Nonreciprocal Charge Transport in an Iron‐Based Superconductor with Broken Inversion Symmetry Engineered by a Hydrogen‐Concentration Gradient

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Authors: Takayuki Nagai, Yukito Nishio, Jumpei Matsumoto, Kota Hanzawa, Hidenori Hiramatsu, Hideo Hosono, Tsuyoshi Kimura
Cited by: 0
References: 44

Abstract

The breaking of spatial inversion symmetry in condensed matter gives rise to intriguing physical properties, such as ferroelectricity, piezoelectricity, spin-momentum locking, and nonreciprocal responses. Here, we propose that a concentration gradient, which often persists as a quasi-stable nonequilibrium state with long relaxation times in solids, can serve as a general platform for inversion symmetry breaking. We demonstrate this concept in an epitaxial thin film of the hydrogen-doped SmFeAsO (Sm1111:H) superconductor with a depthwise hydrogen-concentration gradient introduced via an optimized topotactic reaction. This film exhibits nonreciprocal charge transport-that is, current-direction-dependent resistance-which serves as a key signature of broken inversion symmetry. A pronounced nonreciprocal signal emerges in the vicinity of the superconducting transition, which we attribute to vortex-motion nonreciprocity arising from an asymmetric pinning landscape created by the hydrogen-concentration gradient. Owing to the high critical temperature of Sm1111:H, vortex-origin nonreciprocity is observed above 40 K, representing the highest temperature reported to date among single bulk materials without an artificially hetero-layered structure. Our findings establish concentration-gradient engineering as a versatile and broadly applicable route for realizing inversion-broken states in otherwise centrosymmetric hosts, opening pathways toward a broader landscape of odd-parity-driven functionalities.

Fields of Study & Subjects

Iron-based superconductors research Physics of Superconductivity and Magnetism Electronic and Structural Properties of Oxides

Publication details

Journal / source
Advanced Science
Volume
13
Issue
22
Pages
e24270–e24270
Publication date
15 February 2026
Language
EN