Nickel–cadmium battery

The nickel-cadmium battery (Ni-Cd battery or NiCad battery) is a type of rechargeable battery using nickel oxide hydroxide and metallic cadmium as electrodes. The abbreviation Ni-Cd is derived from the chemical symbols of nickel (Ni) and cadmium (Cd): the abbreviation NiCad is a registered trademark of SAFT Corporation, although this brand name is commonly used to describe all Ni-Cd batteries. Wet-cell nickel-cadmium batteries were invented in 1899. A Ni-Cd battery has a terminal voltage during discharge of around 1.2 volts which decreases little until nearly the end of discharge. The maximum electromotive force offered by a Ni-Cd cell is 1.3 V. Ni-Cd batteries are made in a wide range of sizes and capacities, from portable sealed types interchangeable with carbon-zinc dry cells, to large ventilated cells used for standby power and motive power. Compared with other types of rechargeable cells they offer good cycle life and performance at low temperatures with a fair capacity bu

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Structural Reversibility and Nickel Particle stability in Lanthanum Iron Nickel Perovskite-Type Catalysts

Davide Ferri, Debora Foppiano, Andre Heel, Oliver Kröcher

Perovskite-type oxides have shown the ability to reversibly segregate precious metals from their structure. This reversible segregation behavior was explored for a commonly used catalyst metal, Ni, to prevent Ni sintering, which is observed on most catalyst support materials. Temperature-programmed reduction, X-ray diffraction, X-ray absorption spectroscopy, electron microscopy, and catalytic activity tests were used to follow the extent of reversible Ni segregation. LaFe1-xNixO3-delta (0

Wiley-V C H Verlag Gmbh2017

Impact of Anion Asymmetry on Local Structure and Supercooling Behavior of Water-in-Salt Electrolytes

Corsin Battaglia, David Reber

Salts with asymmetric (fluorosulfonyl)(trifluoromethanesulfonyl)imide (FTFSI) anions have recently been shown to suppress crystallization of water-in-salt electrolytes, enabling low-temperature operation of high-voltage aqueous rechargeable batteries. To clarify the underlying mechanism for the kinetic suppression of crystallization, we investigate the local solution structures and dynamic behaviors of water-in-salt electrolytes based on the asymmetric FTFSI anion and its symmetric anion analogues by Raman spectroscopy and molecular dynamics simulations. We find that monodentate coordination of FTFSI to cations leads to high rotational mobility of the uncoordinated SO2CF3 group. We conclude that the peculiar, coordination-dependent, local dynamics in the asymmetric FTFSI anion, manifested by enhanced intramolecular bond rotation, enables the strong supercooling behavior.

AMER CHEMICAL SOC2020

Increased nickel exsolution from LaFe0.8Ni0.2O3 perovskite-derived CO2 methanation catalysts through strontium doping

Davide Ferri

Perovskite-derived Ni catalysts offer the remarkable benefit of redox stability that allows their regeneration after deactivation through poisoning or Ni particle growth. Here, the catalytic activity of LaFe0.8Ni0.2O3 towards CO2 methanation was improved by increasing Ni reducibility and segregation to the perovskite surface through partial substitution of La by Sr (La1-xSrxFe0.8Ni0.2O3-delta, 0

ELSEVIER2020

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