Anomalous Crystallinity and Magnetism in Chemically Disordered Coherent Heterostructures

S Saeed S. I. Almishal S Sai Venkata Gayathri Ayyagari (Department of Materials Science and Engineering) A Aaron Pearre (Department of Physics The Pennsylvania State University University Park Pennsylvania USA) P Pat Kezer (Department of Electrical Engineering and Computer Science, University of Michigan 1 , Ann Arbor, Michigan 48109,) M Matthew Furst C Christina M. Rost (Department of Materials Science and Engineering) B Binghai Yan N Nasim Alem (Department of Materials Science and Engineering) T Timothy Charlton (Neutron Science Division Oak Ridge National Laboratory Oak Ridge Tennessee USA) Z Zhiqiang Mao (Department of Physics, The Pennsylvania State University, University Park, PA, USA.) J John T. Heron (Department of Materials Science and Engineering) J Jon‐Paul Maria (Department of Materials Science and Engineering The Pennsylvania State University University Park Pennsylvania USA)

Abstract

ABSTRACT High‐entropy oxide (HEO) thin films uniquely superimpose exceptional chemical disorder with exceptional crystalline quality and coherence—an intersection we term anomalous crystallinity that arises from coupled structural, chemical, and valence degrees of freedom unique to the high‐entropy and entropy‐stabilized conditions. Here, we demonstrate unexpected and predictive control of this state using formulation, epitaxial constraints, and kinetic arrest of metastable macrostates. Specifically, aliovalent cation substitutions, tightly controlled substrate temperatures, and conditions favoring significant adatom kinetic energy, can program the out‐of‐plane lattice parameter of coherent rock salt HEOs while preserving in‐plane epitaxial pinning to MgO. We highlight the exemplar (ScMgCoNiCuZn)O/(CrMgCoNiCuZn)O (JSc/JCr) system where Sc and Cr substitution into the rock salt structure produces pseudomorphic heterostructures between individual antiferromagnets, sustaining an exceptional 5.5% out‐of‐plane lattice parameter difference and enabling abrupt interfaces across which the Co valence switches from mostly 2 + to an even 2 + /3 + mixture. The JSc/JCr valence interface heterostructure is accompanied by a 2 × exchange bias boost compared to single‐layer constituents, that could be attributed to enhanced uncompensated spins in the layers themselves or around the buried JSc/JCr interface. These results establish pseudomorphic valence interfaces with anomalous crystallinity as a source of new magnetic macrostates that host emergent magnetic and spintronic functionality.

Article Details

Volume / Issue Vol. 38, Issue 47
Published August 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (12)

S

Saeed S. I. Almishal

S

Sai Venkata Gayathri Ayyagari

Department of Materials Science and Engineering

A

Aaron Pearre

Department of Physics The Pennsylvania State University University Park Pennsylvania USA

P

Pat Kezer

Department of Electrical Engineering and Computer Science, University of Michigan 1 , Ann Arbor, Michigan 48109,

M

Matthew Furst

C

Christina M. Rost

Department of Materials Science and Engineering

B

Binghai Yan

N

Nasim Alem

Department of Materials Science and Engineering

T

Timothy Charlton

Neutron Science Division Oak Ridge National Laboratory Oak Ridge Tennessee USA

Z

Zhiqiang Mao

Department of Physics, The Pennsylvania State University, University Park, PA, USA.

J

John T. Heron

Department of Materials Science and Engineering

J

Jon‐Paul Maria

Department of Materials Science and Engineering The Pennsylvania State University University Park Pennsylvania USA