Amphiphilic Polymer Electrolyte Blocking Lattice Oxygen Evolution from High‐Voltage Nickel‐rich Cathodes for Ultra‐Thermal Stabile Batteries

Author:

Chen Jialiang1,Lin Yan2,Li Qiang3,Ren Hao1,Zhang Linchen1,Sun Yuanyuan1,Zhang Siyu1,Shang Xinchao1,Zhou Weidong4ORCID,Wu Mingbo1,Li Zhongtao1

Affiliation:

1. State Key Laboratory of Heavy Oil Processing College of Chemical Engineering China University of Petroleum (East China) Qingdao 266580 China

2. Department of Chemistry Tsinghua University Beijing 100084 China

3. College of Physics Qingdao University Qingdao, Shandong 266071, China

4. State Key Laboratory of Organic-Inorganic Composites Beijing University of Chemical Technology Beijing 100029 China

Abstract

AbstractNi‐rich cathodes have been intensively adopted in Li‐ion batteries to pursuit high energy density, which still suffering irreversible degradation at high voltage. Some unstable lattice O2− species in Ni‐rich cathodes would be oxidized to singlet oxygen 1O2 and released at high volt, which lead to irreversible phase transfer from the layered rhombohedral (R) phase to a spinel‐like (S) phase. To overcome the issue, the amphiphilic copolymers (UMA‐Fx) electrolyte were prepared by linking hydrophobic C−F side chains with hydrophilic subunits, which could self‐assemble on Ni‐rich cathode surface and convert to stable cathode–electrolyte interphase layer. Thereafter, the oxygen releasing of polymer coated cathode was obviously depressed and substituted by the Co oxidation (Co3+→Co4+) at high volt (>4.2 V), which could suppressed irreversible phase transfer and improve cycling stability. Moreover, the amphiphilic polymer electrolyte was also stable with Li anode and had high ion conductivity. Therefore, the NCM811//UMA‐F6//Li pouch cell exhibited outstanding energy density (362.97 Wh/kg) and durability (cycled 200 times at 4.7 V), which could be stalely cycled even at 120°C without short circuits or explosions.

Funder

National Key Research and Development Program of China

Publisher

Wiley

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