电化学
催化作用
材料科学
氨生产
吸附
氨
范德瓦尔斯力
氮气
贵金属
可逆氢电极
剥脱关节
无机化学
化学工程
纳米技术
分子
化学
电极
石墨烯
有机化学
工作电极
物理化学
工程类
作者
Chuang Wang,Jian Gao,Jinggeng Zhao,Du‐Juan Yan,Xiaodong Zhu
出处
期刊:Small
[Wiley]
日期:2020-04-13
卷期号:16 (18)
被引量:49
标识
DOI:10.1002/smll.201907091
摘要
The electrochemical nitrogen reduction reaction (NRR) is a promising strategy of nitrogen fixation into ammonia under ambient conditions. However, the development of electrochemical NRR is highly bottlenecked by the expensive noble metal catalysts. As a representative 2D nonmetallic material, black phosphorus (BP) has the valence electron structure similar to nitrogen, which can effectively adsorb the inactive nitrogen molecule and activate its triple bond. In addition, the relatively weak hydrogen adsorption can restrict the competitive and vigorous hydrogen evolution reaction. Herein, ultrafine BP quantum dots (QDs) are prepared via liquid-phase exfoliation and then assembled on catalytically active MnO2 nanosheets through van der Waals interactions. The obtained BP QDs/MnO2 catalyst demonstrates admirable synergetic effects in electrochemical NRR. The monodisperse BP QDs providing major activity manifest excellent ammonia production steadily with high selectivity, which benefits from the robust confinement of the BP QDs on the wrinkled MnO2 nanosheets with decent activity. A high ammonia yield rate of 25.3 µg h-1 mgcat.-1 and faradic efficiency of 6.7% can be achieved at -0.5 V (vs RHE) in 0.1 m Na2 SO4 electrolyte, which are dramatically superior to either component. The isotopic labelling and other control tests further exclude the external contamination possibility and attest the genuine activity.
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