NiO Nanodots on Graphene for Efficient Electrochemical N2 Reduction to NH3

被引:147
|
作者
Chu, Ke [1 ]
Liu, Ya-ping [1 ]
Wang, Jing [1 ]
Zhang, Hu [2 ]
机构
[1] Lanzhou Jiaotong Univ, Sch Mat Sci & Engn, Lanzhou 730070, Gansu, Peoples R China
[2] Univ Sci & Technol Beijing, Sch Mat Sci & Engn, Beijing 100083, Peoples R China
基金
中国国家自然科学基金;
关键词
electrochemical NH3 synthesis; N-2 reduction reaction; NH3; yield; NiO nanodots; graphene hybrid; density functional theory; N-2; adsorption; MECHANICAL-PROPERTIES; NITROGEN REDUCTION; INTERFACE; COMPOSITES; AMMONIA; CATALYSTS; ELECTRODE; DEFECTS; DESIGN;
D O I
10.1021/acsaem.9b00102
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Current artificial NH3 synthesis relies heavily on the Haber-Bosch process that involves enormous energy consumption and huge CO2 emission. The electrochemical N-2 reduction reaction (NRR) offers an ecofriendly and sustainable alternative but demands cost-effective and efficient NRR electrocatalysts. Herein, NiO nanodots nm) supported on graphene (NiO/G) were developed as a high-performance NRR electrocatalyst at ambient conditions. Electrochemical tests indicated that the NiO/G exhibited a high NH3 yield (18.6 mu g h(-1) mg(-1)) and Faradaic efficiency (7.8%) at -0.7 V vs reversible hydrogen electrode, outperforming the most reported NRR electrocatalysts. Experimental and density functional theory (DFT) results revealed that NiO was the dominating active center, and nanodot structure enabled the NiO to expose more active sites. DFT results further demonstrated that the distal associative route was the preferable NRR pathway with *N-2 -> *NNH being the rate-determining step.
引用
收藏
页码:2288 / 2295
页数:15
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