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Electrochemical properties of carbon nanotube-supported metallic catalysts prepared by changing a sweep- or step-applied potential

机译:通过改变扫描或分步施加的电势制备的碳纳米管负载的金属催化剂的电化学性质

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The electrochemical deposition of Pt nanoparticles on carbon nanotube (CNTs) supports and their catalytic activities for an electro-oxidation were investigated. Pt catalysts of 4–12 nm average crystalline size were grown on supports by changing applied potential methods such as sweep-potential or step-potential. Electroplating of 24-min time by a step-applied potential was enough to obtain small crystalline-size 4.6-nm particles, resulting in good electrochemical activity. The catalysts’ loading contents could be controlled by increasing the deposition time. The crystalline sizes and structures of the Pt/support catalysts were analyzed using X-ray diffraction (XRD). The electrochemical properties of the Pt/support catalysts were studied according to their characteristic current–potential curves in a methanol solution. As a result, the electrochemical activity was increased by enlarging the plating time. The activity reached the maximum at 24 min and then decreased. The enhanced electroactivity for catalysts by step-potential methods could be explained by the changes of the crystalline size and crystalline structures of the catalysts.
机译:研究了碳纳米管(CNTs)载体上Pt纳米颗粒的电化学沉积及其对电氧化的催化活性。通过改变施加电势方法(例如扫描电势或阶梯电势),可以在载体上生长4-12 nm平均晶体尺寸的Pt催化剂。用分步施加的电位电镀24分钟的时间足以获得小晶体尺寸的4.6 nm颗粒,从而具有良好的电化学活性。可以通过增加沉积时间来控制催化剂的负载量。使用X射线衍射(XRD)分析了Pt /载体催化剂的晶体尺寸和结构。根据Pt /载体催化剂在甲醇溶液中的特征电流-电位曲线研究了其电化学性质。结果,通过延长镀敷时间来提高电化学活性。活性在24分钟时达到最大值,然后降低。逐步电位法提高的催化剂电活性可以用催化剂的晶体尺寸和晶体结构的变化来解释。

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