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Identification of Non-Faradaic Processes by Measurement of the Electrochemical Peltier Heat during the Silver Underpotential Deposition on Au(111)

机译:通过测量Au(111)上银欠电位沉积过程中的电化学帕尔贴热量来鉴定非法拉第过程

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We measured the heat which is reversibly exchanged during the course of an electrochemical surface reaction, i.e., the deposition/dissolution of the first two monolayers of Ag on a Au(111) surface in (bi)sulfate and perchlorate containing electrolytes. The reversibly exchanged heat corresponds to the Peltier heat of the reaction and is linearly related to its entropy change, including also non-Faradaic side processes. Hence, the measurement of the Peltier heat provides thermodynamic information on the electrochemical processes which is complementary to the current-potential relations usually obtained by conventional electrochemical methods. From the variation of the molar Peltier heat during the various stages of the deposition reaction we inferred that co-adsorption processes of anions and Ag do not play a prominent role, while we find strong indications for a charge neutral substitution reaction of adsorbed anions by hydroxide, which would not show up in cyclic voltammetry.
机译:我们测量了在电化学表面反应过程中可逆交换的热量,即在含(双)硫酸盐和高氯酸盐的电解质中,Ag的前两个单层在Au(111)表面上的沉积/溶解。可逆交换的热对应于反应的珀耳帖热,并且与它的熵变线性相关,包括非法拉第副过程。因此,珀耳帖热量的测量提供了有关电化学过程的热力学信息,该信息与通常通过常规电化学方法获得的电流-电位关系互补。从沉积反应各个阶段的珀尔帖热摩尔变化,我们推断出阴离子和Ag的共吸附过程没有发挥重要作用,而我们发现强烈的迹象表明被氢氧化物吸附的阴离子具有电荷中性取代反应,这在循环伏安法中不会出现。

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