Nickel

About: Nickel is a research topic. Over the lifetime, 79308 publications have been published within this topic receiving 1210058 citations. The topic is also known as: Ni & element 28.

Nanoporous Nitrogen-Doped Graphene Oxide/Nickel Sulfide Composite Sheets Derived from a Metal-Organic Framework as an Efficient Electrocatalyst for Hydrogen and Oxygen Evolution

Abstract: Engineering of controlled hybrid nanocomposites creates one of the most exciting applications in the fields of energy materials and environmental science. The rational design and in situ synthesis of hierarchical porous nanocomposite sheets of nitrogen-doped graphene oxide (NGO) and nickel sulfide (Ni7S6) derived from a hybrid of a well-known nickel-based metal-organic framework (NiMOF-74) using thiourea as a sulfur source are reported here. The nanoporous NGO/MOF composite is prepared through a solvothermal process in which Ni(II) metal centers of the MOF structure are chelated with nitrogen and oxygen functional groups of NGO. NGO/Ni7S6 exhibits bifunctional activity, capable of catalyzing both the hydrogen evolution reaction (HER) and the oxygen evolution reaction (OER) with excellent stability in alkaline electrolytes, due to its high surface area, high pore volume, and tailored reaction interface enabling the availability of active nickel sites, mass transport, and gas release. Depending on the nitrogen doping level, the properties of graphene oxide can be tuned toward, e.g., enhanced stability of the composite compared to commonly used RuO2 under OER conditions. Hence, this work opens the door for the development of effective OER/HER electrocatalysts based on hierarchical porous graphene oxide composites with metal chalcogenides, which may replace expensive commercial catalysts such as RuO2 and IrO2.

Mesoporous nickel/nickel oxide-a nanoarchitectured electrode

Abstract: Metallic nickel was electrodeposited from aqueous nickel(II) acetate dissolved in the lyotropic liquid crystalline phases of Brij 56 and Brij 78 surfactant templates to form metal films with hexagonal arrays of nanometer-sized channels. The applicability of these materials as inexpensive, large area and low-resistance current collectors was demonstrated by cyclic voltammetry. The redox charge capacity of the surface oxide in aqueous KOH was enhanced by 2 orders of magnitude over that of a nontemplated sample with no detectable impedance of the reaction rate.

Bimetallic Au-Ni nanoparticles embedded in SiO2 nanospheres: synergetic catalysis in hydrolytic dehydrogenation of ammonia borane.

Abstract: Gold-nickel nanoparticles (NPs) of 3-4 nm diameter embedded in silica nanospheres of around 15 nm have been prepared by using [Au(en)(2)Cl(3)] and [Ni(NH(3))(6)Cl(2)] as precursors in a NP-5/cyclohexane reversed-micelle system, and by in situ reduction in an aqueous solution of NaBH(4)/NH(3)BH(3). Compared with monometallic Au@SiO(2) and Ni@SiO(2), the as-synthesized Au-Ni@SiO(2) catalyst shows higher catalytic activity and better durability in the hydrolysis of ammonia borane, generating a nearly stoichiometric amount of hydrogen. During the generation of H(2), the synergy effect between gold and nickel is apparent: The nickel species stabilizes the gold NPs and the existence of gold helps to improve the catalytic activity and durability of the nickel NPs.

The use of different metal catalysts for the simultaneous production of carbon nanotubes and hydrogen from pyrolysis of plastic feedstocks

Abstract: Nickel, iron, cobalt and copper catalysts were prepared by impregnation and used to produce carbon nanotubes and hydrogen gas from a LDPE feedstock. A two stage catalytic pyrolysis process was used to enable large yields of both products. Plastics samples were pyrolysed in nitrogen at 600 °C, before the evolved gases were passed to a second stage and allowed to deposit carbon onto the catalyst at a temperature of 800 °C. Carbon nanotubes were successfully generated on nickel, iron and cobalt but were barely observed on the copper catalyst. Iron and nickel catalysts gave the largest yield of both hydrogen and carbon nanotubes as a result of metal-support interactions which were neither too strong, like cobalts, nor too weak like copper. These metal support interactions proved a key factor in CNT production. A nickel catalyst with a weaker interaction was prepared using a lower calcination temperature. Yields of both carbon nanotubes and hydrogen gas were lower on the Ni-catalyst prepared at the lower calcination temperature, as a result of sintering of the nickel particles. In addition, the catalyst prepared at a lower calcination temperature produced metal particles which were too large for CNT growth, producing amorphous carbons which deactivate the catalyst instead. Overall the iron catalyst gave the largest yield of CNTs, which is attributed to both its good metal-support interactions and irons large carbon solubility.