非阻塞I/O
亚硝酸盐
煅烧
催化作用
氨
法拉第效率
产量(工程)
氧化镍
化学
镍
无机化学
复合数
化学工程
材料科学
电化学
电极
冶金
硝酸盐
复合材料
有机化学
物理化学
工程类
作者
Talshyn Begildayeva,Jayaraman Theerthagiri,Ahreum Min,Cheol Joo Moon,Myong Yong Choi
标识
DOI:10.1016/j.cej.2024.150041
摘要
Herein, we report the pioneering synthesis of the cobalt–nickel coordination frameworks (Co(H2O)2·Ni(CN)4, CoNi-CF) via pulsed laser irradiation in liquids (PLIL). The distinctive morphology of CoNi-CF has attracted considerable attention as a potential template to produce Co3O4/NiO composites with varying Co and Ni ratios. After subjecting CoNi-CF to a high-temperature calcination process at 400 °C, the resulting Co3O4/NiO composites displayed dual-active canters for efficient electrochemical nitrite (NO2−) reduction to ammonia (NH3). Optimizing the Co:Ni ratio at 1:0.75 yielded Co3O4/NiO with exceptional performance, achieving a remarkable 99.4 % Faradaic efficiency in NH3 production while maintaining a 96.1 % mass balance at − 1.2 V vs. Ag/AgCl. Furthermore, this composite displayed long-term stability, degrading 60.82 % of NO2− in 180 min, with high NH3 yield rates (2012.03 μM h−1 cm−2) at − 1.6 V vs. Ag/AgCl. The superior performance in NO2− reduction to NH3 can be attributed to the unique structural features inherited from CoNi-CF, including well-defined and self-standing Co3O4 and NiO phases. Synergistic effects at the oxide interface enhance electrochemical performance and facilitate efficient charge transfer kinetics of Co3O4/NiO, underscoring the unique potential of these composite materials.
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