Nitrogen fixation is an essential process for sustaining life. Tremendous efforts have been made on the photodriven fixation of nitrogen into ammonia. However, the disproportionation of dinitrogen to ammonia and nitrate under ambient conditions has remained a grand challenge. In this work, the photodriven disproportionation of nitrogen is realized in water under visible light and ambient conditions using Fe-doped TiO microspheres. The oxygen vacancies associated with the Fe dopants activate chemisorbed N molecules, which can then be fixed into NH with H O as the oxidation product. The generated H O thereafter oxidizes NH into nitrate. This disproportionation reaction can be turned to the reductive one by loading plasmonic Au nanoparticles in the doped TiO microspheres. The generated H O can be effectively decomposed by the Au nanoparticles, resulting in the transformation of the disproportionation reaction to the completely reductive nitrogen photofixation.
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http://dx.doi.org/10.1002/anie.202010192 | DOI Listing |
Angew Chem Int Ed Engl
January 2021
Department of Chemistry, The Chinese University of Hong Kong, Shatin, Hong Kong SAR, China.
Nitrogen fixation is an essential process for sustaining life. Tremendous efforts have been made on the photodriven fixation of nitrogen into ammonia. However, the disproportionation of dinitrogen to ammonia and nitrate under ambient conditions has remained a grand challenge.
View Article and Find Full Text PDFChemistry
November 2019
van 't Hoff Institute for Molecular Sciences, University of Amsterdam, Science Park 904, Amsterdam, 1098 XH, The Netherlands.
Artificial photosynthesis-the direct photochemical generation of hydrogen from water-is a promising but scientifically challenging future technology. Because nature employs membranes for photodriven reactions, the aim of this work is to elucidate the effect of membranes on artificial photocatalysis. To do so, a combination of electrochemistry, photocatalysis, and time-resolved spectroscopy on vesicle-embedded [FeFe]hydrogenase mimics, driven by a ruthenium tris-2,2'-bipyridine photosensitizer, is reported.
View Article and Find Full Text PDFACS Cent Sci
November 2017
Department of Chemistry and Chemical Biology, Cornell University, Ithaca, New York 14853, United States.
Compared with their monometallic counterparts, bimetallic nanoparticles often show enhanced catalytic activity associated with the bimetallic interface. Direct quantitation of catalytic activity at the bimetallic interface is important for understanding the enhancement mechanism, but challenging experimentally. Here using single-molecule super-resolution catalysis imaging in correlation with electron microscopy, we report the first quantitative visualization of enhanced bimetallic activity within single bimetallic nanoparticles.
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