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PEM电解水用多孔钛表面改性及性能优化研究

Study on surface modification and performance optimization of porous titanium for PEM water electrolysis

  • 摘要: 为满足质子交换膜(PEM)电解水用多孔钛扩散层的高效率制氢需求,本文以不同粒度的Ti粉为原料,采用粉末轧制技术制备了多孔钛板,并通过湿法喷涂-烧结工艺获得了梯度多孔钛扩散层,然后利用扫描电子显微镜、孔径分析检测仪、电化学工作站等手段,研究了烧结温度对其孔结构和耐腐蚀性能的影响规律。研究结果表明:相比于基材,梯度多孔钛扩散层的孔结构进一步优化,其最大孔径和平均孔径有所减小,自腐蚀电位分别向正偏移了218.4 mV、2.3 mV、12.2 mV,自腐蚀电流密度由204.50 μA·cm-2分别减小到2.99 μA·cm-2、46.29 μA·cm-2、131.70 μA·cm-2,耐腐蚀性能得以提高;随着烧结温度的升高,梯度多孔钛扩散层的平均孔径逐渐增大,最大孔径总体减小,自腐蚀电位和自腐蚀电流密度分别呈现降低和增加的趋势;当烧结温度为900 ℃时,Ti91梯度多孔钛扩散层具有最佳的耐腐蚀性能,其自腐蚀电位和自腐蚀电流密度分别为-65.1 mV和2.99 μA·cm-2。这主要归因于其表面稳定钝化膜的存在,避免了试样与腐蚀介质直接接触,减缓了腐蚀介质的侵入,从而降低了腐蚀速率。

     

    Abstract: To meet the high-efficiency hydrogen production requirements of porous titanium diffusion layer for proton exchange membrane (PEM) water electrolysis, this paper used Ti powders with different powder sizes as the raw material to prepare porous titanium plate through powder rolling technology. Subsequently, the gradient porous titanium diffusion layer was obtained via wet spraying and sintering method. The effects of sintering temperature on its pore structure and corrosion resistance were then studied using scanning electron microscope, pore size analyzers, and electrochemical workstation. The results show that compared to the base material, the pore structure of the gradient porous titanium diffusion layers is further optimized, and its maximum and average pore size decrease, and the self-corrosion potential is shifted to the positive direction by 218.4 mV, 2.3 mV and 12.2 mV, respectively, and the self-corrosion current density is reduced from 204.50 μA cm-2 to 2.99 μA·cm-2, 46.29 μA·cm-2 and 131.70 μA·cm-2, respectively, thereby enhancing its corrosion resistance. With the increase of sintering temperature, its average pore size increases, the maximum pore size decreases, the self-corrosion potential and self-corrosion current density show a trend of decrease and increase, respectively. When it sintered at 900 ℃, the Ti91 gradient porous titanium diffusion layer has excellent corrosion resistance, and its self-corrosion potential and self-corrosion current density are -65.1 mV and 2.99 μA·cm-2, respectively.It is mainly due to the presence of a stable passivation film on its surface, which avoids direct contact between the specimen and the corrosive medium, slows down the intrusion of the corrosive medium, and thus reduces the corrosion rate.

     

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