Magnetically tunable selectivity in methane oxidation enabled by Fe-embedded liquid metal catalysts

利用铁嵌入液态金属催化剂实现甲烷氧化反应的磁性可调选择性

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Abstract

As they are liquids at room temperature, gallium-based metal substrates allow catalytic metal atoms to move freely without lattice constraints, thereby facilitating the development of catalysts with reconfigurable structures. Here we design an iron-embedded liquid metal catalyst that enables reversible switching of the aggregation and electron spin of iron atoms by controlling an external magnetic field. This facilitates a reversible conversion of the primary liquid products, methyl hydroperoxide (CH(3)OOH) and acetic acid (CH(3)COOH), under ambient conditions. The catalyst achieves promising production rates (CH(3)OOH, 1,679.6  mmol gFe-1 h-1 ; CH(3)COOH, 790.5  mmol gFe-1 h-1 ) and high selectivities (CH(3)OOH, 99.9%; CH(3)COOH, 91.7%). In the absence of the magnetic field, iron atoms are atomically dispersed, leading to the C1 pathway without C-C bond coupling. When a magnetic field is applied, iron atoms cluster, favouring CH(3)COOH production in the C2 pathway. The product distribution can be finely and reversibly tuned with magnetic field intensity adjustments ranging from 0 to 500 G. Our findings highlight the potential for using an external magnetic field to precisely control catalytic pathways.

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