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Cobalt

About: Cobalt is a research topic. Over the lifetime, 69899 publications have been published within this topic receiving 1242058 citations. The topic is also known as: Co & Element 27.


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Journal ArticleDOI
TL;DR: In this paper, a high-sensitivity cobalt speciation method was developed and applied to a profile in the North Atlantic, which included examining the redox chemistry of the analytical system and calibrating the electroactive cobalt ligand dimethylglyoxime (DMG) using EDTA as a model ligand.

191 citations

Journal ArticleDOI
TL;DR: This work uncovered the influence of oxygen anion charge distribution on the electronic structure of the redox-active building block Co-O, and found that the OER activity can be promoted by pushing more Co into the octahedral site or shifting the oxygen charge towards the redbox-active metal center in CoO6 octahedra.
Abstract: Cobalt spinel oxides are a class of promising transition metal (TM) oxides for catalyzing oxygen evolution reaction (OER). Their catalytic activity depends on the electronic structure. In a spinel oxide lattice, each oxygen anion is shared amongst its four nearest transition metal cations, of which one is located within the tetrahedral interstices and the remaining three cations are in the octahedral interstices. This work uncovered the influence of oxygen anion charge distribution on the electronic structure of the redox-active building block Co-O. The charge of oxygen anion tends to shift toward the octahedral-occupied Co instead of tetrahedral-occupied Co, which hence produces strong orbital interaction between octahedral Co and O. Thus, the OER activity can be promoted by pushing more Co into the octahedral site or shifting the oxygen charge towards the redox-active metal center in CoO6 octahedra.

191 citations

Journal ArticleDOI
Xiaobo Peng1, Kang Cheng1, Jincan Kang1, Bang Gu1, Yu Xiang1, Qinghong Zhang1, Ye Wang1 
TL;DR: It is demonstrated that effective control of hydrogenolysis by using mesoporous zeolite Y-supported cobalt nanoparticles can enhance the diesel fuel selectivity while keeping methane selectivity low.
Abstract: Selectivity control is a challenging goal in Fischer–Tropsch (FT) synthesis. Hydrogenolysis is known to occur during FT synthesis, but its impact on product selectivity has been overlooked. Demonstrated herein is that effective control of hydrogenolysis by using mesoporous zeolite Y-supported cobalt nanoparticles can enhance the diesel fuel selectivity while keeping methane selectivity low. The sizes of the cobalt particles and mesopores are key factors which determine the selectivity both in FT synthesis and in hydrogenolysis of n-hexadecane, a model compound of heavier hydrocarbons. The diesel fuel selectivity in FT synthesis can reach 60 % with a CH4 selectivity of 5 % over a Na-type mesoporous Y-supported cobalt catalyst with medium mean sizes of 8.4 nm (Co particles) and 15 nm (mesopores). These findings offer a new strategy to tune the product selectivity and possible interpretations of the effect of cobalt particle size and the effect of support pore size in FT synthesis.

191 citations

Journal ArticleDOI
TL;DR: In this article, cloud point extraction has been used for the preconcentration of cobalt and nickel, after the formation of a complex with 1-(2-thiazolylazo)-2-naphthol (TAN), and later analysis by flame atomic absorption spectrometry using octylphenoxypolyethoxyethanol (Triton X-114) as surfactant.

191 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
20232,622
20225,202
20212,220
20202,950
20193,215
20183,007