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101.
生物体内的细胞通常会分泌各种各样的蛋白质,这些蛋白质在生物体中发挥着重要作用,尤其是可被用于诊断各种疾病的发生和发展。多肽具有良好选择性、空间适应能力和识别灵活的特点,可与不同类型的蛋白分子形成非共价键,用于蛋白质的生物检测。将多肽与电化学生物传感器结合用于蛋白质的广谱检测具有良好的发展前景。本文介绍了多肽修饰的电化学传感器在不同蛋白质检测方面的研究进展,分析了待测蛋白质的不同对多肽修饰的电化学传感器分类的影响及其优缺点,提出了基于多肽的电化学传感器在不同蛋白质检测中存在的问题,并展望了其未来发展。 相似文献
102.
K. Alagumalai R. Shanmugam T.-W. Chen S.-M. Chen M. Balamurugan S.S. Choi M.A. Ali A.M. Al-Mohaimeed C.-H. Fan 《Materials Today Chemistry》2022
In this work, we developed a perovskite structured samarium cobalt oxide nanoparticles (SmCoO3 NPs) with the aid of the co-precipitation method. The rare earth metal (Sm) and cobalt oxide combined to form a perovskite lattice structure. One-pot route synthesized SmCoO3 NPs were scrutinized successfully through various physicochemical techniques. Concerning its effective thermal stability and electrical properties, the synthesized SmCoO3 NPs have been effectively implemented in the electrochemical evaluation of promethazine hydrochloride (PHY) using cyclic voltammetry. The electrochemical detection of PHY was performed through SmCoO3 NPs-modified glassy carbon electrode (GCE) and unmodified GCE. The electron transfer kinetics, effect of scan rate, the influence of pH, electroactive surface area, selectivity, and sensitivity have been studied. The electron charge transfer rate (Rct) and electrolyte resistance (Rs) were calculated to be 105.59 (Ω) and 150 (Ω) in the ferricyanide probe, indicating great facilitation of the electron transfer between PHY and SmCoO3 NPs deposited on the electrode surface. Further, the optimized SmCoO3-modified GCE exemplifies excellent selectivity, storage stability, reproducibility, repeatability, detection limit (5 nM), sensitivity (0.594 μA μM?1 cm?2), and wide consecutive linear ranges, respectively. Besides, the proposed method has been effectively employed for the detection of PHY in the various real samples which reveals good recoveries of 95.40–99.17%. 相似文献
103.
《Journal of Saudi Chemical Society》2022,26(4):101514
A facile, single-step hydrothermal route is followed to prepare ZnS nanowires with large aspect ratios. The obtained ZnS nanowires deposited on nickel foam (ZnS/Ni-foam) exhibit a specific capacitance of 781 F/g at a current density of 0.5 A/g. An asymmetric supercapacitor fabricated from ZnS/Ni-foam as a positive electrode and jute derived activated carbon coated on Ni-foam (JAC/Ni-foam) as a negative electrode attains a high specific capacitance of 573 F/g at a current density of 0.5 A/g, with an accompanying high energy density of 51 Wh/kg at a power density of 200 W/kg in an extensive operating potential window of 1.2 V. In addition, the ZnS//JAC asymmetric supercapacitor reveals long-term cyclic stability, after 10,000 GCD cycles the device sustain around ~87 % of the initial specific capacitance. These results shed enlighten a new opportunity for promising electrode materials in supercapacitors. 相似文献
104.
