Concentration Of Zn2 Research Articles

Ionic buffer layer design for stabilizing Zn electrodes in aqueous Zn-based batteries

Aqueous Zn-based batteries (AZBs) are hindered by issues associated with the Zn electrodeposition process (ZEDP) on electrode surfaces, including passivation, dendrite formation, and hydrogen evolution. One of the important reasons is the drastic fluctuation in the concentration of Zn2+ ions on the electrode surface during the charging and discharging process. In this work, an electrolyte with Zn2+ ion buffer layer (EZIBL) is proposed to regulate the ZEDP. First, numerical simulations and corresponding experiments are conducted to assess the impact of different thicknesses of the Zn2+ ion buffer layer (ZIBL) on the variation in Zn2+ ion concentration, from which the optimal thickness of the ZIBL is determined. Then, the regulation role of EZIBL in the cycling process is demonstrated by a Zn-Cu half cell. Further, combined with the potential profile of the symmetric cell and the experimental phenomena, the regulation role of EZIBL in ZEDP is systematically explained at the mechanistic level through the analysis of key parameters. Finally, a full battery composed of Zn-LiMn2O4 is assembled to evaluate the practical applicability of the EZIBL in real battery cycles, which shows great enhancement in capacity retention and coulombic efficiency. This work proposes the design of the EZIBL used to regulate the ZEDP and provides a simple, low-cost regulation method for the development of high-performance AZBs.

Trap Depth Engineering from Persistent Luminescence Phosphors Mg2-xZnxSnO4 for Dynamic Optical Information Encryption Application.

Traditional information encryption materials that rely on fluorescent/phosphorescent molecules are facing an increasing risk of counterfeiting or tampering due to their static reading mode and advances in counterfeiting technology. In this study, a series of Mg2-xZnxSnO4 (x = 0.55, 0.6, 0.65, 0.7 0.75, 0.8) that realizes the writing, reading, and erasing of dynamic information is developed. When heated to 90 °C, the materials exhibit a variety of dynamic emission changes with the concentration of Zn2+ ions. As the doping concentration increased, the ratio of the shallow trap to deep trap changed from 7.77 to 20.86. When x = 0.55, the proportion of deep traps is relatively large, resulting in a higher temperature and longer time required to read the information. When x = 0.80, the proportion of shallow traps is larger and the encrypted information is easier to read. Based on the above features, encryption binary codes device was designed, displaying dynamic writing, reading, and erasing of information under daylight and heating conditions. Accordingly, this work provides reliable guidance on advanced dynamic information encryption.

Upconversion luminescence and temperature sensing performance of Zn2+-doped Ba2GdAlO5: Yb3+, Er3+ phosphors

Although upconversion luminescence (UCL) materials have attracted considerable attention in biomedical, lighting, anti-counterfeiting, and solar cells due to their excellent fluorescence properties, reports of the dibarium gadolinium aluminum oxide (Ba2GdAlO5) are scarce. Herein, we synthesized the single-phase Ba2GdAlO5 material with non-stoichiometric Ba2Gd1.06Al0.94O5 (denoted as BGAO, hereafter). The X-ray Rietveld refinement reveals that the substitution of Gd for Al accounts for the non-stoichiometry. Notably, the UCL properties of BGAO are realized by doping with Yb3+ and Er3+ ion pair, and it can be further enhanced significantly by co-doping with appropriate Zn2+ ions. The SEM images show that the particle size increases as the concentration of Zn2+ ions increases. The X-ray Rietveld refinement results of the Zn-doped BGAO: 0.1 Yb3+, 0.03Er3+ phosphor indicate the substitution of Zn2+ for Ba2+ and Al3+ ions simultaneously. Grain growth and lattice distortion account for the improvement of UCL properties after Zn2+ ions doping. In addition, the temperature sensing performance of the Zn2+-doped sample has been researched based on the fluorescence intensity ratio (FIR) technique, and the maximum absolute and relative sensitivities (SA-max and SR-max) are obtained to be 4.8 × 10−3 K−1 at 498 K and 1.1% K−1 at 298 K, respectively. This work provides a candidate with high UCL intensity for potential applications in optical temperature sensors.

