异质结
光催化
苄胺
材料科学
高分辨率透射电子显微镜
纳米晶材料
电子转移
吸收(声学)
光化学
相(物质)
光电子学
纳米技术
化学
催化作用
透射电子显微镜
复合材料
药物化学
有机化学
生物化学
作者
Yicong Wang,Jun Zhou,Xuqiang Hao,Ying Wang,Zhigang Zou
标识
DOI:10.1016/j.apsusc.2018.06.181
摘要
Constructing Z-scheme system is a promising way to fabricate efficient photocatalysts for solar light utilization. In this study, a novel all-solid direct Z-scheme photocatalyst PTCDA-C3N4 was synthesized and characterized by several methods. XRD and HRTEM confirmed the strong π-π interaction between PTCDA(Perylene-3,4,9,10-tetracarboxylic dianhydride) and g-C3N4 induced the crystal transformation of PTCDA from β-phase to α-phase, self-assembling and reconstructing into nanocrystalline of 5 nm. UV–vis and photoelectronic measurements illustrated that the coupling of PTCDA on g-C3N4 not only dramatically broadened visible light absorption, but also accelerated the charge transfer of g-C3N4. Both the theoretical calculation and active species trapping experiments verified the Z-scheme mechanism of PTCDA-C3N4 heterostructure, which endows the hole of PTCDA-C3N4 much strong oxidizability and effective electron-hole separation, thus eight times higher activity than that of pristine g-C3N4 for benzylamine oxidation under solar driven. Our current work paves a facile way for synthesis efficient Z-scheme photocatalysts.
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