作者：W. Li,* X. Chu, F. Wang, Y. Dang, X. Liu, X. Wang,* C. Wang*
关键字：Simulated solar light, Hydrogen evolution reaction, Precious metal, Three-dimensional porous structure, Electron acceptor
论文来源：期刊
具体来源：https://doi.org/10.1016/j.apcatb.2021.120034
发表时间：2021年

Photocatalytic hydrogen production is regarded as an ideal strategy to solve energy issues. Graphene phase carbon nitrogen compound (g-C₃N₄) is commonly used to prepare improved photocatalysts due to its typical structural advantages. However, it generally presents low photostability of functional cocatalysts (e.g. precious metals) for simple 2D-layered structure of 2D g-C₃N₄. Herein, graphene oxide (GO) is applied to construct 3D porous g-C₃N₄/GO (p-CNG) skeleton via a thermal treatment aiding by template technique. Then, precious-metal (Au, Pd, Pt) cocatalysts were respectively immobilized to the 3D p-CNG skeleton to construct the 3D p-CNG-M (Au, Pd, Pt) composite catalysts. The typical 3D porous structure and bonding interaction between g-C₃N₄ and GO increase the specific surface area and improve the anchoring stability of cocatalysts. Meanwhile, precious-metal cocatalysts acted as the electron acceptors remarkably increase the active sites and promote the electron-hole separation. Thereby, the resultant 3D p-CNG-M composite catalysts present remarkably enhanced hydrogen evolution reaction (HER) activities under simulated solar light (SSL), and the optimal 3D p-CNG-Pt composite catalyst possesses the prominent HER activity (2565.81 μmol·g^-1·h^-1) at pH = 10.5 for the stronger cocatalyst-support interaction, which is about 136-fold greater of 3D p-CNG skeleton (18.93 μmol·g^-1·h^-1). Furthermore, its AQY is about 21.6% under illumination (λ = 420 nm). Especially, the excellent durability and reproducibility were achieved during long time photoinduction and multi-recycling. This study provides a potential strategy for enhancing the photostability and improving the SSL-induced HER performance of precious-metal modified photocatalyst.