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    Spatial expression of a mercury-inducible green fluorescent protein within a nanoporous latex-based biosensor coating
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    Nanoporous
    Aluminium oxides
    Nanopore
    Anodic Aluminum Oxide
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    Abstract The preparation of nanoporous metal structures has received a substantial amount of attention because of the unique properties and various applications of these structures. In this work, the preparation of nanoporous Pt structures by modification of nanoporous gold (NPG) surfaces with Pt was achieved. An atomic layer electrodeposition (ALED) technique previously reported for the modification of flat Au surfaces with Pt was applied to the NPG surfaces to produce Pt‐modified NPG structures. The optimal ALED parameters, such as deposition potential, time, and number of cycles, for the preparation of Pt‐modified NPG structures were investigated. Scanning electron microscopy and energy‐dispersive X‐ray analysis confirmed the successful preparation of nanoporous Pt structures by ALED techniques. The Pt‐modified NPG performed well as a pH sensor with a Nernstian slope and negligible hysteresis. The method of preparing the nanoporous Pt structures reported in this work could be utilized in various applications such as electrocatalysis and electroanalysis.
    Nanoporous
    Hysteresis
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    有 nano 规模毛孔尺寸的 Nanoporous 铜被 dealloying Mn-Cu 先锋合金用一个免费腐蚀方法综合。结果的 nanoporous 铜的合金阶段,形态学和作文上的 Mn-Cu 先锋的热处理的效果被调查。作文在体积 Mn-Cu 先锋同类地散布,这被揭示,它因而充分导致更多为形成 nanoporous 铜的 dealloying。从到热的 Cu0.33Mn0.67 的 non-thermally 对待的先锋的 Cu0.49Mn0.51 和 Cu0.21Mn0.79 的合金阶段变化对待合金。在 nanoporous 铜的剩余 Mn 内容从 12.97% ~ 2.04% 被减少(臼齿的部分) 没有并且与 95 h 热处理,用先锋做了。dealloying 准备的 nanoporous 铜的典型毛孔形状没有热处理的先锋被划分成二个不同地区:一致双性人连续的结构地区并且模糊或没有毛孔结构地区。Nanoporous 铜具有用对待热的先锋做的一致像海绵的形态学,并且平均系带直径是 40 nm,比那远小从 non-thermally 对待的先锋,平均系带直径在被估计是大约 70 nm。
    Nanoporous
    Morphology
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    For the application of high-surface-area nanoporous platinum (Pt) to catalytic device, electrodes and sensors, dealloying technique, which can synthesize nanoporous Pt, was combined with surface alloying technique. As a result, nanoporous structure with ligament and pore sizes below 10 nm was successfully fabricated on the Pt plate surface. Cyclic voltammetry in H2SO4 indicated that the nanoporous structure increases the true surface area by 170 times. The approximation by spherical pore model suggested that the nanoporous surface layer has a thickness of 200 nm.
    Nanoporous
    Surface structure
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    This work reports the effects of metallic glass precursors on the catalytic performance of nanoporous metals. Pd-based multicomponent nanoporous metals with similar nanoporous structure were successfully fabricated by electrochemically dealloying the Pd20Ni60P17B3 and Pd20Ni20Cu40P17B3 metallic glass precursors at the critical dealloying potentials. It was found that the glassy precursors with different chemical compositions result in different doping elements in the as-obtained nanoporous metals and thus lead to different catalytic activities.
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    3D nanoporous graphene shows excellent physics and electrochemical performance in the fields of energy storage and conversion due to its high-quality and unique interconnected structure. Nanoporous metals, especially nanoporous Ni and nanoporous Cu, have high catalysis for the synthesis of high-quality 3D nanoporous graphene. This chapter presents an overview of the most recent research about the 3D nanoporous graphene, heteroatoms-doped nanoporous graphene, and the nanoporous graphene-based composite materials synthesized by using nanoporous Ni and nanoporous Cu.
    Nanoporous
    Heteroatom
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    Objective To establish a stable expressing green fluorescence protein(GFP) COS-7 cell line and to provide a convenient control for some experiments.Method COS-7 cells were cultured by the conventional method.The pEGFP-N3 plasmid was transfected into COS-7 cells,and cells were screened by G418 until the stable G418-resistant monoclonal cells(COS7-GFP cells) were acquired.The GFP-expression cells were tracked by fluorescent microscope.Results The optimum G418 concentration for screening drug-resistant cell line is 500 μg/mL.All the selected COS7-GFP cells maintain stable biology character and display bright green fluorescence under fluorescent microscope,and GFP protein produced in these cells can be detected by western blotting.Conclusion Stable GFP-expression COS-7 cell line(COS7-GFP cell line) was established successfully.This cell line can be handily used as a control for some experiments.
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