4.6 Article

Tuning product selectivity in nitrobenzene reduction over a single Bi2MoO6 photocatalyst in one pot: Mechanisms and roles of reaction compositions

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.jphotochem.2022.114099

关键词

Bi2MoO6; Photocatalyst; Nitrobenzene; Aniline; Azobenzene; Visible light

资金

  1. Science Achievement Scholarship of Thailand
  2. Center of Excellence in Materials Science and Technology
  3. Chiang Mai University
  4. National Research Council of Thailand (NRCT) [N41A640085]
  5. Kurita Asia Research Grant [21Pth001-33R]
  6. Kurita Water and Environment Foundation
  7. Center of Excellence for Innovation in Chemistry (PERCH-CIC)
  8. Ministry of Higher Education, Science, Research and Innovation

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In this article, the authors demonstrate for the first time the possibility of selectively preparing three different valuable compounds using a single bismuth molybdate photocatalyst without catalyst modification. They compare two widely used bismuth molybdate photocatalysts and study the effects of additives on the reaction. Through this research, they discover the capability to control product selectivity over a single photocatalyst.
Poor product selectivity of metal oxide photocatalysts is one of crucial issues limiting their application in photocatalytic organic synthesis particularly when multiple parallel reactions as well as several intermediates and products are involved, as in the reduction of nitrobenzene (NB) in this present study. Accordingly, catalyst modification is often needed. Herein, we first demonstrate that without catalyst modification it is feasible to control product selectivity over a single bismuth molybdate photocatalyst to selectively prepare three different valuable compounds including aniline (AN), azobenzene (AZO) and azoxybenzene (AZX) with high efficacy. Two widely used bismuth molybdate photocatalysts, namely Bi2MoO6 and Bi4MoO9, were studied and compared. Bi2MoO6 offers better visible-light-driven photocatalytic performance than Bi4MoO9 partly due to its narrow band gap energy and efficient charge carrier separation and transfer as evidenced from UV-vis DRS, EIS, and transient photocurrent studies. The roles of hydrazine hydrate, alcohol solvent, and KOH additive on the transfer hydrogenation of NB were examined and their concentrations were optimized to solely obtain the three different products with excellent selectivity (> 98%). Based on UV-vis DRS and Mott-Schottky analysis, the band energy level of Bi2MoO6 and plausible reactions at solid-liquid interface are proposed. The capability to control product selectivity over a single photocatalyst in one pot demonstrated in this work would make the process more practical especially for continuous flow photochemical systems.

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