Unlocking Surface Sodiation Threshold of Titanium Dioxide via Coupled Electrochemical‐Thermal Activation

D Dafu Tang (State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Materials, Xiamen University, Xiamen 361005, China) S Sicheng Fan C Chao Li Z Zerui Yan Y Yuting Song Z Zhangbin Xie (State Key Laboratory of Physical Chemistry of Solid Surfaces Fujian Key Laboratory of Surface and Interface Engineering for High Performance Materials College of Materials Xiamen University Xiamen P. R. China) W Weihan Lin (State Key Laboratory of Physical Chemistry of Solid Surfaces Fujian Key Laboratory of Surface and Interface Engineering for High Performance Materials College of Materials Xiamen University Xiamen P. R. China) J Jiuhui Han (Tianjin Key Laboratory of Advanced Functional Porous Materials, Institute for New Energy Materials and Low-Carbon Technologies, School of Materials Science and Engineering) D Dong‐Liang Peng (State Key Laboratory of Physical Chemistry of Solid Surfaces Fujian Key Laboratory of Surface and Interface Engineering for High Performance Materials College of Materials Xiamen University Xiamen P. R. China) Q Qiulong Wei (State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Materials, Xiamen University, Xiamen 361005, China)

Abstract

ABSTRACT Titanium dioxide anodes for sodium‐ion batteries undergo an electrochemically‐induced phase transformation from crystalline to active amorphous phase in a thin surface layer, resulting in surface‐dependent capacities. The origins of this limited active layer remain unclear. Herein, we reveal that the sluggish movement of the amorphous|crystalline boundary during initial sodiation determines the thickness of the surface‐active layer. To unlock surface sodiation threshold, we propose a coupled electrochemical‐thermal activation protocol to promote the continuous movement of the amorphous|crystalline boundary during the initial cycle, thereby permanently increasing the reversible sodiation capacity. The anatase TiO 2 ‐35 nm anode delivers an enhanced capacity from 116 to 190 mAh g −1 at 0.1 A g −1 after electrochemical‐thermal activation, accompanied by its high‐rate capability and long‐term cyclability. The electrochemical‐thermal activation is also efficient for enhancing the Li + /Na + storage capacities of rutile TiO 2 anodes. This work opens a pathway for enhancing electrochemically‐induced irreversible phase transformations with enhanced charge storage performance.

Article Details

Volume / Issue Vol. 65, Issue 27
Published July 01, 2026
ISSN 1433-7851
Publisher Wiley

Journal Info

Angewandte Chemie International Edition

Wiley

ISSN: 1433-7851 Physical Sciences

Authors (10)

D

Dafu Tang

State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Materials, Xiamen University, Xiamen 361005, China

S

Sicheng Fan

C

Chao Li

Z

Zerui Yan

Y

Yuting Song

Z

Zhangbin Xie

State Key Laboratory of Physical Chemistry of Solid Surfaces Fujian Key Laboratory of Surface and Interface Engineering for High Performance Materials College of Materials Xiamen University Xiamen P. R. China

W

Weihan Lin

State Key Laboratory of Physical Chemistry of Solid Surfaces Fujian Key Laboratory of Surface and Interface Engineering for High Performance Materials College of Materials Xiamen University Xiamen P. R. China

J

Jiuhui Han

Tianjin Key Laboratory of Advanced Functional Porous Materials, Institute for New Energy Materials and Low-Carbon Technologies, School of Materials Science and Engineering

D

Dong‐Liang Peng

State Key Laboratory of Physical Chemistry of Solid Surfaces Fujian Key Laboratory of Surface and Interface Engineering for High Performance Materials College of Materials Xiamen University Xiamen P. R. China

Q

Qiulong Wei

State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Materials, Xiamen University, Xiamen 361005, China