TNTs) have been considered as one of the most promising material in the field of photoelectrochemical water splitting, hydrophobic coatings, solar cells etc owing to their outstanding properties such as unidirectional charge transfer, high surface to volume ratio along with the non-toxicity, corrosion resistance, high thermal and chemical stabilities. In the present study, TNTs were successfully fabricated using a simple and low cost electrochemical anodization technique at 30 V and 60 V. The morphological and structural information of the TiO2 nanotube arrays were investigated through SEM and XRD analysis. This analysis revealed that fabricated nanotubes were having a set of length and pores diameters (2.5 μm, 70 nm), (17 μm, 120 nm) respectively for 30 V TNTs and 60 V TNTs samples. Electronic band gap and surface functional groups of TNTs were examined by diffuse reflectance and attenuation total reflection spectroscopy studies. This analysis divulged that fabricated sample surface was free from chemicals and energy band gap found to be around 3.2 eV. The contact angle measurement revealed that as-fabricated 30 V TNTs sample has shown an enhanced hydrophobic nature (135.9°) and whereas annealed 60 V TNTs sample has shown an enhancement in the photocurrentdesnity (70.7 μA.cm−2). These findings show that fabricated TNTs can be used in hydrophobic coatings along with photocatalytic applications.

Long-Term Stability of Light-Induced Ti3+ Defects in TiO2 Nanotubes for Amplified Photoelectrochemical Water Splitting.

This study shows that the simple approach of keeping anodic TiO2 nanotubes at 70 °C in ethanol for 1 h results in improved photoelectrochemical water splitting activity due to initiation of crystallization in the material amplified by the light-induced formation of a Ti3+ -Vo states under UV 365 nm illumination. For the first time, the light-induced Ti3+ -Vo states are generated when oxygen is present in the reaction solution and are stable when in contact with air (oxygen) for a long time (two months). We confirmed here that the amorphous or nearly amorphous structure of titania supports the survival of Ti3+ species in contact with oxygen. It is also shown that the ethanol treatment substantially improves the morphology of the titania nanotube arrays, specifically, less surface cracking and surface purification from C- and F-based contamination from the electrolyte used for anodizing.

Crystallization of amorphous anodized TiO2 nanotube arrays.

Anodized TiO2 nanotube arrays (TNTAs) prepared by anodization have garnered widespread attention due to their unique structure and properties. In this study, we prepared TNTAs of varying lengths by controlling the anodization time. Among them, the nanotubes anodized for 2 h have an inner diameter of approximately 92 nm and a wall thickness of approximately 12 nm. Then we subjected amorphous TNTAs prepared by the anodization method to annealing treatments, systematically analyzing the evolution of morphology and structure with varying annealing temperatures. As the annealing temperature increases, the amorphous successively undergoes transitions to the anatase phase and then to the rutile phase. During the transition to the anatase phase, the structure of the nanotube array remains intact, with the complete preservation of the tubular array structure. However, during the transition to the rutile phase, the tubular array structure is destroyed. To address why the tubular array remains undamaged during the amorphous-to-anatase transition, we subjected amorphous TNTAs to annealing at 300 °C for different durations. Raman spectroscopy was employed for fit analysis, providing insights into the evolution of the molecular structure during the anatase phase transition. Finally, TNTAs annealed at different temperatures were incorporated into lithium-ion batteries. By combining XRD for semi-quantitative phase content and anatase particle size calculations, we established a correlation between structure and electrochemical performance. The results indicate a significant improvement in electrochemical performance for an amorphous-anatase structure obtained through annealing at 300 °C, providing insights for the design of high-performance energy storage materials.

