光催化
异质结
可见光谱
材料科学
固态
氢
催化作用
光电子学
光化学
化学
物理
物理化学
量子力学
生物化学
作者
Bifang Li,Wenjing Wang,Jiwu Zhao,Zhaoyu Wang,Bo Su,Yidong Hou,Zhengxin Ding,Wee‐Jun Ong,Sibo Wang
摘要
The construction of NiTiO3/Cd0.5Zn0.5S heterostructures is presented as all-solid-state direct Z-scheme photocatalysts for the efficient and stable hydrogen production under visible light. The NiTiO3/Cd0.5Zn0.5S hybrids are assembled by growing Cd0.5Zn0.5S nanoparticles on the surface of NiTiO3 nanorods via a co-precipitation and hydrothermal coupled method. The compositional and structural features of the NiTiO3/Cd0.5Zn0.5S composites are fully disclosed via diverse physicochemical characterizations. The NiTiO3/Cd0.5Zn0.5S heterostructures are revealed to effectively capture the optical spectrum in the visible region as well as enhance the transfer and separation of photogenerated charge carriers through the Z-schematic pathway. Consequently, the optimized NiTiO3/Cd0.5Zn0.5S photocatalyst shows a high H2 production rate of 1058 μmol h−1 (26.45 mmol h−1 g−1), which is independent of any cocatalysts (such as Pt), together with a high apparent quantum yield (AQY) of 34% under monochromatic light irradiation at 420 nm. Besides, the NiTiO3/Cd0.5Zn0.5S composites also exhibit a high stability for the H2 evolution photocatalysis mainly due to the fact that the Z-schematic charge separation and migration can enable the efficient consumption of light-induced holes of Cd0.5Zn0.5S to prevent the photocorrosion effect. Finally, a possible photocatalytic H2 evolution mechanism over the Z-schematic NiTiO3/Cd0.5Zn0.5S heterostructures is also presented based on the results of the band structures, density functional theory (DFT) calculations and electron spin resonance (ESR) tests.
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