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首页> 外文期刊>Journal of Materials Chemistry, A. Materials for energy and sustainability >Unlocking the potential of ruthenium catalysts for nitrogen fixation with subsurface oxygen
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Unlocking the potential of ruthenium catalysts for nitrogen fixation with subsurface oxygen

机译:解锁钌催化剂的施氮,用于用地下氧固定

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摘要

As a clean, eco-friendly and sustainable process, electrocatalysis has potential to replace the energy-consuming and environment-polluting Haber-Bosch process for N-2 fixation. Although ruthenium (Ru) is generally considered as the best electrocatalyst for this process, its low faradaic efficiency greatly hampers the practical applications. Considering the solvent effects, our ab initio calculations and micro-kinetic simulations indicate that doping oxygen into the sublayer of Ru(0001) can turn some surface Ru-0 atoms into positively charged Ru+, significantly boosting the reduction of N-2. The overpotential can be dramatically reduced to 0.18 V only for Ru(0001) with 1.00 ML subsurface oxygen. Notably, the calculated turnover frequency (TOF) is 3.64 x 10(-2) per s per site at 700 K and 100 bar, which is hundreds of times greater than that of the pure Ru(0001) surface. In terms of experimental progress on the successful incorporation of subsurface oxygen into the Ru(0001) surface, our work offers a practical and feasible route to boost electrochemical reduction of N-2 to ammonia.
机译:电催化作为一种清洁、环保、可持续的N-2固定工艺,有望取代能耗高、污染环境的哈伯-博世法。虽然钌(Ru)通常被认为是这一过程的最佳电催化剂,但其较低的法拉第效率极大地阻碍了实际应用。考虑到溶剂效应,我们的从头算计算和微观动力学模拟表明,在Ru(0001)的亚层中掺杂氧可以将一些表面Ru-0原子转变为带正电的Ru+,显著促进N-2的还原。只有Ru(0001)和1.00 ML地下氧气的情况下,过电位才能显著降低至0.18 V。值得注意的是,在700K和100bar条件下,计算出的翻转频率(TOF)为3.64x10(-2)次/s,是纯Ru(0001)表面的数百倍。根据成功地将地下氧引入Ru(0001)表面的实验进展,我们的工作为促进N-2电化学还原为氨提供了一条切实可行的途径。

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