Conventional lateral flow immunoassay (LFIA) usually suffers from poor antimatrix interference, unsatisfactory sensitivity, and lack of quantitative ability for target analyte detection in food matrices. In response to these limits, here, multifunctional nanomaterial ZnFe2O4 nanoparticles (ZFOs) were developed and integrated into LFIA for powerful magnetic separation/enrichment and colorimetric/photothermal target sensing. Under optimum conditions, the detection for clenbuterol (CL) with magnetic enrichment achieves 9-fold higher sensitivity compared to that without enrichment and 162-fold higher sensitivity compared to that based on traditional colloidal golds. Attributing the improved performances of ZFOs, CL can be detected at ultralow levels in pork and milk with 10 min of immunoreaction time. The vLODs were 0.01 μg kg-1 for two modes, and the cutoff values of CL were about 5 and 3 μg kg-1, respectively. More importantly, the enrichment ZFO-mediated LFIA (ZE-LFIA) exhibits a similar limit of detection (LOD) in both buffer solution and food matrix, demonstrating a universal resistance to the food matrix. The multitudinous performance merits of this ZE-LFIA with high sensitivity, matrix tolerance, accuracy, and specificity have ensured a broad application potential for target detection of clenbuterol and can serve as an experience for other veterinary drug residues\' detection.

Herein, SnO2QDs (<10 nm) with small size instead of conventional nanoparticles was employed to modify ZnFe2O4to synthesize porous and heterogeneous SnO2/ZnFe2O4(ZFSQ) composites for gas sensing. By an immersion process combined with calcination treatment, the resultant porous ZFSQ composites with different contents of SnO2QDs were obtained, and their sensing properties were investigated. Compared with bare ZnFe2O4and SnO2QDs, porous ZFSQ composites based-sensors showed much improved sensor response to acetone. For contrast, the sensor performance of ZFSQ composites was also compared with that of ZnFe2O4sphere modified by SnO2nanoparticles with different size. The porous ZFSQ composite with 5 wt% SnO2QDs (ZFSQ-5) showed a better acetone sensing response than that of other ZFSQ composites, and it exhibited a high response value of 110-100 ppm of acetone and a low detection limit of 0.3 ppm at 240 °C. In addition to the rich heterojunctions and porous structure, the size effect of SnO2QDs was other indispensable reasons for the improved sensor performance. Finally, the ZFSQ-5 composite sensor was attempted to be applied for acetone sensing in exhaled breath, suggesting its great potential in monitoring acetone.

Methylene blue (MB) is hazardous in natural water because this dye causes serious diseases that endangers public health and ecosystems. Photocatalytic degradation is a prominent technique for achieving the effective elimination of dye pollutants from wastewater and contribute vitally to ecology and environmental safety. Herein, Cu2+-substituted ZnFe2O4 nanomaterials (CuxZn1-xFe2O4; x = 0, 0.1, 0.2, 0.3, 0.4, 0.6) were synthesized, characterized, and applied for the photocatalytic degradation of MB dye beneath visible light with the assistance of hydrogen peroxide (H2O2). The feature of the photo-catalysts was determined by XRD, EDX, FTIR, DRS, BET, SEM, and TEM techniques. Incorporation of Cu2+ ions changed the crystalline phase, particle size, morphology, and surface area. The photocatalysis condition was optimized with the following major factors, the amout of doping Cu2+ ions, H2O2 concentration, adsorbent dosage, and MB concentration. As a result, the photocatalytic MB degradation efficiency by Cu0.6Zn0.4Fe2O4 catalyst was 99.83% within 90 min under LED light (λ ≥ 420 nm), which was around 4 folds higher than that of pure ZnFe2O4. The photo-Fenton kinetics were in accordance with the pseudo-first-order kinetic model (R2 = 0.981), giving the highes rate constant of 0.034 min-1. It can be, therefore, concluded that Cu2+ substitution considerably boosted the photocatalytic activity of CuxZn1-xFe2O4 ZnFe2O4, suggesting a bright prospect of Cu0.6Zn0.4Fe2O4 as a photo-catalyst in the dyes wastewater treatment.

