Abstract
Manipulating topotactic phase transformations via orderly ion transfer in complex oxides ABO x is ubiquitous in advanced applications such as ionotronics, ion-batteries and catalysts. Most of such ion-mediated transformations are accomplished by the transfer of oxygen or A-site ions. However, implementing the transformation via the transfer of B-site ions, despite the great challenge to overcome a large cohesive energy, has unique advantage since they host most functional properties of materials. Here, we present a tri-state phase transformation from perovskite (P) to brownmillerite (BM) and to single-layered perovskite (SL) structure via the concerted migration of oxygen and B-site Co-ions in La 0.7 Sr 0.3 CoO 3 thin films. Ac-STEM, XPS, XAS, PNR, magnetic and electric measurements demonstrated that presented B-site Co-cation transfer is along the CoO 4 tetrahedral sub-layer of the BM film, which leads to the reconfiguration of 3 d -electrons and spin state in remanent Co ions and causes tremendous changes in magnetic and electric properties: from canted-antiferromagnetic insulator in BM phase to ferromagnetic insulator in SL phase. First-principles calculations revealed that the La 3+ -doping at A-site largely reduces the cohesive energy of Co-ions in CoO 4 and destabilize the CoO 4 tetrahedron of BM phase, which explains the formation of Co-ions transfer channel in the CoO 4 tetrahedral sub-layer. The present study highlights the effectiveness of regulating topotactic transformation via B-site ions transfer and provides a new pathway for manipulating the topotactic transformation with diverse functionalities. Tri-state topotactic transformation induced by B-site Co ion transfer was firstly realized in La 0.7 Sr 0.3 CoO 3 film. A unique transfer channel for Co-ions is demonstrated to be facilitated by the instability of CoO 4 due to A-site La-doping. The reconfiguration of 3d-electrons due to Co transfer leads to tremendous changes in magnetic and electric properties. Such new topotactic transformation driven by B-site ion transfer offers opportunity to exploit new types of electrocatalyst with rich functionalities. • Tri-state topotactic transformation induced by B-site Co ion transfer was firstly realized in La 0.7 Sr 0.3 CoO 3 film. • A unique transfer channel for Co-ions is demonstrated to be facilitated by the instability of CoO 4 due to A-site La-doping. • The concerted transfer of Co and O ions drive tremendous changes in magnetic and electric properties. • Such B-site ion transfer provides a new pathway for exploiting electrocatalyst with diverse functionalities.
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