g-C3N4/Bi4O5I2 heterojunction with I3-/I- redox mediator for enhanced photocatalytic CO2 conversion

被引:260
作者
Bai, Yang [1 ]
Ye, Liqun [1 ,2 ]
Wang, Li [2 ]
Shi, Xian [1 ]
Wang, Pingquan [1 ]
Bai, Wei [1 ,3 ]
Wong, Po Keung [4 ]
机构
[1] Southwest Petr Univ, Sch Oil & Nat Gas Engn, Chengdu 610500, Peoples R China
[2] Nanyang Normal Univ, Coll Chem & Pharmaceut Engn, Key Lab Ecol Secur Water Source Reg Midline Proje, Nanyang 473061, Peoples R China
[3] Chinese Acad Sci, Chengdu Inst Organ Chem, Chengdu 610041, Peoples R China
[4] Chinese Univ Hong Kong, Sch Life Sci, Shatin, Hong Kong, Peoples R China
基金
中国国家自然科学基金;
关键词
g-C3N4; Bi4O5I2; I-3(-)/I-; Photocatalysis; CO2; conversion; VISIBLE-LIGHT IRRADIATION; Z-SCHEME; BIOX X; ELECTRONIC-STRUCTURES; I PHOTOCATALYSTS; HYDROGEN GENERATION; BISMUTH OXYBROMIDE; DFT CALCULATIONS; KYOTO PROTOCOL; WATER;
D O I
10.1016/j.apcatb.2016.04.052
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
Heterojunction is an effectively construction to improve the photocatalytic activity due to the excellent photo-induced carrier separation efficiency. In this paper, g-C3N4/Bi4O5I2 heterojunction was prepared and characterized by X-ray diffraction patterns (XRD), field emission scanning electron microscope (FESEM), transmission electron microscopy (TEM), UV-vis diffuse reflectance spectra (DRS) and X-ray photoelectron spectroscopy (XPS). The photocatalytic data showed that g-C3N4/Bi4O5I2 heterojunction had higher activity than pure g-C3N4 and Bi4O5I2. At an optimal ratio of 1.0 mol% (11.4 wt% of Bi4O5I2), g-C3N4/Bi4O5I2 photocatalyst showed the highest photocatalytic reduction activity for CO2 conversion with 45.6 mu mol h(-1) g(-1) CO generation. Photocurrent and electrochemical impedance (EIS) spectroscopy revealed that higher photo-induced carrier separation efficiency of g-C3N4/Bi4O5I2. Z-scheme charge transfer mode was proved by redox mediator existence and superoxide radical (O-2(center dot-)) and hydroxyl radical ((OH)-O-center dot) quantification experiments. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:98 / 104
页数:7
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