Shared hairpin structure electrochemiluminescence biosensor based on Au@Ni-Co metal organic frameworks for simultaneous detection of Pb(II) and S.aureus.

The excessive content of lead (Pb(II)) and Staphylococcus aureus (S.aureus) seriously harms the quality of aquatic products. In this paper, a highly sensitive electrochemiluminescence (ECL) biosensor was constructed using the synergistic effect of Au NPs@Nickel-Cobalt-Metal-organic frameworks (Au@Ni-Co-MOFs) and double potential resolution function of urchin-like Au@luminol and Cadmium sulfide quantum dots (CdS QDs) for synchronous detection of Pb(II) and S.aureus in aquatic products. Au@Ni-Co-MOFs as the base material, its cube structure can improve the surface active area and sensitivity of the sensor, providing more catalytic active sites for the two functional probes. Urchin-like Au@luminol binding aptamer DNA2 specifically recognizes Pb(II), CdS QDs binding aptamer DNA3 specifically recognizes S.aureus, which collaboratively catalyzed hydrogen peroxide reduction to produce two electrochemiluminescence signals. The shared hairpin structure DNA1 binds stably to Au@Ni-Co-MOFs via the Au-S bond, and the two functional probes are complementary paired with the DNA1 respectively to ensure the specificity of the aptamer. According to the ECL intensity changes of different potentials signal sources, the synchronous detection of Pb(II) and S.aureus with different concentrations is realized. The sensor realizes the detection of two targets in aquatic products and provides a new strategy for the simultaneous detection of multiple targets.

Growth of bimetallic Ni-Co MOFs on a skeleton of electrospun PAN nanofibers and coating on a thin film for SPME of amitriptyline and nortriptyline in urine and plasma samples.

In this research, composited bimetallic organic framework-polyacrylonitrile (Ni-Co MOFs-PAN) was applied for thin-film solid phase microextraction (TF-SPME) of tricyclic antidepressant (TCA) drugs from biological samples. The separation and quantification of the analytes were accomplished by HPLC-UV. First, seeded nanofibers with organic ligands were electrospun on a sheet of foil. Then, with the uniform in-situ solvothermal growth of Ni-Co MOFs on the skeletal surface of nanofibers, the nanoparticles were successfully attached to the surfaces without effective bonds and produced a thin layer with a high flexibility, large active surface and abundant functional groups for adsorption. The characteristics of the produced nanocomposite were investigated by Fourier-transform infrared spectroscopy, field emission-scanning electron microscopy, X-ray diffraction, energy dispersive X-ray spectroscopy and Brunauer-Emmett-Teller analysis. The stirring rate, pH, ionic strength, adsorption and desorption time along with type and volume of desorption solvents as influential factors on extraction efficiencies of the analytes, were optimized by one variable at a time method. Under optimized conditions, wide linear range for analytes in water and plasma matrices were obtained from 0.2 to 1000.0 µg L-1 and 1.0-1000.0 µg L-1, respectively, with R2 ≥ 0.9925. The limits of detection were in the range of 0.06-0.3 µg L-1 in different media. Good repeatability and reproducibility were attained within intra-day, inter-day and film-to-film RSDs% (n = 3) below 3.3 %, 3.9 % and 4.7 %, respectively. Since desirable relative recoveries were calculated between 91.4 % and 100.4 %. The method can be used for the successful extraction and measurement of amitriptyline and nortriptyline as its metabolite in different sampling time from urine and plasma matrices.

Lightweight and efficient luffa sponge carbon/Co composites with adjustable electromagnetic wave absorption properties.

Biomass material has gained significant popularity due to its potential to meet the requirements of green and sustainable development in modern times. It is widely used in various fields, especially for absorbing electromagnetic waves (EMW). In this study, we used luffa sponge carbon (CLS) as a lightweight and porous carbon source. Through a static reaction and heat treatment process, we successfully loaded coral sheet cobalt onto the surface of CLS to create lightweight and efficient luffa sponge carbon/cobalt (CLS/Co) composites for EMW absorption. We controlled the microstructure and electromagnetic properties of the CLS/Co composites by adjusting the pyrolysis temperature. At 700 °C, the CLS/Co composites showed a minimum reflection loss (RLmin) of -60.81 dB and an effective absorption bandwidth (EAB) of 5.56 GHz at a very thin thickness of 1.68 mm. Moreover, at a pyrolysis temperature of 800 °C, the absorption strength of the CLS/Co composites reached -50 dB at various thicknesses.

Lightweight Co3O4/CC Composites with High Microwave Absorption Performance.

