Highly Efficient Spatially–Temporally Synchronized Construction of Robust Li3PO4‐rich Solid–Electrolyte Interphases in Aqueous Li‐ion Batteries

Author:

Zhu Xiangzhen123ORCID,Lin Zejing1,Lai Jingning4,Lv Tianshi1,Lin Ting1,Pan Hongyi1,Feng Jingnan1,Wang Qiyu1,Han Shuai1,Chen Renjie4,Chen Liquan1,Suo Liumin123ORCID

Affiliation:

1. Beijing National Laboratory for Condensed Matter Physics Institute of Physics Chinese Academy of Sciences Beijing 100190 China

2. Center of Materials Science and Optoelectronics Engineering University of Chinese Academy of Sciences Beijing 100049 China

3. Yangtze River Delta Physics Research Center Co. Ltd. Changzhou, Liyang 213300 China

4. Beijing Key Laboratory of Environmental Science and Engineering School of Material Science & Engineering Beijing Institute of Technology Beijing 100081 China

Abstract

AbstractSolid electrolyte interphase (SEI) makes the electrochemical window of aqueous electrolytes beyond the thermodynamics limitation of water. However, achieving the energetic and robust SEI is more challenging in aqueous electrolytes because the low SEI formation efficiency (SFE) only contributed from anion‐reduced products, and the low SEI formation quality (SFQ) negatively impacted by the hydrogen evolution, resulting in a high Li loss to compensate for SEI formation. Herein, we propose a highly efficient strategy to construct Spatially‐Temporally Synchronized (STS) robust SEI by the involvement of synergistic chemical precipitation‐electrochemical reduction. In this case, a robust Li3PO4‐rich SEI enables intelligent inherent growth at the active site of the hydrogen by the chemical capture of the OH stemmed from the HER to trigger the ionization balance of dihydrogen phosphate (H2PO4) shift to insoluble solid Li3PO4. It is worth highlighting that the Li3PO4 formation does not extra‐consume lithium derived from the cathode but makes good use of the product of HER (OH), prompting the SEI to achieve 100 % SFE and pushing the HER potential into −1.8 V vs. Ag/AgCl. This energetic and robust SEI offers a new way to achieve anion/concentration‐independent interfacial chemistry for the aqueous batteries.

Funder

National Key Research and Development Program of China

National Natural Science Foundation of China

Publisher

Wiley

Subject

General Chemistry,Catalysis

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