Jesús Ramsés Cardona-Canto, J. Cruz-Argüello, Danna Lizeth Trejo-Arroyo, Daniel Canté-Góngora
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引用次数: 0
摘要
氢是一种有吸引力的能量载体,电解水是最有效的制氢工艺。阳极的OER是研究的极限反应。本文采用两种化学还原合成的机械混合物,分别以100、70:30、50:50、30:70的机械混合比例制备了基于IrO2和WO3的工作材料。将6.25 mM的IrCl3溶解在异丙醇中,用1M NaOH调节pH,用0.5 mol NH4OH还原剂调节碱性pH为13,得到IrO2。过滤得到的前驱体,在400℃下煅烧1hr。将10mM WCl6溶解于异丙醇和聚乙二醇中得到WO3,生成W (OH)x的前驱体,然后在500℃下煅烧1hr。用CV、LV和EIS电化学技术对材料进行了表征。IrO2-WO3(50:50)材料在室温下具有较低的过电位活化能,在1.8V vs Hg/Hg2SO4下的最大电流密度接近20 mA /cm2。
Aplicación de nanopartículas de IrO2-WO3 como material anódico para la Reacción de Evolución de Oxígeno en un medio ácido
The hydrogen is an attractive energy carrier and electrolysis of water is the most efficient to H2 production process. The OER in the anode is the limiting reaction being the case of study. In the present work materials based on IrO2 and WO3 were developed in different mechanical mixing 100, 70:30, 50:50, 30:70, respectively, by means of a mechanical mixture from two chemical reduction syntheses. The IrO2 was obtained by 6.25 mM of IrCl3 dissolved in isopropyl alcohol by adjusting the pH with 1M NaOH and a 0.5 mol NH4OH reductant was applied by adjusting a basic pH of 13. The obtained precursor was filtered and calcined at 400 ° C for 1hr. WO3 was obtained from 10mM WCl6 dissolved in isopropyl alcohol and polyethylene glycol, generating a precursor of W (OH)x followed by a calcination process at 500 ° C for 1hr. The material was characterized by electrochemical techniques of CV, LV and EIS. The IrO2-WO3 (50:50) material has lower activation energy of overpotential at room temperature, and a maximum current density close to 20 mA /cm2 at 1.8V vs Hg/Hg2SO4.