Ye Cuizhu, Guo Ziyi, Zhou Yongfang, Shen Yi
School of Food Science and Engineering, South China University of Technology, Guangzhou 510640, China; China-Singapore International Joint Research Institute, Guangzhou Knowledge City, Guangzhou 510663, China.
School of Food Science and Engineering, South China University of Technology, Guangzhou 510640, China.
J Colloid Interface Sci. 2025 Jan;677(Pt B):933-941. doi: 10.1016/j.jcis.2024.08.124. Epub 2024 Aug 16.
Electrochemical nitrate (NO) reduction reaction (NORR) to ammonium (NH) or nitrogen (N) provides a green route for nitrate remediation. However, nitrite generation and hydrogen evolution reactions hinder the feasibility of the process. Herein, dual single atom catalysts were rationally designed by introducing Ag/Bi/Mo atoms to atomically dispersed NiNC moieties supported by nitrogen-doped carbon nanosheet (NCNS) for the NORR. Ni single atoms loaded on NCNS (Ni/NCNS) tend to reduce NO to valuable NH with a high selectivity of 77.8 %. In contrast, the main product of NORR catalyzing by NiAg/NCNS, NiBi/NCNS, and NiMo/NCNS was changed to N, giving rise to N selectivity of 48.4, 47.1 and 47.5 %, respectively. Encouragingly, Ni/NCNS, NiBi/NCNS, and NiAg/NCNS showed excellent durability in acidic electrolytes, leading to nitrate conversion rates of 70.3, 91.1, and 93.2 % after a 10-h reaction. Simulated wastewater experiments showed that NiAg/NCNS could remove NO up to 97.8 % at -0.62 V after 9-h electrolysis. This work afforded a new strategy to regulate the reaction pathway and improve the conversion efficiency of the NORR via engineering the dual atomic sites of the catalysts.
电化学硝酸盐(NO)还原反应(NORR)生成铵(NH)或氮气(N)为硝酸盐修复提供了一条绿色途径。然而,亚硝酸盐生成和析氢反应阻碍了该过程的可行性。在此,通过将Ag/Bi/Mo原子引入到由氮掺杂碳纳米片(NCNS)负载的原子分散的NiNC部分中,合理设计了双单原子催化剂用于NORR。负载在NCNS上的Ni单原子(Ni/NCNS)倾向于以77.8%的高选择性将NO还原为有价值的NH。相比之下,由NiAg/NCNS、NiBi/NCNS和NiMo/NCNS催化的NORR的主要产物变为N,N选择性分别为48.4%、47.1%和47.5%。令人鼓舞的是,Ni/NCNS、NiBi/NCNS和NiAg/NCNS在酸性电解质中表现出优异的耐久性,在10小时反应后硝酸盐转化率分别为70.3%、91.1%和93.2%。模拟废水实验表明,NiAg/NCNS在-0.62 V下电解9小时后可去除高达97.8%的NO。这项工作通过设计催化剂的双原子位点,为调节反应途径和提高NORR的转化效率提供了一种新策略。