Photocurrent response loss of dye sensitized solar cells owing to top surface nanograss growth and bundling of anodic TiO2 nanotubes

In this research, the effect of anodization time on the length of the titanium oxide nanotube arrays (TNAs) and photovoltaic parameters of back-side illuminated dye-sensitized solar cells (DSSCs) were investigated. The TNAs were characterized using X-ray diffraction (X-ray) or (XRD), and scanning electron microscopy (SEM). Anodic TNAs having tube lengths from 7.9 to 20.17 μm were produced in ethylene glycol containing ammonium fluoride-NH4F by increasing the anodizing time from 20 min to 6 h. Based on I–V curves, the power conversion efficiency (PCE) of back-side illuminated dye sensitized solar cells (DSSCs) increased for TNAs grown for up to 120 min, but decreased afterward. Using electrochemical impedance spectroscopy (EIS), we understand that the resistance of the TNAs decreased from 94.82 Ω cm−2 for TNAs anodized for 20 min down to 50.43 Ω cm−2 for those TNAs anodized for 120 min, however, it increases for TNAs anodized for longer periods of time. Furthermore, the short circuit current density (Jsc) increased from 3.14 to 5.67 mA cm−2 during 2 h anodic oxidation for TNAs, and leading to enhanced efficiency of about 200 % (from 1.19 % to 2.45 %). We interpret this behaviour with the top surface morphology evolution of TNAs as a function of anodization time which is associated with the formation of top surface nanograss and bundling the tubes for specific durations.

Can electrodeposited Ti replace rolled Ti as substrate for the growth of anodic TiO2 nanotube layers?

This study conducted a deep investigation of TiO2 nanotube (TNT) layers of two different thicknesses anodically grown on electrodeposited Ti films. The Ti films were grown from molten salts on Ni foils. The structure of the starting metals was compared by XRD (X-Ray Diffraction) and EBSD (Electron Backscatter Diffraction analyses), which showed a strong orientation towards the titanium (101) for the electrodeposited substrate, compared to the rather polycrystalline structure of the rolled Ti. The photoelectrochemical and electrochemical properties of 1 μm and 5 μm thick TNT layers anodically grown on these substrates were examined and compared with TNT layers of the same thickness. No significant morphological and compositional differences were found using SEM (Scanning Electron Microscopy) and XPS (X-ray Photoelectron Spectroscopy) between the TNT layers grown on the two substrates. However, higher photocurrent densities and ICPE values were observed for TNT layers grown on electrodeposited Ti. An in-depth investigation using Cyclic Voltammetry (CV) and Electrochemical Impedance Spectroscopy (EIS) analyses showed increased conductivity of the TNT layers produced on electrodeposited Ti compared to their counterparts. The carrier density (ND) for the TNT layers on electrodeposited Ti, calculated from Mott-Schottky measurements, showed a higher doping level than the TNT layers grown on Ti foils. This increase in ND results in more optimal photoelectrochemical performance of the TNT layers grown on electrodeposited Ti. All in all, the results presented herein pave the way for the use of electrodeposited Ti, with all its inherent benefits, and allow the further study of its promising properties in a wide range of applications.

Sn–3Ag–0.5Cu/TiO2/Ti wire-tube structure with memristive response by ultrasonic soldering

High-performance memristors have become the next generation of memory devices with potential application to ultra-high-speed, large-capacity, high-density computing requirements. However, devices with low operating voltage, high switching ratio, and long cycle life have not yet been achieved. A novel Sn–3Ag–0.5Cu/TiO2/Ti wire-tube memristor was fabricated using ultrasonic soldering. Ultrasound application changes the wetting conditions of the filler by using the instantaneous high temperature and pressure generated by ultrasonic cavitation, which induces Sn–3Ag–0.5Cu filler metal into anodized TiO2 nanotubes to prepare a wire-tube structure. The Sn–3Ag–0.5Cu/TiO2/Ti device showed bipolar hysteresis with a clear storage window. The maximum switching ratio was 33, which is slightly lower than the value of 36 for a Ag/TiO2/Ti device made using a conventional anodizing method. Seventeen cycles were achieved, which is 143% higher that of the Ag/TiO2/Ti device. The operating voltage of the Cu–3Ag–0.5Cu/TiO2/Ti device was significantly lower than that of the Ag/TiO2/Ti device. The structure and electrochemical performance of the device was evaluated by Raman spectrometry (LAMAN), X-ray photoelectron spectroscopy (XPS) and Electrochemical impendence spectroscopy (EIS) analysis. Formation of the conductive channels of the TiO2 wire-tube structure memristor was studied using transmission electron microscopy and high-resolution transmission electron microscopy, and a model of the mechanism of formation of the conductive filaments was established.