Facile preparation of a robust, transparent superhydrophobic ZnO coating with self-cleaning, UV-blocking and bacterial anti-adhesion properties

Transparent superhydrophobic coating has been widely investigated for their great potential applications in self-cleaning windows, solar panels, lenses, and optoelectronic devices. Herein, we reported a robust ZnO coating with high transmittance and superhydrophobicity, which was prepared by a facile sol-gel method and post-modification with hexadecyltrimethoxysilane. To well control the surface morphology and roughness of the ZnO coating, CTAB was added in the precursor. When the concentration of Zn2+ was 1.2 mol/L, and the ratio of CTAB/Zn2+ was 0.1, the prepared ZnO coating showed 91.2 % transmittance at a wavelength of 600 nm. A drop of water with a near spherical shape on the coating exhibited a water contact angle of 162.0° ± 1.7° and rebounding back and forth for 7 times in 260.3 ms. Moreover, the ZnO coating shows remarkable stability against water dripping impact, sand impact abrasion and scratching test, while retaining its superhydrophobicity. Furthermore, the ZnO coating also shows self-cleaning, UV-blocking and anti-bioadhesion properties. The prepared transparent superhydrophobic ZnO coating may open a new gate to a variety of practical applications, including windshields, eyeglasses, windows for tall buildings and medical glass, ect.

Characterization of Zn2+ Selective Fluorescence Probe Based on Pyrene Derivatives

A Zn2+-selective fluorescent probe derived from pyrene derivatives was synthesized and characterized based on c=N isomerization which indicated that the O and N atoms in P indeed played important roles in the course of binding with Zn2+. The fluorescence intensity of the probe at 522 nm was enhanced with the addition of Zn2+ over other metal ions. In the concentration range of 1-9 μM, there was an obvious linear correlation between the fluorescent intensity at 522 nm and the concentration of Zn2+. The limit of detection (LOD) was obtained as low as 0.33 μM of Zn2+. The UV-vis spectra also indicated the binding of between the probe and Zn2+. The design concept will provide ideas for the development of fluorescent probes.

Effects of exogenous zinc (ZnSO4·7H2O) on photosynthetic characteristics and grain quality of hybrid rice

Rice is an important food crop and zinc (Zn) is a beneficial microelement. However, there are few reports on the effect of zinc on yield and physiological characteristics of rice. In this study, exogenous zinc (ZnSO4·7H2O) was applied on plant to explore the effects of zinc on rice yield, quality and photosynthetic capacity. The results showed that appropriate concentration of zinc could increase the net photosynthetic rate (Pn) of rice leaves, and Zn2 (2 mg/L ZnSO4•7H2O) treatment was the most significant. However, the Zn treatment had no positive effect on rice yield except under the concentration of Zn2. Meanwhile, the result showed that Zn treatment could increase chalkiness degree (CD) and chalky grain rate (CGR), decreased amylose content (AC), increased protein content and changed protein composition of rice. The above indexes were most significant in Zn2 treatment. In addition, the Zn2 treatment significantly increased rapid viscosity analyzer (RVA) of rice. In conclusion, the results of this study suggested that Zn treatment could enhance the photosynthetic capacity of rice leaves, and improve the processing quality, taste quality and nutritional quality of rice. However, it will have a negative impact on the appearance quality of rice and cannot be used to increase rice production. This study will provide a basis for the application of zinc in rice production.

Preparation and properties of Schiff base fluorescent hydrogels with high strength and toughness based on multiple hydrogen bonding and hydrophobic association

AbstractThe preparation of hydrogels with excellent mechanical properties by the synergistic interaction of various non‐covalent bonds is one of the research focuses. However, the emerging applications put forward requirements on the function, in addition to the mechanical properties. Therefore, we prepared a physically cross‐linked Schiff base fluorescent hydrogel Poly(methacrylic acid‐co‐poly(ethylene glycol) methyl ether acrylate‐co‐(Z)‐N‐(4‐(2‐((1H‐indol‐3‐yl)methylene)hydrazino‐1‐carbonyl)phenyl)methacrylamide) (P(MAA‐PEGA‐IHPMA)) by solvent exchange method, which greatly improved the mechanical properties of the hydrogel, and realized the versatility of the hydrogel. The hydrogel improved the binding energy and crosslinking density through the synergistic effects of non‐covalent bonds such as hydrophobic association, hydrogen bonding and metal complexation. Therefore, the hydrogel had excellent mechanical properties (the maximum tensile fracture stress and strain are 1.45 MPa and 401%, respectively, and the maximum toughness was 3.41 MJ/m3), and could be regulated by changing the content of IHPMA. Moreover, its fluorescence properties could be controlled by the concentration of Zn2+. In addition, P(MAA‐PEGA‐IHPMA) hydrogel also showed temperature response, solvent‐responsive fluorescence, antibacterial properties and shape memory function. The fluorescent hydrogel with high strength and toughness had potential applications in temperature control materials, anti‐fatigue materials and flexible sensors.

