Manipulating Electric Double Layer Adsorption for Stable Solid‐Electrolyte Interphase in 2.3 Ah Zn‐Pouch Cells

Author:

Wang Yu12,Liang Bochun1,Zhu Jiaxiong1,Li Geng3,Li Qing1,Ye Ruquan3,Fan Jun1,Zhi Chunyi12454ORCID

Affiliation:

1. Department of Materials Science and Engineering City University of Hong Kong Kowloon 999077 Hong Kong SAR China

2. Hong Kong Center for Cerebro-Cardiovascular Health Engineering (COCHE) Shatin N. T. 999077 Hong Kong SAR China

3. Department of Chemistry City University of Hong Kong Kowloon 999077 Hong Kong SAR China

4. Hong Kong Institute for Advanced Study City University of Hong Kong Kowloon Hong Kong 999077 China

5. Hong Kong Institute for Clean Energy City University of Hong Kong Kowloon Hong Kong 999077 China

Abstract

AbstractConstructing a reliable solid‐electrolyte interphase (SEI) is imperative for enabling highly reversible zinc metal (Zn0) electrodes. Contrary to conventional “bulk solvation” mechanism, we found the SEI structure is dominated by electric double layer (EDL) adsorption. We manipulate the EDL adsorption and Zn2+ solvation with ether additives (i.e. 15‐crown‐5, 12‐crown‐4, and triglyme). The 12‐crown‐4 with medium adsorption on EDL leads to a layer‐structured SEI with inner inorganic ZnFx/ZnSx and outer organic C−O−C components. This structure endows SEI with high rigidness and strong toughness enabling the 100 cm2 Zn||Zn pouch cell to exhibit a cumulative capacity of 4250 mAh cm−2 at areal‐capacity of 10 mAh cm−2. More importantly, a 2.3 Ah Zn||Zn0.25V2O5n H2O pouch cell delivers a recorded energy density of 104 Wh Lcell−1 and runs for >70 days under the harsh conditions of low negative/positive electrode ratio (2.2 : 1), lean electrolyte (8 g Ah−1), and high‐areal‐capacity (≈13 mAh cm−2).

Publisher

Wiley

Subject

General Medicine

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