El-Taib Heakal F, Abd-Ellatif W R, Tantawy N S, Taha A A
Chemistry Department, Faculty of Science, Cairo University Giza 12613 Egypt
Faculty of Women for Arts, Science and Education, Ain Shams University Cairo 11566 Egypt.
RSC Adv. 2018 Nov 26;8(69):39321-39333. doi: 10.1039/c8ra06899b. eCollection 2018 Nov 23.
Electrochemical characterization of anodically grown thin ZnO films on pure zinc metal was studied in pH 9.2 bicarbonate/carbonate buffer solution. The different undoped passive films were formed potentiostatically in pH 9.2 borate buffer solution at processing anodic voltage ( ) of -1.04, -1.02, -1.0 and -0.99 V ( Ag/AgCl). While, various doped ZnO films were fabricated by anodizing the metal at a fixed potential of -1.00 V in the same borate buffer solution containing different amounts of LiCl or InCl. The electrochemical and semiconducting properties of all formed films were investigated using chronoamperometric measurements, EIS and Mott-Schottky analysis supported by scanning electron microscopy. The impedance results showed a direct correlation between and the value of either total resistance ( ) of undoped passive film or its thickness ( ). It is evident that anodization can afford better conditions for forming thicker compact passive films with more advanced barrier properties. On the other hand, decreases with increasing Li-doping level in the oxide film, and increases in case of In-doping. Interestingly, values of the doped films are always lower when compared to its value for the undoped film grown at -1.00 V, likely due to possible change in the film microstructure upon doping. For both undoped and doped ZnO films, Mott-Schottky plots reveals unintentional n-type conductivity with high electron density. Moreover, with increasing dopant level in ZnO host materials, Mott-Schottky analysis revealed a parallel correlation between charge carrier donor concentration ( ) and the passive film thickness ( ), where the trend of their values are to decrease for Li-doped and to increase for In-doped films.
在pH 9.2的碳酸氢盐/碳酸盐缓冲溶液中研究了在纯锌金属上阳极生长的ZnO薄膜的电化学特性。在pH 9.2的硼酸盐缓冲溶液中,通过恒电位法在-1.04、-1.02、-1.0和-0.99 V(Ag/AgCl)的处理阳极电压( )下形成不同的未掺杂钝化膜。同时,通过在含有不同量LiCl或InCl的相同硼酸盐缓冲溶液中以-1.00 V的固定电位对金属进行阳极氧化来制备各种掺杂的ZnO薄膜。使用计时电流测量、电化学阻抗谱(EIS)和莫特-肖特基分析,并辅以扫描电子显微镜,研究了所有形成薄膜的电化学和半导体性能。阻抗结果表明 与未掺杂钝化膜的总电阻( )值或其厚度( )之间存在直接相关性。显然,阳极氧化可以提供更好的条件来形成具有更先进阻挡性能的更厚致密钝化膜。另一方面,随着氧化膜中Li掺杂水平的增加, 降低,而In掺杂时 增加。有趣的是,与在-1.00 V下生长的未掺杂膜相比,掺杂膜的 值总是更低,这可能是由于掺杂后膜微观结构的可能变化。对于未掺杂和掺杂的ZnO薄膜,莫特-肖特基图显示出具有高电子密度的无意n型导电性。此外,随着ZnO主体材料中掺杂剂水平的增加,莫特-肖特基分析揭示了电荷载流子施主浓度( )与钝化膜厚度( )之间的平行相关性,其中Li掺杂膜的值呈下降趋势,而In掺杂膜的值呈上升趋势。