《Arabian Journal of Chemistry》2022,15(9):104026
Organic carbonyl-based compounds with redox-active site have recently gained full attention as organic cathode material in lithium-ion batteries (LIBs) owing to its high cyclability, low cost, high abundance, tunability of their chemical structure compared to traditionally used inorganic material. However, the utilization of organic carbonyl-based compounds in LIBs is limited to its poor charge capacity and dissolution of lower molecular weight species in electrolytes. In this study, we theoretically investigated five set of cyclohexanone derivatives (denoted as: H1, H2, H3, H4, and H5) and influence of functional groups (-F and -NH2) on their electrochemical properties using advanced level density functional theory (DFT) with the Perdew-Burke-Ernzenhof hybrid functional (PBE0) at 6-31+G(d,p) basis set. In line with the result gotten, the HOMO-LUMO results revealed that compound H5 is the most reactive among the studied cyclohexanone derivatives exhibiting energy gap values of 0.552, 0.532, 0.772 eV for free optimized structures and structurally engineered structures with electron withdrawing group (EWG) and electron donating group (EDG) respectively. Also, results from electrochemical properties of the studied compounds lithiated with only one lithium atom displayed that compound H2 exhibited interesting redox potential and energy density for all the studied structures in free optimized state (1108.28 W h kg?1, 4.92 V vs Li/Li+), with EWG (648.22 W h kg?1, 3.313 V Li/Li+), and with EDG (1002.4 W h kg?1, 5.011 V vs Li/Li+). From our result, we can infer that compound H2 and H3 with corresponding redox potential, energy density and theoretical charge capacity value of 4.92 V vs Li/Li+, 1108.28 W h kg?1, 225.26 mA h g?1 and 5.168 V, 1041.61 W h kg?1, 201.55 mA h g?1 lithiated with only one lithium atom in free optimized state are the most suitable compounds to be employed as organic cathode material in lithium-ion batteries among all the investigated cyclohexanone derivatives. 相似文献
105.
Herein, we investigated the analytical features of potentiometric immunosensors for detection of alpha-fetoprotein (AFP) in hepatocellular carcinoma at different electrodes, such as carbon fiber microelectrode (CFME) and carbon-disk electrode (CDE), respectively. To construct such an immunosensor, anti-AFP capture antibodies were first conjugated covalently onto the activated electrodes through typical carbodiimide coupling. Thereafter, one-step immunoreaction protocol was successfully introduced to develop a new potentiometric immunoassay upon addition of AFP. Accompanying the antigen-antibody reaction, the surface charges of the modified electrodes were changed for the readout of electric potential. Results indicated that the linear range of CDE-based immunosensor was 0.1–100 ng mL−1 AFP, whereas the assay sensitivity by using CFME could be further increased to 3.2 pg mL−1 with the linear range from 0.01 to 500 ng mL−1 AFP. Meanwhile, CFME-based immunosensor showed high sensitivity, good reproducibility and specificity, and could be utilized for the analysis of human serum specimens with consistent results relative to commercialized ELISA kit. 相似文献
106.
Tien Song Hiep Pham Shinichi Hasegawa Peter Mahon Katia Guérin Marc Dubois Aimin Yu 《Electroanalysis》2022,34(3):435-444
Three reduced graphene oxide nanocomposites were employed to achieve the simultaneous electrochemical determination of multi-drugs including acetaminophen (ACTM), carbendazim (CB) and ciprofloxacin (CFX). All nanocomposite modified electrodes showed improved current responses for three drugs. Notably cauliflower-like platinum nanoparticles decorated reduced graphene oxide modified electrode (or Pt−RGO/GCE) exhibited the best performance in terms of electrochemical stability. Using Pt−RGO/GCE, the linear detect ranges of 30–120 μM, 25–115 μM and 10–25 μM, and detection limit values of 3.49, 2.96, and 1.53 μM were achieved for ACTM, CB and CFX respectively. The electrode was further used for the successful determination of above drugs in tap and river water using differential pulse voltammetry. From the obtained results, we believe that Pt-RGO/GCE is highly promising for the fabrication of robust electrochemical sensors for simultaneously determining ACTM, CB and CFX or similar types of drugs in the future. 相似文献
107.
Taking advantage of large conjugated structure and reductivity of boron-doped graphenethe palladium nanoparticles/boron-doped graphene catalyst was prepared by electroless deposition method using boron-doped graphene as reductant and stabilizer. The average size of palladium nanoparticles highly dispersed on the surface of boron-doped graphene was about 6.5 nm. The electrochemical sensor was prepared by modifying the as-formed catalyst on the surface of glassy carbon electrode. The obtained electrochemical sensor exhibited an excellent electrochemical catalytic activity for H2 O2 . It exhibited high sensitivity with the detection limit as low as 830 nmol/L and good linearity in the range of 2.5-300 μµmol/L for detection of H2 O2 . It could be utilized for the determination of H2 O2 in milk samples. © 2022, Youke Publishing Co.,Ltd. All rights reserved. 相似文献
108.
