4.8 Article

High performance red phosphorus electrode in ionic liquid-based electrolyte for Na-ion batteries

期刊

JOURNAL OF POWER SOURCES
卷 363, 期 -, 页码 404-412

出版社

ELSEVIER SCIENCE BV
DOI: 10.1016/j.jpowsour.2017.07.089

关键词

Sodium-ion batteries; Phosphorus; Ionic liquid electrolyte; Solid electrolyte interphase

资金

  1. Ministry of Education, Culture, Sports, Science, and Technology (MEXT) under the Elements Strategy Initiative for Catalysis and Batteries (ESICB), JSPS KAKENHI Grant [JP16K14103, JP16H04225]
  2. Grants-in-Aid for Scientific Research [16H04225] Funding Source: KAKEN

向作者/读者索取更多资源

Electrochemical performance of the red phosphorus electrode was examined in ionic-liquid electrolyte, 0.25 mol dm(-3) sodium bisfluorosulfonylamide (NaFSA) dissolved N-methyl-N-propylpyridinium-bis-fluorosulfonylamide (MPPFSA), at room temperature. We compared its electrochemical performance to conventional EC/PC/DEC, EC/DEC, and PC solutions containing 1 mol dm(-3) NaPF6. The electrode in NaFSA/MPPFSA demonstrated a reversible capacity of 1480 mAh g(-1) and excellent capacity retention of 93% over 80 cycles, which is much better than those in the conventional electrolytes. The difference in capacity retention for the electrolytes correlates to the different solid electrolyte interphase (SEI) layer formed on the phosphorus electrode. To understand the SEI formation in NaFSA/MPPFSA and its evolution during cycling, we investigate the surface layer of the red phosphorus electrodes with hard X-ray photoelectron spectroscopy (HAXPES) and time-of-flight secondary ion mass spectrometry (TOF-SIMS). A detailed analysis of HAXPES spectra demonstrates that SEI layer consists of major inorganic and minor organic species, originating from decomposition of MPP+ and FSA(-). Homogenous surface layer is formed during the first cycle in NaFSA/MPPFSA while in alkyl carbonate ester electrolytes, continuous growth of surface film up to the 20th cycle is observed. Possibility of red phosphorous electrode for battery applications with pure ionic liquid is discussed. (C) 2017 Elsevier B.V. All rights reserved.

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