量子点
材料科学
电化学
离解(化学)
催化作用
氨生产
法拉第效率
氨
氧气
分子
氢
氮气
化学工程
纳米技术
可逆氢电极
析氧
无机化学
电极
产量(工程)
量子产额
制氢
化学
嵌入
氢键
协同催化
作者
Manduo Huang,Yushu Gou,Jiujiang Xian,Yuanming Mu,Yuyao Ji
标识
DOI:10.1021/acsanm.5c05454
摘要
The traditional Haber–Bosch ammonia synthesis process is expected to be replaced with a sustainable and green electrochemical ammonia synthesis method. However, the bond energy of nitrogen molecules is high, making them extremely difficult to decompose. Therefore, it is necessary to develop highly active electrocatalysts to accelerate the dissociation of nitrogen gas and efficiently synthesize ammonia. Herein, we report the development of the Bi 2 WO 6 quantum dots/WO 3 (Bi 2 WO 6 QD/WO 3 ). Their synergistic effect can effectively inhibit the competitive hydrogen evolution reaction, enhancing catalytic activity for NH 3 synthesis. In 0.1 mol/L Na 2 SO 4, compared with pure WO 3, Bi 2 WO 6 QD/WO 3 achieve a higher Faradaic efficiency (FE) (10.1%) and a larger NH 3 yield (43.5 μg h –1 mg cat –1 ) at −0.5 V. Meanwhile, Bi 2 WO 6 QD-WO 3 attain the lowest FEs of hydrogen evolution reaction (HER), further illustrating that Bi 2 WO 6 QD-WO 3 can effectively inhibit the HER. Theoretical calculations and experimental results indicate that the embedding of quantum dots can effectively regulate the concentration of oxygen vacancies, accelerate interface charge transfer, and improve nitrogen reduction reaction performance.
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