4.8 Article

Improving high-capacity Li1.2Ni0.15Mn0.55Co0.1O2-based lithium-ion cells by modifiying the positive electrode with alumina

期刊

JOURNAL OF POWER SOURCES
卷 233, 期 -, 页码 346-357

出版社

ELSEVIER
DOI: 10.1016/j.jpowsour.2013.01.082

关键词

Lithium-ion; Atomic layer deposition; Al2O3; Coating; Secondary ion mass spectrometry; Layered oxide

资金

  1. U.S. Department of Energy's Vehicle Technologies Program [DE-AC02-06CH11357]
  2. DOE Vehicle Technologies Program (VTP) within the core funding of the Applied Battery Research (ABR) for Transportation Program
  3. U. S. Department of Energy, Office of Science, Office of Basic Energy Sciences [DE-AC02-06CH11357]

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Practical high-capacity Li-ion cells containing Li1.2Ni0.15Mn0.55Co0.1O2-based positive and graphite-based negative electrodes show substantial capacity loss and impedance rise when repeatedly cycled to, or held for extended periods, at voltages exceeding 4.5 V. Their performance can be effectively improved by modifying the positive electrode. The positive composite electrodes are modified here in two different ways: by (i) alumina coatings of up to similar to 4 nm applied via atomic layer deposition (ALD), and (ii) addition of nanoscale alumina powder. Thicknesses of the ALD coatings are estimated via X-ray photoelectron spectroscopy (XPS). Electrochemical cycling reveals that capacity retention is better, and impedance rise is smaller for cells containing ALD-coated electrodes. Cells with alumina-powder modified electrodes show also improved capacity retention, but without improvements in impedance. Improved capacity retention is primarily due to reduced Li trapping on the negative electrode. Lower impedance growth, in ALD modified cells, is attributed to improved electro-mechanical integrity and altered surface films inside the positive electrode. The alumina coating inhibits, but does not prevent, transition metal dissolution. The coating also reduces electrolyte oxidation. Significant accumulation of Al on the negative electrode indicates electrochemical crosstalk between the electrodes and chemical instability of the ALD coatings during extended cycling. (C) 2013 Elsevier B.V. All rights reserved.

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