Novel visible light induced Co3O4-g-C3N4 heterojunction photocatalysts for efficient degradation of methyl orange

被引:372
作者
Han, Changcun [1 ,2 ]
Ge, Lei [1 ,2 ]
Chen, Changfeng [2 ]
Li, Yujing [2 ]
Xiao, Xinlai [2 ]
Zhang, Yuanna [2 ]
Guo, Lele [2 ]
机构
[1] China Univ Petr Being, Coll Sci, Key Lab Heavy Oil Proc, Beijing 102249, Peoples R China
[2] China Univ Petr Being, Coll Sci, Dept Mat Sci & Engn, Beijing 102249, Peoples R China
来源
APPLIED CATALYSIS B-ENVIRONMENTAL | 2014年 / 147卷
基金
美国国家科学基金会;
关键词
Graphitic carbon nitride; Cobalt oxides; Photocatalysis; Heterojunction photocatalysts; IN-SITU SYNTHESIS; HYDROGEN EVOLUTION; COMPOSITE PHOTOCATALYSTS; G-C3N4; PERFORMANCE; WATER; PHOTODEGRADATION; IRRADIATION; GRAPHENE; ARRAY;
D O I
10.1016/j.apcatb.2013.09.038
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070305 [高分子化学与物理];
摘要
Novel visible-light-induced Co3O4-g-C3N4 heterojunction photocatalysts were synthesized via a facile mixing-and-heating method. The as-prepared samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), ultraviolet-visible diffuse reflection spectroscopy (DRS), electron spin resonance (ESR) and photoluminescence spectroscopy (PL). The heterojunction photocatalysts exhibit a significantly enhanced photocatalytic activity in degrading methyl orange (MO). The optimal Co3O4 content with the highest photocatalytic activity was determined to be 0.2 wt%. The synergetic effect between Co3O4 and g-C3N4 plays an important role in promoting photo-generated carrier separation. The ESR and PL results reveals that the enhanced photocatalytic activity of Co3O4-g-C3N4 was mainly due to the superior amount and longer lifetime of oxidative radicals (O-.(2)-), as well as the efficient separation of charge carriers. Possible mechanism is proposed for the high photocatalytic activity of heterojunction structures, to guide the design of photocatalysts. (C) 2013 Elsevier B.V. All rights reserved.
引用
收藏
页码:546 / 553
页数:8
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