Electrochemical Co-reduction of N2 and CO2 to Urea Using Bi2S3 Nanorods Anchored to N-Doped Reduced Graphene Oxide

被引:18
|
作者
Xing, Pingxing [1 ]
Wei, Shenqi [1 ]
Zhang, Yulu [1 ]
Chen, Xinyi [1 ]
Dai, Liyi [1 ,2 ]
Wang, Yuanyuan [1 ,2 ]
机构
[1] East China Normal Univ, Shanghai Key Lab Green Chem & Green Proc, Shanghai 200241, Peoples R China
[2] Inst Ecochongming, Shanghai 202162, Peoples R China
基金
中国国家自然科学基金; 国家重点研发计划;
关键词
N-doped reduced graphene oxide; N2 and CO2 adsorption and activation; electrocatalytic synthesis of urea; couple C-N bond; CARBON-DIOXIDE; ELECTROCATALYTIC REDUCTION; AMMONIA-SYNTHESIS; NITRITE IONS; 3D GRAPHENE; N-2; EFFICIENT; PERFORMANCE; CONVERSION; COMPOSITE;
D O I
10.1021/acsami.3c01405
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Producing "green urea" using renewable energy, N2, and CO2 is a long-considered challenge. Herein, an electrocatalyst, Bi2S3/N-reduced graphene oxide (RGO), was synthesized by loading the Bi2S3 nanorods onto the N-RGO via a hydrothermal method. The Bi2S3/N-RGO composites exhibit the highest yield of urea (4.4 mmol g-1 h-1), which is 12.6 and 3.1 times higher than that of Bi2S3 (0.35 mmol g-1 h-1) and that of N-RGO (1.4 mmol g-1 h-1), respectively. N-RGO, because of its porous and open-layer structure, improves the mass transfer efficiency and stability, while the basic groups (-OH and-NH2) promote the adsorption and activation of CO2. Bi2S3 promotes the absorption and activation of inert N2. Finally, the defect sites and the synergistic effect on the Bi2S3/N-RGO composites work simultaneously to form urea from N2 and CO2. This study provides new insights into urea synthesis under ambient conditions and a strategy for the design and development of a new material for green urea synthesis.
引用
收藏
页码:22101 / 22111
页数:11
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