M
M. Schmidt
Researcher at Merck KGaA
Publications - 31
Citations - 2941
M. Schmidt is an academic researcher from Merck KGaA. The author has contributed to research in topics: Electrolyte & Ethylene carbonate. The author has an hindex of 23, co-authored 26 publications receiving 2774 citations. Previous affiliations of M. Schmidt include University of Regensburg.
Papers
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Journal ArticleDOI
GroE facilitates refolding of citrate synthase by suppressing aggregation.
Johannes Buchner,M. Schmidt,Miriam Fuchs,Rainer Jaenicke,Rainer Rudolph,Franz X. Schmid,Thomas Kiefhaber +6 more
TL;DR: The molecular chaperone GroE facilitates correct protein folding in vivo and in vitro, and inhibits aggregation reactions that compete with correctprotein folding, as indicated by specific suppression of light scattering.
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On the capacity fading of LiCoO2 intercalation electrodes
TL;DR: In this paper, the electrochemical behavior and surface chemistry of LiCoO 2 intercalation cathodes as a function of cycling and storage at 25, 45, and 60°C was studied.
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On the application of ionic liquids for rechargeable Li batteries: High voltage systems
TL;DR: In this paper, the authors examined the possible use of the following ionic liquids all having the same anion, bis(trifluoromethylsulfonyl)imide (TFSI) and the following cations: 1hexyl-3-methyl imidazolium (HMITFSI), 1-(2-methoxyethyl)-3 -methyl iminidazolate (MEMITFSI).
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Symmetric complexes of GroE chaperonins as part of the functional cycle.
M. Schmidt,Kerstin Rutkat,Reinhard Rachel,Günter Pfeifer,Rainer Jaenicke,Paul V. Viitanen,George H. Lorimer,Johannes Buchner +7 more
TL;DR: The existence of symmetric chaperonin complexes is not predicted by current models of the functional cycle for GroE-mediated protein folding, but they are proposed to be functionally significant.
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Lithium fluoroalkylphosphates: a new class of conducting salts for electrolytes for high energy lithium-ion batteries
TL;DR: In this article, a new class of conducting salts for electrolytes for high energy lithium-ion batteries was introduced and the results of electrochemical studies of Li[(C2F5)3PF3] in organic carbonates in comparison to LiPF6 including electrochemical stability and charge-discharge efficiency were reported.