Evidence for an Interface of Hybrid Cocatalysts Favoring Photocatalytic Hydrogen Evolution Kinetics
Yingpeng Xie, Junhua Chang, Peng Zheng, Lili Zhang, Tengfeng Xie, Renzheng Jiang, Zhanguo Zhang, Yongqiang Yang, Mengke Zou, Lichang Yin, Chao Zhen, Fei Han, Kaikai Ba, Guangwen Xu
Abstract
Hybrid cocatalysts have great application potential for improving the photocatalytic hydrogen evolution performance of semiconductors. The interfaces between components of hybrid cocatalysts make a great contribution to the improvement, but the associated mechanisms remain unclear. Herein, we prepared and tested three comparative CdS-based photocatalysts with NiS, NiS/Ni 9 S 8, and Ni 9 S 8 as the cocatalysts separately. The emphasis is placed on investigating the effect of the NiS/Ni 9 S 8 interfaces on the photocatalytic hydrogen evolution performance of CdS. NiS/Ni 9 S 8 exhibits a higher ability than NiS and Ni 9 S 8 in making CdS a more active photocatalyst for water splitting. It shows that NiS, NiS/Ni 9 S 8, and Ni 9 S 8 perform similarly in terms of promoting the charge transfer and separation of CdS based on steady-state and time-resolved photoluminescence studies. At the same time, the linear sweep voltammetry and electrochemical impedance spectroscopy tests combined with the density functional theory calculations reveal that the component interfaces of NiS/Ni 9 S 8 enable us to lower the water splitting activation energy, the charge-transfer resistance from the cocatalyst to sacrificial agent, and hydrogen adsorption Gibbs free energy. It is evidenced from this work that component interfaces of hybrid cocatalysts play a vital role in accelerating the dynamics of hydrogen evolution reactions.