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ELECTRODEPOSITED Ni-Fe-C CATHODES FOR HYDROGEN EVOLUTION

机译:电沉积Ni-Fe-C阴极的氢逸出

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Tailoring of active nickel alloy cathodes for hydrogen evolution in a hot concentrated hydroxide solution was attempted by electrodeposition. Electrodeposited iron is naturally more active for hydrogen evolution than nickel, but Ni-Fe alloys show further high activity for hydrogen evolution, although the rate-determining step being assumed as proton discharge is not changed. The carbon addition to iron or nickel remarkably enhances the activity for hydrogen evolution and changes the mechanism of hydrogen evolution. Ternary Ni-Fe-C alloys show the highest activity for hydrogen evolution, and the Tafel slope of hydrogen evolution is about 30 mV/decade, suggesting the rate-determining step of desorption of adsorbed hydrogen by recombination. XPS analysis reveals that the charge transfer occurs from nickel to iron in alloys and the carbon addition particularly enhances the charge transfer. Accelerated proton discharge due to enhanced charge transfer from nickel to iron is responsible for the high activity of the Ni-Fe-C alloys for hydrogen evolution.
机译:试图通过电沉积对活性镍合金阴极进行定制,以使其在热的浓氢氧化物溶液中析出氢。电沉积的铁自然比镍具有更强的氢析出活性,但是镍铁合金显示出更高的氢析出活性,尽管假设质子放电的速率确定步骤不变。向铁或镍中添加碳可显着提高氢释放的活性并改变氢释放的机理。三元Ni-Fe-C合金具有最高的析氢活性,析氢的Tafel斜率约为30 mV /十倍,表明通过重组解吸吸附氢的速率决定步骤。 XPS分析表明,合金中的电荷从镍发生转移到铁,碳的添加特别增强了电荷转移。由于镍到铁的电荷转移增强,质子放电加速,这是Ni-Fe-C合金产生氢的高活性的原因。

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