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用于可持续、灵活供电的高能耐用全聚合物水电池。

Energetic and durable all-polymer aqueous battery for sustainable, flexible power.

作者信息

Hong Yang, Jia Kangkang, Zhang Yueyu, Li Ziyuan, Jia Junlin, Chen Jing, Liang Qimin, Sun Huarui, Gao Qiang, Zhou Dong, Li Ruhong, Dong Xiaoli, Fan Xiulin, He Sisi

机构信息

School of Science, Harbin Institute of Technology (Shenzhen), Shenzhen, China.

Department of Chemistry and Biotechnology, School of Engineering, The University of Tokyo, Tokyo, Japan.

出版信息

Nat Commun. 2024 Nov 5;15(1):9539. doi: 10.1038/s41467-024-53804-2.

DOI:10.1038/s41467-024-53804-2
PMID:39496602
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11535528/
Abstract

All-polymer aqueous batteries, featuring electrodes and electrolytes made entirely from polymers, advance wearable electronics through their processing ease, inherent safety, and sustainability. Challenges persist with the instability of polymer electrode redox products in aqueous environments, which fail to achieve high performance in all-polymer aqueous batteries. Here, we report a polymer-aqueous electrolyte designed to stabilize polymer electrode redox products by modulating the solvation layers and forming a solid-electrolyte interphase. Polyaniline is selected as an example for its dual functionality as a cathode or anode working by p/n doping mechanisms. This approach pioneers the application of polyaniline as an anode and enhances the high-voltage stability of polyaniline cathode in an aqueous electrolyte. The resulting all-polymer aqueous sodium-ion battery with polyaniline as symmetric electrodes exhibits a high capacity of 139 mAh/g, energy density of 153 Wh/kg, and a retention of over 92% after 4800 cycles. Spectroscopic characterizations have elucidated the hydration structure, solid-electrolyte interphase, and dual-ion doping mechanism. Large-scale all-polymer flexible batteries are fabricated with excellent flexibility and recyclability, heralding a paradigmatic approach to sustainable, wearable energy storage.

摘要

全聚合物水系电池的电极和电解质完全由聚合物制成,因其易于加工、固有安全性和可持续性而推动了可穿戴电子产品的发展。然而,聚合物电极氧化还原产物在水性环境中的不稳定性仍然是一个挑战,这使得全聚合物水系电池无法实现高性能。在此,我们报道了一种聚合物水系电解质,其设计目的是通过调节溶剂化层和形成固体电解质界面来稳定聚合物电极氧化还原产物。聚苯胺因其通过p/n掺杂机制作为阴极或阳极工作的双重功能而被选为例证。这种方法开创了聚苯胺作为阳极的应用,并提高了聚苯胺阴极在水性电解质中的高压稳定性。由此产生的以聚苯胺为对称电极的全聚合物水系钠离子电池表现出139 mAh/g的高容量、153 Wh/kg的能量密度,并且在4800次循环后保留率超过92%。光谱表征阐明了水化结构、固体电解质界面和双离子掺杂机制。大规模的全聚合物柔性电池被制造出来,具有优异的柔韧性和可回收性,预示着一种可持续、可穿戴储能的范例方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d834/11535528/27e62924c4ef/41467_2024_53804_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d834/11535528/014ebbd41c3e/41467_2024_53804_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d834/11535528/e18d9e8c2795/41467_2024_53804_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d834/11535528/b0ca9374f731/41467_2024_53804_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d834/11535528/05bcdb0d575e/41467_2024_53804_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d834/11535528/27e62924c4ef/41467_2024_53804_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d834/11535528/014ebbd41c3e/41467_2024_53804_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d834/11535528/e18d9e8c2795/41467_2024_53804_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d834/11535528/b0ca9374f731/41467_2024_53804_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d834/11535528/05bcdb0d575e/41467_2024_53804_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d834/11535528/27e62924c4ef/41467_2024_53804_Fig5_HTML.jpg

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本文引用的文献

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Alkaline-based aqueous sodium-ion batteries for large-scale energy storage.用于大规模储能的碱性水系钠离子电池。
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Various states of water species in an anion exchange membrane characterized by Raman spectroscopy under controlled temperature and humidity.在可控温度和湿度条件下,通过拉曼光谱表征阴离子交换膜中各种水物种的状态。
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Strong Solvent and Dual Lithium Salts Enable Fast-Charging Lithium-Ion Batteries Operating from -78 to 60 °C.
强溶剂和双锂盐使锂离子电池能够在-78至60°C的温度下快速充电。
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Enabling long-cycling aqueous sodium-ion batteries via Mn dissolution inhibition using sodium ferrocyanide electrolyte additive.通过使用亚铁氰化钠电解液添加剂抑制锰溶解来实现长循环水系钠离子电池。
Nat Commun. 2023 Jun 16;14(1):3591. doi: 10.1038/s41467-023-39385-6.
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