Polyphosphates‐Based Cathode‐Electrolyte Interphase for 4.65 V LiCoO <sub>2</sub>

H Hengyu Ren (School of Advanced Materials) X Xiaohu Wang (School of Advanced Materials) W Wenwei Cai 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) K Kunchen Xie (School of Advanced Materials Peking University Shenzhen Graduate School Peking University Shenzhen China) D Dongwen Zou (GuangDong Engineering Technology Research Center of Multi‐Dimensional Optoelectronic Materials, Shenzhen Graduate School Peking University Shenzhen 518055 P.R. China) T Tao Zeng F Funing Yu (College of Physics and Energy Fujian Normal University Fuzhou China) Z Zhikang Deng H Haocong Yi (School of Advanced Materials) C Chunyu Xu (School of Advanced Materials) W Wenhua Zhang S Shunning Li (School of Advanced Materials) Q Qinghe Zhao (School of Advanced Materials) F Feng Pan

Abstract

ABSTRACT The stable interfacial chemistry of LiCoO 2 (LCO) is the cornerstone for its high‐voltage operation. However, interfacial side reactions, originating from the Co/O catalytic sites, lead to ethylene carbonate (EC) oxidation, lithium hexafluorophosphate (LiPF 6 ) hydrolysis, and LCO surface degradation. Herein, we propose that the formation of functional phosphate derivatives (FPD) in the electrolyte, which are generated from the reaction between tris(trimethylsilyl) phosphate (TMSP) and PF 6 − anions, can achieve targeted regulation of the polyphosphates cathode‐electrolyte interphase (CEI). During cycling, the FPD spontaneously forms covalent interactions with surface Co/O sites, triggering in situ polymerization that constructs a robust and full‐coverage CEI on LCO. The resulting CEI is enriched with polyphosphates and LiF/Li 2 O, which ensures high thermodynamic stability and fast Li + transport kinetics simultaneously. Consequently, the LCO with optimized electrolyte (1.0 M LiPF 6 in fluoroethylene carbonate (FEC)‐based solvents with 2.0 wt.% TMSP) demonstrates exceptional cell performance with a high capacity retention of 81.0% after 3000 cycles within 3.0–4.6 V (vs. Li/Li + ), 81.6% after 2000 cycles within 3.0–4.65 V, and shows the feasibility in the LCO||graphite pouch cell with a retention of 80.0% after 500 cycles. This work provides a new insight into the uniform CEI construction for high‐voltage LCO cathodes through functional electrolyte engineering.

Article Details

Volume / Issue Vol. 38, Issue 27
Published May 01, 2026
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (15)

H

Hengyu Ren

School of Advanced Materials

X

Xiaohu Wang

School of Advanced Materials

W

Wenwei Cai

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

K

Kunchen Xie

School of Advanced Materials Peking University Shenzhen Graduate School Peking University Shenzhen China

D

Dongwen Zou

GuangDong Engineering Technology Research Center of Multi‐Dimensional Optoelectronic Materials, Shenzhen Graduate School Peking University Shenzhen 518055 P.R. China

T

Tao Zeng

F

Funing Yu

College of Physics and Energy Fujian Normal University Fuzhou China

Z

Zhikang Deng

H

Haocong Yi

School of Advanced Materials

C

Chunyu Xu

School of Advanced Materials

W

Wenhua Zhang

S

Shunning Li

School of Advanced Materials

Q

Qinghe Zhao

School of Advanced Materials

F

Feng Pan