A Self‐Regulated Interface toward Highly Reversible Aqueous Zinc Batteries
Aqueous zinc batteries, that demonstrate high safety and low cost, are considered promising candidates for large‐scale energy storage. However, Zn anodes suffer from rapid performance deterioration due to the severe Zn dendrite growth and side reactions. Herein, with a low‐cost ammonium acetate (NH4...
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Published in: | Advanced energy materials Vol. 12; no. 9 |
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01-03-2022
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Abstract | Aqueous zinc batteries, that demonstrate high safety and low cost, are considered promising candidates for large‐scale energy storage. However, Zn anodes suffer from rapid performance deterioration due to the severe Zn dendrite growth and side reactions. Herein, with a low‐cost ammonium acetate (NH4OAc) additive, a self‐regulated Zn/electrolyte interface is built to address these problems. The NH4+ induces a dynamic electrostatic shielding layer around the abrupt Zn protuberance to make the Zn deposition uniform, and the OAc− acts as an interfacial pH buffer to suppress the proton‐induced side reactions and the precipitation of insoluble by‐products. As a result, in the electrolyte with the NH4OAc additive, Zn anodes exhibit a long cycling stability of 3500 h at 1 mA cm−2, an impressive cumulative areal capacity of 5000 mAh cm−2 at 10 mA cm−2, and a high Coulombic efficiency of ≈99.7%. A prototype full cell coupled with a NH4V4O10 cathode performs much better in terms of capacity retention than the additive‐free case. The findings pave the way for developing practical Zn batteries.
A self‐regulated interface is built using a dual‐functional ammonium acetate additive to address zinc dendrite growth and proton‐induced side reactions simultaneously, thus enabling an Zn anode with long cycling stability of 3500 h, an impressive cumulative areal capacity of 5000 mAh cm−2 at 10 mA cm−2, and a high Coulombic efficiency of 99.7%. |
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AbstractList | Aqueous zinc batteries, that demonstrate high safety and low cost, are considered promising candidates for large‐scale energy storage. However, Zn anodes suffer from rapid performance deterioration due to the severe Zn dendrite growth and side reactions. Herein, with a low‐cost ammonium acetate (NH4OAc) additive, a self‐regulated Zn/electrolyte interface is built to address these problems. The NH4+ induces a dynamic electrostatic shielding layer around the abrupt Zn protuberance to make the Zn deposition uniform, and the OAc− acts as an interfacial pH buffer to suppress the proton‐induced side reactions and the precipitation of insoluble by‐products. As a result, in the electrolyte with the NH4OAc additive, Zn anodes exhibit a long cycling stability of 3500 h at 1 mA cm−2, an impressive cumulative areal capacity of 5000 mAh cm−2 at 10 mA cm−2, and a high Coulombic efficiency of ≈99.7%. A prototype full cell coupled with a NH4V4O10 cathode performs much better in terms of capacity retention than the additive‐free case. The findings pave the way for developing practical Zn batteries. Abstract Aqueous zinc batteries, that demonstrate high safety and low cost, are considered promising candidates for large‐scale energy storage. However, Zn anodes suffer from rapid performance deterioration due to the severe Zn dendrite growth and side reactions. Herein, with a low‐cost ammonium acetate (NH 4 OAc) additive, a self‐regulated Zn/electrolyte interface is built to address these problems. The NH 4 + induces a dynamic electrostatic shielding layer around the abrupt Zn protuberance to make the Zn deposition uniform, and the OAc − acts as an interfacial pH buffer to suppress the proton‐induced side reactions and the precipitation of insoluble by‐products. As a result, in the electrolyte with the NH 4 OAc additive, Zn anodes exhibit a long cycling stability of 3500 h at 1 mA cm −2 , an impressive cumulative areal capacity of 5000 mAh cm −2 at 10 mA cm −2 , and a high Coulombic efficiency of ≈ 99.7%. A prototype full cell coupled with a NH 4 V 4 O 10 cathode performs much better in terms of capacity retention