铁电性
材料科学
极化(电化学)
矫顽力
薄膜
化学气相沉积
电介质
矿物学
化学工程
分析化学(期刊)
纳米技术
光电子学
化学
物理化学
凝聚态物理
有机化学
物理
工程类
作者
Takayuki Watanabe,Takashi Kojima,Tomohiro Sakai,Hiroshi Funakubo,Minoru Osada,Yuji Noguchi,Masaru Miyayama
摘要
The site engineering approach based on site-selective substitutions was utilized to improve the ferroelectric properties in Bi4Ti3O12 thin film. Thin films of (Bi4−xNdx)(Ti3−yVy)O12 with both A- and B-sites substitutions were deposited on (111)Pt/Ti/SiO2/Si substrates at 600 °C by metalorganic chemical vapor deposition. Although the films substituted for the A site by Nd, (Bi4−xNdx)Ti3O12, showed no significant improvement in ferroelectricity, additional substitution for the B site by V contributed to a large ferroelectricity. Superior properties compared to (Bi4−xLax)(Ti3−yVy)O12 were confirmed for (Bi4−xNdx)(Ti3−yVy)O12 films. We also showed orientation control using Ru-based substrates. (104)-preferred orientation was obtained on (111)Pt/Ti/SiO2/Si substrates, while (110) and (111) orientations with an advantage for large polarization were stabilized on (001)Ru/SiO2/Si substrates and actually a larger ferroelectricity was obtained; the remanent polarization (2Pr) and coercive field (2Ec) of the (Bi3.35Nd0.65)(Ti2.87V0.13)O12 film were 34 μC/cm2 and 290 kV/cm, respectively. No fatigue phenomenon was also observed for the (Bi3.35Nd0.65)(Ti2.87V0.13)O12 film up to 109 switching cycles.
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