Freestanding 2D Oxide Perovskites --- a new playground for strongly correlated 2D phases

Speaker: Yuefeng Nie, Nanjing University

When: August 2, 2019 (Fri), 12:00PM to 01:00PM (add to my calendar)
Location: SCI 352
Hosted by: Wanzheng Hu

This event is part of the Biophysics/Condensed Matter Seminar Series.

Two-dimensional (2D) materials such as graphene and transition metal dichalcogenides (TMD) have demonstrated how the new electronic phases emerge when a bulk crystal is thinned down to a mono-layer. As transition metal oxide perovskites host a variety of correlated phases, realizing the analogs with transition metal oxide perovskite materials would open the door to a rich spectrum of exotic 2D correlated phases that have not yet been explored. Here we report on the fabrication of freestanding perovskite films with high crystalline quality down to a single unit cell[1]. Using the recently developed method based on water-soluble Sr3Al2O6 as the sacrificial buffer layer[2,3] we synthesize freestanding SrTiO3 and BiFeO3 ultrathin films by reactive molecular beam epitaxy (MBE) and transfer them to different substrates such as crystalline silicon wafers and holey carbon films. We find that freestanding BiFeO3 films exhibit an unexpected giant tetragonality and polarization when approaching the ultimate 2D limit. Our results demonstrate the absence of critical thickness for stabilizing the crystalline order in the freestanding ultrathin oxide films. The ability to synthesize and transfer crystalline freestanding perovskite films without thickness limitation onto any desired substrate opens a new field for the 2D correlated electronic phases and interfacial phenomena that technically have not yet been accessible.

In this talk, I will also present our recent works on the atomically precise engineering of the crystalline and electronic structure of titanates[4] and iridates[5,6] by a combination of oxide MBE and in situ angle-resolved photoemission spectroscopy (ARPES).

[1] D.X. Ji, et al. Nature 570 87–90 (2019) [2] D. Lu, et al., Nat. Mater. 15, 1255 (2016) [3] S. S. Hong, et al. Sci. Adv. 3, eaao5173 (2017) [4] H.Y. Sun, et al., Nat. Commun. 9.1, 2965 (2018) [5] Y.F. Nie, et al. Phys. Rev. Lett. 114, 016401 (2015) [6] W. Guo, et al. in preparation