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-C 3 N 4 and NiS using a facile precipitation method. The results demonstrated that nanocarbons played trifunctional roles in boosting the photocatalytic H 2 evolution over g-C 3 N 4, 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-C 3 N 4, thus facilitating the fast oxidation of triethanolamine and charge-carrier separation. Particularly, in all five ternary multiheterostructured systems, the g-C 3 N 4 -0.5%CB-1.0%NiS (weight ratio) and g-C 3 N 4 -0.5%AB-1.0%NiS photocatalysts exhibited the highest H 2 -evolution rates of 366.4 and 297.7 μmol g –1 h –1, which are 3.17 and 2.57 times higher than that of g-C 3 N 4 -1.0%NiS, respectively. Apparently, the significantly enhanced H 2 -evolution activity of multiheterostructured g-C 3 N 4 /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-C 3 N 4 and NiS co-catalysts for maximizing the H 2 generation. This work may give a new mechanistic insight into the development of multiheterostructured g-C 3 N 4 -based composite photocatalysts using the combination of trifunctional nanocarbon bridges and earth-abundant co-catalysts/semiconductors for various photocatalytic applications.
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Wen et al. (2017) studied this question.
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