Understanding the Self-Templating of Hierarchically Porous Carbon Electrocatalysts Using Group 2 Coordination Polymers

Abstract

Self-templating of hierarchical porosity in carbon materials can be realized by the pyrolysis of well-designed metal-organic precursors. While this strategy is elegant and scalable, detailed mechanistic understanding of the self-templating process is lacking. We now present a systematic investigation of the microstructural evolution in porous carbons, including hierarchically micro-/meso-/macroporous materials with variable mesopore size. We focus on a homologous series of well-defined metal-organic coordination polymers, combining the highly abundant Group 2 ions (Mg2+, Ca2+, Sr2+, Ba2+) with a common ligand. To understand the role of the metal ion in directing the morphology of the ultimate N-doped carbons, we performed a detailed investigation using electron microscopy (HRSEM, HRTEM, EDS), N2 porosimetry, XRD, XPS and Raman spectroscopy. The rich morphological variations in the carbons determine their activity as metal-free electrocatalysts towards the oxygen reduction reaction. In particular, the reaction selectivity (2e – vs. 4e – pathways) is directed by competition between kinetics and mass transfer, due to confinement in mesopores. Figure 1