Selective oxidation of aromatic alcohols to aromatic aldehydes by BN/metal sulfide with enhanced photocatalytic activity

被引:157
作者
Meng, Sugang [1 ]
Ye, Xiangju [2 ]
Ning, Xiaofeng [1 ]
Xie, Mengli [1 ]
Fu, Xianliang [1 ]
Chen, Shifu [1 ,2 ]
机构
[1] Huaibei Normal Univ, Dept Chem, Huaibei 235000, Anhui, Peoples R China
[2] Anhui Sci & Technol Univ, Dept Chem, Fengyang 233100, Anhui, Peoples R China
关键词
Selective oxidation; Aromatic alcohols; BN nanosheets; In2S3; Visible light; VISIBLE-LIGHT; TITANIUM-DIOXIDE; LOW-TEMPERATURE; BORON-NITRIDE; TIO2; WATER; SEMICONDUCTORS; NANOCOMPOSITE; PERFORMANCE; NANOSTRUCTURES;
D O I
10.1016/j.apcatb.2015.09.030
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
BN/metal sulfide composite (BN/In2S3) was prepared by a facile in situ one-pot hydrothermal method. The as-synthesized photocatalyst was characterized by X-ray powder diffraction (XRD), UV-vis diffuse reflection spectroscopy (DRS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), N-2-sorption analysis, electron spin resonance (ESR), photoluminescence emission spectra (PL) and X-ray photoelectron spectroscopy (XPS). The results show that compared with single In2S3, the BN/In2S3 photocatalyst exhibits excellent photocatalytic performance for selective oxidation of aromatic alcohols to aromatic aldehydes under visible light irradiation. The enhanced photocatalytic activity of BN/In2S3 composite is mainly attributed to the unique physicochemical properties of BN nanosheet, which acts as a promoter for photoexcited holes transfer, thereby improving the charge separation efficiency and prolonging photoexcited electrons lifetime. Effects of the type of aromatic alcohol and the added scavenger on the photocatalytic efficiency were also investigated. O-center dot(2)- radicals and photogenerated holes play decisive roles for photocatalytic oxidation of aromatic alcohols to aromatic aldehydes. This approach is versatile for constructing other high efficiency photocatalysts such as BN/CdS, BN/Cd(x)Z(1-x)S and BN/ZnIn2S4. It is hoped that this work could provide new insights to construct the BN-based composites for extensive photocatalytic applications. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:356 / 368
页数:13
相关论文
共 65 条
[1]  
ANELLI PL, 1987, J ORG CHEM, V52, P2559
[2]  
[Anonymous], 2014, Angew. Chem. Int. Ed., DOI DOI 10.1002/ange.201403611
[3]  
[Anonymous], ANGEW CHEM, DOI DOI 10.1002/ANGE.200900322
[4]   STUDY OF SUPEROXIDE RADICAL CHEMISTRY BY STOPPED-FLOW RADIOLYSIS AND RADIATION-INDUCED OXYGEN-CONSUMPTION [J].
BIELSKI, BHJ ;
RICHTER, HW .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1977, 99 (09) :3019-3023
[5]   PHOTOELECTROLYSIS AND PHYSICAL-PROPERTIES OF SEMICONDUCTING ELECTRODE WO3 [J].
BUTLER, MA .
JOURNAL OF APPLIED PHYSICS, 1977, 48 (05) :1914-1920
[6]   Photocatalysis by titanium dioxide and polyoxometalate/TiO2 cocatalysts.: Intermediates and mechanistic study [J].
Chen, CC ;
Lei, PX ;
Ji, HW ;
Ma, WH ;
Zhao, JC ;
Hidaka, H ;
Serpone, N .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2004, 38 (01) :329-337
[7]   Enhancement of photocatalytic H2 evolution on ZnIn2S4 loaded with in-situ photo-deposited MoS2 under visible light irradiation [J].
Chen, Guoping ;
Ding, Ning ;
Li, Fan ;
Fan, Yuzun ;
Luo, Yanhong ;
Li, Dongmei ;
Meng, Qingbo .
APPLIED CATALYSIS B-ENVIRONMENTAL, 2014, 160 :614-620
[8]   Low-Temperature and Template-Free Synthesis of ZnIn2S4 Microspheres [J].
Chen, Zhixin ;
Li, Danzhen ;
Zhang, Wenjuan ;
Chen, Chun ;
Li, Wenjuan ;
Sun, Meng ;
He, Yunhui ;
Fu, Xianzhi .
INORGANIC CHEMISTRY, 2008, 47 (21) :9766-9772
[9]   Low temperature synthesis of ZnIn2S4 microspheres as a visible light photocatalyst for selective oxidation [J].
Chen, Zhixin ;
Xu, Jingjing ;
Ren, Zhuyun ;
He, Yunhui ;
Xiao, Guangcan .
CATALYSIS COMMUNICATIONS, 2013, 41 :83-86
[10]   Harnessing single-active plasmonic nanostructures for enhanced photocatalysis under visible light [J].
Cheng, Hefeng ;
Fuku, Kojirou ;
Kuwahara, Yasutaka ;
Mori, Kohsuke ;
Yamashita, Hiromi .
JOURNAL OF MATERIALS CHEMISTRY A, 2015, 3 (10) :5244-5258