Fabricating the Robust g-C3N4 Nanosheets/Carbons/NiS Multiple Heterojunctions for Enhanced Photocatalytic H2 Generation: An Insight into the Trifunctional Roles of Nanocarbons

被引:233
作者
Wen, Jiuqing [1 ,2 ,3 ]
Xie, Jun [1 ,2 ,3 ]
Yang, Zhuohong [1 ,3 ]
Shen, Rongchen [1 ,2 ,3 ]
Li, Huiyi [1 ,2 ,3 ]
Luo, XingYi [1 ,3 ]
Chen, Xiaobo [4 ]
Li, Xin [1 ,2 ,3 ]
机构
[1] South China Agr Univ, Coll Mat & Energy, Guangzhou 510642, Peoples R China
[2] South China Agr Univ, Coll Forestry & Landscape Architecture, Guangzhou 510642, Peoples R China
[3] South China Agr Univ, Inst New Energy & New Mat, Key Lab Biomass Energy Guangdong Regular Higher E, Key Lab Energy Plants Resource & Utilizat,Minist, Guangzhou 510642, Peoples R China
[4] Univ Missouri, Dept Chem, Kansas City, MO 64110 USA
基金
中国国家自然科学基金;
关键词
Photocatalytic hydrogen evolution; NiS co-catalysts; g-C3N4; Trifunctional nanocarbons; Graphene; GRAPHITIC CARBON NITRIDE; GRAPHENE-BASED PHOTOCATALYSTS; HYDROGEN-EVOLUTION; WATER; REDUCTION; COMPOSITE; SEMICONDUCTOR; COCATALYST; TIO2; CO2;
D O I
10.1021/acssuschemeng.6b02490
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
In this work, robust nanocarbons, including graphite (G), carbon nanotube (CNT), reduced graphene oxide (rGO), carbon black (CB), and acetylene black (AB), have been successfully coupled into the interfaces between g-C3N4 and NiS using a facile precipitation method. The results demonstrated that nanocarbons played trifunctional roles in boosting the photocatalytic H-2 evolution over g-C3N4, which can not only act as effective H-2-evolution co-catalysts but can also serve as conductive electron bridges to collect photogenerated electrons and boost the H-2-evolution kinetics over the NiS co-catalysts. More interestingly, the nanocarbons can also result in the downshift of valence band of g-C3N4, thus facilitating the fast oxidation of triethanolamine and charge-carrier separation. Particularly, in all five ternary multiheterostructured systems, the g-C3N4-0.5%CB-1.0% NiS (weight ratio) and g-C3N4-0.5%AB-1.0%NiS photocatalysts exhibited the highest H-2-evolution rates of 366.4 and 297.7 mu mol g(-1) h(-1), which are 3.17 and 2.57 times higher than that of g-C3N4-1.0%NiS, respectively. Apparently, the significantly enhanced H-2-evolution activity of multiheterostructured g-C3N4/carbon/NiS composite photocatalysts can be mainly ascribed to the trifunctional nanocarbons, which serve as the conductive electron bridges rather than the general co-catalysts. More importantly, it is revealed that the amorphous carbons with higher electrical conductivity and weaker electrocatalytic H-2-evolution activity are more suitable interfacial bridges between g-C3N4 and NiS co-catalysts for maximizing the H-2 generation. This work may give a new mechanistic insight into the development of multiheterostructured g-C3N4-based composite photocatalysts using the combination of trifunctional nanocarbon bridges and earth-abundant co-catalysts/semiconductors for various photocatalytic applications.
引用
收藏
页码:2224 / 2236
页数:13
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