Dual‐Sulfite Electrolytes for Stable Sodium Metal Batteries with a Low N/P Ratio

K Kejia Zhang Q Qi Kang J Junyi Hua (State Key Laboratory of Silicon and Advanced Semiconductor Materials School of Materials Science and Engineering Zhejiang University Hangzhou China) Z Zhongqiang Wang (Centre For Advanced Optoelectronic Functional Materials Research Northeast Normal University Changchun China) Y Yongping Shi (Institute of New Energy for Vehicles School of Materials Science and Engineering Tongji University Shanghai 201804 P. R. China) H Haikuo Zhang (State Key Laboratory of Silicon and Advanced Semiconductor Materials, School of Materials Science and Engineering) J Jinze Wang (State Key Laboratory of Silicon and Advanced Semiconductor Materials, School of Materials Science and Engineering) H Haotian Zhu (State Key Laboratory of Silicon and Advanced Semiconductor Materials, School of Materials Science and Engineering) R Ruhong Li (State Key Laboratory of Silicon and Advanced Semiconductor Materials, School of Materials Science and Engineering) X Xueying Zheng (Department of Mechanical Engineering) G Guangxu Zhang (Key Laboratory of High-Precision Computation and Application of Quantum Field Theory of Hebei Province, College of Physics Science and Technology, Hebei University 1 , Baoding 071002,) L Liqiang Huang X Xiulin Fan (State Key Laboratory of Silicon and Advanced Semiconductor Materials, School of Materials Science and Engineering) W Wei Luo

Abstract

Abstract Grasping the intricacies of the solid electrolyte interphase (SEI) on sodium (Na) metal anodes is critical for developing sodium metal batteries (SMBs). Conventional carbonate electrolytes suffer from poor Na compatibility, forming organic‐rich SEIs that degrade cycling stability. Here, A dual‐sulfite electrolyte (DSE) is presented, where the synergistic effect of sp 3 hybridization in –SO 3 and p 2 –pd hybridization in S═O enables a higher solvent coordination number, promoting the formation of a favored solvent‐derived, inorganic‐dominant SEI. The designed DSE accelerates the passivation process of Na anodes, yielding sulfide complexes in the SEI layer. As a result, paired with a high‐loading layered oxide cathode (NaNi 1/3 Fe 1/3 Mn 1/3 O 2 , 2.6 mAh cm −2 ) and thin Na (100 µm), the DSE enables SMBs to achieve an 85% capacity retention after 450 cycles at an N/P ratio of 4.3. Even with thinner Na (50 µm, N/P = 2.2), the cell retains 86% capacity after 200 cycles.

Article Details

Volume / Issue Vol. 38, Issue 6
Published January 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (14)

K

Kejia Zhang

Q

Qi Kang

J

Junyi Hua

State Key Laboratory of Silicon and Advanced Semiconductor Materials School of Materials Science and Engineering Zhejiang University Hangzhou China

Z

Zhongqiang Wang

Centre For Advanced Optoelectronic Functional Materials Research Northeast Normal University Changchun China

Y

Yongping Shi

Institute of New Energy for Vehicles School of Materials Science and Engineering Tongji University Shanghai 201804 P. R. China

H

Haikuo Zhang

State Key Laboratory of Silicon and Advanced Semiconductor Materials, School of Materials Science and Engineering

J

Jinze Wang

State Key Laboratory of Silicon and Advanced Semiconductor Materials, School of Materials Science and Engineering

H

Haotian Zhu

State Key Laboratory of Silicon and Advanced Semiconductor Materials, School of Materials Science and Engineering

R

Ruhong Li

State Key Laboratory of Silicon and Advanced Semiconductor Materials, School of Materials Science and Engineering

X

Xueying Zheng

Department of Mechanical Engineering

G

Guangxu Zhang

Key Laboratory of High-Precision Computation and Application of Quantum Field Theory of Hebei Province, College of Physics Science and Technology, Hebei University 1 , Baoding 071002,

L

Liqiang Huang

X

Xiulin Fan

State Key Laboratory of Silicon and Advanced Semiconductor Materials, School of Materials Science and Engineering

W

Wei Luo