scispace - formally typeset
U

Udo Heider

Researcher at Merck & Co.

Publications -  38
Citations -  3452

Udo Heider is an academic researcher from Merck & Co.. The author has contributed to research in topics: Cyclic voltammetry & Lithium. The author has an hindex of 14, co-authored 38 publications receiving 3270 citations. Previous affiliations of Udo Heider include Merck KGaA & Bar-Ilan University.

Papers
More filters
Journal ArticleDOI

On the use of vinylene carbonate (VC) as an additive to electrolyte solutions for Li-ion batteries

TL;DR: In this article, the authors used a 1:1 mixture of ethylene and dimethyl carbonates (EC-DMC) for Li-ion batteries and found that VC is a reactive additive that reacts on both the anode and the cathode surfaces.
Journal ArticleDOI

Common Electroanalytical Behavior of Li Intercalation Processes into Graphite and Transition Metal Oxides

TL;DR: In this paper, the electroanalytical behavior of graphite,,, and spinel electrodes was compared using slow scan rate cyclic voltammetry (SSCV), potentiostatic intermittent titration (PITT), and electrochemical impedance spectroscopy.
Journal ArticleDOI

Solid‐State Electrochemical Kinetics of Li‐Ion Intercalation into Li1 − x CoO2: Simultaneous Application of Electroanalytical Techniques SSCV, PITT, and EIS

TL;DR: In this paper, the electroanalytical behavior of thin electrodes is elucidated by the simultaneous application of three electro analytical techniques: slow scan-rate cyclic voltammetry (SSCV), potentiostatic intermittent titration technique, and electrochemical impedance spectroscopy.
Journal ArticleDOI

The Study of Surface Phenomena Related to Electrochemical Lithium Intercalation into Li x MO y Host Materials (M = Ni, Mn)

TL;DR: In this article, a comparative study of LiNiO(sub 2) and LiMn{sub 2}O{sub 4} electrodes in three salt solutions was performed.
Journal ArticleDOI

On electrochemical impedance measurements of LixCo0.2Ni0.8O2 and LixNiO2 intercalation electrodes

TL;DR: In this paper, Li ion migration through a surface layer covering the active mass particles and interfacial charge transfer was attributed to Li ion charge transfer, and the absolute values of the double-layer capacity (several mF per 1 cm 2 of visible surface area) can be rationalized in terms of the porous structure of the composite electrodes.