Rapid and template-free synthesis of copper(I) oxide-graphitic carbon nitride heterojunction for photocatalytic degradation of orange II dye in water

被引:18
|
作者
Koiki, Babatunde A. [1 ,3 ]
Orimolade, Benjamin O. [1 ,3 ]
Peleyeju, Gbenga M. [1 ,3 ]
Arotiba, Omotayo A. [1 ,2 ,3 ]
机构
[1] Univ Johannesburg, Dept Chem Sci, Johannesburg, South Africa
[2] Univ Johannesburg, Ctr Nanomat Sci Res, Johannesburg, South Africa
[3] Univ Johannesburg, Dept Appl Chem, Johannesburg, South Africa
基金
新加坡国家研究基金会;
关键词
Copper(I) oxide; Graphitic carbon nitride; Heterojunction photocatalyst; Photocatalytic degradation; Orange II dye; IN-SITU PREPARATION; PERFORMANCE; MECHANISMS; COMPOSITE; OXIDATION; SHELL;
D O I
10.1016/j.solidstatesciences.2019.105994
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Herein, we report the synthesis of a p-n heterojunction catalyst comprising Cu2O and g-C3N4 via a novel rapid, template-free and facile one-pot approach. The pristine semiconductors and their composite were characterised by X-ray diffraction (XRD), N-2 adsorption-desorption isotherms (BET), UV-vis diffuse reflectance spectroscopy, transmission electron microscopy (TEM), field emission scanning electronic microscopy (FESEM) and energy dispersive X-ray spectrometry (EDX). From the Mott-schottky plot, the flat-band potential and carrier density were estimated. Band gap energies of 2.03 and 2.65 eV were calculated for Cu2O and g-C3N4 respectively, which indicate that both catalysts possess excellent optical absorption in the visible region of the solar spectrum. The pn heterojunction produced a type-II band alignment which promotes the efficient separation of photogenerated electron-hole pairs. The photocatalytic property of the material was evaluated by employing it for the degradation of orange II dye in water. Different mass ratios of Cu2O-g-C3N4 such as 1:1, 3:2, 7:3 and 9:1 were employed in the degradation process. However, Cu2O-g-C3N4 with mass ratio 9:1 displayed the best photocatalytic performance, giving a removal efficiency that is 3.6 times higher than the pristine Cu2O. The decolourisation and mineralisation efficiencies were 85% and 60% after 4 h of treatment. Scavenger studies further revealed the photogenerated holes as the main oxidant species in the photocatalytic reaction.
引用
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页数:8
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