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Journal article

Catalytic reduction of nitrogen to produce ammonia by bismuth-based catalysts: State of the art and future prospects

From

University of Technology Sydney1

Department of Energy Conversion and Storage, Technical University of Denmark2

Atomic Scale Materials Modelling, Department of Energy Conversion and Storage, Technical University of Denmark3

Curtin University4

University of New South Wales5

University of Sydney6

Ammonia is a key industrial raw material for fertilisers, chemicals and energy. The annual artificial ammonia synthesis via the Haber-Bosch process results in about 2% of global energy consumption and can lead to 1.6% CO2 emission. Hence, it is urgent to develop low-cost and environmentally friendly approaches for artificial ammonia synthesis under ambient conditions.

Recently, bismuth (Bi)-based catalysts have attracted great interest due to their excellent nitrogen fixation performance in electrochemical and photocatalytic fields. However, there is still a lack of a comprehensive review on Bi-based nitrogen-fixation materials focusing on their crystal structure, surface engineering and modification methods, which is highly desirable for facilitating their further development towards applications.

Herein, we provide an up-to-date review on Bi-based nitrogen-fixation materials and classify them as metallic Bi, bismuth oxide, bismuth oxyhalide, and Bi-based polyoxometalates. Starting from the underlying crystal structure, we analyse the internal electric field, surface engineering and modification methods of Bi-based nitrogen fixation materials.

Then, we highlight the latest achievements of Bi-based materials and reveal the challenges and obstacles in the development and application of Bi-based nitrogen-fixation materials. More importantly, this review presents the surface and structure engineering strategies, and future directions for the development of new Bi-based nitrogen-fixation materials under ambient conditions.

Language: English
Year: 2020
Pages: 1014-1029
ISSN: 20516355 and 20516347
Types: Journal article
DOI: 10.1039/c9mh01668f
ORCIDs: 0000-0001-9981-7499 , 0000-0002-8256-6053 , 0000-0003-1179-2763 , 0000-0002-5215-0487 , 0000-0001-5633-3945 and 0000-0002-1129-7837

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