A ThT Derivative as Zn2+ Sensor Based on DNA G-quadruplex.

In this report, we developed a sensing strategy based on ThT-E(a ThT derivative) and DNA G-quadruplex for the label-free detection of Zn2+. In the absence of Zn2+, there was a fluorescence enhancement of ThT-E by interaction with human telomere sequence. On the addition of Zn2+, Zn2+ induced a more compact antiparallel G-quadruplex to release ThT-E, resulting in fluorescence quenching. The detection limit was 0.6996μM, and the fluorescence intensity showed a good linear relationship with the concentration of Zn2+ in the range of 0-10μM. This sensing strategy which only needs to mix two kinds of materials has the characteristics of label-feel, simple operation, short response time, economical and efficient.

Fluorescent Turn-On Sensing of Zinc(II) and Alkaline Phosphatase Activity Using a Pyridoxal-5'-Phosphate Derived Schiff Base.

A novel Zn2+ ion and alkaline phosphatase (ALP) selective fluorescence turn-on sensor L was developed by reacting pyridoxal 5'-phosphate (PLP) with hydrazine. Sensor L shows significant flurescence enhancement at 476nm due to the formation of a L-Zn2+ complex in 1:1 binding stoichiometry with the association constant of 3.1⋅104M- 1. Using L, the concentration of Zn2+ can be detected down to 2.34 µM, and the practical utility of L was validated by quantifying Zn2+ in real water samples. Additionally, the receptor L was applied to mimic the dephosphorylation reaction catalysed by the enzyme ALP and the resulted fluorescence change was monitored to detect the ALP activity.

Revealing Photocatalytic Performance of ZnxCd1-xS Nanoparticles Depending on the Irradiation Wavelength.

Photocatalysts are useful for various applications, including the conservation and storage of energy, wastewater treatment, air purification, semiconductors, and production of high-value-added products. Herein, ZnxCd1-xS nanoparticle (NP) photocatalysts with different concentrations of Zn2+ ions (x = 0.0, 0.3, 0.5, or 0.7) were successfully synthesized. The photocatalytic activities of ZnxCd1-xS NPs varied with the irradiation wavelength. X-ray diffraction, high-resolution transmission electron microscopy, energy-dispersive X-ray spectroscopy, and ultraviolet-visible spectroscopy were used to characterize the surface morphology and electronic properties of the ZnxCd1-xS NPs. In addition, in situ X-ray photoelectron spectroscopy was performed to investigate the effect of the concentration of Zn2+ ions on the irradiation wavelength for photocatalytic activity. Furthermore, wavelength-dependent photocatalytic degradation (PCD) activity of the ZnxCd1-xS NPs was investigated using biomass-derived 2,5-hydroxymethylfurfural (HMF). We observed that the selective oxidation of HMF using ZnxCd1-xS NPs resulted in the formation of 2,5-furandicarboxylic acid via 5-hydroxymethyl-2-furancarboxylic acid or 2,5-diformylfuran. The selective oxidation of HMF was dependent on the irradiation wavelength for PCD. Moreover, the irradiation wavelength for the PCD depended on the concentration of Zn2+ ions in the ZnxCd1-xS NPs.

From lab-scale to pilot-scale treatment of real wastewater from the production of rayon fiber

The subject of our study involved the treatment of real process wastewater from the production of rayon fiber. During the annual monitoring of the production facility, we performed a mass balance of three problematic sources of process wastewater and analyzed them repeatedly. All three sources showed high values of COD = 0.4–30 g/L, TOC = 0.09–7.1 g/L and the concentration of Zn2+ 0.09–0.5 g/L. At a total volume of 1.84 million m3, this represents a significant pollution source for the Elbe River. At lab-scale, we tested a combination of filtration, microfiltration, and oxidation using the Fenton, electro-assisted Fenton, and the electrochemical oxidation methods, both on the plate and newly developed macroporous BDD electrodes on a ceramic substrate, along with the final adsorption of Zn2+ emissions on the strongly acidic cation exchange resin Lewatit Mono plus S108. It was tested in Na+ and H+ cycles. Using an optimized technological sequence, we have achieved a COD reduction of up to 98%, and a TOC reduction of 85%. During the H+ cycle cation regeneration by sulfuric acid, Zn2+ emissions were converted to zinc sulfate that can be recycled in the spinning bath of the production process. The method was verified at a pilot scale.

