氨生产
固氮酶
氨
催化作用
氮气
固氮
电催化剂
化学
生化工程
纳米技术
材料科学
电化学
有机化学
电极
工程类
物理化学
作者
Shelby L. Foster,Sergio I. Perez Bakovic,Royce D. Duda,Sharad Maheshwari,Ross D. Milton,Shelley D. Minteer,Michael J. Janik,Julie Renner,Lauren F. Greenlee
出处
期刊:Nature Catalysis
[Springer Nature]
日期:2018-07-11
卷期号:1 (7): 490-500
被引量:1227
标识
DOI:10.1038/s41929-018-0092-7
摘要
The production of synthetic ammonia remains dependent on the energy- and capital-intensive Haber–Bosch process. Extensive research in molecular catalysis has demonstrated ammonia production from dinitrogen, albeit at low production rates. Mechanistic understanding of dinitrogen reduction to ammonia continues to be delineated through study of molecular catalyst structure, as well as through understanding the naturally occurring nitrogenase enzyme. The transition to Haber–Bosch alternatives through robust, heterogeneous catalyst surfaces remains an unsolved research challenge. Catalysts for electrochemical reduction of dinitrogen to ammonia are a specific focus of research, due to the potential to compete with the Haber–Bosch process and reduce associated carbon dioxide emissions. However, limited progress has been made to date, as most electrocatalyst surfaces lack specificity towards nitrogen fixation. In this Review, we discuss the progress of the field in developing a mechanistic understanding of nitrogenase-promoted and molecular catalyst-promoted ammonia synthesis and provide a review of the state of the art and scientific needs for heterogeneous electrocatalysts. The artificial synthesis of ammonia remains one of the most important catalytic processes worldwide, over 100 years after its development. In this Review, recent developments in enzymatic, homogeneous and heterogeneous catalysis towards the conversion of nitrogen to ammonia are discussed, with a particular focus on how mechanistic understanding informs catalyst design.
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