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Gradient Interfacial Layer Design for Zinc Metal Anode: Breaking the Trade-Off Between Zincophilicity and Zincophobicity  ( SCI-EXPANDED收录 EI收录)  

文献类型:期刊文献

英文题名:Gradient Interfacial Layer Design for Zinc Metal Anode: Breaking the Trade-Off Between Zincophilicity and Zincophobicity

作者:Zhang, Zekai[1];Liu, Mochou[1];Jin, Yimei[1];Li, Jingkun[1];Mu, Hongchun[1];Han, Xia[1];Liu, Honglai[1];Lian, Cheng[1]

机构:[1]East China Univ Sci & Technol, Shanghai Engn Res Ctr Hierarch Nanomat, Frontiers Sci Ctr Materiobiol & Dynam Chem, Sch Chem & Mol Engn,State Key Lab Chem Engn, Shanghai, Peoples R China

年份:2026

外文期刊名:ADVANCED ENERGY MATERIALS

收录:;EI(收录号:20262821064176);Scopus(收录号:2-s2.0-105043940263);WOS:【SCI-EXPANDED(收录号:WOS:001812836200001)】;

基金:We greatly appreciate the financial support of the Shanghai Pilot Program for Basic Research (22T01400100-18), and 21C Innovation Laboratory, Contemporary Amperex Technology Ltd. by project (No. 21C-OP-202312).

语种:英文

外文关键词:dendrite-free Zn anode; gradient interface layer; zinc-ion hybrid capacitor; zincophilicity; zincophobicity

摘要:The sluggish kinetics and poor thermodynamic stability significantly hinder the practical application of zinc (Zn) metal anodes. The artificial zincophilic interface accelerates Zn2+ deposition but induces intense side reactions, whereas the zincophobic one exhibits the opposite effect. Herein, we innovatively construct a gradient zincophobic-zincophilic interface layer on the zinc anode (PDA-PSBMA@Zn) via self-assembly to break the above trade-off. The aromatic rings and alkyl chains accumulating at the electrode-facing side enhance the thermodynamic stability, while the abundant sulfonate groups near the electrolyte-facing side accelerate Zn2+ desolvation, transport, and deposition kinetics, thereby inducing uniform deposition along the (002) plane. Consequently, symmetric cells with PDA-PSBMA@Zn demonstrate stable cycling for 4200 h at a current density of 1 mA cm-2 and 820 h at 20 mA cm-2. Zinc-ion hybrid capacitors assembled with PDA-PSBMA@Zn and activated carbon retain 97.74% capacity retention after 40 000 cycles at 5 A g-1. This work provides a feasible strategy for balancing the kinetic rate and thermodynamic stability of metal anodes in aqueous energy storage devices.

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