journal article·2023-11Open access

Mild Methane Electrochemical Oxidation Boosted via Plasma Pre‐Activation

Xiaogang Sun, Pengtang Wang, Kenneth Davey, Yao Zheng, Shi‐Zhang Qiao

Small· Volume 19· Issue 45

Abstract

Abstract Obtaining partial methane oxidation reaction (MOR) with various oxygenates via a mild electrochemical method is practically difficult because of activation of stable C─H bond and consequent reaction pathway regulation. Here, a real‐time tandem MOR with cascaded plasma and electrocatalysis to activate and convert the methane (CH4) synergistically is reported for the first time. Boosted CH4 conversion is demonstrated toward value‐added products including, alcohols, carboxylates, and ketone via use of commercial Pd‐based electrocatalysts. Compared with hash industrial processes, a mild condition, that is, anode potential < 1.0 V versus RHE (reversible hydrogen electrode) is used that mitigates overoxidation of oxygenates and obviates competing reaction(s). One evidence that Pd(II) sites and surface adsorbed hydroxyls are important in facilitating activated‐CH4 species conversion, and establish a reaction mechanism for conversion(s) that involves coupling reactions between adsorbed hydroxyls, carbon monoxide and C1/C2 alkyls. One conclude that pre‐activation is important in boosting electrochemical partial MOR under mild conditions and will be of benefit in the development of sustainable CH4 conversion technology.
Source: crossref · Quality: baseline

Research context

OpenAlex topics: CO2 Reduction Techniques and Catalysts · Catalytic Processes in Materials Science · Electrocatalysts for Energy Conversion

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

School of Chemical Engineering The University of Adelaide Adelaide SA 5005 Australia

Funding

Australian Research Council

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