Abstract
We have demonstrated a two-step wet chemical approach for synthesizing ternary Ag/Ag(2)S/CdS heterostructures for efficient photocatalytic hydrogen evolution. The CdS precursor concentrations and reaction temperatures are crucial in determining the efficiency of photocatalytic water splitting under visible light excitation. In addition, the effect of operational parameters (such as the pH value, sacrificial reagents, reusability, water bases, and light sources) on the photocatalytic hydrogen production of Ag/Ag(2)S/CdS heterostructures was investigated. As a result, Ag/Ag(2)S/CdS heterostructures exhibited a 3.1-fold enhancement in photocatalytic activities compared to bare CdS nanoparticles. Furthermore, the combination of Ag, Ag(2)S, and CdS can significantly enhance light absorption and facilitate the separation and transport of photogenerated carriers through the surface plasma resonance (SPR) effect. Furthermore, the Ag/Ag(2)S/CdS heterostructures in seawater exhibited a pH value approximately 2.09 times higher than in de-ionized water without an adjusted pH value under visible light excitation. The ternary Ag/Ag(2)S/CdS heterostructures provide new potential for designing efficient and stable photocatalysts for photocatalytic hydrogen evolution.