Acetylenic bond-driven efficient hydrogen production of a graphdiyne based catalyst

The presence of acetylenic bonds in graphdiyne (GDY) endow this type of carbon allotrope with high intrinsic catalytic activity, which is significantly superior to traditional carbon materials. Here, a synthetic strategy has been developed to study the influence of active acetylenic bond ratio and spatial distribution on the hydrogen evolution reaction (HER) catalytic performance. Two kinds of GDY, namely tetraphenylmethane-graphdiyne (TPM-GDY) and triphenylamine-graphdiyne (TPN-GDY), have been rationally synthesized via a bottom-to-up synthetic strategy. From the structural view, both TPM-GDY and TPN-GDY possess the 1,4-diphenylbuta-1,3-diyne skeleton composed of electrocatalytic active sp carbon. TPM-GDY possesses more active sp carbon exposed to the surface than TPN-GDY, which makes the TPM-GDY electrode exhibit better HER performance. Besides, some other properties of GDY-based carbon materials such as morphology, surface area, and pore distribution can also be efficiently adjusted. The above-mentioned results indicate that the distribution of active sites in the carbon framework plays a critical role in improving the catalytic performances, which offers a new strategy for creating highly active and stable electrocatalysts.

Automated summary

The presence of acetylenic bonds in graphdiyne endows it with high intrinsic catalytic activity, and the distribution and ratio of these active bonds play a critical role in influencing the catalytic performance. Among the two synthesized GDY materials, TPM-GDY showed better performance in the hydrogen evolution reaction due to its higher exposure of active carbon. Adjusting the morphology, surface area, and pore distribution of GDY-based carbon materials can also enhance their catalytic properties.