TY - JOUR
T1 - High-valent cation-mediated inorganic-rich gradient SEI for highly stable solid state polymer lithium metal batteries
AU - Zhai, Pengfei
AU - Qu, Shuangquan
AU - Cao, Zidan
AU - Mao, Heng
N1 - Publisher Copyright:
© 2025 Elsevier B.V.
PY - 2025/9
Y1 - 2025/9
N2 - Solid-state polymer lithium metal batteries (SSPLMBs) are widely regarded as the most promising next-generation energy storage technologies due to the high energy density and intrinsic safety. However, common organic-rich solid electrolyte interphase (SEI) exhibits the inhomogeneous and sluggish Li+ transport at the lithium anode interface, and the high nucleation barrier for lithium atoms, collectively promoting Li dendritic growth, thereby hindering the large-scale deployment of SSPLMBs. Herein, we propose a high-valence cation-mediated strategy to construct an inorganic-rich gradient (SEI) by introducing In(NO3)3 as an additive into a polyethylene oxide-based electrolyte (PEO-In(NO3)3). Specifically, trivalent In3+ reacts with lithium to form a lithiophilic Li-In alloy underlayer, while simultaneously mediating anion enrichment at the lithium anode interface via enhanced electrostatic attraction, which facilitates formation of a lithiophobic top layer enriched with anion-derived LiF/Li3N components. The inorganic-rich gradient SEI architecture is established, and superior Li+ diffusion kinetics and reduced energy barrier for lithium atom nucleation are achieved, synergistically enabling homogeneous lithium deposition morphology. Consequently, over one order of magnitude improvement in the lifespan of Li|PEO-In(NO3)3|LFP cell is achieved, demonstrating a 78.3 % capacity retention after 1000 cycles at 1 C, as compared to Li|PEO|LFP cell with common SEI. This study presents a novel avenue to the rational design of inorganic-rich gradient SEI.
AB - Solid-state polymer lithium metal batteries (SSPLMBs) are widely regarded as the most promising next-generation energy storage technologies due to the high energy density and intrinsic safety. However, common organic-rich solid electrolyte interphase (SEI) exhibits the inhomogeneous and sluggish Li+ transport at the lithium anode interface, and the high nucleation barrier for lithium atoms, collectively promoting Li dendritic growth, thereby hindering the large-scale deployment of SSPLMBs. Herein, we propose a high-valence cation-mediated strategy to construct an inorganic-rich gradient (SEI) by introducing In(NO3)3 as an additive into a polyethylene oxide-based electrolyte (PEO-In(NO3)3). Specifically, trivalent In3+ reacts with lithium to form a lithiophilic Li-In alloy underlayer, while simultaneously mediating anion enrichment at the lithium anode interface via enhanced electrostatic attraction, which facilitates formation of a lithiophobic top layer enriched with anion-derived LiF/Li3N components. The inorganic-rich gradient SEI architecture is established, and superior Li+ diffusion kinetics and reduced energy barrier for lithium atom nucleation are achieved, synergistically enabling homogeneous lithium deposition morphology. Consequently, over one order of magnitude improvement in the lifespan of Li|PEO-In(NO3)3|LFP cell is achieved, demonstrating a 78.3 % capacity retention after 1000 cycles at 1 C, as compared to Li|PEO|LFP cell with common SEI. This study presents a novel avenue to the rational design of inorganic-rich gradient SEI.
KW - High-valent cation mediation
KW - Inorganic-rich gradient SEI
KW - Lithium dendrite
KW - Solid polymer electrolyte
KW - Uniform lithium deposition
UR - http://www.scopus.com/pages/publications/105011697832
U2 - 10.1016/j.ensm.2025.104493
DO - 10.1016/j.ensm.2025.104493
M3 - Article
AN - SCOPUS:105011697832
SN - 2405-8297
VL - 81
JO - Energy Storage Materials
JF - Energy Storage Materials
M1 - 104493
ER -