光催化
三元运算
异质结
石墨氮化碳
可见光谱
化学
甲基橙
降级(电信)
光化学
化学工程
材料科学
催化作用
光电子学
有机化学
计算机科学
电信
程序设计语言
工程类
作者
Fangzhou Wu,Ying Liu,Xiyu Chen,Jun Han,De Hu,Wei Wang,Shufen Wang
标识
DOI:10.1002/jccs.202300373
摘要
Abstract Photocatalysis technology driven by solar energy is considered to be promising for solving energy crisis and environmental problems. Graphitic carbon nitride has been widely researched in the photocatalysis field due to its suitable band positions, non‐toxicity, easy synthesis, high stability, and low cost. However, the slow separation and rapid recombination of photogenerated carriers, the poor visible light response and the low specific surface area seriously limit the photocatalytic activity of g‐C 3 N 4 . Here, firstly, g‐C 3 N 4 nanosheets with a large specific surface area of 152.2 m 2 g −1 which provide more surface‐active sites for photocatalysis were prepared by secondary calcination method. Next, MoS 2 and metal–organic framework (MIL‐101(Cr)) were tightly bonded on g‐C 3 N 4 nanosheets to form ternary g‐C 3 N 4 /MoS 2 /MIL‐101(Cr) heterojunction photocatalyst. In which, a ternary dual Z‐scheme heterojunction photocatalyst composed of g‐C 3 N 4 , MoS 2 , and MIL‐101(Cr) was constructed to facilitate the separation and the migration of photogenerated charges. At the same time, MoS 2 enhanced the visible light response of the ternary photocatalyst. The optimal ternary photocatalyst displayed the highest activity for methyl orange degradation (degradation efficiency of 98% in 60 min) under visible light irradiation. Finally, a photocatalytic mechanism of a dual Z‐scheme electron transfer channel and h + ‐·O 2 − double oxidation sites were proposed and discussed.
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