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Electrochemical properties of Rubpy-reduced graphene oxide synergized by ultrasonication for label-free quercetin sensing

机译:用超声波促进摩尔多瓦斯的石墨烯氧化物的电化学性能,用于无标记的槲皮素感应

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摘要

Tuning the interfacial properties of oxygenated graphene and reduced graphene oxide (rGO) with optical/electrochemically active molecules are highly useful for sensor studies. Herein, we demonstrate the ultra-sonochemical mediated simultaneous reduction of oxygenated graphene and adsorption of ruthenium bipyridine complex (Rubpy) on the planes of rGO nanosheets. Different weight percentage ratio of Rubpy was decorated on the planes of rGO by simple alteration in the sonication parameters. Intercalation of Rubpy complex influences the electron cloud of inherent graphitic carbon network and intermolecular oxygenated functional moieties on the rGO matrix. Activation of C=N network derived from bipyridine ligands of organometallic coordination compound, Rubpy, on the rGO planes enable an amplified electron mobility at the interface of electrode beneficial for electrocatalytic analysis. rGO-Rubpy modified electrode enabled direct electrochemical redox reaction of quercetin, exhibiting a linear detection range of 0.05-50 mu M, with a lowest detection limit of 0.002 mu M. Demonstrated label-free sensor platform display selectivity toward quercetin even in the presence of interferents and sensitivity in the real sample, promising for complementary analytical application.
机译:用光/电化学活性分子调节含氧石墨烯和氧化石墨烯(RGO)的界面性质对传感器研究非常有用。在此,我们证明了超声化学介导的含氧石墨烯同时降低,并在RGO纳米片的平面上对钌联吡啶复合物(Rubpy)的吸附。通过简单的超声处理参数更改,在RGO的平面上装饰不同的重量百分比比例。粗糙复合物的嵌入影响固有的石墨碳网络和分子间含氧功能部分对RGO基质的电子云。在RGO平面上激活来自有机金属配位化合物的Bi0赖氨酸配体,ROMPY,在RGO平面上使得在电极的界面处能够在有利的电催化分析的界面处实现扩增的电子迁移率。 rgo-rubpy改性电极使槲皮素的直接电化学氧化还原反应直接,表现出0.05-50μm的线性检测范围,最低检测限为0.002μmm。即使在存在的情况下,无标签的传感器平台显示出对槲皮素的选择性。即使存在真实样本的干扰和敏感性,有希望用于互补的分析应用。

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