Abstract

Production of value-added chemicals from oriented methane conversion under mild conditions is of great significance for utilization of the energy resources, which, however, remains a great challenge due to its difficulty in the selective activation of C–H bond. Herein, we report a highly selective and efficient methane conversion to formic acid on atomically dispersed Fe sites confined in the nano-channels of ZSM-5. The turnover frequency for producing C1 liquid oxygenates reaches 84,200 h−1 with a high selectivity of 91% to formic acid at 80 °C, which outperforms all previously reported catalysts. Electron paramagnetic resonance analysis and density functional theory calculations demonstrate that the ZSM-5-confined Fe-O active centers can facilely dissociate the C–H bonds and catalyze successive oxidation of methane to formic acid via free radical mechanisms under mild conditions. This study opens a new path of engineering the microenvironment of confined Fe sites within nano-channels toward highly selective methane conversion with low energy input.

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