Suppr超能文献

极化作用下非晶态钛酸钡薄膜中的巨大应变与诱导铁电性

Giant Strain and Induced Ferroelectricity in Amorphous BaTiO₃ Films under Poling.

作者信息

Vaghefi Pegah Mirzadeh, Baghizadeh Ali, Lourenço Armando A C S, Amaral Vitor S, Kholkin Andre L

机构信息

Department of Physics & CICECO-Aveiro Institute of Materials, University of Aveiro, 3810-193 Aveiro, Portugal.

Department of Materials and Ceramics Engineering & CICECO-Aveiro Institute of Materials, University of Aveiro, 3810-193 Aveiro, Portugal.

出版信息

Materials (Basel). 2017 Sep 20;10(9):1107. doi: 10.3390/ma10091107.

Abstract

We report an effect of giant surface modification of a 5.6 nm thick BaTiO₃ film grown on Si (100) substrate under poling by conductive tip of a scanning probe microscope (SPM). The surface can be locally elevated by about 9 nm under -20 V applied during scanning, resulting in the maximum strain of 160%. The threshold voltage for the surface modification is about 12 V. The modified topography is stable enough with time and slowly decays after poling with the rate ~0.02 nm/min. Strong vertical piezoresponse after poling is observed, too. Combined measurements by SPM and piezoresponse force microscopy (PFM) prove that the poled material develops high ferroelectric polarization that cannot be switched back even under an oppositely oriented electric field. The topography modification is hypothesized to be due to a strong Joule heating and concomitant interface reaction between underlying Si and BaTiO₃. The top layer is supposed to become ferroelectric as a result of local crystallization of amorphous BaTiO₃. This work opens up new possibilities to form nanoscale ferroelectric structures useful for various applications.

摘要

我们报道了在扫描探针显微镜(SPM)的导电尖端极化下,生长在Si(100)衬底上的5.6 nm厚的BaTiO₃薄膜的巨大表面改性效应。在扫描过程中施加-20 V电压时,表面可局部升高约9 nm,导致最大应变达160%。表面改性的阈值电压约为12 V。改性后的形貌随时间足够稳定,极化后会缓慢衰减,速率约为0.02 nm/min。极化后也观察到强烈的垂直压电响应。SPM和压电响应力显微镜(PFM)的联合测量证明,极化后的材料会产生高铁电极化,即使在相反方向的电场下也无法反转回来。形貌改性被推测是由于强烈的焦耳热以及底层Si与BaTiO₃之间伴随的界面反应。顶层被认为是由于非晶态BaTiO₃的局部结晶而变成铁电体。这项工作为形成可用于各种应用的纳米级铁电结构开辟了新的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8494/5615760/9ed7db35d279/materials-10-01107-g001.jpg

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验