Effect of Zn2+ on emodin molecules studied by time-resolved fluorescence spectroscopy and quantum chemical calculations

Emodin is a natural drug for treating neurodegenerative diseases and plays a vital role in the mitigation of nerve damage. Metal ions can modify the drug properties of emodin, where Zn2+ can synergize with the emodin molecule and enhance the drug effect of emodin. Besides, complex changes can be observed in the fluorescence intensity and fluorescence lifetime of the emodin molecule as the concentration of Zn2+ increases. Herein, the synergistic effects of ligand structural in Zn(II)-Emodin complexes and the electronic effects of metal elements on the antioxidant properties of the complexes are discussed in detail based on UV–vis absorption spectroscopy, fluorescence spectroscopy, time-correlated single photon counting (TCSPC) technique and quantum chemical calculations at the B3LYP/6-31G(d) level. The experimental results confirm that Zn2+ can coordinate with the hydroxyl groups on the emodin to make the molecule structure more rigid, thus inhibiting the non-radiative processes such as high-frequency vibrations of the emodin molecule in solution. The suppression of non-radiative processes leads to an increase in the average fluorescence lifetime of the emodin molecule, and finally results in the enhanced fluorescence intensity. The chemical softness of Zn(II)-Emodin is then confirmed to be higher than that of emodin by Gaussian calculations, indicating its higher chemical reactivity and lower stability. The stronger electron donating ability of Zn(II)-Emodin compared to emodin may explain the higher antioxidant activity of Zn(II)-Emodin, which gives it a stronger pharmacological activity. The results of this study show that emodin can well complex with Zn2+ to remove excess Zn2+ in human body and the resulting complex has better antioxidant properties, which helps to understand the role of Zn2+ in drug-metal coordination and provides guidance for the design of new drugs.

A Fluorescent Turn-On Sensor Toward Multiple Heavy Metal Ions Based on Meso-anisole Modified BODIPY Scaffold.

A fluorescent turn-on sensor (BOPA) was configured by anchoring bis(pyridin-2-ylmethyl)-amine (DPA) unit to the BODIPY scaffold. It exhibits highly sensitivity and selectivity towards Pb2+, Ba2+, Cr3+, Cd2+, Hg2+, Zn2+ against the competent metal ions. Job's plot analysis supports the 1:1 stoichiometry of BOPA and metal ions. And linear relationship between fluorescence intensity and concentration of Zn2+ (representative metal ion) was observed over the range 0 ~ 20μM Zn2+. The limit detection of BOPA in recognition of Pb2+, Ba2+, Cr3+, Cd2+, Hg2+, Zn2+ was ranged from 15.99 to 43.57nM. Photo induced transfer (PET) in the excited state of BOPA determines the emission "off/on". Coordination of metal ions by DPA significantly weakened the electron-donating ability of nitrogen atom and inhibits the PET, recovering emission of BODIPY. In addition, the attachment of anisole at meso-position of BODIPY finely modulated the recognition of metal ions category.

Fabrication of pH-Responsive Zn2+-Releasing Glass Particles for Smart Antibacterial Restoratives.

The on-demand release of antibacterial components due to pH variations caused by acidogenic/cariogenic bacteria is a possible design for smart antibacterial restorative materials. This study aimed to fabricate pH-responsive Zn2+-releasing glass particles and evaluate their solubilities, ion-releasing characteristics, and antibacterial properties in vitro. Three kinds of silicate-based glass particles containing different molar ratios of Zn (PG-1: 25.3; PG-2: 34.6; PG-3: 42.7 mol%) were fabricated. Each particle was immersed in a pH-adjusted medium, and the solubility and concentration of the released ions were determined. To evaluate the antibacterial effect, Streptococcus mutans was cultured in the pH-adjusted medium in the presence of each particle, and the bacterial number was counted. The solubility and concentration of Zn2+ released in the medium increased with a decrease in medium pH. PG-3 with a greater content of Zn demonstrated higher concentrations of released Zn2+ compared with PG-1 and PG-2. PG-2 exhibited bactericidal effects at pH 5.1, whereas PG-3 demonstrated bactericidal effects at pH values of 5.1 and 6.1, indicating that PG-3 was effective at inhibiting S. mutans even under slightly acidic conditions. The glass particle with 42.7 mol% Zn may be useful for developing smart antibacterial restoratives that contribute to the prevention of diseases such as caries on root surfaces with lower acid resistance.

