Uracil-Doped Graphitic Carbon Nitride for Enhanced Photocatalytic Performance
Source abstract
Abstract
g-C3N4 is a visible-light photocatalyst with a suitable band gap and good stability. Moreover, g-C3N4 is considered to be earth-abundant, which makes it an appealing photocatalyst. However, due to its small specific surface area, low utilization of visible light, and high photogenerated electron–hole pair recombination rate, the photocatalytic activity of g-C3N4 remains unsatisfactory. In this work, a highly efficient nonmetallic photocatalyst, i.e., g-C3N4 doped with uracil (denoted U-C3N4) was successfully developed. Based on the various characterizations and calculations, it is shown that the triazine group in g-C3N4 is replaced with the diazine group in uracil. This occurrence leads to the formation of a new electron-transfer pathway between triazine groups, which can promote the separation of photogenerated electrons and holes. Concurrently, due to the ultrathin structure of the as-prepared U-C3N4, the material possessed a larger specific surface area than pristine g-C3N4, which can provide more active sites. Furthermore, the transfer pathway between the electron and hole was also shortened, and the recombination of the electron and hole was inhibited. According to the results, an optimal hydrogen evolution rate of 31.7 mol h–1 g–1 was achieved by U-C3N4, which is 5.1 times higher as compared to that achieved by pristine g-C3N4 (6.26 mol h–1 g–1). For the photocatalytic degradation of rhodamine B, the reaction rate constant of U-C3N4 (11.3 × 10–2 min–1) is about 5.5 times that of g-C3N4 (2.07 × 10–2 min–1). Furthermore, the uracil-doped catalyst was also able to demonstrate good stability after five successive runs.
Source: openalex_inverted_index · Quality: baseline
Research context
OpenAlex topics: Advanced Photocatalysis Techniques · 2D Materials and Applications · Gas Sensing Nanomaterials and Sensors
SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.
Affiliations
College of Environment & Resource Sciences, Zhejiang University, Hangzhou 310058, P. R. China
Funding
Ministry of Science and Technology of the People's Republic of China · Zhejiang Province
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