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DOI 10.1002/advs.202404323

Медицинская библиотека · Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2024

Easy-to-Lay Poly-N Heterocyclic Additives Enable Long-Term Stabilization of Zinc-Ion Capacitor Anodes under Deep Plating/Stripping.

Bu Yongfeng, Kang Qin, Zhu Zhaomin, Zhang Hongyu, Li Yuman, Wang Shihao, Tang Shengda, Pan Li, Yang Lijun, Liang Hongyu

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Аннотация

Addition of organic compounds containing O/N heteroatoms to aqueous electrolytes such as ZnSO4 (ZS) solutions is one of the effective strategies to inhibit Zn anode dendrites and side reactions. However, addressing the stability of Zn plating/stripping at high current densities and areal capacities by this method is still a challenge, especially in capacitors known for high power and long life. Herein, an organic heterocyclic compound of 1, 4, 7, 10-tetraazacyclododecane (TC) containing four symmetrically distributed N atoms is employed as ZS additive, expanding the life of Zn anodes from ≈ 30 h to 1000 and 240 h at deep plating/stripping conditions of 10 and 20 mA cm-2/mAh cm-2, respectively; the cumulative capacity is as high as 5.0 Ah cm-2 with 99% Coulombic efficiency, far exceeding reported additives. TC with higher binding energies than H2O for Zn species tends to adsorb to Zn (002) in a lying manner and participate in the solvation shell of Zn2+, thus avoiding Zn dendrites and side-reaction damage, especially at high current densities. The TC-endowed Zn anode's stability under such extreme conditions is verified in Zn-ion capacitors (i.e., > 94.6% capacity retention after 28 000 cycles), providing new insights into the development of high-power Zn-based energy storage devices.

Для цитирования: Bu Yongfeng, Kang Qin, Zhu Zhaomin, Zhang Hongyu, Li Yuman, Wang Shihao, Tang Shengda, Pan Li, Yang Lijun, Liang Hongyu. Easy-to-Lay Poly-N Heterocyclic Additives Enable Long-Term Stabilization of Zinc-Ion Capacitor Anodes under Deep Plating/Stripping.. Advanced science (Weinheim, Baden-Wurttemberg, Germany). 2024. DOI: 10.1002/advs.202404323.
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