4.7 Article

Photocatalytic conversion of nitrogen to ammonia with water on triphase interfaces of hydrophilic-hydrophobic composite Bi4O5Br2/ZIF-8

Journal

CHEMICAL ENGINEERING JOURNAL
Volume 371, Issue -, Pages 796-803

Publisher

ELSEVIER SCIENCE SA
DOI: 10.1016/j.cej.2019.03.283

Keywords

Bi4O5Br2/ZIF-8; Photocatalyst; Triphase interface; Hydrophilic-hydrophobic structure; Nitrogen fixation

Funding

  1. National Natural Science Foundation of China [21808151, 21506144, 21676178]
  2. Natural Science Foundation of Shanxi Province for Young Scientists [201701D221037]
  3. Foundation of State Key Laboratory of Coal Conversion [J18-19-605]

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Photocatalysis can produce NH3 using N-2 and H2O at room temperature and atmospheric pressure, which has been considering as a safe, clean, and sustainable NH3 synthesis. However, the poor solubility and slow diffusion rate of N-2 in water severely limited the nitrogen activation efficiency. Herein, we solve this problem by developing a hydrophilic-hydrophobic structure photocatalyst with gas-liquid-solid triphase reaction interface, where hydrophilic Bi4O5Br2 is deposited on the surface of hydrophobic ZIF-8 to form a novel Bi4O5Br2/ZIF-8 composite photocatalyst. Such triphase interface architecture allows the direct delivery of N-2 from gas phase to the photocatalytic reaction interface replaced the diffusion of N-2 through the liquid phase. This rapid supply of N-2 can efficiently capture photoinduced electrons, thereby promoting the utilization efficiency of photo-induced electrons and the nitrogen fixation activation. This novel Bi4O5Br2/ZIF-8(30%) composite photocatalyst with good triphase contact performance shows obviously improved photocatalytic nitrogen fixation activity 327.338 mu mol.L-1.h(-1).g(-1) (3.6 times than that of Bi4O5Br2). Furthermore, efficient molecular nitrogen activation by Bi4O5Br2/ZIF-8 further brings out an attractive potential to improve other gas-consumption reactions, such as CO2 reduction, according to this concept of triphase direct contact.

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