Robust Nanoscale Anode Protective Layers toward Fast‐Charge High‐Energy‐Density Lithium Metal Batteries

C Chuanfa Li Y Yin Cui (Future Technology School Shenzhen Technology University Shenzhen China) S Shenghao Lin (PCFM Lab School of Chemistry Sun Yat‐sen University Guangzhou 510006 P. R. China) P Pengwei Ma Y Yiwei Ji (Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou 510006 P.R. China) Z Zongheng Cen (Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou 510006 P.R. China) G Guofang Yu (PCFM Lab School of Chemistry Sun Yat‐sen University Guangzhou 510006 P. R. China) S Shimei Li (Department of Mechanical Engineering) S Shaohong Liu (Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou P. R. China) D Dingcai Wu

Abstract

AbstractMechanically stable and structurally homogeneous lithium–electrolyte interfacial layers are crucial in stabilizing lithium (Li) anodes for practical Li metal batteries. Herein, an ultrathin (≈84 nm) and robust artificial protective layer is constructed with reactive two‐dimensional (2D) molecular brushes as building blocks. The artificial protective layer can in situ react with underlying Li metal to produce a nanoscale poly(lithium styrenesulfonate)‐grafted graphene oxide (GO‐g‐PSSLi) layer on the outermost surface and an infinite Li–Ag solid solution in the anode. The nanoscale GO‐g‐PSSLi layer well integrates a large number of single Li‐ion conducting PSSLi chains and 2D robust GO backbones, thereby enabling molecular‐level homogeneous and fast Li‐ion diffusion as well as remarkable mechanical strength. Meanwhile, the simultaneously formed Li–Ag solid solution is beneficial for rapid Li transport in the anode to reduce the Li nucleation barrier and facilitate homogeneous deposition of Li. With such artificial protective layers, a prototype pouch cell with a thin Li metal anode (50 µm) and a high‐loading cathode (21.6 mg cm−2) delivers an impressive cycle life of over 350 cycles with 69% capacity retention under harsh conditions. Remarkably, ultrahigh charging power density of 456 W kg−1 and energy density of 325 Wh kg−1 can be simultaneously achieved in an Ah‐level pouch cell.

Article Details

Volume / Issue Vol. 37, Issue 11
Published March 01, 2025
ISSN 0935-9648
Publisher Unknown Publisher

Journal Info

Advanced Materials

Unknown Publisher

ISSN: 0935-9648 Physical Sciences

Authors (10)

C

Chuanfa Li

Y

Yin Cui

Future Technology School Shenzhen Technology University Shenzhen China

S

Shenghao Lin

PCFM Lab School of Chemistry Sun Yat‐sen University Guangzhou 510006 P. R. China

P

Pengwei Ma

Y

Yiwei Ji

Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou 510006 P.R. China

Z

Zongheng Cen

Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou 510006 P.R. China

G

Guofang Yu

PCFM Lab School of Chemistry Sun Yat‐sen University Guangzhou 510006 P. R. China

S

Shimei Li

Department of Mechanical Engineering

S

Shaohong Liu

Key Laboratory for Polymeric Composite and Functional Materials of Ministry of Education School of Chemistry Sun Yat‐sen University Guangzhou P. R. China

D

Dingcai Wu