Fossil fuels are expected to be the major source of energy for the next few decades. However, combustion of nonrenewable resources leads to the release of large quantities of CO2, the primary greenhouse gas. Notably, the concentration of CO2 in the atmosphere is increasing annually at an astounding rate. Electrochemical CO2 reduction (ECR) to value-added fuels and chemicals using electricity from intermittent renewable energy sources is a carbon-neutral method to alleviate anthropogenic CO2 emissions. Despite the steady progress in the selective generation of C1 products (CO and formic acid), the production of multi-carbon species still suffers from low selectivity and efficiency. As an ECR product, ethylene (C2H4) has a higher energy density than do C1 species and is an important industrial feedstock in high demand. However, the conversion of CO2 to C2H4 is plagued by low productivity and large overpotential, in addition to the severe competing hydrogen evolution reaction (HER) during the ECR. To address these issues, the design and development of advanced electrocatalysts are critical. Here, we demonstrate fine-tuning of ECR to C2H4 by taking advantage of the prominent interaction of Cu with shape-controlled CeO2 nanocrystals, that is, cubes, rods, and octahedra predominantly covered with (100), (110), and (111) surfaces, respectively. We found that the selectivity and activity of the ECR depended strongly on the exposed crystal facets of CeO2. The overall ECR Faradaic efficiency (FE) over Cu/CeO2(110) (FE ≈ 56.7%) surpassed that of both Cu/CeO2(100) (FE ≈ 51.5%) and Cu/CeO2(111) (FE ≈ 48.4%) in 0.1 mol·L-1 KHCO3 solutions with an H-type cell. This was in stark contrast to the exclusive occurrence of the HER over pure carbon paper, CeO2(100), CeO2(110), and CeO2(111). In particular, the FE toward C2H4 formation and the partial current density increased in the sequence Cu/CeO2(111) < Cu/CeO2(100) < Cu/CeO2(110) within applied bias potentials from -1.00 to -1.15 V (vs. the reversible hydrogen electrode), reaching 39.1% over Cu/CeO2(110) at a mild overpotential (1.13 V). The corresponding values for Cu/CeO2(100) and Cu/CeO2(111) were FEC2H4 ≈ 31.8% and FEC2H4 ≈ 29.6%, respectively. The C2H4 selectivity was comparable to that of many reported Cu-based electrocatalysts at similar overpotentials. Furthermore, the FE for C2H4 remained stable even after 6 h of continuous electrolysis. The superior ECR activity of Cu/CeO2(110) to yield C2H4 was attributed to the metastable (110) surface, which not only promoted the effective adsorption of CO2 but also remarkably stabilized Cu+, thereby boosting the ECR to produce C2H4. This work offers an alternative strategy to enhance the ECR efficiency by crystal facet engineering. 相似文献
109.
本文开发了基于纳米金修饰的碳纤维超微电极(CFME)用于儿茶素的定量检测。通过使用柠檬酸三钠还原氯金酸制得纳米金粒子(AuNPs),采用恒电位电沉积法将纳米金修饰在CFME表面。在pH 2.00的Tris-HCl缓冲溶液中,采用差分脉冲法和循环伏安法考察了修饰前后电极对儿茶素的电催化性能。结果表明,纳米金修饰电极对儿茶素具有明显的电催化效果。在优化实验条件下,纳米金修饰的碳纤维超微电极(AuNPs/CFME)与儿茶素浓度在1.00×10-3~10.0μmol/L范围内呈良好的线性关系,且AuNPs/CFME的电化学性能非常稳定,具有良好的重现性。该方法操作简单,准确性高,可用于对儿茶素进行定量检测。 相似文献
110.