光催化
异质结
材料科学
氮化碳
量子点
纳米技术
石墨氮化碳
半导体
聚合物
碳纤维
氮化物
化学工程
复合数
光电子学
化学
催化作用
复合材料
图层(电子)
生物化学
工程类
作者
Dandan Zheng,Guigang Zhang,Xinchen Wang
标识
DOI:10.1016/j.apcatb.2015.05.060
摘要
Inorganic quantum dots (QDs) have been introduced onto the exterior surface of hollow carbon nitride spheres (HCNS) to construct an inorganic-polymeric curved heterostructure for solar energy conversion. This hybrid nanoheterostructure cooperates well with cofactors to achieve efficient hydrogen evolution under visible light illumination. The enhanced photocatalytic performance of the heterostructure can be attributed to the unique three-dimensional (3D) hollow architectural framework of HCNS as a polymeric scaffold to form intimate interfacial contact with the QDs by a self-assembly strategy to facilitate surface kinetics of charge separation and mass transfer. Such inorganic-polymer hybrid nanoarchitectures based on controlled deposition of stiff QDs onto the flexible HCNS surface provide a valuable platform for constructing stable photoredox systems for solar-to-chemical conversion. This result promises the great potentials of biostructurally-mimic hollow soft semiconductors in developing photofunctional architectures, with an ample choice of secondary guest species to selectively engineer the interface physicochemistry of the hollow sphere for solar application.
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