1. In situ growth of g-C3N4 on clay minerals of kaolinite, sepiolite, and talc for enhanced solar photocatalytic energy conversion
- Author
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Liping Wen, He’an Luo, Jikai Liu, Jinxin Chen, and Yunhui Chen
- Subjects
Materials science ,Sepiolite ,Composite number ,Geology ,Talc ,Chemical engineering ,Geochemistry and Petrology ,Specific surface area ,medicine ,Photocatalysis ,Kaolinite ,Water splitting ,Clay minerals ,medicine.drug - Abstract
The clay mineral/g-C3N4 composites were prepared through a simple one-pot synthesis with acid-treated clay minerals and melamine as precursors. Three typical clay minerals, e.g., kaolinite, sepiolite, and talc, were adopted as photocatalyst carriers. Notably, the acid-treated clay minerals coupled with g-C3N4 in three different ways. The kaolinite/g-C3N4 composite, in particular, proceeded with an intercalation reaction due to the in situ growth of g-C3N4 within the layers of acid-treated kaolinite, leading to the expansion of kaolinite layers and a prominently large specific surface area of 61.9 m2 g−1. The resultant composites were used in photocatalytic H2 generation by water splitting and CO2 reduction, exhibiting superior photocatalytic performance to the g-C3N4. Among the obtained composites, the optimized kaolinite/g-C3N4 showed the best photocatalytic activities, e.g. 3.03 μmol g−1 h−1 of CO evolution and 385 μmol g−1 h−1 of H2 evolution, compared with merely 0.91 μmol g−1 h−1 of CO evolution and 96.4 μmol g−1 h−1 of H2 evolution for bare g-C3N4. The superior performance of kaolinite/g-C3N4 can be ascribed to the large specific surface area and better distribution of g-C3N4, which can enhance the light absorption, increase the number of active sites and favor the charge separation.
- Published
- 2022