热解
材料科学
纳米颗粒
氮气
碳纤维
多孔性
法拉第效率
化学工程
产量(工程)
兴奋剂
无机化学
纳米技术
电化学
化学
电极
有机化学
复合数
复合材料
物理化学
光电子学
工程类
作者
Zhaobing Lu,Hui Wang,Yinghao Tao,Sheng Zhu,Weiju Hao,Xinjuan Liu,Yulin Min,Jinchen Fan
出处
期刊:Nanoscale
[Royal Society of Chemistry]
日期:2023-01-01
卷期号:15 (36): 14847-14857
被引量:3
摘要
The electrocatalytic nitrogen reduction reaction (eNRR) is a sustainable and green alternative to the traditional Haber-Bosch process. However, the chemical inertness of nitrogen gas and the competitive hydrogen evolution reaction significantly limit the catalytic performance of eNRR. Although tungsten oxide-based eNRR catalysts could donate unpaired electrons to the antibonding orbitals of N2 and accept lone electron pairs from N2 to dissociate NN triple bonds, the low electrical conductivity and the influence of the variable valence of W still affect the catalytic activity. Herein, a high-performance eNRR catalyst WOx nanoparticle/nitrogen-doped porous carbon (WOx/NPC) was prepared by a one-step thermal pyrolysis method. The results reveal that WOx gradually changes from the dominant WO2 phase to the WO3 phase. WOx/NPC-700 °C with WO2 NPs anchored on the surfaces of NPC via W-N bonding could deliver a high NH3 yield of 46.8 μg h-1 mg-1 and a high faradaic efficiency (FE) of 10.2%. The edge W atomic site on WOx/NPC is demonstrated to be the active center which could activate a stable NN triple bond with an electron-donating ability. Benefiting from the covalent interaction between the WOx nanoparticles and NPC, WOx/NPC also shows high electrocatalytic stability.
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