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Search: onr:"swepub:oai:research.chalmers.se:93948006-4e51-4329-9580-d58268e5091c" > The Influence of PM...

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The Influence of PMS-Additive on the Electrode/Electrolyte Interfaces in LiFePO4/Graphite Li-Ion Batteries

Ciosek Högström, Katarzyna (author)
Uppsala universitet,Strukturkemi
Malmgren, Sara, 1985- (author)
Uppsala universitet,Strukturkemi
Hahlin, Maria (author)
Uppsala universitet,Strukturkemi
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Rensmo, Håkan (author)
Uppsala universitet,Molekyl- och kondenserade materiens fysik
Thebault, Frederic, 1978 (author)
Chalmers tekniska högskola,Chalmers University of Technology,Chalmers university of technology,applied physics
Johansson, Patrik, 1969 (author)
Chalmers tekniska högskola,Chalmers University of Technology,Chalmers university of technology,applied physics
Edström, Kristina, 1958- (author)
Uppsala universitet,Strukturkemi
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 (creator_code:org_t)
2013-10-28
2013
English.
In: Journal of Physical Chemistry C. - : American Chemical Society (ACS). - 1932-7447 .- 1932-7455. ; 117:45, s. 23476-23486
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The influence of a film-forming additive, propargyl methanesulfonate (PMS), on electrochemical performance and electrode/electrolyte interface composition of LiFePO4/graphite Li-ion batteries has been studied. Combined use of in-house X-ray photoelectron spectroscopy (XPS) and soft and hard X-ray photoelectron spectroscopy (PES) enabled nondestructive depth profiling at four different probing depths in the 2-50 nm range. Cells cycled with PMS and LiPF6 in ethylene carbonate/diethyl carbonate (EC/DEC) were compared to a reference sample cycled without PMS. In the first cycle, PMS cells showed a higher irreversible capacity, which is explained by formation of a thicker solid electrolyte interphase (SEI). After three cycles, the SET thicknesses were determined to be 19 and 25 nm for the reference and PMS samples, respectively. After the initial cycling, irreversible losses shown by the PMS cells were lower than those of the reference cell. This could be attributed to a different SET composition and lower differences in the amount of lithium between lithiated and delithiated electrodes for the PMS sample. It was suggested that PMS forms a triple-bonded radical on reduction, which further reacts with the electrolyte. The PMS additive was shown to influence the chemical composition at the positive electrode/electrolyte interface. Thicker interface layers with higher C-O and smaller LiF contributions were formed on LiFePO4 cycled with PMS.

Subject headings

TEKNIK OCH TEKNOLOGIER  -- Materialteknik (hsv//swe)
ENGINEERING AND TECHNOLOGY  -- Materials Engineering (hsv//eng)
NATURVETENSKAP  -- Kemi -- Materialkemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Materials Chemistry (hsv//eng)

Keyword

functional electrolytes
ray photoelectron-spectroscopy
graphite-electrodes
sei
electrochemical-behavior
ethylene carbonate
surface-chemistry
lithium
mechanisms
thermal-stability

Publication and Content Type

art (subject category)
ref (subject category)

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