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Ulrich Von Sacken

Bio: Ulrich Von Sacken is an academic researcher. The author has contributed to research in topics: Lithium & Electrochemical cell. The author has an hindex of 4, co-authored 4 publications receiving 1314 citations.

Papers
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Journal ArticleDOI
TL;DR: In this paper, Li/graphite and Li/petroleum coke cells using a in a 50:50 mixture of propylene carbonate (PC) and ethylene carbonates (EC) electrolyte exhibit irreversible reactions only on the first discharge.
Abstract: Li/graphite and Li/petroleum coke cells using a in a 50:50 mixture of propylene carbonate (PC) and ethylene carbonate (EC) electrolyte exhibit irreversible reactions only on the first discharge. These irreversible reactions are associated with electrolyte decomposition and cause the formation of a passivating film or solid electrolyte interphase on the surface of the carbon. The amount of electrolyte decomposition is proportional to the specific surface area of the carbon electrode. When all the available surface area is coated with the film of decomposition products, further decomposition reactions stop. In subsequent cycles, these cells exhibit excellent reversibility and can be cycled without capacity loss.

1,245 citations

Patent
25 Mar 1991
TL;DR: In this article, Li x Ni 2-x-y M y O 2, with x being between about 0.8 and about 1.0, M being one or more transition metal selected from cobalt, iron, chromium, titanium, manganese and vanadium, and y being less than about 2.2, with the proviso that y is less than 0.5 for cobalt.
Abstract: Lithiated nickel dioxide cathode-active materials for electrochemical cellsaving the formula Li x Ni 2-x-y M y O 2 , with x being between about 0.8 and about 1.0, M being one or more metals selected from cobalt, iron, chromium, titanium, manganese and vanadium, and y being less than about 0.2, with the proviso that y is less than about 0.5 for cobalt, which material is substantially free of lithium hydroxide and lithium carbonate. The materials are prepared by providing a substantially homogeneous dry intermediate mixture of a starting material containing a nickel compound selected from nickel oxide, nickel hydroxide, and mixtures thereof, and optionally including one or more oxides or hydroxides of a transition metal selected from cobalt, iron, chromium, titanium, manganese and vanadium, together with between about a 10 and about a 25% stoichiometric excess of lithium hydroxide. The mixture is heat treated at a temperature above about 600° C. in an atmosphere substantially free of carbon dioxide and having a partial pressure ratio of oxygen to water vapor greater than about 15, after which any lithium hydroxide or lithium carbonate present in the mixture is removed. Thermally stable lithiated nickel dioxide having a BET surface area less than about 3.0 m 2 /g, and is also disclosed, as well as electrochemical cells prepared from the disclosed lithiated nickel dioxides.

144 citations

Patent
14 Dec 1995
TL;DR: Carbonaceous insertion compounds and methods for preparation are described in this article, wherein the compounds comprise a highly disordered, impurity free, hard pregraphitic carbonaceous host.
Abstract: Carbonaceous insertion compounds and methods for preparation are described wherein the compounds comprise a highly disordered, impurity free, hard pre-graphitic carbonaceous host. Carbonaceous insertion compounds can be prepared which have large reversible capacity for lithium yet low irreversible capacity and voltage hysteresis. Such insertion compounds can be prepared by simple pyrolysis of suitable epoxy, phenolic resin, or carbohydrate precursors at an appropriate temperature. These insertion compounds may be suitable for use as high capacity anodes in lithium ion batteries.

23 citations

Patent
06 Dec 1995
TL;DR: In this paper, a two-step heating method was used to prepare spinel insertion compounds Li1+x Mn2-x-y My O4 for use as a cathode in a lithium battery.
Abstract: Spinel insertion compounds Li1+x Mn2-x-y My O4 wherein M is a transition metal, 0