Structure engineering of magnetic-dielectric multi-components is emerging as an effective approach for presuming high-performance electromagnetic (EM) absorption, but still faces bottlenecks due to the ambiguous regulation mechanism of surface morphology. Here, a novel wrinkled surface structure is tailored on the ZnFe2O4 microsphere via a spray-pyrolysis induced Kirkendall diffusion effect, the conductivity of the sample is affected, and a better impedance matching is adjusted by modulating the concentration of metal nitrate precursors. Driven by a vapor phase polymerization, conductive polypyrrole (PPy) shell are in situ decorated on the ZnFe2O4 microsphere surfaces, ingeniously constructing a core-shell ZnFe2O4@PPy composites. Moreover, a systematic investigation reveals that this unique wrinkled surface structure is highly dependent on the metal salt concentration. Optimized wrinkle ZnFe2O4@PPy composite exhibits a minimum reflection loss (RLmin) reached -41.0 dB and the effective absorption bandwidth (EAB) can cover as wide as 4.1 GHz. The enhanced interfacial polarization originated from high-density ZnFe2O4-PPy heterostructure, and the conduction loss of PPy contributes to the boosted dielectric loss capability. This study gives a significant guidance for preparing high-performance EM composites by tailoring the surface wrinkle structure.

The development of photocatalysts with a wide spectral response and effective carrier separation capability is essential for the green degradation of tetracycline hydrochloride. In this study, a magnetic recyclable Z-scheme ZnO/ZnFe2O4 heterojunction (ZZF) was successfully constructed via the solid phase method, using MIL-88A(Fe)@Zn as the precursor. An appropriate band gap width and Z-scheme charge transfer mechanism provide ZZF with excellent visible light absorption performance, efficient charge separation, and a strong redox ability. Under visible light irradiation, the degradation efficiency of tetracycline hydrochloride for the optimal sample can reach 86.3% within 75 min in deionized water and 92.9% within 60 min in tap water, exhibiting superior stability and reusability after five cycles. Moreover, the catalyst in the water can be conveniently recovered by magnetic force. After visible light irradiation for 70 min, the temperature of the reaction system increased by 21.9 °C. Its degradation constant (35.53 × 10-3 min-1) increased to 5.1 times that at room temperature (6.95 × 10-3 min-1). Using thermal energy enhances the kinetic driving force of the reactants and facilitates carrier migration, meaning that more charge is available for the production of •O2- and •OH. This study provides a potential candidate for the efficient degradation of tetracycline hydrochloride by combining thermal catalysis with a photocatalytic heterojunction.

The synthesis of ZnFe2O4 nanoparticles was performed using the solution combustion method with three types of fuel, namely urea, glycine, and ethylenediamine tetra-acetic acid (EDTA) with precursors (Zn(NO3)2.6H2O and Fe(NO3)3.9H2O. The combustion process was conducted in an open space at 300 °C for ± 1 h, resulting in a brownish-black ZnFe2O4. Meanwhile, the fuel type used in the process affects the physicochemical properties of ZnFe2O4. XRD analysis showed that ZnFe2O4 synthesized using urea, glycine, and EDTA had spinel structures with crystal sizes of 10.19, 20.34, and 27.21 nm, respectively. The FTIR spectra of ZnFe2O4 synthesized using the three fuel types had Zn-O and Fe-O stretching vibrations. Furthermore, the morphology of ZnFe2O4 synthesized using urea was more homogeneous than glycine and EDTA. The saturation magnetization of ZnFe2O4 synthesized using EDTA was 54.63 emu/g compared to glycine and urea, 50.93 and 44.73 emu/g, respectively. Finally, the surface area of synthesized ZnFe2O4 using urea, glycine, and EDTA were 116.4, 100.6, and 94.2 m2/g, respectively.

The interaction between cathode and anode materials is critical for developing a high-performance asymmetric supercapacitor (SC). Significant advances have been made for cathode materials, while the anode is comparatively less explored for SC applications. Herein, we proposed a high-performance binder-free anode material composed of two-dimensional ZnFe2O4 nanoflakes supported on carbon cloth (ZFO-NF@CC). The electrochemical performance of ZFO-NF@CC as an anode material for supercapacitor application was examined in a KOH solution via a three-electrode configuration. The ZFO-NF@CC electrode demonstrated a specific capacitance of 509 F g-1 at 1.5 A g-1 and was retained 94.2% after 10,000 GCD cycles. The ZFO-NF@CC electrode showed exceptional charge storage properties by attaining high pseudocapacitive-type storage. Furthermore, an asymmetric SC device was fabricated using ZFO-NF@CC as an anode and activated carbon on CC (AC@CC) as a cathode with a KOH-based aqueous electrolyte (ZFO-NF@CC||AC@CC). The ZFO-NF@CC||AC@CC yielded a high specific capacitance of 122.2 F g-1 at a current density of 2 A g-1, a high energy density of 55.044 Wh kg-1 at a power density of 1801.44 W kg-1, with a remarkable retention rate of 96.5% even after 4000 cycles was attained. Thus, our results showed that the enhanced electrochemical performance of ZFO-NF@CC used as an anode in high-performance SC applications can open new research directions for replacing carbon-based anode materials.

