A molecular selenium iodide cathode and hybrid electrolyte for solid-state Na–Se2I2 batteries

S Shufeng Song (College of Aerospace Engineering, Chongqing University 1 , Chongqing 400044,) H Hongyang Shan (College of Aerospace Engineering, Chongqing University 1 , Chongqing 400044,) W Wei Xue (Key Laboratory of Biomaterials of Guangdong Higher Education Institutes, Engineering Technology Research Center of Drug Carrier of Guangdong, Department of Biomedical Engineering) Z Zhixu Long (College of Aerospace Engineering, Chongqing University 1 , Chongqing 400044,) C Chengtao Xiang (College of Aerospace Engineering, Chongqing University 1 , Chongqing 400044,) W Weihua Liang (College of Aerospace Engineering, Chongqing University 1 , Chongqing 400044,) C Chaohe Xu (National Engineering Research Center for Magnesium Alloys, Chongqing University 2 , Chongqing 400044,) G Guangsheng Huang (College of Materials Science and Engineering National Engineering Research for Magnesium Alloys Chongqing University Chongqing 40044 China)

Abstract

Challenges such as polyselenide shuttling and poor reaction kinetics persist in sodium–selenium (Na–Se) batteries. While solid-state Na–Se batteries could potentially eliminate the shuttle effect, they have received limited attention due to poor solid–solid interfacial contact and intrinsically sluggish conversion kinetics. Herein, we report a solid-state Na–Se2I2 battery that employs a low-melting point Se2I2 molecular cathode and a tailored hybrid solid electrolyte. At an operating temperature above its melting point, liquid Se2I2 establishes favorable liquid–liquid interfaces and enables a facile liquid–solid conversion pathway. Furthermore, the sodium super ion conductor (NASICON)/poly(ethylene oxide) hybrid electrolyte simultaneously dissolves polyselenides to promote redox kinetics and physically blocks their shuttling to ensure cycling stability. As a result, a reversible six-electron conversion reaction is achieved, and the solid-state Na–Se2I2 battery delivers a high specific capacity of 336 mAh g−1 at 0.1 C and a stable cycling over 200 cycles with 88.2% capacity retention at 0.5 C. The electrochemically active Se2I2 molecular design opens an alternative chemistry for selenium-based electrodes and provides a promising direction for future solid-state battery research.

Article Details

Volume / Issue Vol. 128, Issue 15
Published April 13, 2026
ISSN 0003-6951
Publisher American Institute of Physics

Journal Info

Applied Physics Letters

American Institute of Physics

ISSN: 0003-6951 Physical Sciences

Authors (8)

S

Shufeng Song

College of Aerospace Engineering, Chongqing University 1 , Chongqing 400044,

H

Hongyang Shan

College of Aerospace Engineering, Chongqing University 1 , Chongqing 400044,

W

Wei Xue

Key Laboratory of Biomaterials of Guangdong Higher Education Institutes, Engineering Technology Research Center of Drug Carrier of Guangdong, Department of Biomedical Engineering

Z

Zhixu Long

College of Aerospace Engineering, Chongqing University 1 , Chongqing 400044,

C

Chengtao Xiang

College of Aerospace Engineering, Chongqing University 1 , Chongqing 400044,

W

Weihua Liang

College of Aerospace Engineering, Chongqing University 1 , Chongqing 400044,

C

Chaohe Xu

National Engineering Research Center for Magnesium Alloys, Chongqing University 2 , Chongqing 400044,

G

Guangsheng Huang

College of Materials Science and Engineering National Engineering Research for Magnesium Alloys Chongqing University Chongqing 40044 China