Abstract

Any new oxygen reduction catalysts for practical low-temperature fuel cell applications must compete with the commercial platinum catalysts on efficiency and cost. Mesoporous nitrogen-doped carbon (N:C) has emerged as a leading alternative, mostly due to its high surface area, and the promise for low-cost production. While the best mesoporous N:C catalysts in the literature can operate on par with commercial platinum/carbon composites,1 their synthesis is complex and difficult – increasing their cost and rendering them impractical. We present a particularly simple synthesis of N-doped carbon, starting from magnesium salts of nitrogen-containing ligands. Pyrolysis of the salts proceeds by the little-researched mechanism of self-templating – formation of similarly sized MgO nanoparticle cores, which are then washed out with dilute acid, leaving behind a narrow pore size distribution. These carbons have high surface areas (>1400 m2/gr), nitrogen doping levels topping what is required for catalysis (>4%), and most interestingly, a very narrow pore size distribution (ranging from 10 to 20 nm for different carbons). Tested in alkaline ORR catalysis, these carbons compete successfully with commercial platinum-based electrodes, so they are efficient, cheap, and simple to prepare. (1) W. Wei, H. Liang, K. Parvez, X. Zhuang, X. Feng, K. Müllen, Angew. Chem. 2014, 126, 1596.

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