Artificial Interface Layer for Long-Life Performance NASICON-Based Sodium-Ion Solid-State Batteries

Significant interest has been directed toward sodium metal batteries owing to their high theoretical specific capacity, low cost, and abundant resources. However, the high reactivity of sodium metal leads to dendrite growth and uncontrolled solid electrolyte interphase (SEI) formation, resulting in safety risks and increased impedance. In this work, a zinc–magnesium codoped Na3.65Zr1.675Zn0.2Mg0.125Si2PO12 (NZZMSPO, SE) solid electrolyte with high Na+ conductivity was synthesized. A facile solution-coating method enabled uniform surface modification, allowing in situ formation of a stable artificial SEI at the solid electrolyte|sodium metal interface. This protective layer effectively stabilizes the interface and markedly enhances cycling stability, elucidated by density functional theory (DFT) calculations. Sodium symmetric cells with the artificial SEI exhibited lifetimes exceeding 1200 h at 0.3 mA cm–2, attributed to suppressed dendrite growth and regulated SEI formation. Full cells using Na4Fe3(PO4)2P2O7 cathodes delivered a specific capacity of 78.82 mAh g–1 with 89% capacity retention after 200 cycles, demonstrating the broad potential of this artificial SEI strategy for solid-state sodium-ion batteries.

Authors

Institutions

Publication Details

Journal
ACS Applied Engineering Materials
Published
2026-04-07
DOI
https://doi.org/10.1021/acsaenm.6c00169
Primary Topic
Advanced Battery Materials and Technologies
Type
article
Field-Weighted Citation Impact
0.00

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Artificial Interface Layer for Long-Life Performance NASICON-Based Sodium-Ion Solid-State Batteries

Xiaobo Ji, Mushi Yang, Guoqiang Zou, Wentao Deng et al.
ACS Applied Engineering Materials
Advanced Battery Materials and Technologies
article

Artificial Interface Layer for Long-Life Performance NASICON-Based Sodium-Ion Solid-State Batteries

Xiaobo Ji, Mushi Yang, Guoqiang Zou, Wentao Deng, Hongshuai Hou
article en

Abstract

Significant interest has been directed toward sodium metal batteries owing to their high theoretical specific capacity, low cost, and abundant resources. However, the high reactivity of sodium metal leads to dendrite growth and uncontrolled solid electrolyte interphase (SEI) formation, resulting in safety risks and increased impedance. In this work, a zinc–magnesium codoped Na3.65Zr1.675Zn0.2Mg0.125Si2PO12 (NZZMSPO, SE) solid electrolyte with high Na+ conductivity was synthesized. A facile solution-coating method enabled uniform surface modification, allowing in situ formation of a stable artificial SEI at the solid electrolyte|sodium metal interface. This protective layer effectively stabilizes the interface and markedly enhances cycling stability, elucidated by density functional theory (DFT) calculations. Sodium symmetric cells with the artificial SEI exhibited lifetimes exceeding 1200 h at 0.3 mA cm–2, attributed to suppressed dendrite growth and regulated SEI formation. Full cells using Na4Fe3(PO4)2P2O7 cathodes delivered a specific capacity of 78.82 mAh g–1 with 89% capacity retention after 200 cycles, demonstrating the broad potential of this artificial SEI strategy for solid-state sodium-ion batteries.

ACS Applied Engineering MaterialsVol. 4(4)
Central South University (CN), Powder Metallurgy Institute (BY), State Key Laboratory of Powder Metallurgy
National Natural Science Foundation of China
Responsible consumption and production
Openalex Percentile: Top 24%
Advanced Battery Materials and Technologies
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.