Nucleotide-Based Lanthanide Coordination Polymer Nano-Probe for Turn-On Fluorescence Sensing of Zn2+ in Serum.

Water-dispersed lanthanide coordination polymers (LCPs) have attracted considerable attention owing to their superiority in bioanalysis. However, so far, most of the reported LCPs, due to the employment of water-insoluble and toxic organic molecules as ligands, are only competent in organic solution or the gaseous phase. Therefore, the construction of a water-dispersed, LCP-based, especially LCP nanoparticle (LCPNP)-based, sensor is still lacking and challenging. The aim was to obtain a novel and effective LCPNP-based sensor for Zn2+ by simple self-assembly, utilizing water-soluble guanosine monophosphate (GMP) as ligand and Eu3+ as luminescence center, . In aqueous solutions, Eu-GMP NPs were formed via self-assembly reaction between Eu3+ and GMP, and displayed very weak fluorescence due to low energy transfer from GMP to Eu3+ and the rate constant of nonradiactive deactivation of the excited states caused by the O-H vibration of coordinated water molecules. After the introduce of Zn2+, forming Eu-GMP/Zn, very interestingly, an 8-fold fluorescence enhancement was observed due to the removal of coordination water molecules and fluorescence sensitization of Zn2+. The fluorescence intensity of Eu-GMP NPs at 614 nm showed a linear relationship with the concentration of Zn2+ from 4 to 240 μM with a detection limit of 4 μM. Due to possessing long fluorescence, Eu-GMP showed prominent achievment for application in serum Zn2+ determination. The LCPNP probe exhibited excellent performance for the determination of Zn2+ in serum. For the first time, we developed and designed a kind of water-dispersed, LCPNP-based turn-on fluorescence assay for Zn2+ in serum. High sensitivity and good recoveries were achieved due to long fluorescence life, good water-dispersed behavior, and the turn-on fluorescence response of the LCPNP probe.

High-strength, tough, and anti-swelling Schiff base hydrogels with fluorescent encryption writing, solvent response and double shape memory functions

The preparation of high-strength and tough hydrogels by hydrophobic association strategy is one of the research hotspots, but now the emerging applications put forward requirements in terms of the function and the water stability of the hydrogel in addition to mechanical properties. In order to meet these requirements, we reported anti-swelling fluorescent hydrogels with high strength and toughness, showing antibacterial properties as well as fluorescence encryption writing, underwater storage, fluorescence solvent response and double shape memory functions. The hydrophobic monomer (Z)-N-(4-(2-(quinoline-2-methylene)hydrazine-1-carbonyl) phenyl) methyl acrylamide (QHPMA) containing quinoline Schiff base was successfully introduced into the hydrogel system by solvent exchange method, and P(MAA-QHPMA) hydrogel based on hydrophobic association was prepared. The mechanical properties could be controlled by QHPMA content and Zn2+ concentration. The maximum tensile fracture stress and strain were 1.39 MPa and 162%, respectively. The maximum toughness was 1.21 MJ/m3. Hydrogels had a low swelling rate (201%) and mechanical property stability after soaking for 14 days. In addition, the hydrogel was used as an “off-on” fluorescence sensor. When the concentration of Zn2+ was 0.1 M, the fluorescence intensity was 1851% of that before complexing. The Zn2+-P(MAA-QHPMA) hydrogel had good antibacterial effect due to Zn2+ ions-quinoline Schiff bases coordination. Finally, the fluorescence encryption writing, underwater storage, fluorescence solvent response and double shape memory functions of P(MAA-QHPMA) hydrogel were designed and studied. This high-strength, tough, and anti-swelling fluorescent hydrogel is expected to be used in underwater sensors, solvent detection, shape memory materials and other fields.

The pH dependence of dissolution kinetics of zinc oxide

Zinc oxide (ZnO) powders are used as feed additives for supplementation in diet of animals. Because zinc dissolution rate strongly influences the digestibility of zinc by animals and their stomach has variable pH, the dissolution kinetics of ZnO are studied at the several pH of relevance between 2 and 4. The dissolution of ZnO has been investigated with the help of modeling the dissolution kinetics measured in vitro at various pH. Dissolution is faster in acidic medium. But the acceleration of dissolution at low pH is moderate compared to what would be expected on the basis of the strong pH dependence of ZnO solubility. The concentration of Zn2+ in the quiescent medium at the surface of ZnO particles is much lower than its solubility. It is proposed as a rationale, that hydroxide anions released during dissolution accumulate at the surface of the positively charged ZnO surface, and that the dissolution kinetics is mainly controlled by the diffusion of H+ ions from the bulk solution to the surface.