than the additive‐free case. The findings pave the way for developing practical Zn batteries. Aqueous zinc batteries, that demonstrate high safety and low cost, are considered promising candidates for large‐scale energy storage. However, Zn anodes suffer from rapid performance deterioration due to the severe Zn dendrite growth and side reactions. Herein, with a low‐cost ammonium acetate (NH4OAc) additive, a self‐regulated Zn/electrolyte interface is built to address these problems. The NH4+ induces a dynamic electrostatic shielding layer around the abrupt Zn protuberance to make the Zn deposition uniform, and the OAc− acts as an interfacial pH buffer to suppress the proton‐induced side reactions and the precipitation of insoluble by‐products. As a result, in the electrolyte with the NH4OAc additive, Zn anodes exhibit a long cycling stability of 3500 h at 1 mA cm−2, an impressive cumulative areal capacity of 5000 mAh cm−2 at 10 mA cm−2, and a high Coulombic efficiency of ≈99.7%. A prototype full cell coupled with a NH4V4O10 cathode performs much better in terms of capacity retention than the additive‐free case. The findings pave the way for developing practical Zn batteries. A self‐regulated interface is built using a dual‐functional ammonium acetate additive to address zinc dendrite growth and proton‐induced side reactions simultaneously, thus enabling an Zn anode with long cycling stability of 3500 h, an impressive cumulative areal capacity of 5000 mAh cm−2 at 10 mA cm−2, and a high Coulombic efficiency of 99.7%. |
Author | Zhi, Xing Yang, Quan‐Hong Wang, Zhenxing Mo, Yanbing Cui, Changjun Li, Huan Geng, Chuannan Lu, Haotian Sun, Rui Kang, Feiyu Han, Daliang Liang, Qinghua Zhang, Zhicheng Weng, Zhe Guo, Xiaoxia |
Author_xml | – sequence: 1 givenname: Daliang orcidid: 0000-0002-4094-3279 surname: Han fullname: Han, Daliang organization: Tianjin University – sequence: 2 givenname: Zhenxing surname: Wang fullname: Wang, Zhenxing organization: Tianjin University – sequence: 3 givenname: Haotian surname: Lu fullname: Lu, Haotian organization: International Campus of Tianjin University – sequence: 4 givenname: Huan surname: Li fullname: Li, Huan organization: The University of Adelaide – sequence: 5 givenname: Changjun surname: Cui fullname: Cui, Changjun organization: Tianjin University – sequence: 6 givenname: Zhicheng surname: Zhang fullname: Zhang, Zhicheng organization: Tianjin University – sequence: 7 givenname: Rui surname: Sun fullname: Sun, Rui organization: Tianjin University – sequence: 8 givenname: Chuannan surname: Geng fullname: Geng, Chuannan organization: Tianjin University – sequence: 9 givenname: Qinghua surname: Liang fullname: Liang, Qinghua organization: The University of Melbourne – sequence: 10 givenname: Xiaoxia surname: Guo fullname: Guo, Xiaoxia organization: Tianjin University – sequence: 11 givenname: Yanbing surname: Mo fullname: Mo, Yanbing organization: Tianjin University – sequence: 12 givenname: Xing surname: Zhi fullname: Zhi, Xing organization: The University of Adelaide – sequence: 13 givenname: Feiyu surname: Kang fullname: Kang, Feiyu organization: Tsinghua University – sequence: 14 givenname: Zhe orcidid: 0000-0002-6005-9552 surname: Weng fullname: Weng, Zhe email: zweng@tju.edu.cn organization: Tianjin University – sequence: 15 givenname: Quan‐Hong orcidid: 0000-0003-2882-3968 surname: Yang fullname: Yang, Quan‐Hong organization: International Campus of Tianjin University |
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Snippet | Aqueous zinc batteries, that demonstrate high safety and low cost, are considered promising candidates for large‐scale energy storage. However, Zn anodes... Abstract Aqueous zinc batteries, that demonstrate high safety and low cost, are considered promising candidates for large‐scale energy storage. However, Zn... |
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SubjectTerms | Ammonium acetate Anodes aqueous zinc batteries Dendritic structure dynamic regulation electrolyte additives Electrolytes Electrostatic shielding Energy storage Performance degradation pH buffers Zinc |
Title | A Self‐Regulated Interface toward Highly Reversible Aqueous Zinc Batteries |
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