电合成
材料科学
电催化剂
碳纤维
催化作用
法拉第效率
可逆氢电极
电解质
化学工程
激光烧蚀
氨
氧化还原
水溶液
氨生产
电化学
纳米技术
无机化学
电极
复合数
激光器
工作电极
化学
物理化学
复合材料
有机化学
冶金
光学
工程类
物理
作者
Wenyi Li,Chao Zhang,Miaomiao Han,Yixing Ye,Shengbo Zhang,Yanyan Liu,Guozhong Wang,Changhao Liang,Haimin Zhang
标识
DOI:10.1021/acsami.9b14770
摘要
This work reports the synthesis of core-shell structured Au@C composite through a simple one-step laser ablation technique. The results demonstrate that the Au@C with a mean nanosphere size of ∼8.0 nm is composed of a spherical shaped Au core and 1-2 layered graphitic carbon shell with abundant defects. As a nitrogen reduction reaction (NRR) electrocatalyst, the Au@C gives a large NH3 yield rate of 241.9 μg h-1 mgcat.-1 with a high faradaic efficiency of 40.5% at -0.45 V versus reversible hydrogen electrode in a 0.1 M Na2SO4 electrolyte (pH = 6.3) under ambient conditions, surpassing the performances of most aqueous-based NRR electrocatalysts recently reported. The 15N labeling experimental results demonstrate that the produced NH3 is undoubtedly originated from the NRR process catalyzed by Au@C. The superior NRR performance of Au@C can be ascribed to the ultrathin carbon layer, effectively inhibiting the aggregation of Au nanospheres during the NRR, and the abundant defects such as carbon vacancies existed in the ultrathin carbon layer, providing additional NRR catalytic active sites. Our theoretical calculation results further confirm the role of carbon vacancies in the electrocatalytic NRR.
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