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Ammonia, a core raw material for the global agricultural and chemical industries, faces serious challenges in its conventional synthesis process (the Haber-Bosch method) due to its high energy consumption, high carbon emissions and dependence on fossil fuels. Photocatalytic ammonia synthesis technology provides a revolutionary solution for green ammonia economy by realizing efficient nitrogen reduction under mild conditions with solar energy as the driving force. In this study, we systematically review the mechanism of photocatalytic nitrogen reduction reaction, focusing on the adsorption activation of nitrogen molecules, electron transfer pathways, and intermediate product regulation strategies, and review multiple types of photocatalyst systems including metal oxides, sulfides, bismuth-based materials, and carbon-based materials. Modification strategies such as defect engineering, single-atom modification, heterojunction design and plasma effect can significantly optimize the light absorption range, suppress the carrier recombination and enhance the active site density. It is further pointed out that the existing catalytic systems still face bottlenecks such as low quantum efficiency, photocorrosion, and scale-up reactor design, and future studies are needed to promote the photocatalytic synthesis of ammonia from the laboratory to the industry through multiscale synergistic innovation. This study provides theoretical guidance and a practical framework for the design and development of an efficient and stable photocatalytic ammonia synthesis system, which is scientifically important for achieving the goal of carbon neutrality.
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http://dx.doi.org/10.1039/d5nr02673c | DOI Listing |
J Colloid Interface Sci
September 2025
School of Materials Science and Engineering, Zhejiang Sci-Tech University, Hangzhou 310018, PR China; Zhejiang Sci-Tech University Shengzhou Innovation Research Institute, Shengzhou 312400, PR China. Electronic address:
Suppressing photoinduced charge recombination represents a critical challenge in photocatalytic ammonia (NH) decomposition for hydrogen (H) production. Herein, we propose a dual-cocatalyst system comprising plasmonic silver (Ag) and nickel oxide (NiO), which synergistically construct an Ag → titanium dioxide (TiO) → NiO directional electron cascade on TiO surfaces through work-function-induced interfacial charge transfer. The optimized 3 %Ag-1 %NiO-TiO reaches a significantly photocatalytic H production rate of 2366.
View Article and Find Full Text PDFSmall
September 2025
Department of Chemical Engineering and Technology, School of Chemistry and Chemical Engineering, Nanjing University of Science and Technology, Nanjing, Jiangsu, 210094, P. R. China.
Photocatalytic nitrogen reduction to ammonia (NH) under ambient conditions offers a sustainable alternative to the energy-intensive Haber-Bosch process but faces significant challenges. Inspired by biological nitrogen fixation, a thiosalicylic acid (TSA)-derived Fe-S cluster catalyst with dual active sites (FeS and FeS) is rationally designed and synthesized. Guided by the hard-soft acid-base (HSAB) theory, the Fe⁺/Fe⁺ ratio in the iron source is optimized to regulate the content of these two coordination structures in the catalysts.
View Article and Find Full Text PDFAngew Chem Int Ed Engl
August 2025
Key Laboratory of Photochemical Conversion and Optoelectronic Materials & CAS-HKU Joint Laboratory on New Materials, Technical Institute of Physics and Chemistry, Chinese Academy of Sciences, Beijing, 100190, P.R. China.
Photocatalytic upcycling of polyethylene terephthalate (PET) waste into value-added chemicals represents a sustainable route for plastic valorization. However, previous studies have solely focused on generating oxygenated compounds through intramolecular C─O bond transformations. Achieving heteroatom-containing important chemicals via intermolecular coupling reactions is still challenging.
View Article and Find Full Text PDFAdv Sci (Weinh)
August 2025
Wolfson Catalysis Centre, Department of Chemistry, University of Oxford, Oxford, OX1 3QR, UK.
Photocatalytic ammonia decomposition offers a sustainable route for hydrogen production, but its development is limited by low catalytic efficiency and poorly understood mechanisms. Here, a protonated layered perovskite, HPrNbO (HPNO), is reported as an efficient catalyst for ammonia decomposition under mild photo-thermal conditions. Upon exposure to NH at elevated temperatures, HPNO promotes the in situ formation and intercalation of hydrazine intermediates within its interlayer galleries, enabled by thermally generated oxygen vacancies and hydrogen bonding.
View Article and Find Full Text PDFLangmuir
September 2025
Yangtze Delta Region Institute (Huzhou), University of Electronic Science and Technology of China, Huzhou 313001, China.
As a carbon-free energy carrier with high energy density, ammonia has been extensively utilized across various industrial sectors. However, the conventional Haber-Bosch process for industrial ammonia synthesis faces critical limitations, including harsh operational conditions (high temperature/pressure), excessive energy consumption, and substantial CO emissions, which fundamentally restrict its sustainable development. Photocatalytic nitrogen reduction emerges as a promising alternative strategy, offering advantages of ambient reaction conditions and environmental benignity.
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