Zinc and copper supplements enhance trichloroethylene removal by Pseudomonas plecoglossicida in water

ABSTRACT The effects of two microelements, zinc and copper, on the aerobic co-metabolic removal of trichloroethylene (10 mg/L) by the isolate Pseudomonas plecoglossicida were investigated. The strain was previously isolated from a petroleum-contaminated site using toluene (150 mg/L) as substrate. Different concentrations (1, 10 and 100 mg/L) of microelements provided with SO4 2− and Cl− were tested. The results showed the supplement of Zn2+ and Cu2+ at the low concentration (1 mg/L) significantly enhanced cell growth. The removal efficiencies for toluene and trichloroethylene were also enhanced at the low concentration (1 mg/L) of Zn2+ and Cu2+. Compared to the control without zinc supplement, higher concentrations of zinc (10 and 100 mg/L) enhanced the removal efficiencies for both toluene and trichloroethylene in the first three days but showed some inhibitory effect afterward. However, the higher concentrations of Cu2+ (10 and 100 mg/L) always showed inhibitory to the toluene removal while showing inhibitory to the TCE removal after three days. For both Zn2+ and Cu2+, the anions SO4 2− and Cl− did not show significant difference in their effects on the toluene removal. A possible mechanism for Zn2+ and Cu2+ to enhance the removal of toluene and trichloroethylene would be their involvement in toluene oxygenase-based transformation processes. In addition, high concentrations of Zn2+ and Cu2+ ions could be removed from the liquid by the cells accordingly. The results imply a potential of supplementing low concentrations of zinc and copper to enhance bioremediation of the sites co-contaminated with toluene and trichloroethylene.

Corrosion performance of zinc phosphate coatings deposited on AA6061-HDG steel

Zinc phosphate conversion coating prior to spraying is essential in the automotive industry to enhance corrosion resistance as well as promote the adhesion of the subsequent top coatings. In this work, the corrosion performance of zinc phosphate coatings deposited on aluminium alloy (AA6061) and hot-dip galvanized (HDG) steel has been investigated in 3.5 wt% NaCl solution using potentiodynamic polarization method. The effects of bath parameters (i.e. concentration of Zn2+, and F− ions, temperature, and time) on the morphology of coatings are presented. Scanning electron microscope (SEM) attached to Energy Dispersive spectroscopy (EDS), were used to characterize the coatings. Surface roughness measurements of coated samples were examined with Atomic Force Microscope (AFM). The results show that Zn2+ did not have any significant effect on the coating and corrosion performance of the product mix of AA6061 alloy and HDG steel. Surface analysis of the coatings showed that nucleation and growth of phosphate crystals were faster on HDG steel than on AA6061 for bath conditions considered. The results indicated that phosphate coatings deposited at 45 °C in 118 mg/L fluoride for 90 s were more uniform and continuous on HDG steel and thus had the better corrosion performance in the investigated electrolyte than AA6061 alloy.

Antibacterial Activity Studies of 3D-Printing Polyetheretherketone Substrates with Surface Growth of 2D TiO2/ZnO Rodlike Arrays.

Heterogeneous metal implants have been applied in clinical treatments of skeletal wounds, but their low antibacterial properties and the possibility of a release of metal ions may have harmful influences on the human body. Therefore, a polymer implant with low cost, high safety, an elastic modulus similar to that of human bone, and a good antibacterial property must be produced for orthopedic treatments. In this study, the surface of a 3D-printed polyetheretherketone (PEEK) disk was grown with ZnO/TiO2 rodlike arrays using a chemical bath deposition. X-ray diffraction patterns and transmission electron microscopy images showed that TiO2/ZnO rodlike arrays were deposited onto the PEEK substrate. With the direct absorption of antibiotic agents onto the surface of TiO2/ZnO/PEEK samples, their antibacterial performances greater than the values of minimum inhibitory concentration required to inhibit the growth of 90% of Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus) remained for around 10 days. The concentration of Zn2+ ions in a buffer solution is reduced with the coating of a TiO2 layer on a ZnO rodlike array. The sample with absorption from a mixture containing ampicillin and vancomycin salts with a weight ratio of 1:1 had the best inhibitory effect on the growth of E. coli and S. aureus.