Molecular Engineering of Green Saccharide Additives: From Solvation Structure to Interface Micro‐Environment for Highly Stable Zinc Metal Anodes

ABSTRACT Saccharide additives have recently emerged as a green, low‐cost, and highly efficient strategy to stabilize Zn metal anodes. Previously reported monosaccharides, disaccharides, oligosaccharides, polysaccharides and their derivatives can effectively suppress dendrite growth, prolong cycle life, and push Coulombic efficiency beyond 99.0%. However, most investigations focus on a single saccharide and its specific mechanism, lacking a systematic review and horizontal comparison of the relationship between the molecular structure and regulatory mechanism, which limits the rational design and performance optimization of saccharide additives. This review comprehensively summarizes and deeply analyzes the common principles by which saccharide additives regulate Zn 2+ solvation, suppress hydrogen evolution, construct water‐poor interface layers, optimize interfacial electric field, and induce oriented Zn 2+ deposition. This review elucidates the structure‐function relationships across different categories of saccharide additives. The abundant oxygen‐containing functional groups, steric hindrance effects, and chain length of saccharide additives act synergistically to deliver a “desolvation‐confinement‐orientation” triple function. This review further proposes forward‐looking strategies for molecular engineering and multi‐component synergy to address existing challenges, and aims to provide critical insights for the design and optimization of long‐lasting zinc‐based energy storage systems.

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Publication Details

Journal
Advanced Energy Materials
Published
2025-11-28
DOI
https://doi.org/10.1002/aenm.202505354
Citations
1
Primary Topic
Advanced battery technologies research
Type
article
Field-Weighted Citation Impact
0.73
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article

Molecular Engineering of Green Saccharide Additives: From Solvation Structure to Interface Micro‐Environment for Highly Stable Zinc Metal Anodes

Aibing Chen, Youan Ji, Guoqiang Ma, Kaiqiang Jing et al.
1 citations
Advanced Energy Materials
Advanced battery technologies research
0.73
article

Molecular Engineering of Green Saccharide Additives: From Solvation Structure to Interface Micro‐Environment for Highly Stable Zinc Metal Anodes

Aibing Chen, Youan Ji, Guoqiang Ma, Kaiqiang Jing, Mengke Peng
article en
1 citations

Abstract

ABSTRACT Saccharide additives have recently emerged as a green, low‐cost, and highly efficient strategy to stabilize Zn metal anodes. Previously reported monosaccharides, disaccharides, oligosaccharides, polysaccharides and their derivatives can effectively suppress dendrite growth, prolong cycle life, and push Coulombic efficiency beyond 99.0%. However, most investigations focus on a single saccharide and its specific mechanism, lacking a systematic review and horizontal comparison of the relationship between the molecular structure and regulatory mechanism, which limits the rational design and performance optimization of saccharide additives. This review comprehensively summarizes and deeply analyzes the common principles by which saccharide additives regulate Zn 2+ solvation, suppress hydrogen evolution, construct water‐poor interface layers, optimize interfacial electric field, and induce oriented Zn 2+ deposition. This review elucidates the structure‐function relationships across different categories of saccharide additives. The abundant oxygen‐containing functional groups, steric hindrance effects, and chain length of saccharide additives act synergistically to deliver a “desolvation‐confinement‐orientation” triple function. This review further proposes forward‐looking strategies for molecular engineering and multi‐component synergy to address existing challenges, and aims to provide critical insights for the design and optimization of long‐lasting zinc‐based energy storage systems.

Advanced Energy MaterialsVol. 16(7)
Hebei University of Science and Technology (CN)
Openalex Percentile: Top 21%
Advanced battery technologies research
0.73
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