Overcoming Chemical and Mechanical Instabilities in Lithium Metal Anodes with Sustainable and Eco‐Friendly Artificial SEI Layer

Author:

Song Hyunsub1,Lee Jiyoung123,Sagong Mingyu1,Jeon Jiwon1,Han Yeji1,Kim Jinuk4,Jung Hun‐Gi5,Yu Ji‐Sang6,Lee Jinwoo4,Kim Il‐Doo1ORCID

Affiliation:

1. Department of Materials Science and Engineering Korea Advanced Institute of Science and Technology (KAIST) 291 Daehak‐ro, Yuseong‐gu Daejeon 34141 Republic of Korea

2. Department of Chemical and Biological Engineering Northwestern University Evanston IL 60208 USA

3. Department of Chemical Engineering Ajou University 206 World cup‐ro, Yeongtong‐gu Suwon‐si Gyeonggi‐do 16499 Republic of Korea

4. Department of Chemical and Biomolecular Engineering Korea Advanced Institute of Science and Technology (KAIST) 291 Daehak‐ro, Yuseong‐gu Daejeon 34141 Republic of Korea

5. Energy Storage Research Center Korea Institute of Science and Technology 5 Hwarang‐ro, Seongbuk‐gu Seoul 02792 Republic of Korea

6. Advanced Batteries Research Center Korea Electronic Technology Institute 25 Saenari‐ro, Bundang‐gu Seongnam‐si 13509 Republic of Korea

Abstract

AbstractConstruction of a robust artificial solid‐electrolyte interphase (SEI) layer has proposed an effective strategy to overcome the instability of the lithium (Li). However, existing artificial SEI layers inadequately controlled ion distribution, leading to dendritic growth and penetration. Furthermore, the environmental impact of the manufacturing process and materials of the artificial layer is often overlooked. In this work, a chemically and physically reinforced membrane (C‐Li@P) composed of the biocompatible Li+ coordinated carboxymethyl guar gum (CMGG) and polyacrylamide (PAM) polymers serves as an artificial SEI membrane for dendrite‐free Li. This membrane with hollow channels not only directs ion flux along the interspace of fibers, fostering uniform Li plating but also induces a desirable interface chemistry. Consequently, artificial SEI membrane‐covered Li exhibits stable electrochemical plating/stripping reactions, surpassing the cycle life of ≈750% of bare Li. It demonstrates exceptional capacity retention of ≈93.9%, ≈88.1%, and ≈79.18% in full cells paired with LiNi0.8Mn0.1Co0.1O2 (NMC811), LiNi0.6Mn0.2Co0.2O2 (NMC622) and S cathodes, respectively over 200 cycles at 1 C rate. Additionally, the water‐based green manufacturing and biodegradability of the membrane demonstrated the sustainable development and disposal of electrodes. This work provides a comprehensive framework for the design of an artificial layer chemically and physically regulating dendritic growth.

Publisher

Wiley

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