Boron‐Centered Organic Salts Enabling Na‐Ion Supply and Interfacial Protection for Na‐Ion Batteries

Z Zilong Zheng S Shu Chen G Guanbin Wu Z Ziyang Kang (State Key Laboratory of Molecular Engineering of Polymers, Department of Macromolecular Science, Institute of Fiber Materials and Devices, Research Center of AI for Polymer Science, Collaborative Innovation Center of Chemistry for Energy Materials) W Wenwen Wang X Xinwei Du (State Key Laboratory of Molecular Engineering of Polymers, Department of Macromolecular Science, Institute of Fiber Materials and Devices, Research Center of AI for Polymer Science, Collaborative Innovation Center of Chemistry for Energy Materials) C Chihao Zhao (State Key Laboratory of Molecular Engineering of Polymers Department of Macromolecular Science Institute of Fiber Materials and Devices Research Center of AI For Polymer Science Collaborative Innovation Center of Chemistry for Energy Materials Fudan University Shanghai China) Y Yue Gao

Abstract

Abstract Sodium (Na)‐ion batteries employing hard carbon anodes suffer from a significant irreversible loss of active Na ions (up to 20%) during the initial formation cycle. Conventional Na‐ion compensation methods are hindered by issues such as incomplete decomposition of Na‐ion supply agents, the generation of harmful byproducts, and electrode degradation. To address these challenges, we utilized unsupervised machine learning to develop an organic Na salt, methylboronic acid sodium salt (CH 3 B(ONa) 2 ), which is coated on cathode particles and effectively delivers over 15% Na‐ion compensation. Meanwhile, its decomposition product, sodium metaborate (NaBO 2 ), in situ formed a protective cathode coating that mitigates transition metal dissolution. Spectroscopic and microscopic studies identified a free radical mechanism of CH 3 B(ONa) 2 decomposition reaction and effective inhibition of nickel metal dissolution in cathode due to the presence of NaBO 2 . In addition, no side effects were found in the process of Na‐ion supply. The initial coulombic efficiency of a hard carbon|P2‐Na 0.75 Ni 0.25 Fe 0.25 Mn 0.5 O 2 pouch cell increased from 81% to 97%, with a capacity retention of 81.5% over 700 cycles. This dual‐function approach significantly enhances cycling stability and capacity retention in Na‐ion batteries.

Article Details

Volume / Issue Vol. 64, Issue 48
Published November 24, 2025
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (8)

Z

Zilong Zheng

S

Shu Chen

G

Guanbin Wu

Z

Ziyang Kang

State Key Laboratory of Molecular Engineering of Polymers, Department of Macromolecular Science, Institute of Fiber Materials and Devices, Research Center of AI for Polymer Science, Collaborative Innovation Center of Chemistry for Energy Materials

W

Wenwen Wang

X

Xinwei Du

State Key Laboratory of Molecular Engineering of Polymers, Department of Macromolecular Science, Institute of Fiber Materials and Devices, Research Center of AI for Polymer Science, Collaborative Innovation Center of Chemistry for Energy Materials

C

Chihao Zhao

State Key Laboratory of Molecular Engineering of Polymers Department of Macromolecular Science Institute of Fiber Materials and Devices Research Center of AI For Polymer Science Collaborative Innovation Center of Chemistry for Energy Materials Fudan University Shanghai China

Y

Yue Gao