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The results have shown that the ternary catalysts are highly active for electrocatalytic ORR.
In naphthalene hydrogenation, the separated Ni species are previously reduced to highly-dispersed metallic Ni nanoclusters with size below 1.6 nm, which are highly active for hydrogenation.
Polymerization results indicate that these catalyst systems are highly active for both the homopolymerization of norbornene and the copolymerization of ethylene with norbornene.
Our previous study showed that the VOx/Pt(1 1 1) surfaces are highly active for the complete oxidation of propane.
The results indicate that the H-GaMCM-48 catalysts are highly active for the chosen reaction, and show much higher substrate conversion than many other catalyst systems.
In this report, we investigated potential anode candidates that are highly active for oxygen evolution and structurally stable under near-neutral operation conditions for a typical CO2 electrolyzer.
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Complex 39 is highly active for ethylene polymerization at higher temperature (at 80 °C, the activity of this complex was 2760 kg PE mol cat −1 h−1), and narrow molecular weight distribution (2.0) indicates its single-site nature [26].
We have previously shown that an activated carbon-supported ruthenium catalyst promoted with ReOx (RuRe/AC) is highly active for the hydrodeoxygenation (HDO) of lignin-derived phenols (e.g., guaiacol).
They were also found to be highly active for ultra-deep desulfurization of gasoline and kerosene.
The surface film has a nominal NiS stoichiometry and is highly active for ORR catalysis.
TiO2 P25 (70%anatase/30%% rutile) was found to be highly active for herbicide decomposition.
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