Interface control of surface photochemical reactivity in ultrathin epitaxial ferroelectric films

被引:29
作者
Chen, Jason [1 ,2 ]
Lu, Haidong [3 ]
Liu, Heng-Jui [4 ]
Chu, Ying-Hao [4 ]
Dunn, Steve [5 ]
Ostrikov, Kostya [2 ,6 ]
Gruverman, Alexei [3 ]
Valanoor, Nagarajan [1 ]
机构
[1] Univ New S Wales, Sch Mat Sci & Engn, Sydney, NSW 2052, Australia
[2] CSIRO Mat Sci & Engn, Lindfield, NSW 2070, Australia
[3] Univ Nebraska, Dept Phys & Astron, Lincoln, NE 68588 USA
[4] Natl Chiao Tung Univ, Dept Mat Sci & Engn, Hsinchu, Taiwan
[5] Queen Mary Univ London, Sch Engn & Mat, London E1 4NS, England
[6] Univ Sydney, Sch Phys, Sydney, NSW 2006, Australia
基金
澳大利亚研究理事会; 英国工程与自然科学研究理事会; 美国国家科学基金会;
关键词
TITANIA FILMS; POLARIZATION; REDUCTION; SILVER;
D O I
10.1063/1.4802885
中图分类号
O59 [应用物理学];
学科分类号
摘要
Asymmetrical electrical boundary conditions in (001)-oriented Pb(Zr0.2TiO0.8)O-3 (PZT) epitaxial ultrathin ferroelectric films are exploited to control surface photochemical reactivity determined by the sign of the surface polarization charge. It is shown that the preferential orientation of polarization in the as-grown PZT layer can be manipulated by choosing an appropriate type of bottom electrode material. PZT films deposited on the SrRuO3 electrodes exhibit preferential upward polarization (C+) whilst the same films grown on the (La, Sr)CoO3-electrodes are polarized downward (C-). Photochemical activity of the PZT surfaces with different surface polarization charges has been tested by studying deposition of silver nanoparticles from AgNO3 solution under UV irradiation. PZT surfaces with preferential C+ orientation possess a more active surface for metal reduction than their C- counterparts, evidenced by large differences in the concentration of deposited silver nanoparticles. This effect is attributed to band bending at the bottom interface which varies depending on the difference in work functions of PZT and electrode materials. (C) 2013 AIP Publishing LLC.
引用
收藏
页数:5
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