...
首页> 外文期刊>Chemical engineering journal >Insights into the Mg storage property and mechanism based on the honeycomb-like structured Na3V2(PO4)(3)/C/G in anhydrous electrolyte
【24h】

Insights into the Mg storage property and mechanism based on the honeycomb-like structured Na3V2(PO4)(3)/C/G in anhydrous electrolyte

机译:基于无水电解质中的蜂窝状结构Na3v2(3)/ c / g基于蜂窝状结构的Mg储存性能和机制的洞察力

获取原文
获取原文并翻译 | 示例
           

摘要

The high-voltage cathode material based on the sodium super ionic conductor (NASICON) structured Na3V2(PO4)(3) (NVP) has been found to be a potential candidate for Mg storage. In this work, to improve its electrochemical performance, we construct honeycomb-like structured NVP/C/G with faster electronic and ionic transport by a convenient and universal spray-drying method for the first time. After electrochemically desodiating two Na from the NVP/C/G (ED-NVP/C/G), the ED-NVP/C/G is tested in highly anhydrous Mg electrolyte, and the insights into its Mg storage property and mechanism are carefully studied. An initial capacity of 87 mAh g(-1) with a relatively high average discharge voltage of 2.47 V vs. Mg2+/Mg is obtained at 0.1 C. The X-ray diffraction (XRD) results show that the inserted Mg2+ ions tend to occupy the Na2 (at 18e sites) vacant sites. The investigation of kinetic process by galvanostatic intermittent titration technique (GITT) reveals that the Mg diffusion kinetics is faster during the demagnesiation process. The electrochemical reaction bases on two-phase transition mechanism, and the R-ct value shows a positive relationship to the formation of NaV2(PO4)(3) phase. Finally, a Mg full cell prototype based on the ED-NVP/C/G cathode with Mg metal anode is built. The rational structure design of NVP/C/G improves the electrochemical performance for Mg storage, and our work also gives new understanding into the Mg storage mechanism in the ED-NVP/C/G structure.
机译:已发现基于超离子导体(NASICON)结构Na3v2(PO4)(3)(NVP)的高压阴极材料是MG储存的潜在候选者。在这项工作中,为了提高其电化学性能,我们首次通过方便,通用的喷雾干燥方法构建蜂窝状结构,具有更快的电子和离子运输。从NVP / C / G)电化学脱充两种Na(ED-NVP / C / G)后,在高无水Mg电解质中测试ED-NVP / C / G,并且仔细地测试其Mg储存性能和机构的见解研究过。在0.1℃下获得具有相对高的平均放电电压的87mAhg(-1)的初始容量为2.47V与mg2 + / mg。X射线衍射(XRD)结果表明插入的Mg2 +离子倾向于占据Na2(在18E位点)空置位点。通过电镀间歇性滴定技术(GITT)对动力学过程的研究表明,在脱磁过程中Mg扩散动力学更快。电化学反应基于两相转变机制,R-CT值显示与NAV2(PO4)(3)相的形成的阳性关系。最后,构建了基于ED-NVP / C / G阴极的MG全细胞原型,构建了Mg金属阳极。 NVP / C / G的合理结构设计改善了MG储存的电化学性能,我们的工作还为ED-NVP / C / G结构中的MG存储机制提供了新的理解。

著录项

  • 来源
    《Chemical engineering journal》 |2019年第2019期|共9页
  • 作者单位

    Xiamen Univ Coll Chem &

    Chem Engn State Prov Joint Engn Lab Power Source Technol Ne Collaborat Innovat Ctr Chem Energy Mat State Key Xiamen 361005 Fujian Peoples R China;

    Xiamen Univ Coll Chem &

    Chem Engn State Prov Joint Engn Lab Power Source Technol Ne Collaborat Innovat Ctr Chem Energy Mat State Key Xiamen 361005 Fujian Peoples R China;

    Xiamen Univ Coll Chem &

    Chem Engn State Prov Joint Engn Lab Power Source Technol Ne Collaborat Innovat Ctr Chem Energy Mat State Key Xiamen 361005 Fujian Peoples R China;

    Xiamen Univ Coll Chem &

    Chem Engn State Prov Joint Engn Lab Power Source Technol Ne Collaborat Innovat Ctr Chem Energy Mat State Key Xiamen 361005 Fujian Peoples R China;

    Xiamen Univ Coll Chem &

    Chem Engn State Prov Joint Engn Lab Power Source Technol Ne Collaborat Innovat Ctr Chem Energy Mat State Key Xiamen 361005 Fujian Peoples R China;

    Xiamen Univ Coll Chem &

    Chem Engn State Prov Joint Engn Lab Power Source Technol Ne Collaborat Innovat Ctr Chem Energy Mat State Key Xiamen 361005 Fujian Peoples R China;

    Xiamen Univ Coll Chem &

    Chem Engn State Prov Joint Engn Lab Power Source Technol Ne Collaborat Innovat Ctr Chem Energy Mat State Key Xiamen 361005 Fujian Peoples R China;

  • 收录信息
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 化学工业;
  • 关键词

    Honeycomb-like structure; Na3V2(PO4)(3); Mg storage; Mechanism; Mg full cell;

    机译:蜂窝状的结构;Na3v2(PO4)(3);mg储存;机制;mg全细胞;

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号