Transforming Interfacial Reactivity Into Stability for Durable High‐Current Solid‐State Sodium Batteries

L Le Xiang (School of Materials Science and Engineering Key Laboratory of Structure and Functional Regulation of Hybrid Materials of Ministry of Education Anhui University Hefei China) F Fayang Guan (Key Laboratory for Thermal Science and Power Engineering of Ministry of Education Department of Engineering Mechanics Tsinghua University Beijing China) H Hengxiang Wang (School of Materials Science and Engineering Key Laboratory of Structure and Functional Regulation of Hybrid Materials of Ministry of Education Anhui University Hefei China) X Xiaoxiao Zhu (School of Physics and Information Technology, Shaanxi Normal University , Xi’an 710119,) B Bing Cheng C Chuanqiang Wu (Information Materials and Intelligent Sensing Laboratory of Anhui Province, Institutes of Physical Science and Information Technology) A Aoran Fan (Key Laboratory for Thermal Science and Power Engineering of Ministry of Education, Department of Engineering Mechanics, Tsinghua University) X Xiaodi Ren X Xiaowen Zhan (School of Materials Science and Engineering Key Laboratory of Structure and Functional Regulation of Hybrid Materials of Ministry of Education Anhui University Hefei China) L Lingyun Zhu

Abstract

ABSTRACT Interfacial instability remains the key obstacle to reliable oxide‐based solid‐state batteries (SSBs). Here we demonstrate a monolithic, self‐regulating mixed ionic‐electronic conducting (MIEC) interface that transforms interfacial reactivity into long‐term stability in SSBs. Introducing cobalt into NASICON‐type Na 3 Zr 2 Si 2 PO 12 (NZSP) yields a dual‐phase NaCoPO 4 /NZSP composite electrolyte, which evolves during cycling into a nanoporous interphase containing Co nanoparticles embedded in NASICON matrix. This reaction‑derived interphase enlarges the active area, homogenizes ion flux, and guides uniform sodium deposition. Extending this concept to a tri‐layer electrolyte architecture with Co‐modified outer layers and pristine NZSP core enables a self‐limiting reaction stabilizing both interfaces. Optimized cells achieve a critical current density of 7.3 mA cm −2 at 60°C and sustain symmetric‐cell cycling over 3000 h at 1 mA cm −2 . Full cells deliver >99% capacity retention over 1200 cycles at 2 C. This work establishes interfacial chemistry as a tunable design principle for durable, high‐current solid‐state metal batteries.

Article Details

Volume / Issue Vol. 65, Issue 24
Published June 08, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (10)

L

Le Xiang

School of Materials Science and Engineering Key Laboratory of Structure and Functional Regulation of Hybrid Materials of Ministry of Education Anhui University Hefei China

F

Fayang Guan

Key Laboratory for Thermal Science and Power Engineering of Ministry of Education Department of Engineering Mechanics Tsinghua University Beijing China

H

Hengxiang Wang

School of Materials Science and Engineering Key Laboratory of Structure and Functional Regulation of Hybrid Materials of Ministry of Education Anhui University Hefei China

X

Xiaoxiao Zhu

School of Physics and Information Technology, Shaanxi Normal University , Xi’an 710119,

B

Bing Cheng

C

Chuanqiang Wu

Information Materials and Intelligent Sensing Laboratory of Anhui Province, Institutes of Physical Science and Information Technology

A

Aoran Fan

Key Laboratory for Thermal Science and Power Engineering of Ministry of Education, Department of Engineering Mechanics, Tsinghua University

X

Xiaodi Ren

X

Xiaowen Zhan

School of Materials Science and Engineering Key Laboratory of Structure and Functional Regulation of Hybrid Materials of Ministry of Education Anhui University Hefei China

L

Lingyun Zhu