Conquering Zn Dendrites via Crystal‐Facet Manipulation and Water‐Repellent Interphase Construction
Source abstract
Abstract
Abstract Aqueous zinc‐ion batteries (AZIBs) are impeded by hydrogen evolution and uncontrolled dendrite growth on Zn metal anodes. A simple, solution‐based strategy is proposed to simultaneously direct crystallographic deposition and reduce interfacial water activity. Cinnamaldehyde (CA) is employed as a molecular surface modifier to form an artificial solid‐electrolyte interphase (ASEI) via a brief immersion. The aromatic moiety of CA imparts strong hydrophobicity, further suppressing water‐triggered side reactions. At the meantime, CA exhibits facet‐selective adsorption, preferentially passivating Zn (002) and (100) planes and thereby guiding Zn 2+ deposition along the (101) orientation. The (101) facet provides intermediate surface energy and plating/stripping barriers, promoting uniform epitaxial growth, improved corrosion resistance, and reduced polarization. Consequently, CA‐modified Zn symmetric cells sustain >2000 h at 1 mA cm −2 with 1 mAh cm −2 . In Zn‖NVO full cells, a specific capacity exceeding 160 mAh g −1 can be maintained after 1000 cycles at 1 A g −1 . This facet‐directed ASEI engineering offers a practical and scalable route to long‐life, dendrite‐resistant Zn anodes for AZIBs.
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Research context
OpenAlex topics: Advanced battery technologies research · Electrocatalysts for Energy Conversion · Advancements in Battery Materials
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
School of Chemical and Environmental Engineering China University of Mining and Technology (Beijing) Beijing 100083 P. R. China
Energy Research Institute at Nanyang Technological University (ERI@NTU) Singapore 637553 Singapore
Funding
National Natural Science Foundation of China
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