Journal
CHEMNANOMAT
Volume 6, Issue 8, Pages 1179-1185Publisher
WILEY-V C H VERLAG GMBH
DOI: 10.1002/cnma.202000174
Keywords
NO3- reduction; photocatalysis; Ni2P; Ta3N5; TaON; clean water
Categories
Funding
- U.S. National Science Foundation from the Division of Chemistry, Macromolecular, Supramolecular, and Nanochemistry Program [1905066]
- Division Of Chemistry
- Direct For Mathematical & Physical Scien [1905066] Funding Source: National Science Foundation
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Self-sustaining photocatalytic NO3- reduction systems could become ideal NO3- removal methods. Developing an efficient, highly active photocatalyst is the key to the photocatalytic reduction of NO3-. In this work, we present the synthesis of Ni2P-modified Ta3N5 (Ni2P/Ta3N5), TaON (Ni2P/TaON), and TiO2 (Ni2P/TiO2). Starting with a 2 mM (28 g/mL NO3--N) aqueous solution of NO3-, as made Ni2P/Ta3N5 and Ni2P/TaON display as high as 79% and 61% NO3- conversion under 419 nm light within 12 h, which correspond to reaction rates per gram of 196 mu mol g(-1) h(-1) and 153 mu mol g(-1) h(-1), respectively, and apparent quantum yields of 3-4%. Compared to 24% NO3- conversion in Ni2P/TiO2, Ni2P/Ta3N5 and Ni2P/TaON exhibit higher activities due to the visible light active semiconductor (SC) substrates Ta3N5 and TaON. We also discuss two possible electron migration pathways in Ni2P/semiconductor heterostructures. Our experimental results suggest one dominant electron migration pathway in these materials, namely: Photo-generated electrons migrate from the semiconductor to co-catalyst Ni2P, and upshift its Fermi level. The higher Fermi level provides greater driving force and allows NO3- reduction to occur on the Ni2P surface.
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