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N?N bond cleavage of azobenzene via photocatalytic hydrogenation with Dy-doped Zn(O,S): the progress from hydrogen evolution to green chemical conversion
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Kuo, Dong-Hau
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Natl Taiwan Univ Sci & Technol, Dept Mat Sci & Engn, 43,Sec 4,Keelung Rd, Taipei 10607, Taiwan Natl Taiwan Univ Sci & Technol, Dept Mat Sci & Engn, 43,Sec 4,Keelung Rd, Taipei 10607, Taiwan

Gultom, Noto Susanto
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Natl Taiwan Univ Sci & Technol, Dept Mat Sci & Engn, 43,Sec 4,Keelung Rd, Taipei 10607, Taiwan Natl Taiwan Univ Sci & Technol, Dept Mat Sci & Engn, 43,Sec 4,Keelung Rd, Taipei 10607, Taiwan
机构:
[1] Natl Taiwan Univ Sci & Technol, Dept Mat Sci & Engn, 43,Sec 4,Keelung Rd, Taipei 10607, Taiwan
关键词:
CHEMOSELECTIVE HYDROGENATION;
NI-B;
NITROBENZENE;
REDUCTION;
GOLD;
CATALYSTS;
ANILINE;
D O I:
10.1039/c9cy00502a
中图分类号:
O64 [物理化学(理论化学)、化学物理学];
学科分类号:
070304 ;
081704 ;
摘要:
Hydrogen-evolved Dy-doped Zn(O,S) photocatalysts with different amounts of Dy precursor have been synthesized, characterized and further utilized for hydrogenation reactions. The Dy catalysts are first examined using electrochemical impedance spectroscopy, photo responsivity, and the hydrogen evolution reaction. Dy-doped Zn(O,S) with 10% Dy precursor shows the best photocatalyst performance with the highest H-2 production rate of 8.160 mmol g(-1) h(-1). This catalyst is chosen for conducting the hydrogenation reaction. It is our intention to confirm the correlation between the photocatalytic H-2 production rate and the hydrogenation reactions of 4-nitrophenol to 4-aminophenol and azobenzene to aniline, which is a step further in the hydrogenation reaction to challenge the N?N bond cleavage of azobenzene. A 100% photo conversion of 60 ppm azobenzene to aniline in 6 h was confirmed under a low-power UV light illumination in a 10% ethanol solution. Kinetic steps and kinetic mechanisms are proposed, which involve the important reaction steps of solvation, adsorption, pinning, and surface hydrogenation reaction operating together.
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页码:2651 / 2663
页数:13
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