Cheng Xuetao, Zhao Huilin, Liu Pengfei, Han Ruihong, Wang Yan-Qin
Inner Mongolia Key Laboratory of Rare Earth Catalysis, College of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot 010021, PR China.
Inner Mongolia Key Laboratory of Rare Earth Catalysis, College of Chemistry and Chemical Engineering, Inner Mongolia University, Hohhot 010021, PR China.
J Colloid Interface Sci. 2025 Mar 15;682:703-714. doi: 10.1016/j.jcis.2024.11.204. Epub 2024 Nov 29.
Electrochemical nitrate reduction reaction (ENORR) is a green technology for value-added ammonia production meanwhile treating waste water at ambient conditions. However, it remains a great challenge to construct efficient catalysts due to the complex multiple proton and electron transfer process. Herein, we report a tandem catalyst Cu/FeO@CN composed of N-doped carbon layer coated Cu/FeO heterostructure toward highly efficient electrocatalytic nitrate reduction to ammonia production in alkaline medium. The catalyst can achieve an ammonia Faradaic efficiency and ammonia yield rate as high as 96.57 % and 22104.15 μg h mg at the optimal potential of -0.9 V vs. RHE in 0.1 M KOH. The outstanding ENORR performance outperforms the most of reported transitional metal-based ENORR electrocatalysts. More importantly, Cu/FeO@CN also exhibits excellent stability even under large current density of 200 mA cm, and long-time durability for continuous electrolysis for 36 h. The experimental and theoretical calculations verify the tandem catalysis mechanism of NO → NO → NH through the synergism of the two components Cu and FeO in Cu/FeO@CN. Specifically, Cu has strong NO adsorption capacity which can be reduced into NO, while FeO can boost water dissociation to generate abundant active *H, ensuring the smooth hydrogenation process while suppressing the occurrence of competitive hydrogen evolution reactions (HER). The heterostructure formation between Cu and FeO also significantly reduces the energy barrier of the rate-determining step (*NO → *NOH), which results in the high performance of Cu/FeO@CN.
电化学硝酸盐还原反应(ENORR)是一种在环境条件下同时处理废水并生产增值氨的绿色技术。然而,由于复杂的多质子和电子转移过程,构建高效催化剂仍然是一个巨大的挑战。在此,我们报道了一种由N掺杂碳层包覆的Cu/FeO异质结构组成的串联催化剂Cu/FeO@CN,用于在碱性介质中高效电催化硝酸盐还原制氨。在0.1 M KOH中,相对于可逆氢电极(RHE),该催化剂在-0.9 V的最佳电位下可实现高达96.57%的氨法拉第效率和22104.15 μg h mg的氨产率。其出色的ENORR性能优于大多数已报道的过渡金属基ENORR电催化剂。更重要的是,即使在200 mA cm的大电流密度下,Cu/FeO@CN也表现出优异的稳定性,并具有长达36小时的连续电解长期耐久性。实验和理论计算通过Cu/FeO@CN中Cu和FeO这两种组分的协同作用,验证了NO→NO→NH的串联催化机制。具体而言,Cu具有很强的NO吸附能力,可将其还原为NO,而FeO可促进水的解离以产生丰富的活性*H,确保氢化过程顺利进行,同时抑制竞争性析氢反应(HER)的发生。Cu和FeO之间形成的异质结构也显著降低了速率决定步骤(*NO→*NOH)的能垒,这导致了Cu/FeO@CN的高性能。