Electronic structure regulation inducing robust solid electrolyte interphase for stable anode-free sodium metal batteries

Anode-free sodium metal batteries (AFSMBs) have gained attention as next-generation storage systems with high energy density and cost-effectiveness. However, non-uniform sodium (Na) deposition and an unsteady solid electrolyte interphase (SEI) lead to dendrite-related issues and severe irreversible Na + plating/stripping, greatly aggravating their cycle deterioration. In this study, we effectively modified the 3D current collector’s electronic structure by introducing Zn-N x active sites (Zn-CNF), which enhances lateral Na + diffusion and the Na planar growth, enabling uniform deep Na deposition at an exceptionally high capacity of 10 mA h cm −2 . Furthermore, the Zn-N x bonds enhance the adsorption capacity of PF 6 − and contribute to forming a stable inorganic-rich SEI layer. Consequently, Zn-CNF with the electronic structure regulation endows an ultra-low nucleation overpotential (8 mV) and ultra-high Coulombic efficiency of 99.94% over 1600 cycles. Symmetric cells demonstrate stable Na + plating/stripping behavior for more than 4400 h at 1 mA cm −2 . Moreover, under high cathode loading (7.97 mg cm −2 ), the AFSMBs achieve a high energy density of 374 Wh kg −1 and retain a high discharge capacity of 82.49 mA h g −1 with a capacity retention of 80.4% after 120 cycles. This work proposes a viable strategy to achieving high-energy-density AFSMBs. The introduction of Zn-N x active sites significantly regulates the electronic structure of the 3D current collector, thereby facilitating the formation of a robust inorganic-rich SEI, enhancing lateral Na + diffusion, and promoting planar Na deposition. This enables high cathode loading (7.97 mg cm −2 ) in anode-free sodium metal batteries with a high energy density of 374 Wh kg −1 and 80.4% capacity retention over 120 cycles. • Zn-N x active sites effectively tune the electronic structure of the 3D current collector, facilitating the formation of an anion-derived robust solid electrolyte interphase (SEI) to suppress electrolyte decomposition and interfacial side reactions. • Enhanced lateral Na + diffusion promotes planar Na growth, enabling highly reversible plating/stripping and uniform Na deposition at a high areal capacity of 10 mA h cm −2 . • This strategy effectively regulates Na plating and interphase-depleted Na + ratios during plating/stripping, maintaining a high Na plating proportion (∼80%) over long-term cycling and ensuring superior Na + utilization. • Anode-free sodium metal batteries (N/P = 0) with a high-loading cathode (7.97 mg cm −2 ) achieve a high discharge capacity of 82.49 mA h g −1 with a capacity retention of 80.4% after 120 cycles.

Authors

Institutions

Publication Details

Journal
Advanced Powder Materials
Published
2025-05-19
DOI
https://doi.org/10.1016/j.apmate.2025.100303
Citations
22
Primary Topic
Advancements in Battery Materials
Type
article
Field-Weighted Citation Impact
16.07

Funders

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

Electronic structure regulation inducing robust solid electrolyte interphase for stable anode-free sodium metal batteries

Shuquan Liang, Mulan Qin, Fei Huang, Yinghan Liu et al.
22 citations
Advanced Powder Materials
Advancements in Battery Materials
16.07
article

Electronic structure regulation inducing robust solid electrolyte interphase for stable anode-free sodium metal batteries

Shuquan Liang, Mulan Qin, Fei Huang, Yinghan Liu, Guozhao Fang, Xu Peng
article en
22 citations

Abstract

Anode-free sodium metal batteries (AFSMBs) have gained attention as next-generation storage systems with high energy density and cost-effectiveness. However, non-uniform sodium (Na) deposition and an unsteady solid electrolyte interphase (SEI) lead to dendrite-related issues and severe irreversible Na + plating/stripping, greatly aggravating their cycle deterioration. In this study, we effectively modified the 3D current collector’s electronic structure by introducing Zn-N x active sites (Zn-CNF), which enhances lateral Na + diffusion and the Na planar growth, enabling uniform deep Na deposition at an exceptionally high capacity of 10 mA h cm −2 . Furthermore, the Zn-N x bonds enhance the adsorption capacity of PF 6 − and contribute to forming a stable inorganic-rich SEI layer. Consequently, Zn-CNF with the electronic structure regulation endows an ultra-low nucleation overpotential (8 mV) and ultra-high Coulombic efficiency of 99.94% over 1600 cycles. Symmetric cells demonstrate stable Na + plating/stripping behavior for more than 4400 h at 1 mA cm −2 . Moreover, under high cathode loading (7.97 mg cm −2 ), the AFSMBs achieve a high energy density of 374 Wh kg −1 and retain a high discharge capacity of 82.49 mA h g −1 with a capacity retention of 80.4% after 120 cycles. This work proposes a viable strategy to achieving high-energy-density AFSMBs. The introduction of Zn-N x active sites significantly regulates the electronic structure of the 3D current collector, thereby facilitating the formation of a robust inorganic-rich SEI, enhancing lateral Na + diffusion, and promoting planar Na deposition. This enables high cathode loading (7.97 mg cm −2 ) in anode-free sodium metal batteries with a high energy density of 374 Wh kg −1 and 80.4% capacity retention over 120 cycles. • Zn-N x active sites effectively tune the electronic structure of the 3D current collector, facilitating the formation of an anion-derived robust solid electrolyte interphase (SEI) to suppress electrolyte decomposition and interfacial side reactions. • Enhanced lateral Na + diffusion promotes planar Na growth, enabling highly reversible plating/stripping and uniform Na deposition at a high areal capacity of 10 mA h cm −2 . • This strategy effectively regulates Na plating and interphase-depleted Na + ratios during plating/stripping, maintaining a high Na plating proportion (∼80%) over long-term cycling and ensuring superior Na + utilization. • Anode-free sodium metal batteries (N/P = 0) with a high-loading cathode (7.97 mg cm −2 ) achieve a high discharge capacity of 82.49 mA h g −1 with a capacity retention of 80.4% after 120 cycles.

Advanced Powder MaterialsVol. 4(4)
Central South University (CN), Hunan Institute of Engineering (CN)
Central South University, Fundamental Research Funds for Central Universities of the Central South University
Openalex Percentile: Top 1%
Advancements in Battery Materials
16.07
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.