Enhanced visible-light-driven photocatalytic performance of porous graphitic carbon nitride

被引:50
作者
Chang, Fei [1 ]
Li, Chenlu [1 ]
Luo, Jieru [1 ]
Xie, Yunchao [1 ]
Deng, Baoqing [1 ]
Hu, Xuefeng [2 ]
机构
[1] Univ Shanghai Sci & Technol, Sch Environm & Architecture, Shanghai 200093, Peoples R China
[2] Chinese Acad Sci, Yantai Inst Coastal Zone Res, Key Lab Coastal Environm Proc & Ecol Remediat, Yantai 264003, Shandong, Peoples R China
基金
中国国家自然科学基金;
关键词
Porousg-C3N4; Nitric acid; Photocatalysis; Rhodamine B; Mechanisma; TEMPLATE-FREE SYNTHESIS; HYDROGEN EVOLUTION; QUANTUM DOTS; DOPED G-C3N4; WATER; DEGRADATION; NANOSHEETS; SEMICONDUCTOR; FABRICATION; GENERATION;
D O I
10.1016/j.apsusc.2015.08.124
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
In this study, a series of porous graphitic carbon nitride (g-C3N4) materials were fabricated through a direct pyrolysis of protonated melamine by nitric acid solution. These as-prepared porous samples were characterized by a collection of analytical techniques. It was found that a proper concentration of nitric acid solution involved facilitated to generate samples in tube-like morphology with numerous pores, identified with X-ray diffraction patterns, FT-IR spectra, SEM, TEM, and BET measurements. These g-C3N4 samples were subjected to photocatalytic degradation of dye Rhodamine B (RhB) in aqueous under visible-light irradiation. Under identical conditions, those porous g-C3N4 samples showed significantly improved catalytic performance in comparison with the sample prepared without the introduction of nitric acid. In particularly, the best candidate, sample M1:1, showed an apparent reaction rate nearly 6.2 times that of the unmodified counterpart. The enhancement of photocatalytic performance could be attributed to the favorable porous structure with the enlarged specific surface area and the suitable electronic structure as well. In addition, ESR measurements were conducted for the sake of proposing a photocatalytic degradation mechanism. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:270 / 277
页数:8
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