化学
盐酸四环素
降级(电信)
光催化
四环素
金属
盐酸盐
化学工程
接口(物质)
核化学
分子
有机化学
催化作用
生物化学
电信
吉布斯等温线
计算机科学
工程类
抗生素
作者
Lishuang Zhao,Liguo Wei,Xiaolong Cai,Bingxin Zhao,Li Li,Baojiang Jiang
标识
DOI:10.1016/j.molstruc.2024.140470
摘要
• A in-situ growth method can be used to prepare Ni(Fe/Al)-LDHs/g-C 3 N 4 nanosheets with dual-active-sites for efficient photocatalytic degradation of TCH . • The formation of Fe/Al N bonds, which enables provide an interfacial charge transfer channel in photocatalytic process. • The metal Ni and Fe/Al on the surface of Ni(Fe/Al)-LDHs/g-C 3 N 4 nanosheets can furnish more photocatalytic active sites and interface synergy. To improve the photogenerated electron–hole separation efficiency and the number of reactive oxygen species of g-C 3 N 4 in visible light. Herein, an interface-engineered Ni(Fe/Al)-LDHs/g-C 3 N 4 nanosheets with Fe/Al N bonds were prepared, which shows highly enhanced photocatalytic degradation performance with excellent structural stability. The interfacial structure of g-C 3 N 4 was precisely regulated by metal Fe/Al on the surface of layered double hydroxides (LDHs), which could form Fe/Al N bonds as the interfacial charge transfer channels. In addition, the metal Ni and Fe/Al on the surface of LDHs nanosheets can furnish more photocatalytic active sites and interface synergy. The obtained 7 %NiFe-LDHs/g-C 3 N 4 owns the degradation rate of 99.23 % for tetracycline hydrochloride (TCH) in visible light. This work highlights a rational interface engineering strategy for the formation of a composite structure with interface interaction for efficient photocatalysts.
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