The exploration of earth-abundant and high-efficiency electrocatalysts for the oxygen evolution reaction (OER) is of great significant for sustainable energy conversion and storage applications. Although spinel-type binary transition metal oxides (ABO, A, B = metal) represent a class of promising candidates for water oxidation catalysis, their intrinsically inferior electrical conductivity exert remarkably negative impacts on their electrochemical performances. Herein, we demonstrates a feasible electrospinning approach to concurrently synthesize CoFeO nanoparticles homogeneously embedded in 1D N-doped carbon nanofibers (denoted as CoFeO@N-CNFs). By integrating the catalytically active CoFeO nanoparticles with the N-doped carbon nanofibers, the as-synthesized CoFeO@N-CNF nanohybrid manifests superior OER performance with a low overpotential, a large current density, a small Tafel slope, and long-term durability in alkaline solution, outperforming the single component counterparts (pure CoFeO and N-doped carbon nanofibers) and the commercial RuO catalyst. Impressively, the overpotential of CoFeO@N-CNFs at the current density of 30.0 mA cm negatively shifts 186 mV as compared with the commercial RuO catalyst and the current density of the CoFeO@N-CNFs at 1.8 V is almost 3.4 times of that on RuO benchmark. The present work would open a new avenue for the exploration of cost-effective and efficient OER electrocatalysts to substitute noble metals for various renewable energy conversion/storage applications.
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5700636 | PMC |
http://dx.doi.org/10.1002/advs.201700226 | DOI Listing |
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