Marinho André L A, Comminges Clément, Habrioux Aurélien, Célérier Stéphane, Bion Nicolas, Morais Cláudia
Institut de Chimie des Milieux et Matériaux de Poitiers (IC2MP), University of Poitiers, CNRS UMR 7285, TSA51106 - F86073, Poitiers Cedex 9, France.
Chem Commun (Camb). 2023 Aug 17;59(67):10133-10136. doi: 10.1039/d3cc02693k.
The electrochemical nitrogen reduction reaction (NRR) to produce NH is the most efficient, eco-friendly and cost-effective alternative to the Haber-Bosch process. It is crucial to investigate and develop electrocatalysts selective for NH synthesis. In recent studies, the TiC MXene has emerged as a highly promising electrocatalyst for the NRR process. In this work, we explore the effect of Zif-8 addition over MXene sheets in order to control the rate of hydrogen evolution reaction (HER). Despite the better result obtained for Zif-8@TiC (3.0 μg NH g h at -0.55 V/RHE), the ammonia produced when using Zif-8@TiC as cathode material is shown to be originated from nitrogen atoms contained in the Zif-8 structure instead of those of N. The results shed light to the need to fully understand the N electroreduction process over -containing electrocatalysts.
通过电化学氮还原反应(NRR)制备氨是哈伯-博施法最有效、环保且经济高效的替代方法。研究和开发对氨合成具有选择性的电催化剂至关重要。在最近的研究中,TiC MXene已成为用于NRR过程的极具前景的电催化剂。在这项工作中,我们探索添加Zif-8对MXene片层的影响,以控制析氢反应(HER)速率。尽管Zif-8@TiC在-0.55 V/RHE时获得了更好的结果(3.0 μg NH₃ g⁻¹ h⁻¹),但使用Zif-8@TiC作为阴极材料时产生的氨显示源自Zif-8结构中所含的氮原子,而非N₂中的氮原子。这些结果揭示了充分理解含氮电催化剂上的氮电还原过程势在必行。