SwePub
Sök i LIBRIS databas

  Utökad sökning

(id:"swepub:oai:DiVA.org:uu-219336")
 

Sökning: (id:"swepub:oai:DiVA.org:uu-219336") > The Complex Nature ...

The Complex Nature of the Electrode/Electrolyte Interfaces in Li-ion Batteries : Towards Understanding the Role of Electrolytes and Additives Using Photoelectron Spectroscopy

Ciosek Högström, Katarzyna (författare)
Uppsala universitet,Strukturkemi
Edström, Kristina, Professor (preses)
Uppsala universitet,Strukturkemi
Rensmo, Håkan, Professor (preses)
Uppsala universitet,Molekyl- och kondenserade materiens fysik
visa fler...
Nyholm, Leif, Professor (preses)
Uppsala universitet,Oorganisk kemi
Owen, John, Professor (opponent)
University of Southampton
visa färre...
 (creator_code:org_t)
ISBN 9789155488901
Uppsala : Acta Universitatis Upsaliensis, 2014
Engelska 74 s.
Serie: Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Science and Technology, 1651-6214 ; 1129
  • Doktorsavhandling (övrigt vetenskapligt/konstnärligt)
Abstract Ämnesord
Stäng  
  • The stability of electrode/electrolyte interfaces in Li-ion batteries is crucial to the performance, lifetime and safety of the entire battery system. In this work, interface processes have been studied in LiFePO4/graphite Li-ion battery cells. The first part has focused on improving photoelectron spectroscopy (PES) methodology for making post-mortem battery analyses. Exposure of cycled electrodes to air was shown to influence the surface chemistry of the graphite. A combination of synchrotron and in-house PES has facilitated non-destructive interface depth profiling from the outermost surfaces into the electrode bulk. A better understanding of the chemistry taking place at the anode and cathode interfaces has been achieved. The solid electrolyte interphase (SEI) on a graphite anode was found to be thicker and more inhomogeneous than films formed on cathodes. Dynamic changes in the SEI on cycling and accumulation of lithium close to the carbon surface have been observed.   Two electrolyte additives have also been studied: a film-forming additive propargyl methanesulfonate (PMS) and a flame retardant triphenyl phosphate (TPP). A detailed study was made at ambient and elevated temperature (21 and 60 °C) of interface aging for anodes and cathodes cycled with and without the PMS additive. PMS improved cell capacity retention at both temperatures. Higher SEI stability, relatively constant thickness and lower loss of cyclable lithium are suggested as the main reasons for better cell performance. PMS was also shown to influence the chemical composition on the cathode surface.The TPP flame retardant was shown to be unsuitable for high power applications. Low TPP concentrations had only a minor impact on electrolyte flammability, while larger amounts led to a significant increase in cell polarization. TPP was also shown to influence the interface chemistry at both electrodes.Although the additives studied here may not be the final solution for improved lifetime and safety of commercial batteries, increased understanding has been achieved of the degradation mechanisms in Li-ion cells. A better understanding of interface processes is of vital importance for the future development of safer and more reliable Li-ion batteries.

Ämnesord

NATURVETENSKAP  -- Kemi -- Oorganisk kemi (hsv//swe)
NATURAL SCIENCES  -- Chemical Sciences -- Inorganic Chemistry (hsv//eng)

Nyckelord

Li-ion battery
LiFePO4/graphite cell
interface
electrolyte additives
solid electrolyte interphase (SEI)
photoelectron spectroscopy (PES)
synchrotron
Chemistry with specialization in Inorganic Chemistry
Kemi med inriktning mot oorganisk kemi

Publikations- och innehållstyp

vet (ämneskategori)
dok (ämneskategori)

Hitta via bibliotek

Till lärosätets databas

Sök utanför SwePub

Kungliga biblioteket hanterar dina personuppgifter i enlighet med EU:s dataskyddsförordning (2018), GDPR. Läs mer om hur det funkar här.
Så här hanterar KB dina uppgifter vid användning av denna tjänst.

 
pil uppåt Stäng

Kopiera och spara länken för att återkomma till aktuell vy