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Shufang Ren Runyan Feng Shounian Cheng Qingtao Wang Zhixiang Zheng 《Electroanalysis》2021,33(6):1471-1483
Ti3C2TX MXene was synthesized by exfoliating pristine Ti3AlC2 phase with hydrofluoric acid. The simple methods of mechanical mixing and drop-casting of Ti3C2TX and MWCNTs were carried out to prepare sensing electrode of Ti3C2TX/MWCNTs/GCE. The composite and topography, especially the surface functional groups of Ti3C2TX/MWCNTs were analyzed by XRD, SEM, FTIR, XPS, and Raman spectrum. The results turned out that Ti3C2TX was characteristic by accordion-like 2D nanostructure with the surfaces terminated with −OH, −F, and =O. When combining with acid pretreated, the interaction between the functional groups of Ti3C2TX and MWCNTs facilitated the convenience and reproducibility of the robust modified electrodes and could make Ti3C2TX/MWCNTs/GCE possess good synergistic catalytic acceleration by increasing the electron transfer efficiency as well as adsorption and aggregation of MOP analyte onto the electrode surface. Versatile electrochemical measurements of CV, DPV and EIS were used to investigate the electrochemical performance of Ti3C2TX/MWCNTs/GCE sensing platform. The linear detection range is 0.01–100 μM with the limit of detection of 0.0092 μM (S/N=3). The sensor has good stability, repeatability, reproducibility and anti-interference. In the detection of serum and urine samples, it has a good recovery rate. 相似文献
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Dr. Yue Wang Fang Zhou Prof. Dr. Qingtao Meng Songhe Zhang Dr. Hongmin Jia Dr. Cuiping Wang Dr. Run Zhang Prof. Dr. Zhiqiang Zhang 《化学:亚洲杂志》2021,16(21):3419-3426
The detection of changes in the reactive oxygen species (ROS)/reactive sulfur species (RSS) couple is important for studying the cellular redox state. Herein, we developed a 1,8-naphthalimide-based fluorescence probe ( NI ) for the reversible detection of bisulfite (HSO3−) and hydrogen peroxide (H2O2) in vitro and in vivo. NI has been designed with a reactive ethylene unit which specifically reacts with HSO3− by a Michael addition reaction mechanism, resulting in the quenching of yellow fluorescence at 580 nm and the appearing of green fluorescence at 510 nm upon excitation at 500 nm and 430 nm, respectively. The addition product ( NI−HSO3 ) could be specifically oxidized to form the original C=C bond of NI , recovering the fluorescence emission and color. The detection limits of NI for HSO3− and NI−HSO3 for H2O2 were calculated to be 2.05 μM and 4.23 μM, respectively. The reversible fluorescence response of NI towards HSO3−/H2O2 couple can be repeated for at least five times. NI is reliable at a broad pH range (pH 3.0–11.5) and features outstanding selectivity, which enabled its practical applications in biological and food samples. Monitoring the reversible and dynamic inter-conversion between HSO3− and H2O2 in vitro and in vivo has been verified by fluorescence imaging in live HeLa cells, adult zebrafish and nude mice. Moreover, NI has been successfully applied to detect of HSO3− levels in food samples. 相似文献
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Qingtao Ma Xiaowen Sun Ping Liu Yongyao Xia Xingjiang Liu Jiayan Luo 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2019,131(19):6266-6272
Progress in lithium‐metal batteries is severely hindered by lithium dendrite growth. Lithium is soft with a mechanical modulus as low as that of polymers. Herein we suppress lithium dendrites by forming soft–hard organic–inorganic lamella reminiscent of the natural sea‐shell material nacres. We use lithium as the soft segment and colloidal vermiculite sheets as the hard inorganic constituent. The vermiculite sheets are highly negatively charged so can absorb Li+ then be co‐deposited with lithium, flattening the lithium growth which remains dendrite‐free over hundreds of cycles. After Li+ ions absorbed on the vermiculite are transferred to the lithium substrate, the vermiculite sheets become negative charged again and move away from the substrate along the electric field, allowing them to absorb new Li+ and shuttling to and from the substrate. Long term cycling of full cells using the nacre‐mimetic lithium‐metal anodes is also demonstrated. 相似文献
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Chong Jia Yong Su Qingtao Zhou Minjun Xin Yousheng Lv Weihai Kong 《Applied Surface Science》2008,254(8):2331-2335
Large scale flower-like ZnO nanosheets have been synthesized on Zinc foil by a simple hydrothermal method. Their morphology and microstructures were characterized and analyzed by X-ray spectroscopy (XRD), field emission scanning electron microscopy (FE-SEM) and high-resolution transmission electron microscopy (HRTEM). The as-synthesized flower-like nanosheets are hexagonal phase single crystal with 200-300 nm in width, 50 nm in thickness. The growth process follows the liquid phase epitaxial growth mechanism. In this approach, the ZnO buffer is used as substrate for the growth of flower-like ZnO nanosheets. The growth direction of the nanosheets is the preferential [0 0 0 1] growth direction of ZnO. The photoluminescence spectrum of the sample exhibits only a sharp and strong UV emission centered at 386 nm, which indicates that the flower-like ZnO nanosheets on Zn foil are of good optical property. 相似文献
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Supramolecular gels exhibit potential applications in the areas of sensors, nanodevices, drug and catalyst carriers, and so on. To develop a novel organogel with a multiresponse, we designed a component molecule bearing a pyridyl group for metal coordination and an amide group for the formation of intermolecular hydrogen bonding. A complex building block with a symmetrical structure was selectively constructed by the coordination of a silver cation to the organic component. The coordination existing in the complex and the hydrogen bonding existing between complexes were examined by IR, Raman, and 1H NMR spectroscopy. The gel formation and phase transition were examined by viscosity and differential scanning calorimetry measurements. The selection of metal ions for the formation of a gel has proved to be crucial as only the complex of a binary coordinated metal ion, Ag+, was found to form a gel structure. From the band shift of the L1 solution with different amounts of silver ion, the binding ratio of silver ion to L1 was estimated to be 1:2 and the calculated stability constant was 3.6 x 10(8) M(-2). On the basis of the analysis of X-ray diffraction and transmission electron microscopy results, we proposed a possible stacking structure of the complex in the fibrous aggregates. Of interest is that the organogel exhibits a 3-D network structure of a beltlike fiber composed of ordered lamellar arrangements of the coordinated complex and shows a rapid response to wide chemical stimulations such as anions I-, Br-, and Cl-, gases such as H(2)S and NH(3), and a change of pH. 相似文献
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