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Emergence of bulk-like ferromagnetism in ultrathin freestanding manganite membranes via sacrifice-layer engineering

  • Jinrui Guo
  • , Bin He*
  • , Qinglong Wang
  • , Huan Liu
  • , Weidong Wang
  • , Qingjiao Huang
  • , Haokun Su
  • , Weiming Lü*
  • *Corresponding author for this work
  • University of Jinan
  • School of Physics, Harbin Institute of Technology

Research output: Contribution to journalArticlepeer-review

Abstract

The development of freestanding complex oxide membranes, particularly of strongly correlated manganites, opens new avenues for heterointegration and quantum material design. However, a fundamental challenge remains in understanding the strain evolution upon release from the substrate, given the critical role of electron–lattice coupling. Here, we fabricate (001)-oriented freestanding La0.67Sr0.33MnO3 (FS-LSMO) membranes using water-soluble sacrificial layers with distinct lattice constants, Sr3Al2O6 (SAO) and SrCa2Al2O6 (SCAO). We find that SCAO-released LSMO membranes, subjected to smaller initial interfacial stress, retain a significantly larger saturation magnetization and higher Curie temperature (T C) than SAO-released counterparts. This correlation indicates that the long-range interfacial stress is converted into a short-range internal stress, which may be mediated by morphological adaptation and defect pinning. Most notably, these optimized membranes exhibit a drastically weak thickness dependence, sustaining robust room-temperature ferromagnetism in layers as thin as 8 u.c., overcoming the pervasive “dead-layer” effect. Furthermore, we constructed stacked FS-Pb(Zr0.52Ti0.48)O3 (FS-PZT) on FS-LSMO multiferroic heterostructures, which exhibits excellent ferroelectric properties. Our work establishes a pathway to achieving high-performance, ultrathin manganite membranes for advanced spintronic and quantum architectures.

Original languageEnglish
Article number142401
JournalApplied Physics Letters
Volume128
Issue number14
DOIs
StatePublished - 6 Apr 2026
Externally publishedYes

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