Bond Length as a Unified Descriptor for Stable Iodine Battery

M Mengzi Geng Y Yanyan Wang (Beijing National Laboratory for Molecular Sciences, CAS Laboratory of Colloid and Interface and Thermodynamics, CAS Research/Education Center for Excellence in Molecular Sciences, Center for Carbon Neutral Chemistry, Institute of Chemistry) F Fanbin Zeng (Department of Applied Physics and Research Institute for Advanced Manufacturing The Hong Kong Polytechnic University Kowloon Hong Kong China) Y Yao Liu H Haijin Ni (School of Advanced Materials) B Bolong Hong (College of Semiconductors (National Graduate College for Engineers)) W Wei Xia (State Key Laboratory of Quantum Functional Materials, School of Physical Science and Technology) S Songbai Han Y Yusheng Zhao B Biao Zhang

Abstract

ABSTRACT Dissolution of active materials in the electrolyte and their subsequent shuttling are common challenges for realizing stable electrodes in rechargeable batteries. These issues become particularly pronounced in cathodes with high solubility, including high‐energy iodine electrodes. The interaction strength of iodine with the host electrode and electrolyte is critical for determining electrochemical stability, yet there is a lack of an appropriate parameter to quantify it. Our findings reveal that, as a weak Lewis acid, iodine's interaction strength is highly influenced by the nucleophilicity of surrounding ligands. We propose the I−I bond length, which can be conveniently probed through Raman tests, as a unified descriptor to predict the iodine electrode stability. The asset of this descriptor is demonstrated in (i) rational design of complex electrodes to enhance the binding strength between iodine and host and (ii) efficient screening of electrolyte solvents to minimize the shuttle. The collective effects enable stable cycling of Li−I 2 batteries under the challenging current rate of 0.1 C for over 4000 h. Overall, the unified descriptor provides a powerful means to expedite electrode and electrolyte design for overcoming active material dissolution challenges.

Article Details

Volume / Issue Vol. 1, Issue 1
Published July 02, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (10)

M

Mengzi Geng

Y

Yanyan Wang

Beijing National Laboratory for Molecular Sciences, CAS Laboratory of Colloid and Interface and Thermodynamics, CAS Research/Education Center for Excellence in Molecular Sciences, Center for Carbon Neutral Chemistry, Institute of Chemistry

F

Fanbin Zeng

Department of Applied Physics and Research Institute for Advanced Manufacturing The Hong Kong Polytechnic University Kowloon Hong Kong China

Y

Yao Liu

H

Haijin Ni

School of Advanced Materials

B

Bolong Hong

College of Semiconductors (National Graduate College for Engineers)

W

Wei Xia

State Key Laboratory of Quantum Functional Materials, School of Physical Science and Technology

S

Songbai Han

Y

Yusheng Zhao

B

Biao Zhang