Metal–organic frameworks (MOFs) are ideal precursors/ templates for porous carbons with homogeneous doping of active components for energy storage and conversion applications. Herein, metalloporphyrinic MOFs, PCN‐224‐FeCo, with adjustable molar ratio of Fe II /Co II alternatively residing inside the porphyrin center, were employed as precursors to afford FeCo‐N‐doped porous carbon (denoted as FeCo‐NPC) by pyrolysis. Thanks to the hollow porous structure, the synergetic effect between highly dispersed FeN x and CoN x active sites accompanied with a high degree of graphitization, the optimized FeCo 2 ‐NPC‐900 obtained by pyrolysis at 900 °C exhibits more positive half‐wave potential, higher diffusion‐limited current density, and better stability than the state‐of‐the‐art Pt/C, under both alkaline and acidic media. More importantly, the current synthetic approach based on MOFs offers a rational strategy to structure‐ and composition‐controlled porous carbons for efficient electrocatalysis.
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Fang et al. (2017) studied this question.
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