双金属片
光电流
三元运算
光催化
异质结
纳米棒
材料科学
半导体
分解水
电子转移
硫化锌
制氢
氢
化学工程
纳米技术
计算机科学
化学
光化学
催化作用
光电子学
锌
冶金
工程类
有机化学
程序设计语言
生物化学
金属
作者
Yendrapati Taraka Prabhu,Sai Prasad Ega,B. Moses Abraham,Ujjwal Pal
标识
DOI:10.1016/j.ijhydene.2022.07.233
摘要
Bimetallic semiconductor metal sulphides are promising for harnessing light energy. In this report, a hydrothermally decorated robust ZnO/ZnS/NiS (ZSN) ternary composite was synthesized and employed in photocatalytic H 2 generation. The structurally defined ZnS/NiS on ZnO nanorods have been observed as efficient visible light driven proton reduction system due to its multiple accessible active sites. Benefitting from the synergetic effects between highly active, ZnS and NiS, the ternary composite ZSN exhibited significantly improved performance of H 2 generation with a rate of 8471 μmol g −1 h −1 and AQE of ∼5.5% under solar irradiation. This design in ZSN enables effective transfer of electrons from ZnS to NiS active sites leading to 29 times and 3.4 times increase in hydrogen production and current density when compared with pristine ZnO photocatalyst, respectively. The photocurrent density and transient photocurrent curve show rapid charge transfer as well as the unique electron transfer paths through the contact surface, resulting in efficient charge separation. DFT and photoelectrochemical studies reveal higher HER activity due to the augmented electric field at the dual-interfaces between NiS and ZS complex. • Hydrothermally decorated ternary ZnO/ZnS/NiS photocatalyst. • Bimetallic Sulfides (ZnS/NiS) improved the efficient charge transfer. • High current density of 0.58 mA/cm 2 and fast charge separation occurs in ternary system. • DFT and experimental data corroborates the superior activity of reported catalyst. • High H 2 evolution with a rate 8471 μmol g −1 h −1 and AQY of ∼5.5%.
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