Visible-light-induced hydrogenation of biomass-based aldehydes by graphitic carbon nitride supported metal catalysts

被引:29
|
作者
Dong, Shenghong [1 ,2 ]
Chen, Mingzhe [1 ,2 ]
Zhang, Jiarui [1 ,2 ]
Chen, Jinzhu [2 ,3 ]
Xu, Yisheng [1 ]
机构
[1] East China Univ Sci & Technol, State Key Lab Chem Engn, 130 Meilong Rd, Shanghai 200237, Peoples R China
[2] Jinan Univ, Coll Chem & Mat Sci, Dept Chem, 855 East Xingye Ave, Guangzhou 511443, Peoples R China
[3] Zhejiang Univ, Dept Chem & Biol Engn, Minist Educ, Key Lab Biomass Chem Engn, 38 Zheda Rd, Hangzhou 310027, Peoples R China
基金
中国国家自然科学基金;
关键词
Biomass; Graphitic carbon nitride; Green chemistry; Hydrogenation; Photocatalysis; SELECTIVE HYDROGENATION; FURFURYL ALCOHOL; DOPED G-C3N4; PHOTOCATALYTIC ACTIVITY; ORGANIC FRAMEWORK; EFFICIENT; CONVERSION; CU; PHOTODEGRADATION; NANOCOMPOSITES;
D O I
10.1016/j.gee.2020.07.004
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
The plasmonic photocatalyst of Pd supported on graphitic carbon nitride (Pd/g-C3N4) exhibits excellent catalytic activity in photo-induced hydrogenation of biomass-based aldehydes with environmental benign reagents of formic acid (HCOOH) as proton source and triethylamine (TEA) as sacrificial electron donator. The chemical and configurational properties of the Pd/g-C3N4 were systematically analyzed with XRD, TEM and XPS. Under optimized conditions, 27% yield of furfuryl alcohol with the corresponding turnover frequency (TOF) around 3.72 h(-1) were obtained from furfural and TEA-HCOOH under visible-light irradiation by using Pd/g-C3N4. Our research additionally reveals that Pd atom is the true catalytic active site for the hydrogenation and the photo-promoted reduction mainly occurs through noble metal nanoparticles (NPs)-induced effect of surface plasmon resonance (SPR). The photo-catalytic system of Pd/g-C3N4 thus demonstrates a green and effective method for the hydrogenation of biomass-based aldehydes with sustainable solar energy as a driven force. (C) 2020, Institute of Process Engineering, Chinese Academy of Sciences. Publishing services by Elsevier B.V. on behalf of KeAi Communications Co., Ltd.
引用
收藏
页码:715 / 724
页数:10
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