Ti/TiO2电极开路电位测量

Marcelo J. Avena, Osvaldo R. Cámara, Carlos P. De Pauli
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引用次数: 30

摘要

测定了金属钛热氧化和电化学氧化制备的Ti/TiO2电极在KNO3水溶液中的开路电位(OCP)与pH响应,以确定OCP-pH曲线的斜率是否可以作为TiO2表面电位(ψo)随水溶液pH变化的指标。为了比较起见,我们还从TiO2分散体的酸碱电位滴定得到的表面电荷- ph数据中评估了ψ - ph斜率。Ti/TiO2电极在ph 5 ~ 10范围内呈线性OCP-pH响应,斜率为−0.039±0.005 V ph−1。Ti/TiO2电极的OCP-pH依赖性低于热力学预测。根据描述氧化物/水溶液界面的三层模型,得到的Ti/TiO2电极的OCP-pH斜率不能用ψo随ph的变化来识别。该模型的计算表明,用于评估氧化物表面位置的本征电离常数的单外推法和双外推法都不能给出TiO2表面这些参数的真实值。通过对表面电荷- pH数据的分析和利用三层模型对实验值的预测表明,TiO2表面的ψ - pH斜率必须大于(绝对值)0.041 V pH−1。
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Open circuit potential measurements with Ti/TiO2 electrodes

The open circuit potential (OCP) vs pH response of Ti/TiO2 electrodes prepared by thermal and electrochemical oxidation of metallic titanium was measured in KNO3 aqueous solutions in order to establish whether the slopes of the OCP-pH curves can be used as a measure of the variation of surface potential (ψo) of TiO2 with the pH of the aqueous solution. For comparison purposes, ψo—pH slopes were also evaluated from surface charge-pH data obtained by acid-base potentiometric titrations of TiO2 dispersions.

Ti/TiO2 electrodes showed a linear OCP-pH response in the range of ph 5–10 with slopes of −0.039 ± 0.005 V ph−1. The OCP-pH dependence of Ti/TiO2 electrodes was lower than that predicted thermodynamically. According to the triple-layer model, used to describe the oxide/aqueous solution interface, the OCP-pH slopes obtained for Ti/TiO2 electrodes cannot be identified with the variation of ψo with the pH. Calculations with this model indicated that neither the single nor the double extrapolation methods used to evaluate the intrinsic ionization constant of oxide surface sites render realistic values of these parameters for the TiO2 surface.

The analysis of surface charge—pH data and the use of the triple-layer model to predict experimental values indicated that the ψo—pH slopes of TiO2 surfaces must be greater (in absolute magnitude) than 0.041 V pH−1.

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