Donor-acceptor conjugated heptazine polymers: Boosting the Cr(VI) photoreductions via heteroatom engineering

被引:5
|
作者
Li, Zhen [1 ]
Jiang, Zi-Jian [1 ]
Zheng, Jun-Feng [1 ]
Lin, Mei-Jin [1 ,2 ]
机构
[1] Fuzhou Univ, Coll Chem, Fujian Prov Key Lab Adv Inorgan Oxygenated Mat, Fuzhou 350116, Peoples R China
[2] Fuzhou Univ, Coll Mat Sci & Engn, Fuzhou 350116, Peoples R China
来源
基金
中国国家自然科学基金;
关键词
Conjugated polymers; Heptazines; Donor-Acceptor; Heteroatom engineering; Cr(VI) reduction; GRAPHITIC CARBON NITRIDE; PHOTOCATALYTIC REDUCTION; MICROPOROUS POLYMERS; IN-SITU; DRIVEN; TRIAZINE; FRAMEWORKS; NETWORKS; G-C3N4;
D O I
10.1016/j.mtcomm.2022.103825
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Due to the high photoinduced charge seperations, donor-acceptor (D-A) conjugated heptazine polymers containing fluorene donors have attracted much attention for their high photocatalytic degradations towards organic pollutants. To have an insight into the impact of the electron-donating ability of the donor moieties, herein three D-A conjugated heptazine polymers containing fluorene-like donors with different heteroatoms (dibenzofuran, carbazole, dibenzothiophene, named as CHP-O, CHP-N and CHP-S, respectively) have been synthesized through reversible Friedel-Crafts reactions. Interestingly, the photocatalytic evaluations reveal that all three compounds exhibit an exceptional photocatalytic reduction activity towards hexavalent chromium (Cr(VI)) with the conversion rates of 97%, 95% and 90% for CHP-O, CHP-N and CHP-S, respectively, upon the visible-light irradiation, which is attributed to the narrow band gap and high charge transfer efficiency in the crystalline conjugated systems.
引用
收藏
页数:9
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