Highly Performing Sodium Metal Batteries Reinforced by a Self-Regulated Dual-Layered Solid Electrolyte Interphase via a Metal-Organic Framework
文献类型:期刊论文
| 作者 | Lv, Jiaze1,2,3,4; Wang, Qiannan2,3,4,5; Ouyang, Mingwei1,2,3,4; Cao, Yan1,2,3,4 |
| 刊名 | ACS APPLIED MATERIALS & INTERFACES
![]() |
| 出版日期 | 2024-07-23 |
| 卷号 | 16期号:31页码:41570-41582 |
| 关键词 | sodium metal battery metal-organic framework dual-layered SEI dendrite-free superior durability |
| ISSN号 | 1944-8244 |
| DOI | 10.1021/acsami.4c09387 |
| 通讯作者 | Cao, Yan(caoyan@ms.giec.ac.cn) |
| 英文摘要 | Sodium-metal batteries, heralded for high energy density and cost-effectiveness, are compromised by an unstable solid electrolyte interphase (SEI) and dendrite formation, which hinder practical applications. Herein, a zirconium-based metal-organic framework nanostructure coating (ZMOF-NSC) was constructed in a low-loss, flexible manner. Comprehensive studies show that ZMOF-NSC, with its periodically ordered nanochannels and organized pore structures, enhances ion transport and decreases the Na+ migration energy barrier, thus ensuring uniform ion flux and achieving uniform spherical deposition. Additionally, ZMOF-NSC facilitates partial desolvation, catalyzing the formation of an inorganic-rich, dual-layered SEI that effectively protects the anode and suppresses dendrite formation. Consequently, the ZMOF-NSC@Na symmetric battery exhibits an impressive lifespan of over 2500 h, demonstrating extended operational longevity. The Na3V2(PO4)(3)parallel to ZMOF-NSC@Na batteries demonstrate exceptional cycling stability with 81% capacity retention after 2000 cycles at 10 C, maintaining stability over 3000 cycles at 20 C. Moreover, the NVP parallel to ZMOF-NSC@Na battery achieves an energy density of 370 Wh kg(-1) and a power density of 10,484 W kg(-1), indicating superior durability and performance. This significant finding highlights the significant potential of structured MOFs to induce a dual-layered SEI, advancing the commercialization of durable, dendrite-free sodium metal batteries. The precise design of self-assembled pore structures and surface active sites in MOFs demonstrates significant potential in advancing the commercialization of durable, dendrite-free electrodes of metal-based rechargeable batteries. |
| WOS关键词 | ANODE |
| 资助项目 | National Natural Science Foundation of China[22178339] ; The 2023 Innovation-Driven Development Special Foundation of Guangxi Province[AA23023021] |
| WOS研究方向 | Science & Technology - Other Topics ; Materials Science |
| 语种 | 英语 |
| WOS记录号 | WOS:001275493100001 |
| 出版者 | AMER CHEMICAL SOC |
| 资助机构 | National Natural Science Foundation of China ; The 2023 Innovation-Driven Development Special Foundation of Guangxi Province |
| 源URL | [http://ir.giec.ac.cn/handle/344007/42413] ![]() |
| 专题 | 中国科学院广州能源研究所 |
| 通讯作者 | Cao, Yan |
| 作者单位 | 1.Univ Sci & Technol China, Sch Energy Sci & Engn, Hefei 230026, Peoples R China 2.Chinese Acad Sci, Guangzhou Inst Energy Convers, Guangzhou 510640, Peoples R China 3.Chinese Acad Sci, Key Lab Renewable Energy, Guangzhou 510640, Peoples R China 4.Guangdong Prov Key Lab New & Renewable Energy Res, Guangzhou 510640, Peoples R China 5.Anhui Univ, Coll Chem & Chem Engn, Hefei 230601, Peoples R China |
| 推荐引用方式 GB/T 7714 | Lv, Jiaze,Wang, Qiannan,Ouyang, Mingwei,et al. Highly Performing Sodium Metal Batteries Reinforced by a Self-Regulated Dual-Layered Solid Electrolyte Interphase via a Metal-Organic Framework[J]. ACS APPLIED MATERIALS & INTERFACES,2024,16(31):41570-41582. |
| APA | Lv, Jiaze,Wang, Qiannan,Ouyang, Mingwei,&Cao, Yan.(2024).Highly Performing Sodium Metal Batteries Reinforced by a Self-Regulated Dual-Layered Solid Electrolyte Interphase via a Metal-Organic Framework.ACS APPLIED MATERIALS & INTERFACES,16(31),41570-41582. |
| MLA | Lv, Jiaze,et al."Highly Performing Sodium Metal Batteries Reinforced by a Self-Regulated Dual-Layered Solid Electrolyte Interphase via a Metal-Organic Framework".ACS APPLIED MATERIALS & INTERFACES 16.31(2024):41570-41582. |
入库方式: OAI收割
来源:广州能源研究所
浏览0
下载0
收藏0
其他版本
除非特别说明,本系统中所有内容都受版权保护,并保留所有权利。

