Heterojunction composites of covalent organic frameworks grown on the surface of persistent luminescent nanoparticles for photocatalytic hydrogen evolution and degradation of organic pollutants

被引:1
作者
Li, Boyuan [1 ,2 ]
Abulimiti, Abuduaini [1 ]
Tuerdi, Ailijiang [1 ]
Yan, Peng [1 ]
He, Fenggui [1 ,2 ]
Zhou, Jie [1 ]
Long, Gang [1 ]
Zhang, Minghui [2 ]
Abdukayum, Abdukader [1 ]
机构
[1] Kashi Univ, Coll Chem & Environm Sci, Xinjiang Key Lab Novel Funct Mat Chem, Kashi 844000, Peoples R China
[2] Nankai Univ, Coll Chem, Key Lab Adv Energy Mat Chem, Minist Educ, Tianjin 300071, Peoples R China
基金
中国国家自然科学基金;
关键词
Persistent luminescent nanoparticles; Covalent organic frameworks; Core-shell structure; Heterostructure photocatalyst; Round-the-clock photocatalysis; CRYSTALLINE; ZN2GEO4MN2+; REDUCTION; CATALYSTS; ENERGY;
D O I
10.1016/j.colsurfa.2024.134792
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
Covalent organic frameworks (COFs) have shown great promise for photocatalytic hydrogen evolution from water and photocatalytic degradation of organic pollutants. However, a single COFs suffers from poor photogenerated charge separation efficiency. In this study, we synthesized persistent luminescent nanoparticles (PLNPs)@COFs composites with core -shell heterostructures by the in situ growth of COFs on the surface of PLNPs. The PLNPs@COFs composites demonstrated better photocatalytic performance than pure PLNPs and COFs. The hydrogen production rate of PLNPs@COFs (1:6) was about 35 mmol h-1 g-1 , and the photodegradation efficiency of Rhodamine B by PLNPs@COFs (3:1) reached 100 % in 50 min. Evidently, the combination of COFs with PLNPs to form a core -shell heterostructure with a tight contact interface can effectively improve the photogenerated charge separation efficiency. Our covalent bonding and in situ growth approach is more conducive to the formation of stable core-shell heterostructures. A good match between the persistent luminescence emission spectrum of the PLNPs and the absorption range of the COFs improves the potential of PLNPs@COFs to function as a round-the-clock photocatalyst. This strategy holds excellent promise in the efficient use of solar photocatalytic hydrogen evolution and in environmental purification in the future.
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页数:11
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