JOURNAL ARTICLE

Layered Transition Metal Oxynitride Co<sub>3</sub>Mo<sub>2</sub>O<sub><i>x</i></sub>N<sub>6–<i>x</i></sub>/C Catalyst for Oxygen Reduction Reaction

Li An (399351)Zhonghong Xia (2832425)Peikai Chen (402161)Dingguo Xia (1594594)

Year: 2016 Journal:   OPAL (Open@LaTrobe) (La Trobe University)   Publisher: La Trobe University

Abstract

Transition metal\noxynitrides have now garnered growing interest\nin our quest for highly efficient alternatives to Pt in direct methanol\nalkaline fuel cells. Herein, carbon supported Co<sub>3</sub>Mo<sub>2</sub>O<sub><i>x</i></sub>N<sub>6–<i>x</i></sub> was synthesized via a simple two-step approach wherein the\nreactants undergo refluxing and heat treatment in NH<sub>3</sub>.\nFor the as-prepared Co<sub>3</sub>Mo<sub>2</sub>O<sub><i>x</i></sub>N<sub>6–<i>x</i></sub> catalyst, uniformly\ndispersed on XC-72, with the particle size averaged at 5 nm, the catalytic\nactivities toward oxygen reduction reaction in alkaline media are\nrelated to the commercial Pt/C, such as the comparable onset potential\n(0.9 V vs RHE), half-wave potential (0.8 V vs RHE), and even higher\nspecific activity (82.7 mA cm<sup>–2</sup> at 0.7 V). Significantly,\nthe Co<sub>3</sub>Mo<sub>2</sub>O<sub><i>x</i></sub>N<sub>6–<i>x</i></sub> catalyst was highly stable in terms\nof 95% current retention after 12 h chronoamperometry measurement,\nindicative of favorable prospect for the non-noble cathodic catalyst\nin alkaline fuel cell.

Keywords:
Catalysis Chronoamperometry Transition metal Oxygen reduction reaction Cathodic protection Particle size Carbon fibers Fuel cells Oxygen Oxide

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