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Investigation of the response of separate electrodes in a polymer electrolyte membrane fuel cell without reference electrode

机译:没有参比电极的聚合物电解质膜燃料电池中独立电极的响应研究

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The paper presents electrochemical measurements carried out in a PEMFC with a view to determining the separate kinetics of the electrode reactions. For this purpose, the separate response of one electrode (anode or cathode) was magnified by dilution of the reacting gas, respectively hydrogen and oxygen, and comparison of the experimental data in the form of steady voltage-current variations and impedance spectra. Experiments were carried out at 60 °C and ambient pressure. Water management was thoroughly controlled so that the gases leaving the cell had the same relative humidity in all experiments of one series. Hydrogen oxidation, although rapid, corresponds to overpotentials up to 50 mV at high dilution rates and current densities. Assuming a Tafel–Volmer mechanism, the exchange current density of the anode reaction at the Pt surface is of the order of 1 mA cm−2. The two techniques employed led to Tafel slopes of oxygen reduction ranging from 120 to 150 mV/decade, with an exchange current density near 1 μA cm−2, in good agreement with published data.
机译:本文介绍了在PEMFC中进行的电化学测量,目的是确定电极反应的独立动力学。为此,通过稀释反应气体(分别为氢气和氧气),并以稳定的电压-电流变化和阻抗谱的形式比较实验数据,可以放大一个电极(阳极或阴极)的单独响应。实验在60°C和环境压力下进行。彻底控制水管理,以使离开电解槽的气体在一系列实验中均具有相同的相对湿度。氢氧化虽然很快,但在高稀释率和高电流密度下相当于高达50 mV的过电势。假设采用塔菲尔-沃尔默机制,则在Pt表面的阳极反应的交换电流密度约为1 mA cm-2 。所使用的两种技术导致氧气的Tafel下降斜率范围为120至150 mV /十年,交换电流密度接近1μAcm-2 ,与已发表的数据非常吻合。

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