4.8 Article

NiO/ZnO heterojunction nanorod catalyst for high-efficiency electrochemical conversion of methane

Journal

APPLIED CATALYSIS B-ENVIRONMENTAL
Volume 323, Issue -, Pages -

Publisher

ELSEVIER
DOI: 10.1016/j.apcatb.2022.122129

Keywords

Electrocatalyst; Methane conversion; Heterojunction catalyst; Core; shell nanorod

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Electrochemical conversion shows potential for selective partial oxidation of methane. We propose a NiO/ZnO shell/core nanorod catalyst to enhance electrochemical conversion. The built-in potential at the NiO/ZnO interface and the 1D morphology of the nanorods facilitate fast charge transfer, thereby improving electrochemical methane conversion. By using a 600-nm long NiO/ZnO nanorod catalyst, a high ethanol production rate of 1084.2 mu mol/gNiO/hr with a selectivity of 81% was achieved. Mechanistic analyses with isotopic labeling reactions suggest ethanol production pathways involving the generation of active oxygen, methane activation, and coupling of deprotonated methanol and methane. Enhancement of methane solubility and in situ generation of CO32- from a CH4/CO2 mixture were also explored.
Electrochemical conversion is promising for selective partial oxidation of methane. We present a NiO/ZnO shell/ core nanorod catalyst used to enhance electrochemical conversion. The built-in potential at the NiO/ZnO interface and the 1D morphology of the nanorods allow for fast charge transfer, thereby enhancing electrochemical methane conversion. We achieved a high ethanol production rate of 1084.2 mu mol/gNiO/hr with a selectivity of 81 % for a 600-nm long NiO/ZnO nanorod catalyst. Mechanistic analyses with isotopic labeling reactions suggested ethanol production pathways involving generation of active oxygen by dissociative adsorption of the anionic CO32- oxidant, formation of methanol by methane activation, and coupling of deprotonated methanol and methane. Furthermore, we improved the ethanol yield by improving methane solubility in sulfolane cosolvent mixtures. We also demonstrated conversion with in situ generation of CO32- from a CH4/CO2 mixture.

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