{"title":"Manipulating Charged Domain Wall Arrays in BiFeO<sub>3</sub> Films by Asymmetric Electrical Boundary Conditions.","authors":"Wen-Wen Fan, Shuang-Jie Chen, Li-Xin Yang, ChangJi Li, Jiaqi Liu, Yu-Jia Wang, Yin-Lian Zhu, Xiu-Liang Ma, Yun-Long Tang","doi":"10.1021/acsnano.5c06742","DOIUrl":null,"url":null,"abstract":"<p><p>Charged domain walls (CDWs) in ferroelectric thin films have been identified as reconfigurable functional elements for advanced nanoelectronics, owing to their enhanced electrical conductivity and field-tunable topology. Deterministic control of stable CDWs remains a critical challenge due to insufficient understanding of their atomic-scale mechanisms. Here, we present a method for controllable introduction of CDWs in BiFeO<sub>3</sub> thin films. By making use of atom resolved scanning transmission electron microscopy (STEM), we specified the stabilization principle of head-to-head and tail-to-tail CDW arrays in ultrathin BiFeO<sub>3</sub> epitaxial films governed by asymmetric electrical boundary conditions, which were grown on SrTiO<sub>3</sub> substrates. Atomic scale analysis of the lattice parameters and Fe ion displacements show distinct structural responses at head-to-head and tail-to-tail CDWs. Specifically, a reduction of in-plane lattice constant was observed at head-to-head CDWs, whereas an increase of in-plane lattice constant was identified at tail-to-tail CDWs. Moreover, the in-plane Fe ion displacements exhibit a continuous and periodic variation along the alternating head-to-head and tail-to-tail CDWs. These phenomena are governed by interfacial screening charge asymmetry, which plays a crucial role in stabilizing CDW arrays in dimensionally confined ferroelectrics. Our study advances the manipulation of interfacial screening and polarizations of ferroelectric films, facilitating the development of domain-wall-based nanoelectronic devices.</p>","PeriodicalId":21,"journal":{"name":"ACS Nano","volume":" ","pages":""},"PeriodicalIF":15.8000,"publicationDate":"2025-07-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Nano","FirstCategoryId":"88","ListUrlMain":"https://doi.org/10.1021/acsnano.5c06742","RegionNum":1,"RegionCategory":"材料科学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0
Abstract
Charged domain walls (CDWs) in ferroelectric thin films have been identified as reconfigurable functional elements for advanced nanoelectronics, owing to their enhanced electrical conductivity and field-tunable topology. Deterministic control of stable CDWs remains a critical challenge due to insufficient understanding of their atomic-scale mechanisms. Here, we present a method for controllable introduction of CDWs in BiFeO3 thin films. By making use of atom resolved scanning transmission electron microscopy (STEM), we specified the stabilization principle of head-to-head and tail-to-tail CDW arrays in ultrathin BiFeO3 epitaxial films governed by asymmetric electrical boundary conditions, which were grown on SrTiO3 substrates. Atomic scale analysis of the lattice parameters and Fe ion displacements show distinct structural responses at head-to-head and tail-to-tail CDWs. Specifically, a reduction of in-plane lattice constant was observed at head-to-head CDWs, whereas an increase of in-plane lattice constant was identified at tail-to-tail CDWs. Moreover, the in-plane Fe ion displacements exhibit a continuous and periodic variation along the alternating head-to-head and tail-to-tail CDWs. These phenomena are governed by interfacial screening charge asymmetry, which plays a crucial role in stabilizing CDW arrays in dimensionally confined ferroelectrics. Our study advances the manipulation of interfacial screening and polarizations of ferroelectric films, facilitating the development of domain-wall-based nanoelectronic devices.
期刊介绍:
ACS Nano, published monthly, serves as an international forum for comprehensive articles on nanoscience and nanotechnology research at the intersections of chemistry, biology, materials science, physics, and engineering. The journal fosters communication among scientists in these communities, facilitating collaboration, new research opportunities, and advancements through discoveries. ACS Nano covers synthesis, assembly, characterization, theory, and simulation of nanostructures, nanobiotechnology, nanofabrication, methods and tools for nanoscience and nanotechnology, and self- and directed-assembly. Alongside original research articles, it offers thorough reviews, perspectives on cutting-edge research, and discussions envisioning the future of nanoscience and nanotechnology.