促进电催化硝酸盐还原成氨的镍负载 Co-NC 催化剂

IF 4.4 3区 化学 Q2 CHEMISTRY, PHYSICAL
Fang Zhao, Yidi Liu, Chengjie Li, Zhen Yuan, Qianqian Hua, Liguo Gao, Xuefeng Ren, Peixia Yang, Anmin Liu
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引用次数: 0

摘要

哈伯-博施工艺是合成氨的传统方法,使用的氢气来自碳氢化合物的蒸汽重整;并且涉及高温(300-600 °C)和高压(200-400 atm)的苛刻操作条件,每年消耗大量能源。最近,人们对电化学还原氮过程(NRR)转化为 NH3 产生了浓厚的兴趣,这一过程受到了自然界微生物固氮作用的启发。然而,稳定的 NN 剧烈氢进化反应阻碍了 NRR 的发展。相比之下,电催化硝酸盐还原反应(NO3RR)具有显著优势。NO 所需的解离能(204 kJ mol-1)要低得多;硝酸盐在地表水中广泛存在。本文报道了一种通过简单浸渍法将镍负载到 CoZn@ZIF 上的电催化剂,该催化剂在热解碳化后具有掺氮石墨碳结构。详细实验表明,与 Co-NC 相比,NiCo-NC 催化剂能显著加速 NO3RR 的生成。NiCo-NC 具有显著的 NO3RR 活性。在 -0.6 V 和 -1.1 V 下,氨产量分别为 5.01 mg cm-2 h-1 和 10.12 mg cm-2 h-1,FE 分别达到 92.75% 和 96.65%。在 24 小时电解实验和五次循环稳定性测试中,催化剂表现出优异的电化学稳定性。同时,15N 同位素标记实验进一步验证了 NH4+ 中的 N 来源于 NO3-。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Ni-loaded Co-NC catalysts for promoting electrocatalytic nitrate reduction to ammonia

Ni-loaded Co-NC catalysts for promoting electrocatalytic nitrate reduction to ammonia
The Haber–Bosch process, the traditional method of ammonia synthesis, uses hydrogen derived from steam reforming of hydrocarbons; and involves harsh operating conditions of high temperatures (300–600 °C) and pressures (200–400 atm), expending a vast amount of energy each year. Recently, there has been a lot of interest in the electrochemical nitrogen reduction process (NRR) to NH3, which is inspired by natural microbial nitrogen fixation. However, the stable N[triple bond, length as m-dash]N violent hydrogen evolution reaction hindered the development of the NRR. In comparison, the electrocatalytic nitrate reduction reaction (NO3RR) has significant advantages. The much lower dissociation energy of N[double bond, length as m-dash]O (204 kJ mol−1) is required; nitrate is widespread in surface water. Herein, an electrocatalyst loaded with Ni onto CoZn@ZIF by a simple impregnation method is reported, which possesses a nitrogen-doped graphitic carbon structure after pyrolytic carbonization. Detailed experiments showed that the NiCo-NC catalyst significantly accelerated the NO3RR compared to Co-NC. NiCo-NC exhibited remarkable NO3RR activity. At −0.6 V and −1.1 V, ammonia yields of 5.01 mg cm−2 h−1 and 10.12 mg cm−2 h−1 were obtained, with FEs reaching 92.75% and 96.65%, respectively. The catalyst showed excellent electrochemical stability in 24-hour electrolysis experiments and five-cycle stability tests. Meanwhile, 15N isotope labeling experiments further verified the source of N in NH4+ from NO3.
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来源期刊
Catalysis Science & Technology
Catalysis Science & Technology CHEMISTRY, PHYSICAL-
CiteScore
8.70
自引率
6.00%
发文量
587
审稿时长
1.5 months
期刊介绍: A multidisciplinary journal focusing on cutting edge research across all fundamental science and technological aspects of catalysis. Editor-in-chief: Bert Weckhuysen Impact factor: 5.0 Time to first decision (peer reviewed only): 31 days
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