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A comparative study of electrochemical techniques in investigating the adsorption behaviour of fibrinogen on platinum

机译:电化学技术研究纤维蛋白原在铂上的吸附行为的比较研究

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摘要

The interfacial behaviour of fibrinogen at a platinum electrode/electrolyte interface has been studied using a series of potentiostatic and potentiodynamic dc and ac electrochemical techniques: cyclic voltammetry, electrochemical quartz crystal nanobalance electrochemical impedance spectroscopy, and differential capacitance. It has been shown that the adsorption of fibrinogen on Pt at anodic potentials is a reversible process, accompanied by the transfer of charge. The adsorbed protein layer has been found to influence the capacitance of the electrode double layer and the homogeneity of the Pt/solution interface. The Langmuir adsorption isotherm has been used to describe the adsorption process, and the corresponding thermodynamic adsorption values have been calculated. A highly negative Gibbs energy of adsorption demonstrates that fibrinogen has a high affinity for the Pt surface, and the adsorption process proceeds spontaneously, driven by a positive gain in adsorption entropy. The thermodynamic data obtained in a wide potential region indicate that the change in anodic Pt surface charge does not influence the adsorption equilibrium, once the protein is already adsorbed on the Pt surface at high anodic potentials. Excellent agreement between the thermodynamic values has been obtained using four experimental techniques and five measurement variables.
机译:纤维蛋白原在铂电极/电解质界面上的界面行为已使用一系列恒电位和恒动力直流和交流电化学技术进行了研究:循环伏安法,电化学石英晶体纳米平衡电化学阻抗谱和差分电容。已经表明,纤维蛋白原在阳极电位上在Pt上的吸附是可逆的过程,伴随着电荷的转移。已发现吸附的蛋白质层会影响电极双层的电容和Pt /溶液界面的均匀性。用Langmuir吸附等温线描述了吸附过程,并计算了相应的热力学吸附值。极负的吉布斯吸附能表明,纤维蛋白原对Pt表面具有很高的亲和力,并且在吸附熵的正增益的驱动下,吸附过程自发进行。在较宽的电势区域获得的热力学数据表明,一旦蛋白质已经在高阳极电势上吸附在Pt表面上,则阳极Pt表面电荷的变化不会影响吸附平衡。使用四种实验技术和五个测量变量获得了热力学值之间的极佳一致性。

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