Herein, a facile fabrication process of ZnO-ZnFe2O4 hollow nanofibers through one-needle syringe electrospinning and the following calcination process is presented. The various compositions of the ZnO-ZnFe2O4 nanofibers are simply created by controlling the metal precursor ratios of Zn and Fe. Moreover, the different diffusion rates of the metal oxides and metal precursors generate a hollow nanostructure during calcination. The hollow structure of the ZnO-ZnFe2O4 enables an enlarged surface area and increased gas sensing sites. In addition, the interface of ZnO and ZnFe2O4 forms a p-n junction to improve gas response and to lower operation temperature. The optimized ZnO-ZnFe2O4 has shown good H2S gas sensing properties of 84.5 (S = Ra/Rg) at 10 ppm at 250 °C with excellent selectivity. This study shows the good potential of p-n junction ZnO-ZnFe2O4 on H2S detection and affords a promising sensor design for a high-performance gas sensor.

Based on the fact that the photo-Fenton process can directly use solar energy to degrade various pollutants, it has received widespread attention. However, it has attracted widespread attention due to the rapid recombination of photo-generated carriers and the low light response range. Therefore, the construction of a Z-scheme heterojunction in this paper can effectively enhance the electron-hole separation, increase the reduction and oxidation potential, and enhance the redox capability of the photocatalysis. This paper reports the successful preparation of visible-light-induced ZnFe2O4/BiOI composite photocatalysis. There is a Z-scheme heterojunction structure of ZnFe2O4 and BiOI. At the same time, the PL and UV absorption spectra showed that the light absorption performance of the composite nanomaterials was enhanced, the photo-generated carrier recombination rate was reduced, and the photo-Fenton performance was also significantly improved. And the photocurrent of ZnFe2O4/BiOI is more than 27 times that of pure ZnFe2O4. In addition, ZnFe2O4/BiOI can degrade the simulated pollutant RhB 100% within 20 min under simulated sunlight. It shows that ZnFe2O4/BiOI binary composite has excellent photo-Fenton properties. In addition, ZnFe2O4/BiOI still maintains a high photo-Fenton ability after three cycles. Therefore, it has potential application prospects of the industrial photodegradation of organic pollutants.

In this study, the application of ZnFe2O4, Uio-66 nanoparticles and ZnFe2O4@Uio-66 photocatalytic nanocomposites, with different ratios of each component was synthesized and applied for the photocatalytic degradation of metronidazole (MNZ) antibiotic. The samples were characterized with (FTIR), (XRD), (SEM), (DLS), (VSM), and UV-Vis spectroscopy. The photocatalytic process was performed under visible light in an aqueous solution. The optical studies revealed that the addition of ZnFe2O4 nanoparticles could stimulate the activation wavelength of the nanocomposite, effectively shifting it to the visible light region, and correspondingly reduce the bandgap. To evaluate the ability of ZnFe2O4@Uio-66 magnetic nanocatalyst to degrade metronidazole, effective parameters such as the initial concentration of MNZ in aqueous solution(10-90 mg/L), pH(2-10), the illumination and darkness time and photocatalyst dosage(0.01-0.05 g) were investigated and optimized. It was observed that when ZnFe2O4 concentration was twice that of Uio-66, the degradation efficiency increased. The optimum degradation conditions, at which 93.7% degradation efficiency was achieved, were determined at 120 min brightness, 40 min darkness, pH = 8, initial concentration of 10 ppm, and photocatalyst content of 0.03 g. Based on the results of photocatalytic degradation kinetics, all the samples followed the Langmuir-Hinshelwood pseudo-first-order kinetics model.
BACKGROUND: The online version contains supplementary material available at 10.1007/s40201-021-00713-x.