Hexagonal Porous Zincophilic Alloy Interface for Ultrastable Zinc Metal Anode

The cycling stability of zinc metal anodes (ZMAs) is often hindered by issues including uncontrolled dendritic growth, nonuniform electric field distribution, and parasitic hydrogen evolution reaction (HER). Herein, we report a zinc anode protected by a zinc-tin (ZnSn) alloy layer with a hexagonal porous structure, fabricated via a simple electrochemical etching process in sodium citrate electrolyte followed by an elemental substitution treatment in stannous chloride solution (denoted as SC@ZnSn). This modified anode exhibits an enhanced electrochemical activity and superior corrosion resistance. When paired in an asymmetric cell configuration, the SC@ZnSn anode delivers remarkable cycling stability, maintaining an average Coulombic efficiency of 99.6% over 1800 cycles. Experimental investigations reveal that the hexagonal porous framework provides abundant Zn<sup>2+</sup> adsorption sites and promotes uniform ion flux while the zincophilic ZnSn alloy surface effectively lowers the nucleation barrier. These synergistic effects jointly suppress dendrite growth and ensure excellent long-term reversibility. Furthermore, the SC@ZnSn||<i>I</i><sub>2</sub> full cell demonstrates outstanding durability, achieving stable operation for over 4000 cycles at 1 A g<sup>-1</sup> while maintaining high capacity retention.

Authors

Institutions

Publication Details

Journal
ACS Applied Materials & Interfaces
Published
2026-02-09
DOI
https://doi.org/10.1021/acsami.5c23621
Primary Topic
Advanced battery technologies research
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Hexagonal Porous Zincophilic Alloy Interface for Ultrastable Zinc Metal Anode

Mengliang Hu, Zongtao Qu, Zuomin Lei, Keyu Zhu et al.
ACS Applied Materials & Interfaces
Advanced battery technologies research
article

Hexagonal Porous Zincophilic Alloy Interface for Ultrastable Zinc Metal Anode

Mengliang Hu, Zongtao Qu, Zuomin Lei, Keyu Zhu, Shu‐Shen Lyu, Dong-chuan Mo
article en

Abstract

The cycling stability of zinc metal anodes (ZMAs) is often hindered by issues including uncontrolled dendritic growth, nonuniform electric field distribution, and parasitic hydrogen evolution reaction (HER). Herein, we report a zinc anode protected by a zinc-tin (ZnSn) alloy layer with a hexagonal porous structure, fabricated via a simple electrochemical etching process in sodium citrate electrolyte followed by an elemental substitution treatment in stannous chloride solution (denoted as SC@ZnSn). This modified anode exhibits an enhanced electrochemical activity and superior corrosion resistance. When paired in an asymmetric cell configuration, the SC@ZnSn anode delivers remarkable cycling stability, maintaining an average Coulombic efficiency of 99.6% over 1800 cycles. Experimental investigations reveal that the hexagonal porous framework provides abundant Zn<sup>2+</sup> adsorption sites and promotes uniform ion flux while the zincophilic ZnSn alloy surface effectively lowers the nucleation barrier. These synergistic effects jointly suppress dendrite growth and ensure excellent long-term reversibility. Furthermore, the SC@ZnSn||<i>I</i><sub>2</sub> full cell demonstrates outstanding durability, achieving stable operation for over 4000 cycles at 1 A g<sup>-1</sup> while maintaining high capacity retention.

ACS Applied Materials & InterfacesVol. 18(6)
Sun Yat-sen University (CN), Department of Space (IN), Space Micro (United States) (US), Huizhou University (CN)
Affordable and clean energy
Openalex Percentile: Top 62%
Advanced battery technologies research
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.