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Synthesis of a MoS x –O–PtO x Electrocatalyst with High Hydrogen Evolution Activity Using a Sacrificial Counter‐Electrode

机译:牺牲对电极合成具有高氢释放活性的MoS x –O–PtO x电催化剂

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Water splitting is considered to be a very promising alternative to greenly produce hydrogen, and the key to optimizing this process is the development of suitable electrocatalysts. Here, a sacrificial‐counter‐electrode method to synthesize a MoS x /carbon nanotubes/Pt catalyst (0.55 wt% Pt loading) is developed, which exhibits a low overpotential of 25 mV at a current density of 10 mA cm ?2 , a low Tafel slope of 27 mV dec ?1 , and excellent stability under acidic conditions. The theory calculations and experimental results confirm the high hydrogen evolution activity that is likely due to the fact that the S atoms in MoS x can be substituted with O atoms during a potential cycling process when using Pt as a counter‐electrode, where the O atoms act as bridges between the catalytic PtO x particles and the MoS x support to generate a MoS x –O–PtO x structure, allowing the Pt atoms to donate more electrons thus facilitating the hydrogen evolution reaction process.
机译:水分解被认为是绿色生产氢的非常有前途的替代方法,而优化此过程的关键是开发合适的电催化剂。在这里,开发了一种牺牲对电极方法来合成MoS x /碳纳米管/ Pt催化剂(Pt负载为0.55 wt%),该方法在电流密度为10 mA cm?2时显示出25 mV的低过电势, Tafel斜率低,为27 mV dec?1,在酸性条件下具有出色的稳定性。理论计算和实验结果证实了较高的氢释放活性,这很可能是由于MoS x中的S原子在使用Pt作为反电极的潜在循环过程中可以被O原子取代的事实,充当催化性PtO x颗粒和MoS x载体之间的桥梁,以生成MoS x –O–PtO x结构,使Pt原子能提供更多的电子,从而促进了析氢反应过程。

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