摘要
Since the sluggish kinetics of the oxygen evolution process(OER)at the anode of water splitting remains to be a crucial bottleneckfor hydrogen production, it is imperative to develop low-cost OERelectrocatalysts with high efficiency. Here, (FeSe2 + CoSe2) nanoparticles loaded on nitrogen-doped three-dimensionalporous carbon nanosheets (referred to as (FeSe2 + CoSe2)/N-3DCN) were prepared by freeze-drying, heat treatment andselenization. The favorable affinity and large surface area of N-3DCNenabled the synthesis of the ultrafine (FeSe2 + CoSe2) nanoparticles with a diameter of 10 nm, which were highlydispersed on carbon nanosheets and provided a significant number ofactive sites. The density functional theory (DFT) calculation demonstratedthat the free energy of oxygen-containing intermediates during OERwas optimized by coupling FeSe2 with CoSe2.The overpotential of (FeSe2 + CoSe2)/N-3DCNis 312 mV at 10 mA cm(-2), which is superior to thoseof (FeSe2 + CoSe2) (390 mV), CoSe2/N-3DCN (377 mV), RuO2 (320 mV), and FeSe2/N-3DCN(479 mV). Additionally, after the 80 h stability test, the overpotentialof (FeSe2 + CoSe2)/N-3DCN can still be maintainedat 316 mV.
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单位天津大学