Durable Interphase Engineering on SiO <i> <sub>x</sub> </i> Anodes Through Interfacial‐Enrichment‐Facilitated Polymerization

S Shiming Chen (Department of Chemistry) K Kai Yang W Wenguang Zhao (Institute of Materials Research and Engineering (IMRE), Agency for Science, Technology andResearch (A*STAR), 2 Fusionopolis Way, Innovis #08-03, Singapore 138634, Singapore) W Wei Yang J Jiangxiao Li C Chenyu Yang (National Synchrotron Radiation Laboratory) Z Zhikang Deng Y Yue Zuo (School of Advanced Materials Peking University Shenzhen Graduate School Shenzhen People's Republic of China) X Xiaohu Wang (School of Advanced Materials) Z Zu‐Wei Yin (College of Energy Xiamen University Xiamen 361102 P.R. China) J Junyang Liu (State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering & Institute of Artificial Intelligence & Innovation Laboratory for Sciences and Technologies of Energy Materials of Fujian Province (IKKEM)) M Meng Zhang F Feng Pan L Luyi Yang (School of Advanced Materials)

Abstract

ABSTRACT Constructing a robust solid electrolyte interphase (SEI) is a proven strategy to enhance the performance of Si‐based anodes by accommodating severe volume swings and suppressing interfacial side reactions. However, existing strategies that rely solely on either chemical coating or electrochemical formation struggle to reconcile SEI uniformity and long‐term stability. Here, we propose a synergistic strategy that integrates the interfacial modification with in situ regulated electrolyte decomposition. A conformal layer composed of LiF and Li 3 PO 4 is pre‐formed on SiO x anodes, where LiF serves as a stable mechanical framework for the inorganic‐rich SEI, and Li 3 PO 4 selectively adsorbs fluoroethylene carbonate (FEC), favoring the polymerization of FEC‐derived species via interfacial enrichment to form the high‐molecular‐weight organic species. These electrochemically generated SEI components effectively compensate for the damage to the initial coating caused by volume expansion, enabling the SEI to possess both structural integrity and resilience. Consequently, the modified SiO x anode exhibits benchmark electrochemical performance, delivering excellent cycling stability (1086 mA h g −1 , 81% capacity retention for 300 cycles at 0.8 A g −1 ) and high‐rate capability (1010 mAh g −1 at 2.4 A g −1 ). This work establishes a precedent for the dynamic repair interphase design paradigm for high‐capacity anodes.

Article Details

Volume / Issue Vol. 1, Issue 1
Published August 05, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (14)

S

Shiming Chen

Department of Chemistry

K

Kai Yang

W

Wenguang Zhao

Institute of Materials Research and Engineering (IMRE), Agency for Science, Technology andResearch (A*STAR), 2 Fusionopolis Way, Innovis #08-03, Singapore 138634, Singapore

W

Wei Yang

J

Jiangxiao Li

C

Chenyu Yang

National Synchrotron Radiation Laboratory

Z

Zhikang Deng

Y

Yue Zuo

School of Advanced Materials Peking University Shenzhen Graduate School Shenzhen People's Republic of China

X

Xiaohu Wang

School of Advanced Materials

Z

Zu‐Wei Yin

College of Energy Xiamen University Xiamen 361102 P.R. China

J

Junyang Liu

State Key Laboratory of Physical Chemistry of Solid Surfaces, College of Chemistry and Chemical Engineering & Institute of Artificial Intelligence & Innovation Laboratory for Sciences and Technologies of Energy Materials of Fujian Province (IKKEM)

M

Meng Zhang

F

Feng Pan

L

Luyi Yang

School of Advanced Materials