Ultrathin 1T-MoS Nanoplates Induced by Quaternary Ammonium-Type Ionic Liquids on Polypyrrole/Graphene Oxide Nanosheets and Its Irreversible Crystal Phase Transition During Electrocatalytic Nitrogen Reduction.

Ultrathin nanoplates of metastable 1T-MoS have been successfully stabilized and uniformly distributed on the surface of -butyl triethyl ammonium bromide functionalized polypyrrole/graphene oxide (BTAB/PPy/GO) by a very simple hydrothermal method. BTAB as a typical kind of quaternary ammonium-type ionic liquids (ILs) played a crucial role in the formation of the obtained 1T-MoS/BTAB/PPy/GO. It was covalently linked with PPy/GO and arranged in a highly ordered order at the solid-liquid interface of PPy/GO and HO due to Coulombic interactions and other intermolecular interactions, which would induce and stabilize ultrathin 1T-MoS nanoplates by morphosynthesis. The good electrocatalytic activity toward nitrogen reduction reaction (NRR) with strong durability and good stability can be achieved by 1T-MoS/BTAB/PPy/GO due to their excellent inorganic/organic hierarchical lamellar micro-/nanostructures. Especially, after the long-term electrocatalysis for NRR at a negative potential, metastable 1T-MoS as the catalytic center undergoes two types of irreversible crystal phase transition, which was converted to 1T'-MoS and MoN, caused by the competitive hydrogen evolution reaction (HER) process and the electrochemical reaction between the electroactive 1T-MoS and N, respectively. The new N-Mo bonding prevents Mo atoms from binding to other N atoms in N, resulting in the deactivation of the electrocatalysts to NRR after being used for 18 h. Even so, quaternary ammonium-type ILs would induce the crystal structures of transition-metal dichalcogenides (TMDCs), which might provide a new thought for the reasonable design of electrocatalysts based on TMDCs for electrocatalysis.