Copper-nickel-MOF/nickel foam catalysts grown in situ for efficient electrochemical nitrate reduction to ammonia.

Journal of hazardous materials Pub Date : 2024-12-05 Epub Date: 2024-10-03 DOI:10.1016/j.jhazmat.2024.136036
Chenxia Yang, Ying Tang, Qian Yang, Bo Wang, Xianghao Liu, Yuxiang Li, Weixia Yang, Kunxuan Zhao, Gang Wang, Zongyuan Wang, Feng Yu
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Abstract

Reducing nitrate (NO3-) in an aqueous solution to ammonia under ambient conditions can provide a green and sustainable NH3-synthesis technology and mitigate global energy and pollution issues. In this work, a CuNi0.75-1,3,5-benzenetricarboxylic acid/nickel foam (CuNi0.75-MOF/NF) catalyst grown in situ was prepared via a one-pot method as an efficient cathode material for electrocatalytic nitrate reduction reaction (NO3RR). The CuNi0.75-MOF/NF catalyst exhibited excellent electrocatalytic NO3RR performance at -1.0 V versus a reversible hydrogen electrode, achieving an outstanding faradaic efficiency of 95.88 % and an NH3 yield of 51.78 mg h-1 cm-2. The 15N isotope labeling experiments confirmed that the sole source of N in the electrocatalytic NO3RR was the NO3- in the electrolyte. The reaction pathway for the electrocatalytic NO3RR was derived by in situ Fourier transform infrared spectroscopy and in situ differential electrochemical mass spectrometry. Density functional theory calculations revealed that the Ni element in the CuNi0.75-MOF/NF catalyst had excellent O-H activation ability and strong *H adsorption capacity. These *H species were transferred from the Ni sites to the *NO adsorption intermediates located on the Cu sites, providing a continuous supply of *H to Cu, thereby promoting the formation of *NOH intermediates and enhancing the hydrogenation process of the electrocatalytic NO3RR.

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原位生长的铜镍-MOF/镍泡沫催化剂,用于高效电化学硝酸盐还原成氨。
在环境条件下将水溶液中的硝酸盐(NO3-)还原成氨气,可提供一种绿色、可持续的 NH3 合成技术,并缓解全球能源和污染问题。本研究采用一锅法制备了一种原位生长的铜镍0.75-1,3,5-苯三羧酸/泡沫镍(CuNi0.75-MOF/NF)催化剂,作为电催化硝酸盐还原反应(NO3RR)的高效阴极材料。与可逆氢电极相比,CuNi0.75-MOF/NF催化剂在-1.0 V电压下表现出优异的电催化NO3RR性能,远红外效率达到95.88%,NH3产率为51.78 mg h-1 cm-2。15N 同位素标记实验证实,电催化 NO3RR 中 N 的唯一来源是电解质中的 NO3-。电催化 NO3RR 的反应途径是通过原位傅立叶变换红外光谱法和原位差分电化学质谱法得出的。密度泛函理论计算表明,CuNi0.75-MOF/NF 催化剂中的镍元素具有优异的 O-H 活化能力和较强的 *H 吸附能力。这些 *H 物种从 Ni 位点转移到位于 Cu 位点上的 *NO 吸附中间体,为 Cu 提供了源源不断的 *H,从而促进了 *NOH 中间体的形成,增强了电催化 NO3RR 的氢化过程。
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