在掺杂钴的铜氧化物上促进*NO2加氢用于硝酸选择性氨电合成。

IF 6.6 2区 化学 Q1 CHEMISTRY, MULTIDISCIPLINARY
ChemSusChem Pub Date : 2025-03-06 DOI:10.1002/cssc.202500017
Chang Liu, Chunqi Yang, Wenxuan Zhang, Yuhang Li
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引用次数: 0

摘要

可再生能源驱动的电化学硝酸还原反应(NO3RR)在环境条件下可同时实现硝酸盐降解和氨生成,引起了广泛关注。铜基催化剂因其高活性而应用最广泛,但由于中间亚硝酸盐的积累,其选择性较低。本工作报道了钴掺杂氧化铜(Co/CuO)复合材料,同时引入Co位点加速了氮的加氢。在所制备的Co/CuO复合材料在-0.4 V(相对于RHE)电位下的法拉第效率为93.9%,产氨速率为0.5441 mmol·h-1·cm-2。Co/CuO复合材料的优异稳定性也通过连续的回收试验得到了肯定。原位表征证实了Co位点的存在容易使*NO2转化为*NH2,因此对NO3RR表现出较高的性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Promoting *NO2 Hydrogeneration on Cobalt-Doped Copper Oxides for Selective Ammonia Electrosynthesis from Nitrate

Promoting *NO2 Hydrogeneration on Cobalt-Doped Copper Oxides for Selective Ammonia Electrosynthesis from Nitrate

Electrochemical nitrate reduction reaction (NO3RR) driven by renewable energy has attracted extensive attention, which can realize nitrate degradation and ammonia production simultaneously under ambient conditions. Copper−based catalysts are the most widely used due to their high activity but are subject to low selectivity owing to intermediate nitrite accumulation. This work has reported cobalt-doped copper oxide (Co/CuO) composites, while introduced Co sites accelerate the hydrogenation of nitrogen species. The prepared Co/CuO composites realize a 93.9 % Faradaic efficiency at the applied potential of −0.4 V (vs. RHE), yielding ammonia at 0.5441 mmol⋅h−1 cm−2. The exceptional stability of Co/CuO composites has also been affirmed by following continuous recycling tests. In situ characterization confirms that the existence of Co sites is prone to conversion of *NO2 to *NH2, thus exhibiting high performance for NO3RR.

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来源期刊
ChemSusChem
ChemSusChem 化学-化学综合
CiteScore
15.80
自引率
4.80%
发文量
555
审稿时长
1.8 months
期刊介绍: ChemSusChem Impact Factor (2016): 7.226 Scope: Interdisciplinary journal Focuses on research at the interface of chemistry and sustainability Features the best research on sustainability and energy Areas Covered: Chemistry Materials Science Chemical Engineering Biotechnology
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