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用于实用锌阳极的仿生局部凝胶电解质。

Biomimetic Localized Gel Electrolyte for Practical Zinc Anode.

作者信息

Zhu Yibo, Gao Shengyong, Zhang Shuangbin, Chen Yang, Liu Peng, Meng Haotian, Luo Zhiruo, Chen Xuan, Wen Zhenhai, Wang Lina, Wang Lianzhou, Luo Bin, Zhou Jisheng

机构信息

State Key Laboratory of Chemical Resource Engineering, Beijing Key Laboratory of Electrochemical Process and Technology for Materials Technology, National Engineering Research Center for Fuel Cell and Hydrogen Source, Beijing University of Chemical Technology, Beijing, 100029, P.R. China.

Australia Institute for Bioengineering and Nanotechnology (AIBN), The University of Queensland, Brisbane, QLD, 4072, Australia.

出版信息

Angew Chem Int Ed Engl. 2025 May;64(21):e202501664. doi: 10.1002/anie.202501664. Epub 2025 Mar 22.

DOI:10.1002/anie.202501664
PMID:40074686
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12087840/
Abstract

Incompatible electrode/electrolyte interface often leads to dendrite growth, parasitic reactions, and corrosion, posing significant challenges to the application of Zn anodes. Herein, we introduce a biomimetic antifreeze protein localized gel electrolyte (ALGE) with multifunctional capabilities to address these issues by combining electrolyte modification with interface optimization. ALGE modifies the Zn solvation structure and the hydrogen-bond network adjacent to the zinc anode, effectively suppressing hydrogen evolution. Additionally, ALGE promotes (002) crystal plane-dominated deposition by protein-zinc surface interactions, enabling a long-range dendrite-free deposition. The absence of by-products and inhibited corrosion further highlights the practical potential of ALGE. Symmetric cells with ALGE-modified zinc demonstrate an impressive lifespan of 610  h under a current density of 10 mA cm and a capacity of 10 mAh cm. The pouch cell integrating a manganese dioxide cathode and ALGE-modified Zn anode retains 75.8% of its capacity after 200 cycles at 1 A g. This localized gel electrolyte strategy offers a practical and scalable approach to stabilizing Zn anodes for next-generation energy storage systems.

摘要

不相容的电极/电解质界面常常会导致枝晶生长、寄生反应和腐蚀,这给锌负极的应用带来了重大挑战。在此,我们引入了一种具有多功能的仿生抗冻蛋白局部凝胶电解质(ALGE),通过将电解质改性与界面优化相结合来解决这些问题。ALGE改变了锌的溶剂化结构以及锌负极附近的氢键网络,有效抑制了析氢反应。此外,ALGE通过蛋白质与锌表面的相互作用促进以(002)晶面为主的沉积,实现了无长程枝晶的沉积。没有副产物以及抑制了腐蚀进一步凸显了ALGE的实际应用潜力。采用ALGE改性锌的对称电池在电流密度为10 mA cm²、容量为10 mAh cm²的条件下展现出令人印象深刻的610小时的寿命。集成二氧化锰正极和ALGE改性锌负极的软包电池在1 A g的电流密度下循环200次后仍保留其75.8%的容量。这种局部凝胶电解质策略为稳定下一代储能系统中的锌负极提供了一种实用且可扩展的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fcb/12087840/035d16d8c6bc/ANIE-64-e202501664-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fcb/12087840/ce63d18cb82f/ANIE-64-e202501664-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fcb/12087840/e0d44ffa9913/ANIE-64-e202501664-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fcb/12087840/45e11a78e41e/ANIE-64-e202501664-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fcb/12087840/bfb93d0afb99/ANIE-64-e202501664-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fcb/12087840/8fc142489d86/ANIE-64-e202501664-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fcb/12087840/035d16d8c6bc/ANIE-64-e202501664-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fcb/12087840/ce63d18cb82f/ANIE-64-e202501664-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fcb/12087840/e0d44ffa9913/ANIE-64-e202501664-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fcb/12087840/45e11a78e41e/ANIE-64-e202501664-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fcb/12087840/bfb93d0afb99/ANIE-64-e202501664-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fcb/12087840/8fc142489d86/ANIE-64-e202501664-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1fcb/12087840/035d16d8c6bc/ANIE-64-e202501664-g001.jpg

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本文引用的文献

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Directing Zn Growth with Biased Adsorption of Straight-chain Molecules for Superior Zn Anode Stability.通过直链分子的偏置吸附引导锌生长以实现卓越的锌阳极稳定性。
Angew Chem Int Ed Engl. 2025 Mar 10;64(11):e202421787. doi: 10.1002/anie.202421787. Epub 2024 Dec 20.
2
Hydrogen-Bonded Ionic Co-Crystals for Fast Solid-State Zinc Ion Storage.用于快速固态锌离子存储的氢键离子共晶体
Adv Mater. 2024 Nov;36(47):e2407150. doi: 10.1002/adma.202407150. Epub 2024 Oct 6.
3
Dipole Moment Dictates the Preferential Immobilization in Gel Electrolytes for Ah-level Aqueous Zinc-Metal Batteries.
偶极矩决定了用于安培级水系锌金属电池的凝胶电解质中的优先固定化。
Angew Chem Int Ed Engl. 2025 Jan 10;64(2):e202414702. doi: 10.1002/anie.202414702. Epub 2024 Nov 2.
4
Bidentate Coordination Enables Anions-Regulated Solvation Structure for Advanced Aqueous Zinc Metal Batteries.双齿配位实现用于先进水系锌金属电池的阴离子调控溶剂化结构
Angew Chem Int Ed Engl. 2025 Jan 10;64(2):e202414117. doi: 10.1002/anie.202414117. Epub 2024 Nov 4.
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Advanced electrolytes for high-performance aqueous zinc-ion batteries.用于高性能水系锌离子电池的先进电解质
Chem Soc Rev. 2024 Oct 14;53(20):10335-10369. doi: 10.1039/d4cs00584h.
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The effect of interface heterogeneity on zinc metal anode cyclability.界面异质性对锌金属负极循环性能的影响。
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Anti-Swelling Microporous Membrane for High-Capacity and Long-Life Zn-I Batteries.用于高容量长寿命锌碘电池的抗膨胀微孔膜
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Protein Interfacial Gelation toward Shuttle-Free and Dendrite-Free Zn-Iodine Batteries.用于无穿梭效应和无枝晶锌碘电池的蛋白质界面凝胶化
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Interfacial Biomacromolecular Engineering Toward Stable Ah-Level Aqueous Zinc Batteries.面向稳定的安培级水系锌电池的界面生物大分子工程
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Unlocking Dynamic Solvation Chemistry and Hydrogen Evolution Mechanism in Aqueous Zinc Batteries.揭示水系锌电池中的动态溶剂化化学与析氢机制
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