Bin Wang, Wenqi Li, Siyuan Wang, Peng Xie, Peng Wan, Ying Gui and Ding Chen
{"title":"从金属有机框架中合理设计碳包封硒化锰复合材料,用于稳定的锌锰水性电池","authors":"Bin Wang, Wenqi Li, Siyuan Wang, Peng Xie, Peng Wan, Ying Gui and Ding Chen","doi":"10.1039/D3TA08043A","DOIUrl":null,"url":null,"abstract":"<p >Aqueous zinc ion batteries (AZIBs) have emerged as promising candidates for large-scale energy storage and small electronic devices due to their environmentally friendly, safe, stable, and cost-effective characteristics. Among various cathode materials, manganese-based compounds, particularly manganese oxides, have garnered special attention for their high energy density, non-toxicity, and low cost. However, currently, reported cathode materials generally exhibit mediocre performance in terms of Zn<small><sup>2−</sup></small> storage kinetics and stability. This work proposes a novel cathode material for AZIBs based on manganese selenide nanoparticles (C@MnSe@GO-<em>x</em>) with graphene oxide (GO) encapsulation and <em>in situ</em> transformation of metal–organic frameworks. Upon activation, the C@MnSe@GO-<em>x</em> material transforms into MnO<small><sub><em>x</em></sub></small>, resulting in a high specific capacity of 457.14 mA h g<small><sup>−1</sup></small> (at 100 mA g<small><sup>−1</sup></small>) in AZIBs. Even after 1500 cycles at 2000 mA g<small><sup>−1</sup></small>, the material maintains 86.15% of its specific capacity. The mechanism of the improved electrochemical performance of the C@MnSe@GO-<em>x</em> based electrode was also investigated by a series of electrochemical tests and <em>ex situ</em> XRD, revealing its transformation mechanism during the initial activation process. This research offers novel insights and theoretical backing for the design and optimization of cathode materials in aqueous zinc-ion batteries, contributing to the advancement of these batteries for practical applications.</p>","PeriodicalId":82,"journal":{"name":"Journal of Materials Chemistry A","volume":null,"pages":null},"PeriodicalIF":10.7000,"publicationDate":"2024-02-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Rationally designed carbon-encapsulated manganese selenide composites from metal–organic frameworks for stable aqueous Zn–Mn batteries†\",\"authors\":\"Bin Wang, Wenqi Li, Siyuan Wang, Peng Xie, Peng Wan, Ying Gui and Ding Chen\",\"doi\":\"10.1039/D3TA08043A\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p >Aqueous zinc ion batteries (AZIBs) have emerged as promising candidates for large-scale energy storage and small electronic devices due to their environmentally friendly, safe, stable, and cost-effective characteristics. 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The mechanism of the improved electrochemical performance of the C@MnSe@GO-<em>x</em> based electrode was also investigated by a series of electrochemical tests and <em>ex situ</em> XRD, revealing its transformation mechanism during the initial activation process. 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引用次数: 0
摘要
锌离子水电池(AZIBs)因其环保、安全、稳定和成本效益高的特点,已成为大规模储能和小型电子设备的理想候选材料。在各种阴极材料中,锰基化合物,尤其是锰氧化物,因其能量密度高、无毒、成本低而受到特别关注。然而,目前报道的阴极材料在 Zn2+ 储存动力学和稳定性方面表现一般。本研究提出了一种基于硒化锰纳米颗粒(C@MnSe@GO-x)、氧化石墨烯(GO)封装和金属有机框架原位转化的新型 AZIB 阴极材料。活化后,C@MnSe@GO-x 材料转化为 MnOx,从而使 AZIBs 的比容量高达 457.14 mAh g-1(100 mA g-1)。即使在 2000 mA g-1 下循环 1500 次后,该材料仍能保持 86.15 % 的比容量。此外,还通过一系列电化学测试和原位 XRD 研究了 C@MnSe@GO-x 基电极电化学性能改善的机理,揭示了其在初始活化过程中的转化机制。这项研究为锌离子水电池阴极材料的设计和优化提供了新的见解和理论依据,有助于推动这类电池的实际应用。
Rationally designed carbon-encapsulated manganese selenide composites from metal–organic frameworks for stable aqueous Zn–Mn batteries†
Aqueous zinc ion batteries (AZIBs) have emerged as promising candidates for large-scale energy storage and small electronic devices due to their environmentally friendly, safe, stable, and cost-effective characteristics. Among various cathode materials, manganese-based compounds, particularly manganese oxides, have garnered special attention for their high energy density, non-toxicity, and low cost. However, currently, reported cathode materials generally exhibit mediocre performance in terms of Zn2− storage kinetics and stability. This work proposes a novel cathode material for AZIBs based on manganese selenide nanoparticles (C@MnSe@GO-x) with graphene oxide (GO) encapsulation and in situ transformation of metal–organic frameworks. Upon activation, the C@MnSe@GO-x material transforms into MnOx, resulting in a high specific capacity of 457.14 mA h g−1 (at 100 mA g−1) in AZIBs. Even after 1500 cycles at 2000 mA g−1, the material maintains 86.15% of its specific capacity. The mechanism of the improved electrochemical performance of the C@MnSe@GO-x based electrode was also investigated by a series of electrochemical tests and ex situ XRD, revealing its transformation mechanism during the initial activation process. This research offers novel insights and theoretical backing for the design and optimization of cathode materials in aqueous zinc-ion batteries, contributing to the advancement of these batteries for practical applications.
期刊介绍:
The Journal of Materials Chemistry A, B & C covers a wide range of high-quality studies in the field of materials chemistry, with each section focusing on specific applications of the materials studied. Journal of Materials Chemistry A emphasizes applications in energy and sustainability, including topics such as artificial photosynthesis, batteries, and fuel cells. Journal of Materials Chemistry B focuses on applications in biology and medicine, while Journal of Materials Chemistry C covers applications in optical, magnetic, and electronic devices. Example topic areas within the scope of Journal of Materials Chemistry A include catalysis, green/sustainable materials, sensors, and water treatment, among others.