In-situ hydrothermal synthesis of Ag3PO4/g-C3N4 composite and their photocatalytic decomposition of NOx

被引:37
作者
Zhao, Zhihuan [1 ,2 ]
Fan, Jimin [1 ,2 ]
Liu, Wenhui [1 ]
Xue, Yongqiang [1 ]
Yin, Shu [1 ,2 ]
机构
[1] Taiyuan Univ Technol, Coll Chem & Chem Engn, Taiyuan 030024, Shanxi, Peoples R China
[2] Tohoku Univ, Inst Multidisciplinary Res Adv Mat, Aoba Ku, 2-1-1 Katahira, Sendai, Miyagi 9808577, Japan
基金
中国国家自然科学基金;
关键词
In-situ solvothermal method; Composite Ag3PO4/g-C3N4; Decomposition NOx; Heterojunction; GRAPHITIC CARBON NITRIDE; VISIBLE-LIGHT IRRADIATION; OXYGEN REDUCTION REACTION; G-C3N4; MATERIAL; TIO2; AG3PO4; ELECTROCATALYSTS; NANOPARTICLES; MICROCRYSTALS; PERFORMANCES;
D O I
10.1016/j.jallcom.2016.12.001
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
Ag3PO4 and Ag3PO4/g-C3N4 were successfully synthesized by an in-situ solvothermal method using graphitic carbon nitride obtained by sectional heating of guanidine carbonate and AgNO3 as starting materials. The composites were characterized by XRD, SEM, PL, DRS and BET. The photocatalytic performance was determined by deNOx reaction under different light wavelength irradiation. Ag3PO4/gC(3)N(4) composites with different ratio showed different band gap and morphology, and also decreased the photo-corrosion and self-corrosion by forming heterojunction. The photocatalytic deNOx ability of Ag3PO4/20% g-C3N4 was 15.52% under irradiation of visible light (>400 nm) and could be enhanced to 41.76% under irradiation of 290 nm. With the increment of the g-C3N4 content, high efficiency of charge separation induced by the formation of heterojunction between Ag3PO4 and g-C3N4. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:2812 / 2819
页数:8
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