An excellent electrocatalyst for oxygen reduction in zinc–air batteries: N-, P- and Fe-tridoped nanoporous carbon catalyst, derived from highly available and recyclable corn silk, was prepared. The catalyst exhibited superior electrochemical activity to state-of-the-art 20% Pt/C catalyst for the zinc–air battery application.
Methane dehydroaromatization (MDA) on Mo/ZSM‐5 zeolite catalyst is promising for direct transformation of natural gas. Understanding the nature of active sites on Mo/ZSM‐5 is a challenge for applications. Herein, using 1H{95Mo} double‐resonance solid‐state NMR spectroscopy, we identify proximate dual active sites on Mo/ZSM‐5 catalyst by direct observation of internuclear spatial interaction between Brønsted acid site and Mo species in zeolite channels. The acidic proton–Mo spatial interaction is correlated with methane conversion and aromatics formation in the MDA process, an important factor in determining the catalyst activity and lifetime. The evolution of olefins and aromatics in Mo/ZSM‐5 channels is monitored by detecting their host–guest interactions with both active Mo sites and Brønsted acid sites via 1H{95Mo} double‐resonance and two‐dimensional 1H–1H correlation NMR spectroscopy, revealing the intermediate role of olefins in hydrocarbon pool process during the MDA reaction.
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