Bismuth-rich strategy induced photocatalytic molecular oxygen activation properties of bismuth oxyhalogen: The case of Bi24O31CI10

被引:181
作者
Jin, Xiaoli [1 ]
Ye, Liqun [1 ]
Wang, Hui [2 ,3 ]
Su, Yurong [1 ]
Xie, Haiquan [1 ]
Zhong, Zhiguo [1 ]
Zhang, He [1 ]
机构
[1] Nanyang Normal Univ, Coll Chem & Pharmaceut Engn, Nanyang 473061, Peoples R China
[2] Chinese Acad Sci, CAS Key Lab Nucl Radiat & Nucl Energy Tech, Beijing 100049, Peoples R China
[3] Chinese Acad Sci, Inst High Energy Phys, Multidisciplinary Initiat Ctr, Beijing 100049, Peoples R China
基金
中国国家自然科学基金;
关键词
Bi24O31CI10; Molecular oxygen activation; Photocatalysis; Bismuth-rich strategy; VISIBLE-LIGHT IRRADIATION; SEMICONDUCTOR PHOTOCATALYSIS; BIOI/BIOCL COMPOSITES; ELECTRONIC-STRUCTURE; RHODAMINE-B; BIOX X; WATER; DEGRADATION; REDUCTION; OXIDATION;
D O I
10.1016/j.apcatb.2014.10.075
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
Molecular oxygen activation is very important for photocatalytic degradation of organic pollutants. In this paper, Bi24O31Cl10 nanosheets with {1 0 0} facets exposure were successfully synthesized by hydromel method and characterized. The size of a single nanosheet is about 5 pm in width and 10-30 nm in thickness, which results in a large ratio of surface to thickness and higher exposure ratio of {1 0 0} facets. The Mott-Schottky test revealed that the conduction band minimum (CBM) of Bi24O31Cl10 is more negative than BiOCl due to the bismuth-rich strategy. And the photocatalytic results showed that as-synthesized Bi24O31Cl10 showed higher photocatalytic properties than BiOCl for activate molecular oxygen to generate superoxide radical (O-2 center dot(-)) under visible light (lambda >420 nm) irradiation, and generate hydroxyl radical (center dot OH) under UV-vis light irradiation. This strategy in this work may potentially be extended to other bismuth-based photocatalysts for molecular oxygen activation. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:668 / 675
页数:8
相关论文
共 39 条
[1]   Novel Bi2S3-sensitized BiOCl with highly visible light photocatalytic activity for the removal of rhodamine B [J].
Cao, Jing ;
Xu, Benyan ;
Lin, Haili ;
Luo, Bangde ;
Chen, Shifu .
CATALYSIS COMMUNICATIONS, 2012, 26 :204-208
[2]   PHOTO-DECHLORINATION OF PCBS IN PRESENCE OF TITANIUM-DIOXIDE IN AQUEOUS SUSPENSIONS [J].
CAREY, JH ;
LAWRENCE, J ;
TOSINE, HM .
BULLETIN OF ENVIRONMENTAL CONTAMINATION AND TOXICOLOGY, 1976, 16 (06) :697-701
[3]  
Che G., 2013, MAT RES B, V48, P1256
[4]   Room temperature synthesis and highly enhanced visible light photocatalytic activity of porous BiOI/BiOCl composites nanoplates microflowers [J].
Dong, Fan ;
Sun, Yanjuan ;
Fu, Min ;
Wu, Zhongbiao ;
Lee, S. C. .
JOURNAL OF HAZARDOUS MATERIALS, 2012, 219 :26-34
[5]  
Fan Y., 2011, ENVIRON SCI TECHNOL, V45, P1593
[6]   Exploring the Reactivity of Multicomponent Photocatalysts: Insight into the Complex Valence Band of BiOBr [J].
Fang, Yan-Fen ;
Ma, Wan-Hong ;
Huang, Ying-Ping ;
Cheng, Gen-Wei .
CHEMISTRY-A EUROPEAN JOURNAL, 2013, 19 (09) :3224-3229
[7]   Synthesis of mesoporous BiOBr 3D microspheres and their photodecomposition for toluene [J].
Feng, Yinchang ;
Li, Lei ;
Li, Junwei ;
Wang, Junfeng ;
Liu, Lu .
JOURNAL OF HAZARDOUS MATERIALS, 2011, 192 (02) :538-544
[8]   Visible-light-induced degradation of rhodamine B by nanosized Bi2WO6 [J].
Fu, HB ;
Pan, CS ;
Yao, WQ ;
Zhu, YF .
JOURNAL OF PHYSICAL CHEMISTRY B, 2005, 109 (47) :22432-22439
[9]   Adsorption and degradation performance of Rhodamine B over BiOBr under monochromatic 532 nm pulsed laser exposure [J].
Gondal, Mohammed Ashraf ;
Chang, Xiaofeng ;
Ali, Mohammad Ashraf ;
Yamani, Zain Hassan ;
Zhou, Qin ;
Ji, Guangbin .
APPLIED CATALYSIS A-GENERAL, 2011, 397 (1-2) :192-200
[10]   Chemistry and applications of photocatalytic oxidation of thin organic films [J].
Heller, A .
ACCOUNTS OF CHEMICAL RESEARCH, 1995, 28 (12) :503-508