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An efficient organic magnesium borate-based electrolyte with non-nucleophilic characteristics for magnesium-sulfur battery

  • Aobing Du
  • , Zhonghua Zhang
  • , Hongtao Qu
  • , Zili Cui
  • , Lixin Qiao
  • , Longlong Wang
  • , Jingchao Chai
  • , Tao Lu
  • , Shanmu Dong
  • , Tiantian Dong
  • , Huimin Xu
  • , Xinhong Zhou
  • , Guanglei Cui
  • CAS - Qingdao Institute of Biomass Energy and Bioprocess Technology
  • University of Chinese Academy of Sciences
  • Qingdao University of Science and Technology

Research output: Contribution to journalArticlepeer-review

265 Scopus citations

Abstract

Two-electron transfer chemistry based on earth-abundant Mg and S offers great possibilities of delivering higher energy density than current Li-ion technology. The development of non-nucleophilic electrolytes that reversibly and efficiently plate and strip Mg is believed to be a major obstacle to the implementation of this divalent battery technology. In this study, we present a new type of organic magnesium borate-based electrolyte that primarily comprises tetrakis(hexafluoroisopropyl)borate anions [B(HFP)4]- and solvated cations [Mg4Cl6(DME)6]2+, which was synthesized via a facile in situ reaction of tris(hexafluoroisopropyl)borate [B(HFP)3], MgCl2 and Mg powder in 1,2-dimethoxyethane (DME). Rigorous analyses including NMR, mass spectroscopy and single-crystal XRD were conducted to identify the equilibrium species in the abovementioned solution. The as-prepared Mg-ion electrolyte exhibited unprecedented Mg plating/stripping performance, such as high anodic stability up to 3.3 V (vs. Mg/Mg2+), high ionic conductivity of 5.58 mS cm-1, a low overpotential of 0.11 V for plating processes and Coulombic efficiencies greater than 98%. By virtue of the non-nucleophilic nature of this electrolyte, a fully reversible Mg/S battery was constructed that displayed an extremely low overpotential of 0.3 V and a high discharge capacity of up to 1247 mA h g-1 and yielded a specific energy of approximately 1200 W h kg-1 (10 times higher that of the Chevrel benchmark) based on the weight of active sulfur. More significantly, commonly used sulfur-carbon nanotube (S-CNTs) cathodes with S contents of 80 wt% and S loadings of 1.5 mg cm-2 were demonstrated to withstand more than 100 cycles without obvious capacity decay and to enable fast conversion processes, which achieved a charging current rate of up to 500 mA g-1. Our findings convincingly validate the pivotal role of the newly designed non-nucleophilic Mg-ion electrolyte for practical Mg/S battery chemistry.

Original languageEnglish
Pages (from-to)2616-2625
Number of pages10
JournalEnergy and Environmental Science
Volume10
Issue number12
DOIs
StatePublished - Dec 2017
Externally publishedYes

Bibliographical note

Publisher Copyright:
© The Royal Society of Chemistry.

Funding

This work was financially supported by the National Natural Science Foundation for Distinguished Young Scholars of China (Grant No. 51625204) and the Youth Innovation Promotion Association of CAS (2016193). The authors gratefully acknowledge Mr Zai-yong Zhang (Pharmaceutical Analytical & Solid-State Chemistry Research Center, Shanghai Institute of Materia Medica, Chinese Academy of Sciences, Shanghai 201203, China) and Dr Bingbing Chen (Qingdao Institute of Bioenergy and Bioprocess Technology, Chinese Academy of Sciences, Qingdao 266101, China) for their analysis of the crystal structures.

FundersFunder number
National Natural Science Foundation of China51625204
Youth Innovation Promotion Association of the Chinese Academy of Sciences2016193

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 7 - Affordable and Clean Energy
      SDG 7 Affordable and Clean Energy

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