With the rapid development of electronic and communication technology for military radars, the demand for microwave-absorbing materials in the low-frequency range with thin layers is growing. In this study, flexible Co3O4/CC (carbon cloth) composites derived from Co-MOFs (metal-organic frameworks) and CC are prepared using hydrothermal and thermal treatment processes. The flexible precursors of the Co-MOFs/CC samples are calcined with different calcination temperatures, for which the material structure, dielectric properties, and microwave absorption performance are changed. With the increases in calcination temperature, the minimum reflection loss of the corresponding Co3O4/CC composites gradually moves to the lower frequency with a thinner thickness. In addition, the Co3O4/CC composites with the 25 wt% filler loading ratio exhibit the minimum reflection loss (RL) of -46.59 dB at 6.24 GHz with a 4.2 mm thickness. When the thickness is 3.70 mm, the effective absorption bandwidth is 3.04 GHz from 5.84 to 8.88 GHz. This study not only proves that the Co3O4/CC composite is an outstanding microwave-absorbing material with better flexibility but also provides useful inspiration for research on wideband microwave absorption materials below 10 GHz.

Carbon cloth based flexible electromagnetic wave absorbing materials loaded with Co3O4 array and tunable electromagnetic wave absorption performance.

The demand for flexible electromagnetic wave (EMW) absorbing materials has increased, highlighting the importance of designing efficient and adaptable EMW absorbing materials. In this study, flexible Co3O4/carbon cloth (Co3O4/CC) composites with high EMW absorption properties were prepared via a static growth method and annealing process. The composites exhibited remarkable properties, with the minimum reflection loss (RLmin) and maximum effective absorption bandwidth (EAB, RL ≤ -10 dB) of -54.43 dB and 4.54 GHz, respectively. The flexible carbon cloth (CC) substrates exhibited outstanding dielectric loss due to their conductive networks. Moreover, the uniformly and tightly organized Co3O4 arrays on the flexible CC substrate played a crucial role in fine-tuning the impedance matching and facilitating abundant multiple scattering and interface polarization. This study proposes a promising approach to preparing flexible Co3O4/CC composites with a significant reference value for the field of flexible EMW.

Interfacial Engineering of Bimetallic Ni/Co-MOFs with H-Substituted Graphdiyne for Ammonia Electrosynthesis from Nitrate.

The electrochemical synthesis of ammonia is highly dependent on the coupling reaction between nitrate and water, for which an electrocatalyst with a multifunctional interface is anticipated to promote the deoxygenation and hydrogenation of nitrate with water. Herein, by engineering the surface of bimetallic Ni/Co-MOFs (NiCoBDC) with hydrogen-substituted graphdiyne (HsGDY), a hybrid nanoarray of NiCoBDC@HsGDY with a multifunctional interface has been achieved toward scale-up of the nitrate-to-ammonia conversion. On the one hand, a partial electron transfers from Ni2+ to the coordinatively unsaturated Co2+ on the surface of NiCoBDC, which not only promotes the deoxygenation of *NO3 on Co2+ but also activates the water-dissociation to *H on Ni2+. On the other hand, the conformal coated HsGDY facilitates both electrons and NO3- ions gathering on the interface between NiCoBDC and HsGDY, which moves forward the rate-determining step from the deoxygenation of *NO3 to the hydrogenation of *N with both *H on Ni2+ and *H2O on Co2+. As a result, such a NiCoBDC@HsGDY nanoarray delivers high NH3 yield rates with Faradaic efficiency above 90% over both wide potential and pH windows. When assembled into a galvanic Zn-NO3- battery, a power density of 3.66 mW cm-2 is achieved, suggesting its potential in the area of aqueous Zn-based batteries.

A novel ratiometric fluorescent probe for sensitive detection of jasmonic acid in crops.

Herein, a novel ratiometric fluorescent probe was proposed for sensitive detection of jasmonic acid (JA) based on NCQDs@Co-MOFs@MIPs. The prepared NCQDs, with uniquely dual-emissive performance, are insensitive to JA due to electrostatic repulsion. Interestingly, the introduction of Co-MOFs not only avoided the self-aggregation of NCQDs, but changed the surface charge of NCQDs and triggered the response of NCQDs to JA. More importantly, the imprinted recognition sites from MIPs provided "key-lock" structures to specifically capture JA molecules, greatly improving the selectivity of the probe to JA. Under the synergistic actions of Co-MOFs and MIPs, JA can interact with NCQDs through photo-induced electron transfer (PET), resulting in the changes on emission intensity of the probe at Em = 367 nm and 442 nm. Based on the observations, the quantification of JA was realized in the range of 1-800 ng/mL with the limit of detection (LOD) of 0.35 ng/mL. In addition, the probe was used for detecting JA in rice with satisfactory analysis results, indicating the probe holds great potential for monitoring JA levels in crops. Overall, this strategy provides new insights into the construction of practical probes for sensitive detection of plant hormones in crops.

Co-MOFs as Emerging Pulse Modulators for Femtosecond Ultrafast Fiber Laser.

