Electronic tuning of platinum cocatalysts over g-C3N4 nanosheets through the linker engineering for photocatalytic hydrogen evolution

被引:2
|
作者
Chen, Long [1 ]
Li, Miao [1 ]
Yang, Ying [1 ]
Qiu, Xiaoqing [1 ]
机构
[1] College of Chemistry and Chemical Engineering, Central South University, Hunan, Changsha,410083, China
基金
中国国家自然科学基金;
关键词
Electron density measurement - Error correction - Hydrogen evolution reaction - Photocatalytic activity - Platinum metal compounds;
D O I
10.1016/j.chemosphere.2024.143895
中图分类号
学科分类号
摘要
The strong metal-support interactions (SMSI) can profoundly affect the electronic state of platinum (Pt) cocatalysts, which plays a dominant role for photocatalytic activity in the supported photocatalysts. However, the conventional Pt/g-C3N4 photocatalysts usually shows negligible SMSI effect because of the lack of the reducible species. Herein, we demonstrate that the linker engineering of UiO66-type MOFs can effectively strengthen the SMSI and optimize the electron density of Pt nanoparticles on g-C3N4 nanosheets. The enhancement of electron-donating ability of the ligand functional groups effectively enriches the electron density of Pt cocatalysts, thus accelerating the photocatalytic hydrogen evolution rate. The results show that CN@Pt@UiO66-NA (the electron-donating functional group modified) exhibits the excellent photocatalytic hydrogen evolution activity (4.22 mmol g−1 h−1), which is 2.7 times that of CN@Pt@UiO66-NO2 (the electron-withdrawing functional group modified). © 2024 Elsevier Ltd
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