Abstract
The use of low-cost photocatalysts to split water into H(2) fuel via solar energy is highly desirable for the production of clean energy and a sustainable society. Here three-dimensional graphene oxide (3DG) porous materials were prepared by cross-linking graphene oxide (GO) sheets using aromatic diamines (benzidine, 2,2'-dimethyl-4,4'-biphenyldiamine, 4,4'-diaminodiphenylmethane) that reacted with the carboxyl groups of the GO sheets at room temperature. The prepared 3DG porous materials were used as efficient metal-free photocatalysts for the production of H(2) via water splitting under full-spectrum light, where the photocatalytic activity was highly dependent on the cross-linker and the 3DG reduction level. It was also found that the 3DG prepared with benzidine as the linker demonstrated a significantly higher H(2) evolution rate than the 3DGs prepared using 2,2'-dimethyl-4,4'-biphenyldiamine and 4,4'-diaminodiphenylmethane as the cross-linkers. The photoactivity was further tuned by varying the mass ratio of GO to benzidine. Among the prepared 3DG materials, 3DG-3, with an intermediate C/O ratio of 1.84, exhibited the highest H(2) production rate (690 μmol g(-1) h(-1)), which was significantly higher than the two-dimensional GO (45 μmol g(-1) h(-1)) and the noncovalent 3DG synthesized by a hydrothermal method (128 μmol g(-1) h(-1)). Moreover, this study revealed that the 3DG photocatalytic performance was favored by effective charge separation, while it could be further tuned by changing the reduction level. In addition, these results could prompt the preparation of other 3D materials and the application of new types of photocatalysts for H(2) evolution.