Preparation of a shell nanostructure for highly selective photocatalytic oxidation of organic compounds by wrapping on NiO nanorods exposed {110} facets with ultrathin g-C3N4 nanosheets

被引:23
作者
Liang, Zhi-Yu [1 ,2 ,3 ]
Huang, Ren-Kun [1 ,2 ]
Liang, Ruo-Wen [1 ,2 ]
Chen, Feng [1 ,2 ]
Yu, Yan [4 ]
Yan, Gui-Yang [1 ,2 ,3 ]
机构
[1] Ningde Normal Univ, Coll Chem & Mat, Fujian Prov Key Lab Featured Mat Biochem Ind, Ningde 352100, Fujian, Peoples R China
[2] Ningde Normal Univ, Coll Chem & Mat, Key Lab Green Energy & Environm Catalysis, Fujian Prov Univ, Ningde 352100, Fujian, Peoples R China
[3] Ningde Normal Univ, Fujian Prov Key Lab Toxicol, Ningde 352100, Fujian, Peoples R China
[4] Fuzhou Univ, Fujian Prov Key Lab Ecomat Adv Technol, Fuzhou 350108, Fujian, Peoples R China
基金
中国国家自然科学基金;
关键词
Reactive facets; G-C3N4; nanosheets; NiO nanorods; Photocatalytic oxidation; FACILE SYNTHESIS; PERFORMANCE; CARBON; DRIVEN; WATER; COMPOSITE; SINGLE; HETEROJUNCTION; NANOCOMPOSITE; CONSTRUCTION;
D O I
10.1016/j.apsusc.2019.04.105
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Semiconductor building blocks of varying dimensionality have been used to prepare multifunctional heterostructural photocatalysts that can efficiently separate photo-generated carriers to enhance photocatalytic activity, while exposing the desired reactive facets of the semiconductor via structure engineering remains a fascinating strategy. In this work, ultrathin graphitic-carbon nitride (g-C3N4) nanosheets (NSs) and NiO nanorods (NRs) with exposed {110} facets were utilized as assembly units to strategically construct well-defined g-C3N4@NiO heterostructure via a facile self-assembly, and g-C3N4 NSs were uniformly and intimately enwrapped on the NiO NRs. This shell nanostructure possessed remarkably high photocatalytic activity in the oxidation of organic compounds and in photoelectrochemical reactions. The underlying reasons accounting for the considerably improved photocatalytic oxidation performances of g-C3N4@NiO heterostructure were examined, which resulted from the more efficient charge separation/transfer thanks to the peculiar structural merits of g-C3N4 NSs and NiO NRs, as well as from the intimate interfacial contact and unique spatial integration mode between them. The predominant active species in the photocatalytic oxidation were determined unambiguously, which enabled to elucidate the mechanism of the photocatalytic oxidation.
引用
收藏
页码:424 / 432
页数:9
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