Enhanced Reversibility of Iron Metal Anode with a Solid Electrolyte Interphase in Concentrated Chloride Electrolytes

M Min Soo Jung (Department of Chemistry Oregon State University Corvallis Oregon USA) S Sungjin Yang (Department of Chemistry Oregon State University Corvallis OR 97331 USA) C Cheng Chen S Sathya Narayanan Jagadeesan (SLAC‐Stanford Battery Center SLAC National Accelerator Laboratory Menlo Park California USA) W Weiyin Chen G Guangxia Feng (Department of Materials Science and Engineering) Y Yiming Sui (Department of Chemistry Oregon State University Corvallis OR 97331 USA) Z Ziang Jiang (School of Chemical Sciences) E Emmanuel N. Musa (Department of Chemistry Oregon State University Corvallis OR 97331 USA) N Nan‐Chieh Chiu (Department of Chemistry Oregon State University Corvallis OR 97331 USA) H Hunter Maclennan (Department of Chemistry Oregon State University Corvallis OR 97331 USA) E Elliot Holden (Department of Chemistry Oregon State University Corvallis OR 97331 USA) K Kyriakos C. Stylianou J Ju Li C Chong Fang (Department of Chemistry, Oregon State University) X Xueli Zheng (Department of Materials Science and Engineering) X Xiulei Ji (Department of Chemistry, Oregon State University 2 , Corvallis, Oregon 97331,)

Abstract

AbstractIron is a promising candidate for a cost‐effective anode for large‐scale energy storage systems due to its natural abundance and well‐established mass production. Recently, Fe‐ion batteries (FeIBs) that use ferrous ions as the charge carrier have emerged as a potential storage solution. The electrolytes in FeIBs are necessarily acidic to render the ferrous ions more anodically stable, allowing a wide operation voltage window. However, the iron anode suffers severe hydrogen evolution reaction with a low Coulombic efficiency (CE) in an acidic environment, shortening the battery cycle life. Herein, a hybrid aqueous electrolyte that forms a solid‐electrolyte interphase (SEI) layer on the Fe anode surface is introduced. The electrolyte mainly comprises FeCl2 and ZnCl2 as cosalts, where the Zn‐Cl anionic complex species of the concentrated ZnCl2 allows dimethyl carbonate (DMC) to be miscible with the aqueous ferrous electrolyte. SEI derived from DMC's decomposition passivates the iron surface, which leads to an average CE of 98.3% and much‐improved cycling stability. This advancement shows the promise of efficient and durable FeIBs.

Article Details

Volume / Issue Vol. 37, Issue 18
Published May 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (17)

M

Min Soo Jung

Department of Chemistry Oregon State University Corvallis Oregon USA

S

Sungjin Yang

Department of Chemistry Oregon State University Corvallis OR 97331 USA

C

Cheng Chen

S

Sathya Narayanan Jagadeesan

SLAC‐Stanford Battery Center SLAC National Accelerator Laboratory Menlo Park California USA

W

Weiyin Chen

G

Guangxia Feng

Department of Materials Science and Engineering

Y

Yiming Sui

Department of Chemistry Oregon State University Corvallis OR 97331 USA

Z

Ziang Jiang

School of Chemical Sciences

E

Emmanuel N. Musa

Department of Chemistry Oregon State University Corvallis OR 97331 USA

N

Nan‐Chieh Chiu

Department of Chemistry Oregon State University Corvallis OR 97331 USA

H

Hunter Maclennan

Department of Chemistry Oregon State University Corvallis OR 97331 USA

E

Elliot Holden

Department of Chemistry Oregon State University Corvallis OR 97331 USA

K

Kyriakos C. Stylianou

J

Ju Li

C

Chong Fang

Department of Chemistry, Oregon State University

X

Xueli Zheng

Department of Materials Science and Engineering

X

Xiulei Ji

Department of Chemistry, Oregon State University 2 , Corvallis, Oregon 97331,