摘要
Graphitic carbon nitride (g-C3N4) nanosheets exfoliated from their bulk-sized counterparts are limited by a quantum size effect-induced widened bandgap. In this work, an (NH4)2S2O8 (APS) induced thermal exfoliation approach is introduced to fabricate O-doped g-C3N4 nanosheets (OCNs). During this calcination process, the thermal decomposition products (NH3 and H2SO4) from APS not only efficiently promote delamination, but also introduce O doping into the g-C3N4 structure, realizing the synchronization control of the electronic structure and morphology. Compared to the bulk g-C3N4, OCNs show exceptional enhancement of the photocatalytic degradation of RhB and H2 evolution, owing to their enlarged specific surface area, more active edges exposed, and efficient photogenerated carrier separation.
源语言 | 英语 |
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页(从-至) | 1423-1433 |
页数 | 11 |
期刊 | Inorganic Chemistry Frontiers |
卷 | 9 |
期 | 7 |
DOI | |
出版状态 | 已出版 - 11 2月 2022 |