Synthesis of MnS/MnO Decorated N, S‐Doped Carbon Derived from a Mn(II)‐Coordinated Polymer for the Catalytic Oxidation of H2O2 and Bisphenol A

A way to synthesize a Mn2+‐ coordinated polymer precursor ligated by sulfur atoms with acetate counter ions (Mn‐DTOGA) is proposed, which is achieved by an imine formation reaction between dithiooxamide and glutaraldehyde in the presence of manganese (II) acetate. MnS/MnO decorated N, S‐doped carbon nanoparticles (MnS/O‐SNC) are then prepared by calcination of the Mn ion‐coordinated polymer for the practical applications of catalytic reactions. The Mn‐DTOGA and MnS/O‐SNC structures prepared at different temperatures (700, 800, and 900 °C) are characterized using various physical and electrochemical and chemical analyses. The nanoparticles prepared at 900 °C reveal the best performance for the catalytic oxidation of Hydrogen peroxide (H2O2) and bisphenol A. The decomposition potentials of H2O2 (1.0 mm) and bisphenol A (100.0 µm) on the catalyst modified electrode are observed to be +0.40 and +0.15 V (versus Ag/AgCl), respectively. It is observed that the catalytic performances to the oxidation reactions are mainly related to MnO decorated outside the SNC particles compared to MnS formed inside the particles. The electrode reveals a wide dynamic range with the low detection limits for H2O2 (0.08 (±0.02) µm) and bisphenol A (0.17 (±0.04) µm). This study will provide essential clues for the future catalyst design. A new synthesis method of Mn ion coordinated polymer precursor (Mn‐DTOGA) by an imine formation reaction between dithiooxamide and glutaraldehyde is demonstrated. The MnO/MnS decorated S, N doped‐carbon nanoparticles (MnS/O‐SNC) as an oxidation catalyst is prepared by calcination of Mn‐DTOGA precursor. It will pave the way to find the optimal carbon complex architecture for specific catalytic processes.