Bulk‐Rashba Effect with Suppressed Spin Relaxation in a Polar Phase of Bi <sub>1‐</sub> <i> <sub>x</sub> </i> In <sub>1+</sub> <i> <sub>x</sub> </i> O <sub>3</sub>

D Deokyoung Kang (Rice Advanced Materials Institute) X Xue‐Zeng Lu (Key Laboratory of Quantum Materials and Devices of Ministry of Education School of Physics Southeast University Nanjing Jiangsu China) M Megha Acharya (Department of Materials Science and Engineering University of California, Berkeley Berkeley CA 94720 USA) S Sajid Husain (Department of Materials Science and Engineering) I Isaac Harris P Piush Behera C Ching‐Che Lin (Department of Materials Science and NanoEnginereing Rice University Houston Texas USA) E Ella Banyas (Materials Sciences Division Lawrence Berkeley National Laboratory Berkeley CA 94720 USA) A Alex Smith F Francesco Ricci (Department of Chemical Sciences and Technologies, University of Rome, Tor Vergata, Via della Ricerca Scientifica, Rome 00133, Italy) M Menglin Zhu B Bridget R. Denzer (Department of Materials Science and Engineering Massachusetts Institute of Technology Cambridge MA USA) T Tanguy Terlier (SIMS laboratory, Shared Equipment Authority, Rice University, 6100 Main Street, Houston, Texas 77005, United States) S Shu Wang T Tae Yeon Kim (Department of Materials Science and NanoEngineering, Rice University) L Lucas Caretta (Department of Physics) D Douglas Natelson J James M. LeBeau J Jeffrey B. Neaton R Ramamoorthy Ramesh (Rice Advanced Materials Institute) J James M. Rondinelli (Department of Materials Science and Engineering) L Lane W. Martin (Rice Advanced Materials Institute)

Abstract

Abstract The Rashba effect enables control over the spin degree of freedom, particularly in polar materials where the polar symmetry couples to Rashba‐type spin splitting. The exploration of this effect, however, has been hindered by the scarcity of polar materials exhibiting the bulk‐Rashba effect and rapid spin‐relaxation effects dictated by the D'yakonov–Perel mechanism. Here, a polar LiNbO 3 ‐type R 3 c phase of Bi 1‐ x In 1+ x O 3 with x ≈0.15–0.24 is stabilized via epitaxial growth, which exhibits a bulk‐Rashba effect with suppressed spin relaxation as a result of its unidirectional spin texture. As compared to the previously observed non‐polar Pnma phase, this polar phase exhibits higher conductivity, reduced bandgap, and enhanced dielectric and piezoelectric responses. Combining first‐principles calculations and multimodal magnetotransport measurements, which reveal weak (anti)localization, anisotropic magnetoresistance, planar‐Hall effect, and nonreciprocal charge transport, a bulk‐Rashba effect without rapid spin relaxation is demonstrated. These findings offer insights into spin‐orbit coupling physics within polar oxides and suggest potential spintronic applications.

Article Details

Volume / Issue Vol. 37, Issue 39
Published October 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (22)

D

Deokyoung Kang

Rice Advanced Materials Institute

X

Xue‐Zeng Lu

Key Laboratory of Quantum Materials and Devices of Ministry of Education School of Physics Southeast University Nanjing Jiangsu China

M

Megha Acharya

Department of Materials Science and Engineering University of California, Berkeley Berkeley CA 94720 USA

S

Sajid Husain

Department of Materials Science and Engineering

I

Isaac Harris

P

Piush Behera

C

Ching‐Che Lin

Department of Materials Science and NanoEnginereing Rice University Houston Texas USA

E

Ella Banyas

Materials Sciences Division Lawrence Berkeley National Laboratory Berkeley CA 94720 USA

A

Alex Smith

F

Francesco Ricci

Department of Chemical Sciences and Technologies, University of Rome, Tor Vergata, Via della Ricerca Scientifica, Rome 00133, Italy

M

Menglin Zhu

B

Bridget R. Denzer

Department of Materials Science and Engineering Massachusetts Institute of Technology Cambridge MA USA

T

Tanguy Terlier

SIMS laboratory, Shared Equipment Authority, Rice University, 6100 Main Street, Houston, Texas 77005, United States

S

Shu Wang

T

Tae Yeon Kim

Department of Materials Science and NanoEngineering, Rice University

L

Lucas Caretta

Department of Physics

D

Douglas Natelson

J

James M. LeBeau

J

Jeffrey B. Neaton

R

Ramamoorthy Ramesh

Rice Advanced Materials Institute

J

James M. Rondinelli

Department of Materials Science and Engineering

L

Lane W. Martin

Rice Advanced Materials Institute