14 citations


Cited by
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Journal ArticleDOI
TL;DR: In this paper, the authors reviewed the challenges for further development of Li rechargeable batteries for electric vehicles and proposed a nonflammable electrolyte with either a larger window between its lowest unoccupied molecular orbital and highest occupied molecular orbital (HOMO) or a constituent that can develop rapidly a solid/ electrolyte-interface (SEI) layer to prevent plating of Li on a carbon anode during a fast charge of the battery.
Abstract: The challenges for further development of Li rechargeable batteries for electric vehicles are reviewed. Most important is safety, which requires development of a nonflammable electrolyte with either a larger window between its lowest unoccupied molecular orbital (LUMO) and highest occupied molecular orbital (HOMO) or a constituent (or additive) that can develop rapidly a solid/ electrolyte-interface (SEI) layer to prevent plating of Li on a carbon anode during a fast charge of the battery. A high Li-ion conductivity (σ Li > 10 ―4 S/cm) in the electrolyte and across the electrode/ electrolyte interface is needed for a power battery. Important also is an increase in the density of the stored energy, which is the product of the voltage and capacity of reversible Li insertion/extraction into/from the electrodes. It will be difficult to design a better anode than carbon, but carbon requires formation of an SEI layer, which involves an irreversible capacity loss. The design of a cathode composed of environmentally benign, low-cost materials that has its electrochemical potential μ C well-matched to the HOMO of the electrolyte and allows access to two Li atoms per transition-metal cation would increase the energy density, but it is a daunting challenge. Two redox couples can be accessed where the cation redox couples are "pinned" at the top of the O 2p bands, but to take advantage of this possibility, it must be realized in a framework structure that can accept more than one Li atom per transition-metal cation. Moreover, such a situation represents an intrinsic voltage limit of the cathode, and matching this limit to the HOMO of the electrolyte requires the ability to tune the intrinsic voltage limit. Finally, the chemical compatibility in the battery must allow a long service life.

8,535 citations

Journal ArticleDOI
TL;DR: New strategies are needed for batteries that go beyond powering hand-held devices, such as using electrode hosts with two-electron redox centers; replacing the cathode hosts by materials that undergo displacement reactions; and developing a Li(+) solid electrolyte separator membrane that allows an organic and aqueous liquid electrolyte on the anode and cathode sides, respectively.
Abstract: Each cell of a battery stores electrical energy as chemical energy in two electrodes, a reductant (anode) and an oxidant (cathode), separated by an electrolyte that transfers the ionic component of the chemical reaction inside the cell and forces the electronic component outside the battery. The output on discharge is an external electronic current I at a voltage V for a time Δt. The chemical reaction of a rechargeable battery must be reversible on the application of a charging I and V. Critical parameters of a rechargeable battery are safety, density of energy that can be stored at a specific power input and retrieved at a specific power output, cycle and shelf life, storage efficiency, and cost of fabrication. Conventional ambient-temperature rechargeable batteries have solid electrodes and a liquid electrolyte. The positive electrode (cathode) consists of a host framework into which the mobile (working) cation is inserted reversibly over a finite solid–solution range. The solid–solution range, which is...

6,950 citations

Journal ArticleDOI
TL;DR: The phytochemical properties of Lithium Hexafluoroarsenate and its Derivatives are as follows: 2.2.1.
Abstract: 2.1. Solvents 4307 2.1.1. Propylene Carbonate (PC) 4308 2.1.2. Ethers 4308 2.1.3. Ethylene Carbonate (EC) 4309 2.1.4. Linear Dialkyl Carbonates 4310 2.2. Lithium Salts 4310 2.2.1. Lithium Perchlorate (LiClO4) 4311 2.2.2. Lithium Hexafluoroarsenate (LiAsF6) 4312 2.2.3. Lithium Tetrafluoroborate (LiBF4) 4312 2.2.4. Lithium Trifluoromethanesulfonate (LiTf) 4312 2.2.5. Lithium Bis(trifluoromethanesulfonyl)imide (LiIm) and Its Derivatives 4313

5,710 citations

Journal ArticleDOI
TL;DR: Some of the recent scientific advances in nanomaterials, and especially in nanostructured materials, for rechargeable lithium-ion batteries are reviewed.
Abstract: Energy storage is more important today than at any time in human history. Future generations of rechargeable lithium batteries are required to power portable electronic devices (cellphones, laptop computers etc.), store electricity from renewable sources, and as a vital component in new hybrid electric vehicles. To achieve the increase in energy and power density essential to meet the future challenges of energy storage, new materials chemistry, and especially new nanomaterials chemistry, is essential. We must find ways of synthesizing new nanomaterials with new properties or combinations of properties, for use as electrodes and electrolytes in lithium batteries. Herein we review some of the recent scientific advances in nanomaterials, and especially in nanostructured materials, for rechargeable lithium-ion batteries.

5,441 citations