CO2/NOx-involved Electrochemical C-N Coupling Reactions

被引:0
|
作者
Sui, Xiqing [1 ,2 ]
Wu, Limin [1 ,2 ]
Jia, Shunhan [1 ,2 ]
Jin, Xiangyuan [1 ,2 ]
Sun, Xiaofu [1 ,2 ]
Han, Buxing [1 ,2 ,3 ]
机构
[1] Chinese Acad Sci, Beijing Natl Lab Mol Sci, Key Lab Colloid & Interface & Thermodynam, Ctr Carbon Neutral Chem,Inst Chem, Beijing 100190, Peoples R China
[2] Univ Chinese Acad Sci, Sch Chem Sci, Beijing 100049, Peoples R China
[3] East China Normal Univ, Sch Chem & Mol Engn, Shanghai Key Lab Green Chem & Chem Proc, Shanghai 200062, Peoples R China
基金
北京市自然科学基金; 中国国家自然科学基金;
关键词
CO2; reduction; NOx reduction; C-N coupling; Electrocatalysis; GAS-DIFFUSION ELECTRODES; EFFICIENT UREA ELECTROSYNTHESIS; ELECTROCATALYTIC CO2 REDUCTION; CARBON-DIOXIDE; NITRITE IONS; NITRATE REDUCTION; AMMONIA-SYNTHESIS; BIPOLAR MEMBRANE; ELECTROREDUCTION; CATALYSTS;
D O I
10.1007/s40242-024-4118-1
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
With the excessive use of fossil fuels leading to significant CO2 emissions, and the continuous increase of NOx in water bodies and soils, the use of electrochemical methods for the conversion of CO2 and NOx has garnered widespread attention as a green chemical approach due to its advantages of being environmentally friendly, low-carbon, and straightforward. C-N bonds are widely present in many value-added chemicals, such as urea, amides, and oximes. However, traditional methods for constructing C-N bonds typically involve thermochemical processes. Therefore, using electrochemical methods to catalyze the reduction of CO2 and NOx for C-N bond formation has emerged as a green and sustainable alternative. This paper summarizes the research progress of electrochemical C-N bond construction involving CO2 and NOx from the perspectives of reaction mechanisms and catalytic system construction, reviews the electrochemical synthesis of urea, amines, amides, and oximes through electrochemical C-N bond construction, and finally analyzes the current problems and challenges in the field, providing prospects for its future development.
引用
收藏
页码:764 / 775
页数:12
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