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Self-Established Rapid Magnesiation/De-Magnesiation Pathways in Binary Selenium-Copper Mixtures with Significantly Enhanced Mg-Ion Storage Reversibility

文献类型:期刊论文

作者Zhang, Zhonghua1,2; Chen, Bingbing1; Xu, Huimin3; Cui, Zili1; Dong, Shanmu1; Du, Aobing1,2; Ma, Jun1; Wang, Qingfu1; Zhou, Xinhong3; Cui, Guanglei1
刊名ADVANCED FUNCTIONAL MATERIALS
出版日期2018-01-04
卷号28期号:1
关键词Displacement Reactions High Reversibility Intercalation Reactions Magnesium Batteries Selenium Cathodes
DOI10.1002/adfm.201701718
文献子类Article
英文摘要Rechargeable magnesium/sulfur (Mg/S) and magnesium/selenium (Mg/Se) batteries are characterized by high energy density, inherent safety, and economical effectiveness, and therefore, are of great scientific and technological interest. However, elusive challenges, including the limited charge storage capacity, low Coulombic efficiency, and short cycle life, have been encountered due to the sluggish electrochemical kinetics and severe shuttles of ploysulfides (polyselenide). Taking selenium as model paradigm, a new and reliable Mg-Se chemistry is proposed through designing binary selenium-copper (Se-Cu) cathodes. An intriguing effect of Cu powders on the electrochemical reaction pathways of the active Se microparticles is revealed in a way of forming Cu3Se2 intermediates, which induces an unconventional yet reversible two-stage magnesiation mechanism: Mg-ions first insert into Cu3Se2 phases; in a second step Cu-ions in the Mg2xCu3Se2 lattice exchange with Mg-ions. As expected, binary Se-Cu electrodes show significantly improved reversibility and elongated cycle life. More bracingly, Se/C nanostructures fabricated by facile blade coating Se nanorodes onto copper foils exhibit high output power and capacity (696.0 mAh g(-1) at 67.9 mA g(-1)), which outperforms all previously reported Mg/Se batteries. This work envisions a facile and reliable strategy to achieve better reversibility and long-term durability of selenium (sulfur) electrodes.
WOS关键词POSITIVE ELECTRODE ; CRYSTAL-STRUCTURE ; SULFUR CATHODE ; BATTERIES ; LITHIUM ; ENERGY ; CAPACITY ; XPS
WOS研究方向Chemistry ; Science & Technology - Other Topics ; Materials Science ; Physics
语种英语
WOS记录号WOS:000419025200020
资助机构National Science Fund for Distinguished Young Scholars(51625204) ; National Natural Science Foundation of China(51502319) ; Shandong Provincial Natural Science Foundation(ZR2016BQ18)
源URL[http://ir.qibebt.ac.cn/handle/337004/10015]  
专题青岛生物能源与过程研究所_仿生能源与储能系统团队
作者单位1.Chinese Acad Sci, Qingdao Ind Energy Storage Res Inst, Qingdao Inst Bioenergy & Bioproc Technol, Qingdao 266101, Peoples R China
2.Univ Chinese Acad Sci, Beijing 100190, Peoples R China
3.Qingdao Univ Sci & Technol, Coll Chem & Mol Engn, Qingdao 266042, Peoples R China
推荐引用方式
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Zhang, Zhonghua,Chen, Bingbing,Xu, Huimin,et al. Self-Established Rapid Magnesiation/De-Magnesiation Pathways in Binary Selenium-Copper Mixtures with Significantly Enhanced Mg-Ion Storage Reversibility[J]. ADVANCED FUNCTIONAL MATERIALS,2018,28(1).
APA Zhang, Zhonghua.,Chen, Bingbing.,Xu, Huimin.,Cui, Zili.,Dong, Shanmu.,...&Cui, Guanglei.(2018).Self-Established Rapid Magnesiation/De-Magnesiation Pathways in Binary Selenium-Copper Mixtures with Significantly Enhanced Mg-Ion Storage Reversibility.ADVANCED FUNCTIONAL MATERIALS,28(1).
MLA Zhang, Zhonghua,et al."Self-Established Rapid Magnesiation/De-Magnesiation Pathways in Binary Selenium-Copper Mixtures with Significantly Enhanced Mg-Ion Storage Reversibility".ADVANCED FUNCTIONAL MATERIALS 28.1(2018).

入库方式: OAI收割

来源:青岛生物能源与过程研究所

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