Frédéric Thébault
Chalmers University of Technology
8 Papers
112 Citations
Frédéric Thébault is an academic researcher from Chalmers University of Technology. The author has contributed to research in topics: Hydrogen bond & Electrolyte. The author has an hindex of 6, co-authored 8 publications. Previous affiliations of Frédéric Thébault include University of Nottingham.
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Papers
Control of copper(I) iodide architectures by ligand design: angular versus linear bridging ligands.
Frédéric Thébault,Sarah A. Barnett,Alexander J. Blake,Claire Wilson,Neil R. Champness,Martin Schröder +5 more
TL;DR: A family of coordination polymers formed by the reaction of copper(I) iodide with a range of angular bidentate or tridentate N-donor ligands is reported, which exhibits a highly unusual three-dimensional structure in which the pypm ligand bridges two-dimensional brick-wall (CuI)(infinity) sheets.
84
The influence of PMS-additive on the electrode/electrolyte interfaces in LiFePO4/graphite Li-ion batteries
Katarzyna Ciosek Högström,Sara Malmgren,Maria Hahlin,Håkan Rensmo,Frédéric Thébault,Patrik Johansson,Kristina Edström +6 more
TL;DR: In this paper, 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.
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Synthesis of pyridazinyl ligands for multimetallic complexes
TL;DR: A family of ligands based upon the linking of two or three bis-(2-pyridyl)pyridine (dppz) moieties via the 4 or 4,5 positions of the pyridazine rings has been synthesised using an inverse electron demand Diels-Alder pathway as discussed by the authors.
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2,3,6,7,10,11-Hexamethoxytriphenylene (HMTP): A new organic cathode material for lithium batteries
Jae-Kwang Kim,Frédéric Thébault,Min-Yeong Heo,Dul-Sun Kim,Örjan Hansson,Jou-Hyeon Ahn,Patrik Johansson,Lars Öhrström,Aleksandar Matic,Per Jacobsson +9 more
TL;DR: In this paper, the authors proposed a new organic cathode material for rechargeable lithium battery applications: 2,3,6,7,10,11-hexamethoxytriphenylene (HMTP), which is composed of six methoxy functional groups substituted onto a central triphenylene moiety.
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2,3,6,7,10,11-Hexahydroxytriphenylene tetrahydrate: a new form of an important starting material for supramolecular chemistry and covalent organic frameworks.
TL;DR: In the title compound, C(18)H(12)O(6)·4H(2)O, the 2,3,6,7,10,11-hexahydroxytriphenylene molecule is located on a twofold axis and two water molecules occupy general positions.
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