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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.


Papers
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Journal ArticleDOI
J. H. Sinfelt1, J.L. Carter1, D.J.C. Yates1
TL;DR: In this article, the effect of adding copper to nickel was investigated for the hydrogenolysis of ethane to methane and the dehydrogenation of cyclohexane to benzene over a series of copper-nickel alloys.

585 citations

Journal ArticleDOI
TL;DR: The bagasse fly ash, an industrial solid waste of sugar industry, was used for the removal of cadmium and nickel from wastewater and the adsorption data follow the Langmuir model better then the Freundlich model, indicating endothermic nature of the adsorbent process.

583 citations

Journal ArticleDOI
TL;DR: Density functional theory calculations indicate that the vanadium site of the iron/vanadium co-doped nickel (oxy)hydroxide gives near-optimal binding energies of oxygen evolution reaction intermediates and has lower overpotential compared with nickel and iron sites.
Abstract: It is of great importance to understand the origin of high oxygen-evolving activity of state-of-the-art multimetal oxides/(oxy)hydroxides at atomic level. Herein we report an evident improvement of oxygen evolution reaction activity via incorporating iron and vanadium into nickel hydroxide lattices. X-ray photoelectron/absorption spectroscopies reveal the synergistic interaction between iron/vanadium dopants and nickel in the host matrix, which subtly modulates local coordination environments and electronic structures of the iron/vanadium/nickel cations. Further, in-situ X-ray absorption spectroscopic analyses manifest contraction of metal-oxygen bond lengths in the activated catalyst, with a short vanadium-oxygen bond distance. Density functional theory calculations indicate that the vanadium site of the iron/vanadium co-doped nickel (oxy)hydroxide gives near-optimal binding energies of oxygen evolution reaction intermediates and has lower overpotential compared with nickel and iron sites. These findings suggest that the doped vanadium with distorted geometric and disturbed electronic structures makes crucial contribution to high activity of the trimetallic catalyst.

576 citations

Book
01 Jan 1991

573 citations

Journal ArticleDOI
TL;DR: In this article, an in situ Raman spectroscopic investigation has been carried out to identify the composition of the active phase present on the surface of nickel electrodes used for the electrochemical evolution of oxygen.
Abstract: An in situ Raman spectroscopic investigation has been carried out to identify the composition of the active phase present on the surface of nickel electrodes used for the electrochemical evolution of oxygen. The electrolyte in all cases was 0.1 M KOH. A freshly polished Ni electrode oxidized upon immersion in the electrolyte and at potentials approaching the evolution of oxygen developed a layer of γ-NiOOH. Electrochemical cycling of this film transformed it into β-NiOOH, which was observed to be three times more active than γ-NiOOH. The higher activity of β-NiOOH is attributed to an unidentified Ni oxide formed at a potential above 0.52 V (vs Hg/HgO reference). We have also observed that a submonolayer of Ni oxide deposited on Au exhibits a turnover frequency (TOF) for oxygen evolution that is an order of magnitude higher than that for a freshly prepared γ-NiOOH surface and more than 2-fold higher than that for a β-NiOOH surface. By contrast, a similar film deposited on Pd exhibits a TOF that is similar ...

563 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
20233,184
20226,229
20211,949
20202,693
20193,234
20183,107