The metal organic framework (MOF) has attracted more and more attention due to its unique morphology, functional linkers, and orderly network structure. Zeolitio imidazolata frameworks (ZIFs), which are formed by bivalent transition metals (Zn, Co, etc.) and nitrogen-containing heterocyclic imidazole or purine organic ligands, are a very attractive subclass of MOFs. ZIF-67, obtained by the nucleation growth of dimethylimidazole and Co 2p, has been developed as a precursor for porous nanostructured cobalt-based metal oxides. During material preparation we add rGO because it can be used as a basic element to construct macroscopic three-dimensional carbon structural materials, which self-assemble into a 3D network structure with ZIF-67 through simple van der Waals forces or hydrogen bonds, and some samples contain specific functional groups that are added to the precursor. In this paper, we employ liquid-phase synthesis to generate rGO-ZIF-67 and calcine it at the temperature of 350 °C to obtain rGO-Co3O4. Then we fabricate rGO-Co3O4 and rGO-ZIF-67 modulators based on microfibers and test their nonlinear optical absorption in 1.5 µm range. The modulation depths of rGO-Co3O4 and rGO-ZIF-67 are measured as 10.41% and 6.61%, respectively. By using microfiber-based rGO-Co3O4 modulator, we have obtained a conventional soliton and a soliton molecule in Er3+-doped fiber lasers. The conventional soliton has a pulse width of 793.4 fs and a spectral width of 3.3 at 1558.9 nm, respectively. The obtained soliton molecule has a spectral modulation period of 1.65 nm and temporal separation of 4.94 ps at 1563.2 nm. By employing a microfiber-based rGO-ZIF-67 modulator, we obtain conventional solitons with a spectral width of 1.9 nm at the central wavelength of 1529.8 nm. Our research may expand the MOF-based materials for ultrafast photonics, blazing a new path for fiber laser, optical communications, and optoelectronics, etc.

Ultrasensitive dual-signal electrochemical ratiometric aptasensor based on Co-MOFs with intrinsic self-calibration property for Mucin 1.

The concentration of tumor biomarker Mucin 1 (MUC 1) is highly related with many diseases, which can be employed for the early diagnosis of cancer. In this paper, an electrochemical ratiometric aptasensor with intrinsic self-calibration property for the detection of MUC 1 is presented. In this paper, Co-MOFs themselves were employed as signal substances. This strategy was fabricated by using gold nanoparticles@black phosphorus (BP) as the substrate on the electrode, followed by modification of DNA nanotetrahedrons (DTN) via Au-S bond. The terminal of DTN contains MUC 1 aptamer. In the presence of MUC 1, the signal of DNA-labeled Co-MOFs can be detected. The current signal of Co-MOFs increased and that of thionine (as reference) was unchanged upon the addition of MUC 1. Thus, an intrinsic self-calibration aptasensor was achieved. In order to simplify the modification procedure, the electrolyte solution thionine was employed as an inner reference probe. Moreover, coupling of the hybridization chain reaction (HCR) with these MOFs signal tags presents an enzyme-free method for signal amplification, endowing the proposed ratiometric biosensor detection with high reproducibility and high sensitivity. The current ratio (IIR/ISP) remained stable over 30 individual measurements performed on ten different working electrodes. Even ten repeated scans performed on a single electrode exhibited a constant current ratio. The electrochemical ratiometric aptasensor is highly sensitivity for MUC 1 with the detection limit of 1.34 fM. Our proposed ratiometric sensor has great potential for the detection of cancer-related biomarkers.

In-situ synthesis of graphite carbon nitride nanotubes/Cobalt@Carbon with castor-fruit-like structure as high-efficiency electromagnetic wave absorbers.

The increasingly electromagnetic wave (EMW) pollution has rendered the study and development of new, high-efficiency EMW absorbers a sought-after topic. In this study, graphite carbon nitride nanotubes/cobalt@carbon (GCNNs/Co@C) composites were fabricated using an in-situ synthesis method, which included facile grinding and carbonization pyrolysis. The synthesized GCNNs/Co@C composites exhibited a unique castor-fruit-like structure, that is, GCNNs formed an entwined three-dimensional (3D) network structure on the surface of cobalt@carbon (Co@C), which improved the EMW absorption properties of composites. The obtained GCNNs/Co@C composites exhibited excellent EMW absorption performance. For the fabricated GCNNs/Co@C composites, the minimum reflection loss (RLmin) value reached -63.90 dB at a thickness of 1.96 mm, and the effective absorption bandwidth (EAB, RL ≤  -10 dB) achieved 4.44 GHz at an ultra-thin thickness of 1.51 mm. The EAB covered the entire X and Ku bands (6.96-18.00 GHz) through thickness adjustment from 1.51 to 2.50 mm. Underlying EMW absorption mechanisms were briefly discussed. This study presents a novel design method to prepare light-weight and highly-efficient EMW absorbing absorbers.