Temperature Effect on Hydrogen Evolution Reaction at Au Electrode  

金电极上氢析出反应的温度效应

作　　者：汤志强[1] 廖玲文[1] 郑勇力[1] 康婧[1] 陈艳霞[1] 

机构地区：[1]中国科学技术大学合肥微尺度物质科学国家实验室(筹),化学物理系,合肥230026

出　　处：《Chinese Journal of Chemical Physics》2012年第4期469-474,I0004,共7页化学物理学报（英文）

基　　金：V, ACKNOWLEDGMENTS This work was supported by one Hundred Talents＇ Program of the Chinese Academy of Science, the National Natural Science Foundation of China （No.21073176）, and 973 Program from the Ministry of Science and Technology of China （No.2010CB923302）.

摘　　要：The temperature dependence of hydrogen evolution reaction （HER） at a quasi-single crystalline gold electrode in both 0.1 mol/L HCl04 and 0.1 mol/L KOH solutions was investigated by cyclic voltammetry. HER current displays a clear increase with reaction overpotential （η） and temperature from 278-333 K. In 0.1 mol/L HClO4 the Tafel slopes are found to increases slightly with temperature from 118 mV/dec to 146 mV/dec, while in 0.1 mol/L KOH it is ca. 153±15 mV/dec without clear temperature-dependent trend. The apparent activation energy （Ea） for HER at equilibrium potential is ca. 48 and 34 kJ/mol in 0.1 mol/L HC104 and 0.1 mol/L KOH, respectively. In acid solution, Ea decreases with increase in η, from Ea-37 kJ/mol （η=0.2 V） to 30 kJ/mol （η=0.35 V）. In contrast, in 0.1 mol/L KOH, Ea does not show obvious change with U. The pre-exponential factor （A） in 0.1 mol/L HC104 is ca. 1 order higher than that in 0.1 mol/L KOH. Toward more negative potential, in 0.1 mol/L HC104 A changes little with potential, while in 0.1 mol/L KOH it displays a monotonic increase with U. The change trends of the potential-dependent kinetic parameters for HER at Au electrode in 0.1 mol/L HClO4 and that in 0.1 mol/L KOH are discussed.

关 键 词：Hydrogen evolution reaction Au electrode Temperature effect Activation energy Symmetric factor 

分 类 号：O[理学]